Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 483 |
|---|---|
| ensemblid | ENSG00000069849.11 |
| hgncid | 806 |
| symbol | ATP1B3 |
| name | ATPase Na+/K+ transporting subunit beta 3 |
| refseq_nuc | NM_001679.4 |
| refseq_prot | NP_001670.1 |
| ensembl_nuc | ENST00000286371.8 |
| ensembl_prot | ENSP00000286371.3 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 141876643 |
| end | 141926549 |
| strand | + |
| ver | v1.2 |
| region | chr3:141876643-141926549 |
| region5000 | chr3:141871643-141931549 |
| regionname0 | ATP1B3_chr3_141876643_141926549 |
| regionname5000 | ATP1B3_chr3_141871643_141931549 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 279 | 408 | 92 | 62 | 192 | 16 | 44 | 148 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | copy fasta | chr3 | 141871643 | 141931549 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 840 | 403 | 89 | 62 | 192 | 14 | 44 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | copy fasta | chr3 | 141871643 | 141931549 |
| c0002 | 0/0 | 840 | 2 | 2 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | copy fasta | chr3 | 141871643 | 141931549 |
| c0003 | 0/0 | 840 | 2 | 0 | 0 | 0 | 2 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | copy fasta | chr3 | 141871643 | 141931549 |
| c0004 | 0/0 | 840 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | copy fasta | chr3 | 141871643 | 141931549 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 1007 | 174 | 35 | 23 | 89 | 5 | 21 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | copy fasta | chr3 | 141871643 | 141931549 |
| t0002 | 1/0 | 1008 | 72 | 11 | 13 | 32 | 7 | 8 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | copy fasta | chr3 | 141871643 | 141931549 |
| t0003 | 0/0 | 1008 | 66 | 22 | 18 | 15 | 1 | 10 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | copy fasta | chr3 | 141871643 | 141931549 |
| t0004 | 0/0 | 1007 | 53 | 0 | 4 | 43 | 2 | 4 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | copy fasta | chr3 | 141871643 | 141931549 |
| t0005 | 0/0 | 1007 | 11 | 0 | 3 | 7 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | copy fasta | chr3 | 141871643 | 141931549 |
| t0006 | 0/0 | 1006 | 11 | 11 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | copy fasta | chr3 | 141871643 | 141931549 |
| t0007 | 0/0 | 1007 | 4 | 4 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | copy fasta | chr3 | 141871643 | 141931549 |
| t0008 | 0/0 | 1005 | 3 | 3 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | copy fasta | chr3 | 141871643 | 141931549 |
| t0009 | 0/0 | 1008 | 3 | 3 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | copy fasta | chr3 | 141871643 | 141931549 |
| t0010 | 0/0 | 1008 | 2 | 0 | 0 | 2 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | copy fasta | chr3 | 141871643 | 141931549 |
| t0011 | 0/0 | 1007 | 2 | 2 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | copy fasta | chr3 | 141871643 | 141931549 |
| t0012 | 0/0 | 1007 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | copy fasta | chr3 | 141871643 | 141931549 |
| t0013 | 0/0 | 1008 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | copy fasta | chr3 | 141871643 | 141931549 |
| t0014 | 0/0 | 1007 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | copy fasta | chr3 | 141871643 | 141931549 |
| t0015 | 0/0 | 1005 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | copy fasta | chr3 | 141871643 | 141931549 |
| t0016 | 0/0 | 1008 | 1 | 0 | 0 | 0 | 1 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | copy fasta | chr3 | 141871643 | 141931549 |
| t0017 | 0/0 | 1007 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | copy fasta | chr3 | 141871643 | 141931549 |
| t0018 | 0/0 | 1008 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | copy fasta | chr3 | 141871643 | 141931549 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0003 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0005 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0189 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0357 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0358 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0384 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0385 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0387 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0388 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0389 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0390 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0391 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0392 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0393 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0394 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0395 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0396 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0397 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| g0398 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 840 | 403 | 89 | 62 | 192 | 14 | 44 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | copy fasta | chr3 | 141871643 | 141931549 |
| a0001c0002 | 0/0 | 840 | 2 | 2 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | copy fasta | chr3 | 141871643 | 141931549 |
| a0001c0003 | 0/0 | 840 | 2 | 0 | 0 | 0 | 2 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | copy fasta | chr3 | 141871643 | 141931549 |
| a0001c0004 | 0/0 | 840 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | copy fasta | chr3 | 141871643 | 141931549 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1846 | 171 | 32 | 23 | 89 | 5 | 21 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | copy fasta | chr3 | 141871643 | 141931549 |
| a0001c0001t0002 | 1/0 | 1847 | 70 | 11 | 13 | 32 | 5 | 8 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | copy fasta | chr3 | 141871643 | 141931549 |
| a0001c0001t0003 | 0/0 | 1847 | 66 | 22 | 18 | 15 | 1 | 10 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | copy fasta | chr3 | 141871643 | 141931549 |
| a0001c0001t0004 | 0/0 | 1846 | 53 | 0 | 4 | 43 | 2 | 4 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | copy fasta | chr3 | 141871643 | 141931549 |
| a0001c0001t0005 | 0/0 | 1846 | 11 | 0 | 3 | 7 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | copy fasta | chr3 | 141871643 | 141931549 |
| a0001c0001t0006 | 0/0 | 1845 | 11 | 11 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | copy fasta | chr3 | 141871643 | 141931549 |
| a0001c0001t0007 | 0/0 | 1846 | 4 | 4 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | copy fasta | chr3 | 141871643 | 141931549 |
| a0001c0001t0008 | 0/0 | 1844 | 3 | 3 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | copy fasta | chr3 | 141871643 | 141931549 |
| a0001c0001t0009 | 0/0 | 1847 | 3 | 3 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | copy fasta | chr3 | 141871643 | 141931549 |
| a0001c0001t0010 | 0/0 | 1847 | 2 | 0 | 0 | 2 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | copy fasta | chr3 | 141871643 | 141931549 |
| a0001c0001t0011 | 0/0 | 1846 | 2 | 2 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | copy fasta | chr3 | 141871643 | 141931549 |
| a0001c0001t0012 | 0/0 | 1846 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | copy fasta | chr3 | 141871643 | 141931549 |
| a0001c0001t0013 | 0/0 | 1847 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | copy fasta | chr3 | 141871643 | 141931549 |
| a0001c0001t0014 | 0/0 | 1846 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | copy fasta | chr3 | 141871643 | 141931549 |
| a0001c0001t0015 | 0/0 | 1844 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | copy fasta | chr3 | 141871643 | 141931549 |
| a0001c0001t0016 | 0/0 | 1847 | 1 | 0 | 0 | 0 | 1 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | copy fasta | chr3 | 141871643 | 141931549 |
| a0001c0001t0017 | 0/0 | 1846 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | copy fasta | chr3 | 141871643 | 141931549 |
| a0001c0001t0018 | 0/0 | 1847 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | copy fasta | chr3 | 141871643 | 141931549 |
| a0001c0002t0001 | 0/0 | 1846 | 2 | 2 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | copy fasta | chr3 | 141871643 | 141931549 |
| a0001c0003t0002 | 0/0 | 1847 | 2 | 0 | 0 | 0 | 2 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | copy fasta | chr3 | 141871643 | 141931549 |
| a0001c0004t0001 | 0/0 | 1846 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | copy fasta | chr3 | 141871643 | 141931549 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0003 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0393 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0395 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0396 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0397 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0398 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0189 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0394 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0357 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0358 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0385 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0387 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0388 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0389 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0390 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0391 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0392 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0005g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0005g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0005g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0005g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0005g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0005g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0005g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0005g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0005g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0005g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0005g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0006g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0006g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0006g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0006g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0006g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0006g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0006g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0006g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0006g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0006g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0006g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0007g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0007g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0007g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0007g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0008g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0008g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0008g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0009g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0009g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0009g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0010g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0010g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0011g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0011g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0012g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0013g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0014g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0015g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0016g0384 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0017g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0018g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0002t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0002t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0003t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0003t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0004t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0005 | EUR | GBR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0017 | EUR | GBR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0287 | EUR | FIN | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0122 | EUR | FIN | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0125 | EUR | FIN | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0185 | EUR | FIN | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | CHS | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | CHS | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00423 | hp1 | a0001 | c0001 | t0012 | g0277 | EAS | CHS | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | CHS | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | CHS | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00544 | hp1 | a0001 | c0001 | t0004 | g0362 | EAS | CHS | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | CHS | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00558 | hp1 | a0001 | c0001 | t0004 | g0376 | EAS | CHS | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | CHS | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | CHS | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0126 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00642 | hp2 | a0001 | c0001 | t0018 | g0351 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00673 | hp1 | a0001 | c0001 | t0017 | g0373 | EAS | CHS | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | CHS | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0056 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0063 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0042 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0194 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0190 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01069 | hp2 | a0001 | c0001 | t0004 | g0369 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0118 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01070 | hp2 | a0001 | c0001 | t0005 | g0343 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0119 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0188 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0031 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0187 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0055 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0236 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0298 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0068 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0319 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0062 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0372 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0065 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01256 | hp1 | a0001 | c0001 | t0005 | g0342 | AMR | CLM | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0069 | AMR | CLM | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0038 | AMR | CLM | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01258 | hp1 | a0001 | c0001 | t0005 | g0341 | AMR | CLM | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0053 | AMR | CLM | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0060 | AMR | CLM | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | CLM | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0170 | AMR | CLM | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01515 | hp1 | a0001 | c0003 | t0002 | g0161 | EUR | IBS | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0162 | EUR | IBS | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0241 | EUR | IBS | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01516 | hp2 | a0001 | c0001 | t0004 | g0358 | EUR | IBS | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01517 | hp1 | a0001 | c0001 | t0004 | g0357 | EUR | IBS | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01517 | hp2 | a0001 | c0003 | t0002 | g0160 | EUR | IBS | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0323 | AFR | ACB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01884 | hp2 | a0001 | c0001 | t0006 | g0096 | AFR | ACB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0334 | AFR | ACB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01891 | hp2 | a0001 | c0001 | t0007 | g0308 | AFR | ACB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0057 | AMR | PEL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0033 | AMR | PEL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0322 | AMR | PEL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01978 | hp2 | a0001 | c0001 | t0004 | g0392 | AMR | PEL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0035 | AMR | PEL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0210 | AMR | PEL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0202 | AMR | PEL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PEL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02015 | hp2 | a0001 | c0001 | t0004 | g0336 | EAS | KHV | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | KHV | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02040 | hp1 | a0001 | c0001 | t0004 | g0345 | EAS | KHV | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | KHV | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02055 | hp1 | a0001 | c0001 | t0006 | g0105 | AFR | ACB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | KHV | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02071 | hp1 | a0001 | c0001 | t0004 | g0349 | EAS | KHV | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | KHV | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | KHV | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0061 | EAS | KHV | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02080 | hp1 | a0001 | c0001 | t0013 | g0156 | EAS | KHV | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02080 | hp2 | a0001 | c0001 | t0004 | g0370 | EAS | KHV | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | KHV | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02083 | hp2 | a0001 | c0001 | t0004 | g0389 | EAS | KHV | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0037 | EAS | KHV | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02132 | hp2 | a0001 | c0001 | t0004 | g0361 | EAS | KHV | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | KHV | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02135 | hp2 | a0001 | c0001 | t0004 | g0375 | EAS | KHV | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02145 | hp1 | a0001 | c0001 | t0009 | g0076 | AFR | ACB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0233 | AFR | ACB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | PEL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0205 | AMR | PEL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CDX | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02155 | hp2 | a0001 | c0001 | t0010 | g0198 | EAS | CDX | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0329 | AFR | ACB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0106 | AFR | ACB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02258 | hp1 | a0001 | c0001 | t0006 | g0103 | AFR | ACB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0332 | AFR | ACB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02451 | hp1 | a0001 | c0001 | t0008 | g0094 | AFR | ACB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | KHV | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0302 | AFR | GWD | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0025 | SAS | PJL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0301 | SAS | PJL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02615 | hp2 | a0001 | c0001 | t0006 | g0092 | AFR | GWD | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02647 | hp1 | a0001 | c0001 | t0008 | g0303 | AFR | GWD | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0313 | AFR | GWD | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0279 | SAS | PJL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0335 | AFR | GWD | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0148 | AFR | GWD | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02723 | hp1 | a0001 | c0001 | t0011 | g0178 | AFR | GWD | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0315 | AFR | GWD | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0234 | SAS | PJL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02735 | hp2 | a0001 | c0001 | t0004 | g0337 | SAS | PJL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0325 | SAS | PJL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0075 | SAS | PJL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02809 | hp1 | a0001 | c0001 | t0006 | g0100 | AFR | GWD | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0020 | AFR | GWD | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0169 | AFR | GWD | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0312 | AFR | GWD | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0018 | AFR | GWD | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0164 | AFR | GWD | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0027 | AFR | GWD | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0165 | AFR | GWD | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0039 | AFR | ESN | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02922 | hp2 | a0001 | c0001 | t0006 | g0098 | AFR | ESN | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | ESN | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0310 | AFR | ESN | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0394 | AFR | ESN | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02970 | hp2 | a0001 | c0001 | t0007 | g0317 | AFR | ESN | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02976 | hp1 | a0001 | c0001 | t0006 | g0102 | AFR | ESN | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0058 | SAS | PJL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0041 | AFR | GWD | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03041 | hp2 | a0001 | c0001 | t0007 | g0048 | AFR | GWD | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | MSL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | MSL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | ESN | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03130 | hp2 | a0001 | c0001 | t0009 | g0077 | AFR | ESN | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03139 | hp1 | a0001 | c0001 | t0006 | g0099 | AFR | ESN | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | ESN | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0316 | AFR | ESN | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03195 | hp2 | a0001 | c0001 | t0006 | g0093 | AFR | ESN | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03209 | hp1 | a0001 | c0001 | t0008 | g0101 | AFR | MSL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | MSL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0081 | AFR | MSL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | MSL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0271 | SAS | PJL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0331 | AFR | MSL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0015 | AFR | MSL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03486 | hp2 | a0001 | c0001 | t0007 | g0314 | AFR | MSL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0064 | SAS | PJL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03491 | hp1 | a0001 | c0001 | t0004 | g0356 | SAS | PJL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0306 | AFR | ESN | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | ESN | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0309 | AFR | GWD | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0086 | AFR | GWD | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | MSL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0330 | AFR | MSL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0318 | SAS | PJL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0193 | SAS | PJL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0297 | SAS | STU | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0235 | SAS | STU | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0070 | SAS | PJL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0249 | SAS | PJL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0159 | SAS | PJL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0146 | SAS | PJL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0073 | SAS | BEB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0246 | SAS | BEB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03834 | hp1 | a0001 | c0001 | t0004 | g0338 | SAS | BEB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03834 | hp2 | a0001 | c0001 | t0005 | g0022 | SAS | BEB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03927 | hp1 | a0001 | c0001 | t0004 | g0385 | SAS | BEB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0293 | SAS | BEB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | BEB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0072 | SAS | BEB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | STU | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | STU | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | BEB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0215 | SAS | BEB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0244 | SAS | STU | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0324 | SAS | STU | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0195 | SAS | STU | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | STU | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | YRI | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0397 | AFR | YRI | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18612 | hp1 | a0001 | c0001 | t0004 | g0378 | EAS | CHB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | CHB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | CHB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | CHB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0398 | AFR | YRI | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0307 | AFR | YRI | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18941 | hp1 | a0001 | c0001 | t0004 | g0371 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18943 | hp1 | a0001 | c0001 | t0004 | g0346 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18944 | hp1 | a0001 | c0001 | t0014 | g0291 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18949 | hp1 | a0001 | c0001 | t0004 | g0388 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18952 | hp1 | a0001 | c0001 | t0004 | g0377 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18953 | hp1 | a0001 | c0001 | t0005 | g0059 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18956 | hp2 | a0001 | c0001 | t0004 | g0379 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18959 | hp1 | a0001 | c0001 | t0004 | g0366 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18962 | hp2 | a0001 | c0001 | t0005 | g0029 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18964 | hp1 | a0001 | c0001 | t0004 | g0381 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18966 | hp1 | a0001 | c0001 | t0004 | g0386 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18969 | hp2 | a0001 | c0001 | t0004 | g0382 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18970 | hp1 | a0001 | c0001 | t0004 | g0348 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0396 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18971 | hp2 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0328 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18972 | hp2 | a0001 | c0001 | t0004 | g0367 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18975 | hp1 | a0001 | c0001 | t0004 | g0355 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18977 | hp1 | a0001 | c0001 | t0004 | g0391 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18979 | hp2 | a0001 | c0001 | t0004 | g0363 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18984 | hp1 | a0001 | c0001 | t0004 | g0387 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18986 | hp2 | a0001 | c0001 | t0004 | g0344 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18987 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18988 | hp2 | a0001 | c0001 | t0004 | g0364 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18990 | hp2 | a0001 | c0001 | t0004 | g0380 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0327 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18998 | hp1 | a0001 | c0001 | t0004 | g0374 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18998 | hp2 | a0001 | c0001 | t0005 | g0014 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19000 | hp1 | a0001 | c0001 | t0004 | g0339 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19003 | hp1 | a0001 | c0001 | t0004 | g0352 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0393 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19005 | hp1 | a0001 | c0001 | t0005 | g0046 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19007 | hp2 | a0001 | c0001 | t0004 | g0365 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19009 | hp1 | a0001 | c0001 | t0004 | g0368 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19010 | hp1 | a0001 | c0001 | t0004 | g0383 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19030 | hp1 | a0001 | c0001 | t0009 | g0078 | AFR | LWK | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0023 | AFR | LWK | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19043 | hp1 | a0001 | c0004 | t0001 | g0304 | AFR | LWK | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19043 | hp2 | a0001 | c0001 | t0006 | g0097 | AFR | LWK | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19056 | hp2 | a0001 | c0001 | t0004 | g0354 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19059 | hp1 | a0001 | c0001 | t0005 | g0021 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19059 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19060 | hp1 | a0001 | c0001 | t0004 | g0347 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19063 | hp1 | a0001 | c0001 | t0005 | g0036 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19065 | hp2 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19066 | hp2 | a0001 | c0001 | t0004 | g0350 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19072 | hp1 | a0001 | c0001 | t0010 | g0197 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19076 | hp2 | a0001 | c0001 | t0004 | g0359 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0395 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19082 | hp1 | a0001 | c0001 | t0004 | g0340 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19087 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19088 | hp1 | a0001 | c0001 | t0004 | g0353 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19089 | hp1 | a0001 | c0001 | t0005 | g0054 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19091 | hp1 | a0001 | c0001 | t0004 | g0390 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0305 | AFR | YRI | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0333 | AFR | YRI | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0311 | AFR | ASW | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ASW | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0274 | EUR | TSI | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0321 | EUR | TSI | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA20805 | hp1 | a0001 | c0001 | t0016 | g0384 | EUR | TSI | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0191 | EUR | TSI | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0047 | SAS | GIH | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0030 | SAS | GIH | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01123 | hp1 | a0001 | c0001 | t0004 | g0360 | AMR | CLM | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02486 | hp1 | a0001 | c0001 | t0015 | g0026 | AFR | ACB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02559 | hp2 | a0001 | c0001 | t0011 | g0231 | AFR | ACB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0074 | AFR | MSL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0091 | AFR | MSL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | USA | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | USA | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA20300 | hp1 | a0001 | c0001 | t0006 | g0104 | AFR | USA | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | USA | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | LWK | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | LWK | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0003 | REF | REF | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0189 | REF | REF | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:141876897
|
C | T | 1 | a0001c0003 | 2 | HG01515.hp1 HG01517.hp2 |
synonymous_variant | LOW | c.96C>T | p.Thr32Thr | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/7 | 255/1847 | 96/840 | 32/279 | chr3 | 141876897 | ||
| chr3:141907195
|
C | T | 1 | a0001c0002 | 2 | HG03516.hp1 NA19240.hp1 |
synonymous_variant | LOW | c.267C>T | p.Thr89Thr | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/7 | 426/1847 | 267/840 | 89/279 | chr3 | 141907195 | ||
| chr3:141913770
|
T | C | 1 | a0001c0004 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.465T>C | p.Ser155Ser | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 4/7 | 624/1847 | 465/840 | 155/279 | chr3 | 141913770 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:141876685
|
C | G | 4 | a0001c0001t0004a0001c0001t0016a0001c0001t0017others(1): Show | 56 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(53): Show |
5_prime_UTR_variant | MODIFIER | c.-117C>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/7 | 117 | chr3 | 141876685 | |||||
| chr3:141876722
|
C | G | 1 | a0001c0001t0009 | 3 | HG02145.hp1 HG03130.hp2 NA19030.hp1 |
5_prime_UTR_variant | MODIFIER | c.-80C>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/7 | 80 | chr3 | 141876722 | |||||
| chr3:141876739
|
T | A | 1 | a0001c0001t0012 | 1 | HG00423.hp1 | 5_prime_UTR_variant | MODIFIER | c.-63T>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/7 | 63 | chr3 | 141876739 | |||||
| chr3:141876796
|
C | G | 1 | a0001c0001t0011 | 2 | HG02559.hp2 HG02723.hp1 |
5_prime_UTR_variant | MODIFIER | c.-6C>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/7 | 6 | chr3 | 141876796 | |||||
| chr3:141925782
|
T | C | 1 | a0001c0001t0010 | 2 | HG02155.hp2 NA19072.hp1 |
3_prime_UTR_variant | MODIFIER | c.*81T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 7/7 | 81 | chr3 | 141925782 | |||||
| chr3:141925932
|
G | C | 3 | a0001c0001t0004a0001c0001t0005a0001c0001t0016 | 65 | HG00544.hp1 HG00558.hp1 HG01069.hp2 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*231G>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 7/7 | 231 | chr3 | 141925932 | |||||
| chr3:141925954
|
T | C | 1 | a0001c0001t0008 | 3 | HG02451.hp1 HG02647.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*253T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 7/7 | 253 | chr3 | 141925954 | |||||
| chr3:141925966
|
G | T | 3 | a0001c0001t0003a0001c0001t0007a0001c0001t0018 | 71 | HG00099.hp2 HG00642.hp2 HG00733.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*265G>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 7/7 | 265 | chr3 | 141925966 | |||||
| chr3:141926046
|
TAAC | T | 2 | a0001c0001t0008a0001c0001t0015 | 4 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*349_*351delAAC | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 7/7 | 349 | INFO_REALIGN_3_PRIME | chr3 | 141926046 | ||||
| chr3:141926294
|
TA | T | 11 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(8): Show | 258 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(255): Show |
3_prime_UTR_variant | MODIFIER | c.*604delA | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 7/7 | 604 | INFO_REALIGN_3_PRIME | chr3 | 141926294 | ||||
| chr3:141926430
|
T | C | 6 | a0001c0001t0003a0001c0001t0007a0001c0001t0008others(3): Show | 76 | HG00099.hp2 HG00642.hp2 HG00733.hp1 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*729T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 7/7 | 729 | chr3 | 141926430 | |||||
| chr3:141926437
|
A | G | 1 | a0001c0001t0014 | 1 | NA18944.hp1 | 3_prime_UTR_variant | MODIFIER | c.*736A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 7/7 | 736 | chr3 | 141926437 | |||||
| chr3:141926500
|
TA | T | 1 | a0001c0001t0006 | 11 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*802delA | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 7/7 | 802 | INFO_REALIGN_3_PRIME | chr3 | 141926500 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:141876945
|
C | G | 2 | a0001c0001t0001g0397a0001c0001t0001g0398 | 2 | NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.109+35C>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141876945 | ||||||
| chr3:141877041
|
G | C | 65 | a0001c0001t0001g0024a0001c0001t0001g0032a0001c0001t0001g0043others(62): Show | 65 | HG00099.hp2 HG00733.hp1 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.109+131G>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141877041 | ||||||
| chr3:141877048
|
C | T | 2 | a0001c0001t0001g0395a0001c0001t0001g0396 | 2 | NA18971.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.109+138C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141877048 | ||||||
| chr3:141877058
|
C | G | 1 | a0001c0001t0001g0396 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.109+148C>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141877058 | ||||||
| chr3:141877227
|
A | ACCCCTGC others(13): Show |
65 | a0001c0001t0001g0024a0001c0001t0001g0032a0001c0001t0001g0043others(62): Show | 65 | HG00099.hp2 HG00733.hp1 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.109+320_109+339dup others(20): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141877227 | |||||
| chr3:141877247
|
C | A | 4 | a0001c0001t0001g0079a0001c0001t0009g0076a0001c0001t0009g0077others(1): Show | 4 | HG00735.hp2 HG02145.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.109+337C>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141877247 | ||||||
| chr3:141877249
|
C | G | 1 | a0001c0001t0002g0394 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.109+339C>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141877249 | ||||||
| chr3:141877257
|
C | T | 1 | a0001c0001t0001g0393 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.109+347C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141877257 | ||||||
| chr3:141877258
|
A | G | 58 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(55): Show | 59 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.109+348A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141877258 | ||||||
| chr3:141877345
|
A | G | 1 | a0001c0001t0002g0394 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.109+435A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141877345 | ||||||
| chr3:141877509
|
A | G | 11 | a0001c0001t0001g0079a0001c0001t0001g0330a0001c0001t0001g0331others(8): Show | 11 | HG00735.hp2 HG01891.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.109+599A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141877509 | ||||||
| chr3:141877538
|
G | A | 2 | a0001c0001t0003g0011a0001c0001t0003g0012 | 2 | HG02965.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.109+628G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141877538 | ||||||
| chr3:141877657
|
G | GT | 17 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0001g0320others(14): Show | 17 | HG01167.hp2 HG01884.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.109+761dupT | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141877657 | |||||
| chr3:141877657
|
GT | G | 14 | a0001c0001t0001g0095a0001c0001t0006g0092a0001c0001t0006g0093others(11): Show | 14 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.109+761delT | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141877657 | |||||
| chr3:141877660
|
T | G | 1 | a0001c0001t0002g0329 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.109+750T>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141877660 | ||||||
| chr3:141877661
|
T | G | 13 | a0001c0001t0001g0001a0001c0001t0001g0080a0001c0001t0001g0082others(10): Show | 14 | HG00738.hp2 HG01433.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.109+751T>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141877661 | ||||||
| chr3:141877831
|
C | CT | 148 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(145): Show | 151 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.109+935dupT | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141877831 | |||||
| chr3:141877831
|
C | CTT | 71 | a0001c0001t0001g0299a0001c0001t0001g0300a0001c0001t0001g0301others(68): Show | 72 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.109+934_109+935dup others(2): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141877831 | |||||
| chr3:141877831
|
C | CTTT | 11 | a0001c0001t0002g0307a0001c0001t0003g0309a0001c0001t0003g0310others(8): Show | 11 | HG01891.hp2 HG02647.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.109+933_109+935dup others(3): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141877831 | |||||
| chr3:141877896
|
A | G | 2 | a0001c0002t0001g0305a0001c0002t0001g0306 | 2 | HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.109+986A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141877896 | ||||||
| chr3:141877918
|
G | T | 1 | a0001c0001t0003g0071 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.109+1008G>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141877918 | ||||||
| chr3:141877954
|
C | G | 1 | a0001c0001t0004g0390 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.109+1044C>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141877954 | ||||||
| chr3:141877961
|
C | A | 2 | a0001c0001t0001g0242a0001c0001t0001g0243 | 2 | HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.109+1051C>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141877961 | ||||||
| chr3:141877979
|
T | A | 1 | a0001c0001t0001g0244 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.109+1069T>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141877979 | ||||||
| chr3:141878006
|
G | A | 229 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0024others(226): Show | 232 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(229): Show |
intron_variant | MODIFIER | c.109+1096G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141878006 | ||||||
| chr3:141878029
|
G | C | 229 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0024others(226): Show | 232 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(229): Show |
intron_variant | MODIFIER | c.109+1119G>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141878029 | ||||||
| chr3:141878148
|
C | G | 58 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(55): Show | 59 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.109+1238C>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141878148 | ||||||
| chr3:141878356
|
C | G | 3 | a0001c0001t0003g0302a0001c0001t0008g0303a0001c0004t0001g0304 | 3 | HG02572.hp1 HG02647.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.109+1446C>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141878356 | ||||||
| chr3:141878486
|
C | A | 3 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0245 | 3 | HG03098.hp2 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.109+1576C>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141878486 | ||||||
| chr3:141878503
|
G | C | 2 | a0001c0002t0001g0305a0001c0002t0001g0306 | 2 | HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.109+1593G>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141878503 | ||||||
| chr3:141878509
|
C | T | 1 | a0001c0001t0003g0070 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.109+1599C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141878509 | ||||||
| chr3:141878523
|
C | T | 58 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(55): Show | 59 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.109+1613C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141878523 | ||||||
| chr3:141878602
|
G | A | 12 | a0001c0001t0001g0001a0001c0001t0001g0080a0001c0001t0001g0082others(9): Show | 13 | HG00738.hp2 HG01433.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.109+1692G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141878602 | ||||||
| chr3:141878696
|
A | G | 58 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(55): Show | 59 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.109+1786A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141878696 | ||||||
| chr3:141878784
|
G | C | 11 | a0001c0001t0001g0079a0001c0001t0001g0330a0001c0001t0001g0331others(8): Show | 11 | HG00735.hp2 HG01891.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.109+1874G>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141878784 | ||||||
| chr3:141878812
|
C | T | 3 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0245 | 3 | HG03098.hp2 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.109+1902C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141878812 | ||||||
| chr3:141879011
|
G | T | 67 | a0001c0001t0001g0024a0001c0001t0001g0032a0001c0001t0001g0043others(64): Show | 67 | HG00099.hp2 HG00733.hp1 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.109+2101G>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141879011 | ||||||
| chr3:141879090
|
G | A | 1 | a0001c0001t0004g0336 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.109+2180G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141879090 | ||||||
| chr3:141879332
|
A | G | 73 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0095others(70): Show | 75 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.109+2422A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141879332 | ||||||
| chr3:141879405
|
A | G | 1 | a0001c0001t0001g0294 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.109+2495A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141879405 | ||||||
| chr3:141879448
|
A | G | 1 | a0001c0001t0002g0241 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.109+2538A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141879448 | ||||||
| chr3:141879460
|
G | A | 3 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0245 | 3 | HG03098.hp2 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.109+2550G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141879460 | ||||||
| chr3:141879480
|
A | T | 1 | a0001c0001t0004g0390 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.109+2570A>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141879480 | ||||||
| chr3:141879624
|
A | T | 1 | a0001c0001t0007g0317 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.109+2714A>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141879624 | ||||||
| chr3:141879754
|
G | A | 26 | a0001c0001t0001g0079a0001c0001t0001g0330a0001c0001t0001g0331others(23): Show | 26 | HG00735.hp2 HG01891.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.109+2844G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141879754 | ||||||
| chr3:141879757
|
C | T | 1 | a0001c0001t0002g0329 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.109+2847C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141879757 | ||||||
| chr3:141879777
|
T | TCAAAAAA others(5): Show |
15 | a0001c0001t0002g0307a0001c0001t0003g0106a0001c0001t0003g0302others(12): Show | 15 | HG01891.hp2 HG02257.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.109+2869_109+2880d others(14): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141879777 | |||||
| chr3:141879777
|
T | TCAAAAAA others(6): Show |
10 | a0001c0001t0001g0079a0001c0001t0001g0330a0001c0001t0001g0331others(7): Show | 10 | HG00735.hp2 HG01891.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.109+2879_109+2880i others(15): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141879777 | |||||
| chr3:141879777
|
T | TCAAAAAA others(8): Show |
1 | a0001c0001t0004g0389 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.109+2879_109+2880i others(17): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141879777 | |||||
| chr3:141879777
|
T | TCAAAAAA others(9): Show |
53 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0344others(50): Show | 54 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.109+2879_109+2880i others(18): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141879777 | |||||
| chr3:141879777
|
T | TCAAAAAA others(10): Show |
4 | a0001c0001t0004g0337a0001c0001t0004g0338a0001c0001t0004g0339others(1): Show | 4 | HG02735.hp2 HG03834.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.109+2879_109+2880i others(19): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141879777 | |||||
| chr3:141879778
|
C | CAAAAAAA others(7): Show |
1 | a0001c0001t0009g0076 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.109+2879_109+2880i others(16): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141879778 | |||||
| chr3:141879779
|
A | AAAAAAAA others(7): Show |
4 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0075others(1): Show | 4 | HG02738.hp2 HG03486.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.109+2879_109+2880i others(16): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141879779 | |||||
| chr3:141879779
|
A | AAAAAAAA others(6): Show |
63 | a0001c0001t0001g0024a0001c0001t0001g0032a0001c0001t0001g0043others(60): Show | 63 | HG00099.hp2 HG00733.hp1 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.109+2879_109+2880i others(15): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141879779 | |||||
| chr3:141879779
|
A | AAAAAAAA others(5): Show |
78 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0095others(75): Show | 80 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.109+2870_109+2881d others(14): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141879779 | |||||
| chr3:141879811
|
C | CT | 41 | a0001c0001t0001g0079a0001c0001t0001g0088a0001c0001t0001g0089others(38): Show | 41 | HG00621.hp1 HG00621.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.109+2925dupT | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141879811 | |||||
| chr3:141879811
|
C | CTTT | 14 | a0001c0001t0001g0095a0001c0001t0001g0245a0001c0001t0004g0389others(11): Show | 14 | HG01070.hp2 HG01256.hp1 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.109+2923_109+2925d others(5): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141879811 | |||||
| chr3:141879811
|
C | CTTTT | 34 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0003g0298others(31): Show | 35 | HG00544.hp1 HG00642.hp2 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.109+2922_109+2925d others(6): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141879811 | |||||
| chr3:141879811
|
C | CTTTTT | 25 | a0001c0001t0001g0107a0001c0001t0004g0339a0001c0001t0004g0340others(22): Show | 25 | HG00558.hp1 HG00673.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.109+2921_109+2925d others(7): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141879811 | |||||
| chr3:141879811
|
C | CTTTTTT | 43 | a0001c0001t0001g0024a0001c0001t0001g0032a0001c0001t0001g0043others(40): Show | 43 | HG00741.hp1 HG01081.hp1 HG01257.hp2 others(40): Show |
intron_variant | MODIFIER | c.109+2920_109+2925d others(8): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141879811 | |||||
| chr3:141879811
|
C | CTTTTTTT | 24 | a0001c0001t0002g0394a0001c0001t0003g0012a0001c0001t0003g0015others(21): Show | 24 | HG00733.hp1 HG00735.hp1 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.109+2919_109+2925d others(9): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141879811 | |||||
| chr3:141879811
|
CT | C | 6 | a0001c0001t0001g0080a0001c0001t0001g0108a0001c0001t0001g0109others(3): Show | 6 | HG02451.hp2 HG03225.hp1 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.109+2925delT | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141879811 | |||||
| chr3:141879811
|
CTTTT | C | 56 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0244others(53): Show | 58 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.109+2922_109+2925d others(6): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141879811 | |||||
| chr3:141879833
|
T | A | 1 | a0001c0001t0002g0329 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.109+2923T>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141879833 | ||||||
| chr3:141879944
|
T | G | 1 | a0001c0001t0003g0106 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.109+3034T>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141879944 | ||||||
| chr3:141879972
|
A | T | 1 | a0001c0001t0002g0111 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.109+3062A>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141879972 | ||||||
| chr3:141880059
|
A | G | 1 | a0001c0001t0016g0384 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.109+3149A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141880059 | ||||||
| chr3:141880109
|
T | A | 65 | a0001c0001t0001g0024a0001c0001t0001g0032a0001c0001t0001g0043others(62): Show | 65 | HG00099.hp2 HG00733.hp1 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.109+3199T>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141880109 | ||||||
| chr3:141880242
|
T | TTTTGAGT others(4): Show |
1 | a0001c0001t0001g0292 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.109+3333_109+3343d others(13): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141880242 | |||||
| chr3:141880274
|
A | G | 1 | a0001c0004t0001g0304 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.109+3364A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141880274 | ||||||
| chr3:141880387
|
G | A | 15 | a0001c0001t0001g0095a0001c0001t0001g0107a0001c0001t0006g0092others(12): Show | 15 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.109+3477G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141880387 | ||||||
| chr3:141880663
|
T | C | 58 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(55): Show | 59 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.109+3753T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141880663 | ||||||
| chr3:141880674
|
A | G | 1 | a0001c0001t0001g0217 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.109+3764A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141880674 | ||||||
| chr3:141881002
|
G | C | 6 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(3): Show | 6 | HG00639.hp1 HG01358.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.109+4092G>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141881002 | ||||||
| chr3:141881158
|
G | A | 2 | a0001c0001t0009g0077a0001c0001t0009g0078 | 2 | HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.109+4248G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141881158 | ||||||
| chr3:141881204
|
C | CA | 30 | a0001c0001t0001g0079a0001c0001t0001g0117a0001c0001t0001g0219others(27): Show | 30 | HG00735.hp2 HG01891.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.109+4308dupA | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141881204 | |||||
| chr3:141881204
|
C | CAA | 64 | a0001c0001t0001g0024a0001c0001t0001g0032a0001c0001t0001g0043others(61): Show | 64 | HG00099.hp2 HG00733.hp1 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.109+4307_109+4308d others(4): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141881204 | |||||
| chr3:141881303
|
A | G | 1 | a0001c0001t0014g0291 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.109+4393A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141881303 | ||||||
| chr3:141881433
|
C | T | 12 | a0001c0001t0002g0307a0001c0001t0003g0106a0001c0001t0003g0309others(9): Show | 12 | HG01891.hp2 HG02257.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.109+4523C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141881433 | ||||||
| chr3:141881478
|
G | A | 1 | a0001c0001t0001g0107 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.109+4568G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141881478 | ||||||
| chr3:141881490
|
G | A | 1 | a0001c0001t0002g0394 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.109+4580G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141881490 | ||||||
| chr3:141881830
|
G | A | 1 | a0001c0001t0005g0014 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.109+4920G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141881830 | ||||||
| chr3:141881886
|
A | G | 1 | a0001c0001t0002g0111 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.109+4976A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141881886 | ||||||
| chr3:141881965
|
T | C | 2 | a0001c0001t0002g0118a0001c0001t0002g0119 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.109+5055T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141881965 | ||||||
| chr3:141882270
|
C | G | 3 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0245 | 3 | HG03098.hp2 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.109+5360C>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141882270 | ||||||
| chr3:141882352
|
TATAA | T | 4 | a0001c0001t0001g0079a0001c0001t0009g0076a0001c0001t0009g0077others(1): Show | 4 | HG00735.hp2 HG02145.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.109+5447_109+5450d others(6): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141882352 | |||||
| chr3:141882415
|
G | T | 8 | a0001c0001t0003g0013a0001c0001t0003g0016a0001c0001t0003g0049others(5): Show | 8 | NA18951.hp1 NA18955.hp2 NA18956.hp1 others(5): Show |
intron_variant | MODIFIER | c.109+5505G>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141882415 | ||||||
| chr3:141882455
|
T | C | 349 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(346): Show | 356 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(353): Show |
intron_variant | MODIFIER | c.109+5545T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141882455 | ||||||
| chr3:141882564
|
A | G | 1 | a0001c0001t0007g0048 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.109+5654A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141882564 | ||||||
| chr3:141882570
|
A | C | 3 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0245 | 3 | HG03098.hp2 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.109+5660A>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141882570 | ||||||
| chr3:141882579
|
A | ATTTTG | 3 | a0001c0001t0004g0010a0001c0001t0004g0344a0001c0001t0004g0367 | 4 | NA18971.hp2 NA18972.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.109+5684_109+5688d others(7): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141882579 | |||||
| chr3:141882613
|
C | T | 1 | a0001c0001t0003g0298 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.109+5703C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141882613 | ||||||
| chr3:141882614
|
G | A | 1 | a0001c0001t0001g0107 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.109+5704G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141882614 | ||||||
| chr3:141882687
|
G | A | 2 | a0001c0001t0003g0068a0001c0001t0003g0069 | 2 | HG01167.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.109+5777G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141882687 | ||||||
| chr3:141882743
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.109+5833C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141882743 | ||||||
| chr3:141882863
|
G | A | 2 | a0001c0001t0002g0394a0001c0001t0003g0298 | 2 | HG01109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.109+5953G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141882863 | ||||||
| chr3:141882876
|
G | A | 70 | a0001c0001t0001g0024a0001c0001t0001g0032a0001c0001t0001g0043others(67): Show | 70 | HG00099.hp2 HG00733.hp1 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.109+5966G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141882876 | ||||||
| chr3:141882881
|
C | T | 1 | a0001c0001t0001g0290 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.109+5971C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141882881 | ||||||
| chr3:141883231
|
T | C | 1 | a0001c0001t0001g0107 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.109+6321T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141883231 | ||||||
| chr3:141883269
|
C | G | 1 | a0001c0001t0001g0107 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.109+6359C>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141883269 | ||||||
| chr3:141883277
|
C | G | 12 | a0001c0001t0002g0307a0001c0001t0003g0106a0001c0001t0003g0309others(9): Show | 12 | HG01891.hp2 HG02257.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.109+6367C>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141883277 | ||||||
| chr3:141883286
|
G | A | 1 | a0001c0001t0002g0307 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.109+6376G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141883286 | ||||||
| chr3:141883380
|
C | T | 3 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0014g0291 | 3 | NA18944.hp1 NA18954.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.109+6470C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141883380 | ||||||
| chr3:141883410
|
C | T | 2 | a0001c0001t0001g0080a0001c0001t0002g0081 | 2 | HG02451.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.109+6500C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141883410 | ||||||
| chr3:141883595
|
G | A | 1 | a0001c0001t0001g0120 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.109+6685G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141883595 | ||||||
| chr3:141883773
|
C | T | 1 | a0001c0001t0002g0086 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.109+6863C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141883773 | ||||||
| chr3:141883823
|
T | C | 12 | a0001c0001t0002g0307a0001c0001t0003g0106a0001c0001t0003g0309others(9): Show | 12 | HG01891.hp2 HG02257.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.109+6913T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141883823 | ||||||
| chr3:141883928
|
G | T | 58 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(55): Show | 59 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.109+7018G>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141883928 | ||||||
| chr3:141883960
|
A | C | 3 | a0001c0001t0003g0302a0001c0001t0008g0303a0001c0004t0001g0304 | 3 | HG02572.hp1 HG02647.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.109+7050A>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141883960 | ||||||
| chr3:141884056
|
G | A | 58 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(55): Show | 59 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.109+7146G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141884056 | ||||||
| chr3:141884148
|
C | T | 2 | a0001c0002t0001g0305a0001c0002t0001g0306 | 2 | HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.109+7238C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141884148 | ||||||
| chr3:141884192
|
A | T | 1 | a0001c0001t0001g0287 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.109+7282A>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141884192 | ||||||
| chr3:141884308
|
C | T | 58 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(55): Show | 59 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.109+7398C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141884308 | ||||||
| chr3:141884465
|
A | C | 4 | a0001c0001t0006g0092a0001c0001t0006g0098a0001c0001t0006g0099others(1): Show | 4 | HG02615.hp2 HG02809.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.109+7555A>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141884465 | ||||||
| chr3:141884868
|
C | T | 1 | a0001c0001t0003g0015 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.109+7958C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141884868 | ||||||
| chr3:141884909
|
C | T | 58 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(55): Show | 59 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.109+7999C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141884909 | ||||||
| chr3:141885045
|
G | A | 145 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0024others(142): Show | 147 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.109+8135G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141885045 | ||||||
| chr3:141885063
|
C | T | 15 | a0001c0001t0001g0095a0001c0001t0001g0107a0001c0001t0006g0092others(12): Show | 15 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.109+8153C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141885063 | ||||||
| chr3:141885137
|
C | T | 1 | a0001c0001t0001g0286 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.109+8227C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141885137 | ||||||
| chr3:141885302
|
C | T | 13 | a0001c0001t0001g0001a0001c0001t0001g0080a0001c0001t0001g0082others(10): Show | 14 | HG00738.hp2 HG01433.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.109+8392C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141885302 | ||||||
| chr3:141885437
|
T | C | 2 | a0001c0002t0001g0305a0001c0002t0001g0306 | 2 | HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.109+8527T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141885437 | ||||||
| chr3:141885439
|
CTTTTCTT others(1): Show |
C | 11 | a0001c0001t0001g0079a0001c0001t0001g0330a0001c0001t0001g0331others(8): Show | 11 | HG00735.hp2 HG01891.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.109+8542_109+8549d others(10): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141885439 | |||||
| chr3:141885479
|
G | A | 14 | a0001c0001t0001g0095a0001c0001t0006g0092a0001c0001t0006g0093others(11): Show | 14 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.109+8569G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141885479 | ||||||
| chr3:141885535
|
G | A | 75 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0095others(72): Show | 77 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.109+8625G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141885535 | ||||||
| chr3:141885561
|
G | A | 58 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(55): Show | 59 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.109+8651G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141885561 | ||||||
| chr3:141885682
|
A | G | 1 | a0001c0001t0001g0184 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.109+8772A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141885682 | ||||||
| chr3:141885693
|
C | G | 3 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0245 | 3 | HG03098.hp2 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.109+8783C>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141885693 | ||||||
| chr3:141885880
|
A | AAC | 73 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0024others(70): Show | 76 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.109+9013_109+9014d others(4): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141885880 | |||||
| chr3:141885880
|
A | AACAC | 22 | a0001c0001t0001g0115a0001c0001t0001g0123a0001c0001t0001g0124others(19): Show | 22 | HG00323.hp1 HG00323.hp2 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.109+9011_109+9014d others(6): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141885880 | |||||
| chr3:141885880
|
A | AACACAC | 11 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0122others(8): Show | 11 | HG00280.hp2 HG01167.hp2 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.109+9009_109+9014d others(8): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141885880 | |||||
| chr3:141885880
|
A | AACACACA others(1): Show |
9 | a0001c0001t0001g0112a0001c0001t0001g0121a0001c0001t0001g0220others(6): Show | 9 | HG00099.hp2 HG00639.hp1 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.109+9007_109+9014d others(10): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141885880 | |||||
| chr3:141885880
|
A | C | 1 | a0001c0001t0002g0216 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.109+8970A>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141885880 | ||||||
| chr3:141885880
|
AAC | A | 81 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0084others(78): Show | 83 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.109+9013_109+9014d others(4): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141885880 | |||||
| chr3:141885880
|
AACAC | A | 23 | a0001c0001t0001g0045a0001c0001t0001g0177a0001c0001t0001g0179others(20): Show | 23 | HG00408.hp1 HG01192.hp1 HG01361.hp1 others(20): Show |
intron_variant | MODIFIER | c.109+9011_109+9014d others(6): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141885880 | |||||
| chr3:141885880
|
AACACAC | A | 23 | a0001c0001t0001g0117a0001c0001t0002g0006a0001c0001t0002g0007others(20): Show | 25 | HG00438.hp1 HG01891.hp2 HG01981.hp2 others(22): Show |
intron_variant | MODIFIER | c.109+9009_109+9014d others(8): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141885880 | |||||
| chr3:141885880
|
AACACACA others(1): Show |
A | 17 | a0001c0001t0001g0079a0001c0001t0001g0181a0001c0001t0001g0182others(14): Show | 17 | HG00735.hp2 HG01943.hp2 HG02004.hp1 others(14): Show |
intron_variant | MODIFIER | c.109+9007_109+9014d others(10): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141885880 | |||||
| chr3:141885880
|
AACACACA others(3): Show |
A | 9 | a0001c0001t0001g0330a0001c0001t0001g0332a0001c0001t0002g0307others(6): Show | 9 | HG01891.hp1 HG02258.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.109+9005_109+9014d others(12): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141885880 | |||||
| chr3:141885880
|
AACACACA others(5): Show |
A | 1 | a0001c0001t0003g0047 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.109+9003_109+9014d others(14): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141885880 | |||||
| chr3:141885880
|
AACACACA others(9): Show |
A | 10 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0003g0013others(7): Show | 10 | HG00423.hp2 NA18951.hp1 NA18955.hp2 others(7): Show |
intron_variant | MODIFIER | c.109+8999_109+9014d others(18): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141885880 | |||||
| chr3:141885880
|
AACACACA others(13): Show |
A | 1 | a0001c0001t0002g0215 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.109+8995_109+9014d others(22): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141885880 | |||||
| chr3:141885923
|
AC | A | 4 | a0001c0001t0002g0195a0001c0001t0003g0075a0001c0001t0004g0370others(1): Show | 4 | HG02080.hp2 HG02738.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.109+9017delC | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141885923 | |||||
| chr3:141885949
|
G | T | 12 | a0001c0001t0002g0307a0001c0001t0003g0106a0001c0001t0003g0309others(9): Show | 12 | HG01891.hp2 HG02257.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.109+9039G>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141885949 | ||||||
| chr3:141886024
|
T | C | 1 | a0001c0001t0001g0223 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.109+9114T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141886024 | ||||||
| chr3:141886090
|
A | G | 1 | a0001c0001t0001g0107 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.109+9180A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141886090 | ||||||
| chr3:141886173
|
C | T | 1 | a0001c0001t0003g0040 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.109+9263C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141886173 | ||||||
| chr3:141886232
|
A | T | 2 | a0001c0001t0001g0175a0001c0001t0001g0176 | 2 | NA18992.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.109+9322A>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141886232 | ||||||
| chr3:141886283
|
A | G | 2 | a0001c0001t0002g0394a0001c0001t0003g0298 | 2 | HG01109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.109+9373A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141886283 | ||||||
| chr3:141886354
|
T | C | 1 | a0001c0001t0002g0257 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.109+9444T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141886354 | ||||||
| chr3:141886393
|
C | T | 1 | a0001c0001t0001g0129 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.109+9483C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141886393 | ||||||
| chr3:141886498
|
T | C | 2 | a0001c0001t0003g0025a0001c0001t0003g0075 | 2 | HG02602.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.109+9588T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141886498 | ||||||
| chr3:141886655
|
G | A | 3 | a0001c0001t0002g0333a0001c0001t0002g0334a0001c0001t0002g0335 | 3 | HG01891.hp1 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.109+9745G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141886655 | ||||||
| chr3:141886705
|
GA | G | 4 | a0001c0001t0006g0092a0001c0001t0006g0098a0001c0001t0006g0099others(1): Show | 4 | HG02615.hp2 HG02809.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.109+9801delA | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141886705 | |||||
| chr3:141886774
|
G | A | 15 | a0001c0001t0001g0095a0001c0001t0001g0107a0001c0001t0006g0092others(12): Show | 15 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.109+9864G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141886774 | ||||||
| chr3:141886864
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.109+9954G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141886864 | ||||||
| chr3:141886867
|
T | G | 229 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0024others(226): Show | 232 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(229): Show |
intron_variant | MODIFIER | c.109+9957T>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141886867 | ||||||
| chr3:141886886
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.109+9976C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141886886 | ||||||
| chr3:141886908
|
C | T | 11 | a0001c0001t0003g0106a0001c0001t0003g0309a0001c0001t0003g0310others(8): Show | 11 | HG01891.hp2 HG02257.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.109+9998C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141886908 | ||||||
| chr3:141886980
|
T | G | 58 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(55): Show | 59 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.109+10070T>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141886980 | ||||||
| chr3:141887065
|
A | T | 1 | a0001c0001t0001g0330 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.109+10155A>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141887065 | ||||||
| chr3:141887074
|
A | G | 58 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(55): Show | 59 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.109+10164A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141887074 | ||||||
| chr3:141887119
|
G | A | 58 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0244others(55): Show | 60 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.109+10209G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141887119 | ||||||
| chr3:141887199
|
A | G | 2 | a0001c0001t0001g0331a0001c0001t0001g0332 | 2 | HG02258.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.109+10289A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141887199 | ||||||
| chr3:141887348
|
T | C | 3 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0245 | 3 | HG03098.hp2 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.109+10438T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141887348 | ||||||
| chr3:141887402
|
A | G | 75 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0095others(72): Show | 77 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.109+10492A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141887402 | ||||||
| chr3:141887426
|
TC | T | 3 | a0001c0001t0002g0333a0001c0001t0002g0334a0001c0001t0002g0335 | 3 | HG01891.hp1 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.109+10519delC | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141887426 | |||||
| chr3:141887441
|
C | T | 1 | a0001c0001t0001g0151 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.109+10531C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141887441 | ||||||
| chr3:141887483
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.109+10573A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141887483 | ||||||
| chr3:141887644
|
C | G | 1 | a0001c0001t0003g0017 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.109+10734C>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141887644 | ||||||
| chr3:141887660
|
C | G | 1 | a0001c0001t0001g0217 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.109+10750C>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141887660 | ||||||
| chr3:141887902
|
G | T | 1 | a0001c0001t0001g0180 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.109+10992G>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141887902 | ||||||
| chr3:141887950
|
G | A | 1 | a0001c0001t0001g0286 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.109+11040G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141887950 | ||||||
| chr3:141887998
|
T | G | 3 | a0001c0001t0002g0394a0001c0002t0001g0305a0001c0002t0001g0306 | 3 | HG02970.hp1 HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.109+11088T>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141887998 | ||||||
| chr3:141888138
|
A | G | 1 | a0001c0001t0001g0150 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.109+11228A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141888138 | ||||||
| chr3:141888214
|
A | G | 58 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(55): Show | 59 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.109+11304A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141888214 | ||||||
| chr3:141888272
|
C | G | 1 | a0001c0001t0003g0065 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.109+11362C>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141888272 | ||||||
| chr3:141888304
|
A | G | 1 | a0001c0001t0003g0017 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.109+11394A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141888304 | ||||||
| chr3:141888388
|
G | T | 1 | a0001c0001t0002g0394 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.109+11478G>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141888388 | ||||||
| chr3:141888493
|
A | G | 3 | a0001c0001t0001g0121a0001c0001t0001g0127a0001c0001t0001g0128 | 3 | HG03491.hp2 HG03669.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.109+11583A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141888493 | ||||||
| chr3:141888538
|
A | G | 1 | a0001c0001t0003g0012 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.109+11628A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141888538 | ||||||
| chr3:141888749
|
G | A | 58 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(55): Show | 59 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.109+11839G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141888749 | ||||||
| chr3:141888817
|
C | T | 68 | a0001c0001t0001g0024a0001c0001t0001g0032a0001c0001t0001g0043others(65): Show | 68 | HG00099.hp2 HG00733.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.109+11907C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141888817 | ||||||
| chr3:141888870
|
G | A | 4 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0001g0321others(1): Show | 4 | HG01167.hp2 HG01978.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.109+11960G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141888870 | ||||||
| chr3:141888973
|
C | G | 14 | a0001c0001t0001g0095a0001c0001t0006g0092a0001c0001t0006g0093others(11): Show | 14 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.109+12063C>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141888973 | ||||||
| chr3:141889019
|
T | C | 1 | a0001c0001t0001g0292 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.109+12109T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141889019 | ||||||
| chr3:141889031
|
A | G | 2 | a0001c0001t0001g0256a0001c0001t0001g0275 | 2 | NA18950.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.109+12121A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141889031 | ||||||
| chr3:141889039
|
G | T | 58 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0244others(55): Show | 60 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.109+12129G>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141889039 | ||||||
| chr3:141889050
|
C | T | 15 | a0001c0001t0001g0095a0001c0001t0001g0107a0001c0001t0006g0092others(12): Show | 15 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.109+12140C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141889050 | ||||||
| chr3:141889070
|
GGAGA | G | 65 | a0001c0001t0001g0024a0001c0001t0001g0032a0001c0001t0001g0043others(62): Show | 65 | HG00099.hp2 HG00733.hp1 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.109+12170_109+1217 others(8): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141889070 | |||||
| chr3:141889168
|
C | A | 1 | a0001c0001t0001g0247 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.109+12258C>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141889168 | ||||||
| chr3:141889171
|
A | G | 1 | a0001c0001t0001g0274 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.109+12261A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141889171 | ||||||
| chr3:141889198
|
C | T | 11 | a0001c0001t0001g0079a0001c0001t0001g0330a0001c0001t0001g0331others(8): Show | 11 | HG00735.hp2 HG01891.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.109+12288C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141889198 | ||||||
| chr3:141889307
|
A | G | 8 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0173others(5): Show | 8 | HG00438.hp2 HG02523.hp2 NA18949.hp2 others(5): Show |
intron_variant | MODIFIER | c.109+12397A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141889307 | ||||||
| chr3:141889528
|
A | G | 3 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0245 | 3 | HG03098.hp2 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.109+12618A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141889528 | ||||||
| chr3:141889728
|
C | CA | 21 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0123others(18): Show | 21 | HG00642.hp1 HG01433.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.109+12841dupA | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141889728 | |||||
| chr3:141889728
|
C | CAAAA | 6 | a0001c0001t0001g0001a0001c0001t0001g0082a0001c0001t0001g0083others(3): Show | 7 | HG00738.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.109+12838_109+1284 others(8): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141889728 | |||||
| chr3:141889728
|
CA | C | 16 | a0001c0001t0001g0149a0001c0001t0001g0163a0001c0001t0002g0004others(13): Show | 17 | HG01243.hp2 HG01257.hp1 HG01258.hp2 others(14): Show |
intron_variant | MODIFIER | c.109+12841delA | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141889728 | |||||
| chr3:141889728
|
CAA | C | 25 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0183others(22): Show | 25 | HG00099.hp2 HG00733.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.109+12840_109+1284 others(6): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141889728 | |||||
| chr3:141889728
|
CAAA | C | 11 | a0001c0001t0003g0064a0001c0001t0003g0106a0001c0001t0003g0309others(8): Show | 11 | HG01891.hp2 HG02257.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.109+12839_109+1284 others(7): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141889728 | |||||
| chr3:141889728
|
CAAAA | C | 28 | a0001c0001t0001g0032a0001c0001t0003g0028a0001c0001t0003g0030others(25): Show | 28 | HG00735.hp1 HG01081.hp1 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.109+12838_109+1284 others(8): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141889728 | |||||
| chr3:141889744
|
A | T | 1 | a0001c0001t0002g0329 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.109+12834A>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141889744 | ||||||
| chr3:141889746
|
A | AT | 5 | a0001c0001t0001g0331a0001c0001t0001g0332a0001c0001t0002g0335others(2): Show | 5 | HG02258.hp2 HG02717.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.109+12836_109+1283 others(5): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141889746 | ||||||
| chr3:141889746
|
A | ATAT | 5 | a0001c0001t0004g0338a0001c0001t0004g0363a0001c0001t0004g0364others(2): Show | 5 | HG01069.hp2 HG03834.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.109+12836_109+1283 others(7): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141889746 | ||||||
| chr3:141889746
|
A | ATATAT | 26 | a0001c0001t0002g0333a0001c0001t0002g0334a0001c0001t0004g0340others(23): Show | 26 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.109+12836_109+1283 others(9): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141889746 | ||||||
| chr3:141889746
|
A | ATATATAT | 17 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0344others(14): Show | 18 | HG01070.hp2 HG01123.hp1 HG01258.hp1 others(15): Show |
intron_variant | MODIFIER | c.109+12836_109+1283 others(11): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141889746 | ||||||
| chr3:141889746
|
A | T | 10 | a0001c0001t0001g0024a0001c0001t0001g0079a0001c0001t0001g0330others(7): Show | 10 | HG00735.hp2 HG01256.hp1 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.109+12836A>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141889746 | ||||||
| chr3:141889747
|
A | G | 1 | a0001c0001t0002g0394 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.109+12837A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141889747 | ||||||
| chr3:141889748
|
A | ATAT | 4 | a0001c0001t0001g0245a0001c0001t0003g0298a0001c0001t0004g0359others(1): Show | 4 | HG01109.hp2 HG03130.hp1 NA18941.hp1 others(1): Show |
intron_variant | MODIFIER | c.109+12838_109+1283 others(7): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141889748 | ||||||
| chr3:141889748
|
A | T | 81 | a0001c0001t0001g0024a0001c0001t0001g0043a0001c0001t0001g0045others(78): Show | 82 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.109+12838A>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141889748 | ||||||
| chr3:141889750
|
A | ATATATAT others(2): Show |
3 | a0001c0001t0003g0302a0001c0001t0008g0303a0001c0004t0001g0304 | 3 | HG02572.hp1 HG02647.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.109+12840_109+1284 others(13): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141889750 | ||||||
| chr3:141889750
|
A | T | 120 | a0001c0001t0001g0024a0001c0001t0001g0043a0001c0001t0001g0045others(117): Show | 121 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.109+12840A>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141889750 | ||||||
| chr3:141889751
|
AT | A | 20 | a0001c0001t0001g0244a0001c0001t0001g0259a0001c0001t0001g0260others(17): Show | 21 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(18): Show |
intron_variant | MODIFIER | c.109+12842delT | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141889751 | ||||||
| chr3:141889751
|
ATAT | A | 3 | a0001c0001t0001g0290a0001c0001t0002g0186a0001c0001t0002g0239 | 3 | NA18940.hp1 NA18992.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.109+12842_109+1284 others(7): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141889751 | ||||||
| chr3:141889751
|
ATATAT | A | 7 | a0001c0001t0001g0095a0001c0001t0001g0397a0001c0001t0001g0398others(4): Show | 7 | HG02451.hp1 HG03195.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.109+12842_109+1284 others(9): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141889751 | ||||||
| chr3:141889751
|
ATATATAC | A | 8 | a0001c0001t0006g0092a0001c0001t0006g0098a0001c0001t0006g0099others(5): Show | 8 | HG02055.hp1 HG02258.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.109+12842_109+1284 others(11): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141889751 | ||||||
| chr3:141889752
|
T | A | 49 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0080others(46): Show | 51 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.109+12842T>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141889752 | ||||||
| chr3:141889752
|
T | C | 5 | a0001c0001t0002g0164a0001c0001t0002g0165a0001c0001t0002g0329others(2): Show | 5 | HG01891.hp1 HG02257.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.109+12842T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141889752 | ||||||
| chr3:141889754
|
T | A | 15 | a0001c0001t0001g0244a0001c0001t0001g0258a0001c0001t0001g0259others(12): Show | 15 | HG00423.hp1 HG00423.hp2 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.109+12844T>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141889754 | ||||||
| chr3:141889754
|
T | C | 3 | a0001c0001t0001g0079a0001c0001t0002g0164a0001c0001t0002g0165 | 3 | HG00735.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.109+12844T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141889754 | ||||||
| chr3:141889756
|
T | C | 32 | a0001c0001t0001g0166a0001c0001t0001g0331a0001c0001t0001g0332others(29): Show | 34 | HG01070.hp2 HG01123.hp1 HG01257.hp1 others(31): Show |
intron_variant | MODIFIER | c.109+12846T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141889756 | ||||||
| chr3:141889756
|
T | TAC | 12 | a0001c0001t0001g0120a0001c0001t0001g0124a0001c0001t0001g0138others(9): Show | 12 | HG01346.hp1 HG02559.hp2 HG03579.hp1 others(9): Show |
intron_variant | MODIFIER | c.109+12885_109+1288 others(6): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141889756 | |||||
| chr3:141889756
|
T | TACAC | 15 | a0001c0001t0001g0002a0001c0001t0001g0135a0001c0001t0001g0136others(12): Show | 16 | HG00673.hp1 HG01243.hp1 NA18963.hp2 others(13): Show |
intron_variant | MODIFIER | c.109+12883_109+1288 others(8): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141889756 | |||||
| chr3:141889756
|
T | TACACAC | 8 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0133others(5): Show | 8 | HG00621.hp1 NA18941.hp2 NA18959.hp2 others(5): Show |
intron_variant | MODIFIER | c.109+12881_109+1288 others(10): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141889756 | |||||
| chr3:141889756
|
T | TACACACA others(3): Show |
1 | a0001c0001t0004g0389 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.109+12877_109+1288 others(14): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141889756 | |||||
| chr3:141889756
|
TAC | T | 72 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0112others(69): Show | 76 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.109+12885_109+1288 others(6): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141889756 | |||||
| chr3:141889756
|
TACAC | T | 16 | a0001c0001t0001g0107a0001c0001t0001g0123a0001c0001t0001g0127others(13): Show | 16 | HG03017.hp2 HG03239.hp2 HG03490.hp1 others(13): Show |
intron_variant | MODIFIER | c.109+12883_109+1288 others(8): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141889756 | |||||
| chr3:141889756
|
TACACAC | T | 11 | a0001c0001t0001g0114a0001c0001t0001g0175a0001c0001t0001g0176others(8): Show | 11 | HG00741.hp2 HG01257.hp2 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.109+12881_109+1288 others(10): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141889756 | |||||
| chr3:141889756
|
TACACACA others(3): Show |
T | 1 | a0001c0001t0002g0019 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.109+12877_109+1288 others(14): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141889756 | |||||
| chr3:141889756
|
TACACACA others(5): Show |
T | 3 | a0001c0001t0003g0023a0001c0001t0003g0025a0001c0001t0003g0075 | 3 | HG02602.hp1 HG02738.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.109+12875_109+1288 others(16): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141889756 | |||||
| chr3:141889758
|
C | A | 7 | a0001c0001t0001g0095a0001c0001t0001g0397a0001c0001t0001g0398others(4): Show | 7 | HG02451.hp1 HG03195.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.109+12848C>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141889758 | ||||||
| chr3:141889758
|
C | T | 134 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0001g0043others(131): Show | 136 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.109+12848C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141889758 | ||||||
| chr3:141889760
|
C | A | 9 | a0001c0001t0006g0092a0001c0001t0006g0093a0001c0001t0006g0098others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.109+12850C>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141889760 | ||||||
| chr3:141889760
|
C | T | 159 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(156): Show | 162 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.109+12850C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141889760 | ||||||
| chr3:141889762
|
C | A | 1 | a0001c0001t0006g0102 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.109+12852C>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141889762 | ||||||
| chr3:141889762
|
C | T | 160 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(157): Show | 163 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.109+12852C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141889762 | ||||||
| chr3:141889764
|
C | T | 104 | a0001c0001t0001g0032a0001c0001t0001g0043a0001c0001t0001g0045others(101): Show | 104 | HG00099.hp2 HG00733.hp1 HG00735.hp1 others(101): Show |
intron_variant | MODIFIER | c.109+12854C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141889764 | ||||||
| chr3:141889766
|
C | T | 95 | a0001c0001t0001g0024a0001c0001t0001g0032a0001c0001t0001g0043others(92): Show | 95 | HG00099.hp2 HG00733.hp1 HG00735.hp1 others(92): Show |
intron_variant | MODIFIER | c.109+12856C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141889766 | ||||||
| chr3:141889768
|
C | T | 63 | a0001c0001t0001g0024a0001c0001t0001g0032a0001c0001t0001g0095others(60): Show | 63 | HG00735.hp1 HG01081.hp1 HG01099.hp2 others(60): Show |
intron_variant | MODIFIER | c.109+12858C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141889768 | ||||||
| chr3:141889770
|
C | T | 24 | a0001c0001t0001g0024a0001c0001t0002g0019a0001c0001t0003g0023others(21): Show | 24 | HG01257.hp2 HG01884.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.109+12860C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141889770 | ||||||
| chr3:141889772
|
C | T | 5 | a0001c0001t0001g0024a0001c0001t0002g0019a0001c0001t0003g0023others(2): Show | 5 | HG02602.hp1 HG02622.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.109+12862C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141889772 | ||||||
| chr3:141889774
|
C | T | 4 | a0001c0001t0002g0019a0001c0001t0003g0023a0001c0001t0003g0025others(1): Show | 4 | HG02602.hp1 HG02738.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.109+12864C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141889774 | ||||||
| chr3:141889776
|
C | T | 4 | a0001c0001t0002g0019a0001c0001t0003g0023a0001c0001t0003g0025others(1): Show | 4 | HG02602.hp1 HG02738.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.109+12866C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141889776 | ||||||
| chr3:141889796
|
C | T | 1 | a0001c0001t0012g0277 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.109+12886C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141889796 | ||||||
| chr3:141889830
|
C | CAT | 61 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0150others(58): Show | 63 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.109+12934_109+1293 others(6): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141889830 | |||||
| chr3:141889830
|
C | CATAT | 3 | a0001c0001t0001g0397a0001c0001t0001g0398a0001c0001t0002g0394 | 3 | HG02970.hp1 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.109+12932_109+1293 others(8): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141889830 | |||||
| chr3:141889887
|
CA | C | 3 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0245 | 3 | HG03098.hp2 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.109+12978delA | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141889887 | ||||||
| chr3:141889965
|
G | A | 229 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0024others(226): Show | 232 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(229): Show |
intron_variant | MODIFIER | c.109+13055G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141889965 | ||||||
| chr3:141890070
|
T | C | 1 | a0001c0001t0003g0020 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.109+13160T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141890070 | ||||||
| chr3:141890084
|
T | G | 58 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(55): Show | 59 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.109+13174T>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141890084 | ||||||
| chr3:141890086
|
C | CT | 18 | a0001c0001t0001g0131a0001c0001t0001g0143a0001c0001t0001g0150others(15): Show | 18 | HG00438.hp2 HG00621.hp1 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.109+13198dupT | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141890086 | |||||
| chr3:141890086
|
C | CTT | 12 | a0001c0001t0001g0001a0001c0001t0001g0080a0001c0001t0001g0083others(9): Show | 13 | HG01433.hp1 HG02451.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.109+13197_109+1319 others(6): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141890086 | |||||
| chr3:141890086
|
CT | C | 76 | a0001c0001t0001g0024a0001c0001t0001g0032a0001c0001t0001g0043others(73): Show | 76 | HG00099.hp2 HG00642.hp2 HG00733.hp1 others(73): Show |
intron_variant | MODIFIER | c.109+13198delT | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141890086 | |||||
| chr3:141890086
|
CTT | C | 75 | a0001c0001t0001g0330a0001c0001t0001g0331a0001c0001t0001g0332others(72): Show | 76 | HG00544.hp1 HG00558.hp1 HG00673.hp1 others(73): Show |
intron_variant | MODIFIER | c.109+13197_109+1319 others(6): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141890086 | |||||
| chr3:141890088
|
T | TTTTTC | 8 | a0001c0001t0001g0095a0001c0001t0006g0093a0001c0001t0006g0097others(5): Show | 8 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.109+13182_109+1318 others(9): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141890088 | |||||
| chr3:141890089
|
T | TTTTC | 6 | a0001c0001t0006g0092a0001c0001t0006g0096a0001c0001t0006g0098others(3): Show | 6 | HG01884.hp2 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.109+13182_109+1318 others(8): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141890089 | |||||
| chr3:141890092
|
T | TC | 56 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0244others(53): Show | 58 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.109+13182_109+1318 others(5): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141890092 | ||||||
| chr3:141890093
|
T | C | 1 | a0001c0001t0001g0168 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.109+13183T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141890093 | ||||||
| chr3:141890094
|
T | C | 67 | a0001c0001t0001g0024a0001c0001t0001g0032a0001c0001t0001g0043others(64): Show | 67 | HG00099.hp2 HG00733.hp1 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.109+13184T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141890094 | ||||||
| chr3:141890095
|
T | C | 2 | a0001c0001t0001g0107a0001c0001t0003g0298 | 2 | HG01109.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.109+13185T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141890095 | ||||||
| chr3:141890103
|
T | C | 1 | a0001c0001t0001g0263 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.109+13193T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141890103 | ||||||
| chr3:141890111
|
G | A | 9 | a0001c0001t0004g0010a0001c0001t0004g0344a0001c0001t0004g0345others(6): Show | 10 | HG02040.hp1 HG02071.hp1 NA18943.hp1 others(7): Show |
intron_variant | MODIFIER | c.109+13201G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141890111 | ||||||
| chr3:141890160
|
G | A | 15 | a0001c0001t0002g0307a0001c0001t0003g0106a0001c0001t0003g0302others(12): Show | 15 | HG01891.hp2 HG02257.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.109+13250G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141890160 | ||||||
| chr3:141890160
|
G | GGCTCACT others(17): Show |
1 | a0001c0001t0002g0146 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.109+13253_109+1327 others(28): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141890160 | |||||
| chr3:141890285
|
C | CT | 14 | a0001c0001t0001g0142a0001c0001t0001g0158a0001c0001t0001g0203others(11): Show | 15 | HG00438.hp1 HG01981.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.110-13300dupT | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141890285 | |||||
| chr3:141890285
|
C | CTT | 15 | a0001c0001t0002g0111a0001c0001t0002g0126a0001c0001t0002g0193others(12): Show | 15 | HG00639.hp2 HG00741.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.110-13301_110-1330 others(6): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141890285 | |||||
| chr3:141890285
|
CT | C | 21 | a0001c0001t0001g0115a0001c0001t0001g0120a0001c0001t0001g0137others(18): Show | 22 | HG00408.hp1 HG01071.hp1 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.110-13300delT | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141890285 | |||||
| chr3:141890285
|
CTT | C | 56 | a0001c0001t0001g0002a0001c0001t0001g0085a0001c0001t0001g0088others(53): Show | 57 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.110-13301_110-1330 others(6): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141890285 | |||||
| chr3:141890285
|
CTTT | C | 40 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0082others(37): Show | 42 | HG00280.hp2 HG00639.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.110-13302_110-1330 others(7): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141890285 | |||||
| chr3:141890285
|
CTTTT | C | 6 | a0001c0001t0001g0080a0001c0001t0001g0108a0001c0001t0001g0397others(3): Show | 6 | HG02451.hp2 HG02486.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.110-13303_110-1330 others(8): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141890285 | |||||
| chr3:141890285
|
CTTTTT | C | 24 | a0001c0001t0001g0045a0001c0001t0001g0084a0001c0001t0001g0107others(21): Show | 24 | HG00735.hp1 HG00741.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.110-13304_110-1330 others(9): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141890285 | |||||
| chr3:141890285
|
CTTTTTT | C | 44 | a0001c0001t0001g0024a0001c0001t0001g0032a0001c0001t0001g0043others(41): Show | 44 | HG00099.hp2 HG00733.hp1 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.110-13305_110-1330 others(10): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141890285 | |||||
| chr3:141890285
|
CTTTTTTT | C | 17 | a0001c0001t0001g0255a0001c0001t0001g0258a0001c0001t0001g0259others(14): Show | 17 | HG01361.hp1 HG01884.hp2 HG02027.hp1 others(14): Show |
intron_variant | MODIFIER | c.110-13306_110-1330 others(11): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141890285 | |||||
| chr3:141890285
|
CTTTTTTT others(1): Show |
C | 69 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0246others(66): Show | 71 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.110-13307_110-1330 others(12): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141890285 | |||||
| chr3:141890285
|
CTTTTTTT others(2): Show |
C | 52 | a0001c0001t0001g0247a0001c0001t0001g0253a0001c0001t0001g0264others(49): Show | 53 | HG00558.hp1 HG00642.hp2 HG01069.hp2 others(50): Show |
intron_variant | MODIFIER | c.110-13308_110-1330 others(13): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141890285 | |||||
| chr3:141890285
|
CTTTTTTT others(3): Show |
C | 10 | a0001c0001t0001g0079a0001c0001t0001g0330a0001c0001t0001g0331others(7): Show | 10 | HG00735.hp2 HG02257.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.110-13309_110-1330 others(14): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141890285 | |||||
| chr3:141890285
|
CTTTTTTT others(4): Show |
C | 3 | a0001c0001t0009g0076a0001c0001t0009g0077a0001c0001t0009g0078 | 3 | HG02145.hp1 HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.110-13310_110-1330 others(15): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141890285 | |||||
| chr3:141890285
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0002g0196 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.110-13312_110-1330 others(17): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141890285 | |||||
| chr3:141890285
|
CTTTTTTT others(10): Show |
C | 1 | a0001c0001t0003g0057 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.110-13316_110-1330 others(21): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141890285 | |||||
| chr3:141890285
|
CTTTTTTT others(12): Show |
C | 2 | a0001c0001t0001g0249a0001c0001t0003g0298 | 2 | HG01109.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.110-13318_110-1330 others(23): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141890285 | |||||
| chr3:141890285
|
CTTTTTTT others(13): Show |
C | 1 | a0001c0001t0002g0394 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.110-13319_110-1330 others(24): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141890285 | |||||
| chr3:141890285
|
CTTTTTTT others(14): Show |
C | 3 | a0001c0001t0001g0144a0001c0001t0002g0146a0001c0001t0002g0325 | 3 | HG02698.hp1 HG02738.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.110-13320_110-1330 others(25): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141890285 | |||||
| chr3:141890286
|
T | C | 2 | a0001c0001t0001g0243a0001c0001t0001g0245 | 2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.110-13334T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141890286 | ||||||
| chr3:141890287
|
T | C | 2 | a0001c0001t0001g0242a0001c0002t0001g0305 | 2 | HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.110-13333T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141890287 | ||||||
| chr3:141890288
|
T | C | 1 | a0001c0002t0001g0306 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.110-13332T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141890288 | ||||||
| chr3:141890290
|
T | C | 2 | a0001c0001t0003g0015a0001c0001t0015g0026 | 2 | HG02486.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.110-13330T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141890290 | ||||||
| chr3:141890291
|
T | C | 22 | a0001c0001t0001g0045a0001c0001t0002g0019a0001c0001t0003g0023others(19): Show | 22 | HG00735.hp1 HG00741.hp1 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.110-13329T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141890291 | ||||||
| chr3:141890292
|
T | C | 40 | a0001c0001t0001g0024a0001c0001t0001g0032a0001c0001t0001g0043others(37): Show | 40 | HG00099.hp2 HG00733.hp1 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.110-13328T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141890292 | ||||||
| chr3:141890303
|
T | C | 1 | a0001c0001t0003g0057 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.110-13317T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141890303 | ||||||
| chr3:141890495
|
G | A | 15 | a0001c0001t0002g0307a0001c0001t0003g0106a0001c0001t0003g0302others(12): Show | 15 | HG01891.hp2 HG02257.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.110-13125G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141890495 | ||||||
| chr3:141890549
|
C | T | 1 | a0001c0001t0002g0296 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.110-13071C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141890549 | ||||||
| chr3:141890550
|
G | C | 1 | a0001c0001t0002g0296 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.110-13070G>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141890550 | ||||||
| chr3:141890581
|
GCGTGAGC others(128): Show |
G | 26 | a0001c0001t0001g0079a0001c0001t0001g0330a0001c0001t0001g0331others(23): Show | 26 | HG00735.hp2 HG01891.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.110-12962_110-1282 others(4): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141890581 | |||||
| chr3:141890582
|
C | T | 2 | a0001c0002t0001g0305a0001c0002t0001g0306 | 2 | HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.110-13038C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141890582 | ||||||
| chr3:141890747
|
A | G | 58 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(55): Show | 59 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.110-12873A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141890747 | ||||||
| chr3:141890748
|
T | G | 58 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(55): Show | 59 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.110-12872T>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141890748 | ||||||
| chr3:141890759
|
G | T | 1 | a0001c0001t0001g0184 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.110-12861G>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141890759 | ||||||
| chr3:141890811
|
G | A | 1 | a0001c0001t0004g0379 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.110-12809G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141890811 | ||||||
| chr3:141890862
|
G | A | 2 | a0001c0001t0002g0394a0001c0001t0003g0298 | 2 | HG01109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.110-12758G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141890862 | ||||||
| chr3:141891013
|
G | A | 145 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0024others(142): Show | 147 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.110-12607G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141891013 | ||||||
| chr3:141891042
|
A | C | 75 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0095others(72): Show | 77 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.110-12578A>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141891042 | ||||||
| chr3:141891085
|
T | A | 1 | a0001c0001t0002g0296 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.110-12535T>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141891085 | ||||||
| chr3:141891337
|
A | G | 1 | a0001c0001t0003g0091 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.110-12283A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141891337 | ||||||
| chr3:141891592
|
G | T | 67 | a0001c0001t0001g0024a0001c0001t0001g0032a0001c0001t0001g0043others(64): Show | 67 | HG00099.hp2 HG00733.hp1 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.110-12028G>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141891592 | ||||||
| chr3:141891630
|
C | T | 229 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0024others(226): Show | 232 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(229): Show |
intron_variant | MODIFIER | c.110-11990C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141891630 | ||||||
| chr3:141891702
|
G | A | 58 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(55): Show | 59 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.110-11918G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141891702 | ||||||
| chr3:141891764
|
T | C | 58 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(55): Show | 59 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.110-11856T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141891764 | ||||||
| chr3:141891793
|
A | G | 2 | a0001c0001t0001g0397a0001c0001t0001g0398 | 2 | NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.110-11827A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141891793 | ||||||
| chr3:141891891
|
C | CTT | 56 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(53): Show | 57 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.110-11718_110-1171 others(6): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141891891 | |||||
| chr3:141891911
|
T | C | 12 | a0001c0001t0001g0001a0001c0001t0001g0080a0001c0001t0001g0082others(9): Show | 13 | HG00738.hp2 HG01433.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.110-11709T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141891911 | ||||||
| chr3:141891965
|
A | G | 244 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(241): Show | 248 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(245): Show |
intron_variant | MODIFIER | c.110-11655A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141891965 | ||||||
| chr3:141892031
|
C | T | 1 | a0001c0001t0001g0289 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.110-11589C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141892031 | ||||||
| chr3:141892036
|
G | T | 1 | a0001c0001t0004g0360 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.110-11584G>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141892036 | ||||||
| chr3:141892089
|
T | C | 1 | a0001c0001t0003g0040 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.110-11531T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141892089 | ||||||
| chr3:141892310
|
A | C | 1 | a0001c0001t0002g0206 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.110-11310A>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141892310 | ||||||
| chr3:141892346
|
A | C | 1 | a0001c0001t0001g0219 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.110-11274A>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141892346 | ||||||
| chr3:141892444
|
T | A | 1 | a0001c0001t0001g0281 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.110-11176T>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141892444 | ||||||
| chr3:141892445
|
A | T | 1 | a0001c0001t0001g0281 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.110-11175A>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141892445 | ||||||
| chr3:141892446
|
T | A | 1 | a0001c0001t0001g0281 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.110-11174T>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141892446 | ||||||
| chr3:141892480
|
A | G | 1 | a0001c0001t0003g0072 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.110-11140A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141892480 | ||||||
| chr3:141892550
|
C | G | 1 | a0001c0001t0003g0033 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.110-11070C>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141892550 | ||||||
| chr3:141892568
|
A | G | 1 | a0001c0001t0001g0286 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.110-11052A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141892568 | ||||||
| chr3:141892572
|
T | C | 58 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(55): Show | 59 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.110-11048T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141892572 | ||||||
| chr3:141892588
|
C | CA | 11 | a0001c0001t0001g0079a0001c0001t0001g0330a0001c0001t0001g0331others(8): Show | 11 | HG00735.hp2 HG01891.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.110-11031dupA | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141892588 | |||||
| chr3:141892637
|
C | T | 1 | a0001c0001t0015g0026 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.110-10983C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141892637 | ||||||
| chr3:141892651
|
C | CA | 29 | a0001c0001t0001g0113a0001c0001t0001g0122a0001c0001t0001g0127others(26): Show | 29 | HG00280.hp2 HG00621.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.110-10944dupA | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141892651 | |||||
| chr3:141892651
|
C | CAA | 46 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0173others(43): Show | 48 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.110-10945_110-1094 others(6): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141892651 | |||||
| chr3:141892651
|
C | CAAA | 9 | a0001c0001t0001g0248a0001c0001t0001g0265a0001c0001t0001g0266others(6): Show | 9 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(6): Show |
intron_variant | MODIFIER | c.110-10946_110-1094 others(7): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141892651 | |||||
| chr3:141892651
|
CA | C | 51 | a0001c0001t0001g0001a0001c0001t0001g0024a0001c0001t0001g0079others(48): Show | 54 | HG00438.hp1 HG00735.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.110-10944delA | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141892651 | |||||
| chr3:141892651
|
CAA | C | 83 | a0001c0001t0001g0032a0001c0001t0001g0043a0001c0001t0001g0045others(80): Show | 83 | HG00099.hp2 HG00733.hp1 HG00741.hp1 others(80): Show |
intron_variant | MODIFIER | c.110-10945_110-1094 others(6): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141892651 | |||||
| chr3:141892651
|
CAAA | C | 8 | a0001c0001t0001g0242a0001c0001t0001g0245a0001c0001t0001g0331others(5): Show | 8 | HG00735.hp1 HG01109.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.110-10946_110-1094 others(7): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141892651 | |||||
| chr3:141892651
|
CAAAAAAA others(2): Show |
C | 53 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(50): Show | 54 | HG00544.hp1 HG00642.hp2 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.110-10952_110-1094 others(13): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141892651 | |||||
| chr3:141892651
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0004g0356 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.110-10953_110-1094 others(14): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141892651 | |||||
| chr3:141892651
|
CAAAAAAA others(7): Show |
C | 2 | a0001c0001t0003g0025a0001c0001t0003g0075 | 2 | HG02602.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.110-10957_110-1094 others(18): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141892651 | |||||
| chr3:141892676
|
A | C | 1 | a0001c0001t0002g0211 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.110-10944A>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141892676 | ||||||
| chr3:141892684
|
C | T | 58 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(55): Show | 59 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.110-10936C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141892684 | ||||||
| chr3:141892710
|
G | A | 1 | a0001c0001t0003g0298 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.110-10910G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141892710 | ||||||
| chr3:141892793
|
G | C | 244 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(241): Show | 248 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(245): Show |
intron_variant | MODIFIER | c.110-10827G>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141892793 | ||||||
| chr3:141892857
|
G | T | 3 | a0001c0001t0002g0004a0001c0003t0002g0160a0001c0003t0002g0161 | 4 | HG01257.hp1 HG01258.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.110-10763G>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141892857 | ||||||
| chr3:141892925
|
A | G | 2 | a0001c0001t0001g0397a0001c0001t0001g0398 | 2 | NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.110-10695A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141892925 | ||||||
| chr3:141893042
|
C | G | 1 | a0001c0001t0012g0277 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.110-10578C>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141893042 | ||||||
| chr3:141893242
|
C | T | 3 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0245 | 3 | HG03098.hp2 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.110-10378C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141893242 | ||||||
| chr3:141893277
|
A | G | 58 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(55): Show | 59 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.110-10343A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141893277 | ||||||
| chr3:141893345
|
A | G | 58 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(55): Show | 59 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.110-10275A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141893345 | ||||||
| chr3:141893491
|
G | A | 3 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0245 | 3 | HG03098.hp2 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.110-10129G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141893491 | ||||||
| chr3:141893531
|
C | G | 229 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0024others(226): Show | 232 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(229): Show |
intron_variant | MODIFIER | c.110-10089C>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141893531 | ||||||
| chr3:141893625
|
G | A | 15 | a0001c0001t0002g0307a0001c0001t0003g0106a0001c0001t0003g0302others(12): Show | 15 | HG01891.hp2 HG02257.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.110-9995G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141893625 | ||||||
| chr3:141893646
|
C | G | 2 | a0001c0001t0001g0150a0001c0001t0001g0229 | 2 | HG02027.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.110-9974C>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141893646 | ||||||
| chr3:141893662
|
C | T | 58 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(55): Show | 59 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.110-9958C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141893662 | ||||||
| chr3:141893704
|
A | G | 1 | a0001c0001t0003g0034 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.110-9916A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141893704 | ||||||
| chr3:141893839
|
A | G | 1 | a0001c0001t0002g0307 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.110-9781A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141893839 | ||||||
| chr3:141893909
|
C | T | 2 | a0001c0001t0001g0397a0001c0001t0001g0398 | 2 | NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.110-9711C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141893909 | ||||||
| chr3:141894017
|
A | G | 3 | a0001c0001t0001g0142a0001c0001t0001g0223a0001c0001t0001g0228 | 3 | HG00621.hp2 NA18940.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.110-9603A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141894017 | ||||||
| chr3:141894170
|
A | G | 244 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(241): Show | 248 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(245): Show |
intron_variant | MODIFIER | c.110-9450A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141894170 | ||||||
| chr3:141894274
|
T | C | 15 | a0001c0001t0002g0307a0001c0001t0003g0106a0001c0001t0003g0302others(12): Show | 15 | HG01891.hp2 HG02257.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.110-9346T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141894274 | ||||||
| chr3:141894279
|
A | T | 54 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(51): Show | 55 | HG00544.hp1 HG00558.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.110-9341A>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141894279 | ||||||
| chr3:141894326
|
A | G | 1 | a0001c0001t0003g0018 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.110-9294A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141894326 | ||||||
| chr3:141894326
|
AT | A | 77 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0095others(74): Show | 79 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.110-9283delT | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141894326 | |||||
| chr3:141894337
|
T | A | 3 | a0001c0001t0003g0302a0001c0001t0008g0303a0001c0004t0001g0304 | 3 | HG02572.hp1 HG02647.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.110-9283T>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141894337 | ||||||
| chr3:141894517
|
T | C | 1 | a0001c0001t0001g0168 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.110-9103T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141894517 | ||||||
| chr3:141894903
|
G | T | 1 | a0001c0001t0003g0298 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.110-8717G>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141894903 | ||||||
| chr3:141894987
|
C | G | 1 | a0001c0001t0001g0107 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.110-8633C>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141894987 | ||||||
| chr3:141894988
|
G | A | 58 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0244others(55): Show | 60 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.110-8632G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141894988 | ||||||
| chr3:141895083
|
G | A | 2 | a0001c0001t0001g0259a0001c0001t0001g0265 | 2 | NA18952.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.110-8537G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141895083 | ||||||
| chr3:141895122
|
T | G | 245 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(242): Show | 249 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(246): Show |
intron_variant | MODIFIER | c.110-8498T>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141895122 | ||||||
| chr3:141895188
|
C | CT | 28 | a0001c0001t0001g0095a0001c0001t0001g0107a0001c0001t0001g0184others(25): Show | 28 | HG01515.hp2 HG01884.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.110-8414dupT | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141895188 | |||||
| chr3:141895188
|
CT | C | 22 | a0001c0001t0001g0117a0001c0001t0001g0129a0001c0001t0001g0135others(19): Show | 22 | HG00621.hp2 HG01167.hp2 HG01517.hp2 others(19): Show |
intron_variant | MODIFIER | c.110-8414delT | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141895188 | |||||
| chr3:141895190
|
T | TC | 56 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(53): Show | 57 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.110-8430_110-8429i others(3): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141895190 | ||||||
| chr3:141895191
|
T | C | 1 | a0001c0001t0005g0343 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.110-8429T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141895191 | ||||||
| chr3:141895216
|
T | C | 3 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0014g0291 | 3 | NA18944.hp1 NA18954.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.110-8404T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141895216 | ||||||
| chr3:141895391
|
C | T | 97 | a0001c0001t0001g0024a0001c0001t0001g0032a0001c0001t0001g0043others(94): Show | 97 | HG00099.hp2 HG00733.hp1 HG00735.hp1 others(94): Show |
intron_variant | MODIFIER | c.110-8229C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141895391 | ||||||
| chr3:141895401
|
G | A | 1 | a0001c0001t0001g0332 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.110-8219G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141895401 | ||||||
| chr3:141895577
|
A | G | 8 | a0001c0001t0001g0001a0001c0001t0001g0082a0001c0001t0001g0083others(5): Show | 9 | HG00738.hp2 HG01433.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.110-8043A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141895577 | ||||||
| chr3:141895747
|
T | C | 1 | a0001c0001t0015g0026 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.110-7873T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141895747 | ||||||
| chr3:141895848
|
A | G | 97 | a0001c0001t0001g0024a0001c0001t0001g0032a0001c0001t0001g0043others(94): Show | 97 | HG00099.hp2 HG00733.hp1 HG00735.hp1 others(94): Show |
intron_variant | MODIFIER | c.110-7772A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141895848 | ||||||
| chr3:141895994
|
G | A | 58 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(55): Show | 59 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.110-7626G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141895994 | ||||||
| chr3:141896036
|
C | G | 4 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0290others(1): Show | 4 | NA18974.hp2 NA18992.hp1 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.110-7584C>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141896036 | ||||||
| chr3:141896138
|
G | A | 3 | a0001c0001t0002g0159a0001c0001t0002g0162a0001c0001t0002g0241 | 3 | HG01515.hp2 HG01516.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.110-7482G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141896138 | ||||||
| chr3:141896180
|
C | T | 3 | a0001c0001t0001g0145a0001c0001t0001g0297a0001c0001t0002g0126 | 3 | HG00639.hp2 HG00738.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.110-7440C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141896180 | ||||||
| chr3:141896186
|
C | A | 14 | a0001c0001t0001g0095a0001c0001t0006g0092a0001c0001t0006g0093others(11): Show | 14 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.110-7434C>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141896186 | ||||||
| chr3:141896190
|
T | TGG | 11 | a0001c0001t0001g0079a0001c0001t0001g0330a0001c0001t0001g0331others(8): Show | 11 | HG00735.hp2 HG01891.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.110-7427_110-7426d others(4): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141896190 | |||||
| chr3:141896206
|
C | T | 66 | a0001c0001t0001g0024a0001c0001t0001g0032a0001c0001t0001g0043others(63): Show | 66 | HG00099.hp2 HG00733.hp1 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.110-7414C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141896206 | ||||||
| chr3:141896314
|
C | CA | 27 | a0001c0001t0001g0001a0001c0001t0001g0079a0001c0001t0001g0082others(24): Show | 28 | HG00735.hp2 HG00738.hp2 HG01361.hp1 others(25): Show |
intron_variant | MODIFIER | c.110-7294dupA | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141896314 | |||||
| chr3:141896314
|
C | CAA | 12 | a0001c0001t0002g0307a0001c0001t0003g0106a0001c0001t0003g0309others(9): Show | 12 | HG01891.hp2 HG02257.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.110-7295_110-7294d others(4): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141896314 | |||||
| chr3:141896326
|
A | AT | 3 | a0001c0001t0001g0080a0001c0001t0002g0081a0001c0001t0002g0086 | 3 | HG02451.hp2 HG03225.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.110-7290dupT | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141896326 | |||||
| chr3:141896348
|
C | T | 66 | a0001c0001t0001g0024a0001c0001t0001g0032a0001c0001t0001g0043others(63): Show | 66 | HG00099.hp2 HG00733.hp1 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.110-7272C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141896348 | ||||||
| chr3:141896536
|
A | C | 1 | a0001c0001t0001g0279 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.110-7084A>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141896536 | ||||||
| chr3:141896764
|
T | C | 1 | a0001c0001t0003g0302 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.110-6856T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141896764 | ||||||
| chr3:141896805
|
C | T | 1 | a0001c0001t0003g0070 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.110-6815C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141896805 | ||||||
| chr3:141897147
|
G | A | 58 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0244others(55): Show | 60 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.110-6473G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141897147 | ||||||
| chr3:141897178
|
C | T | 1 | a0001c0001t0002g0394 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.110-6442C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141897178 | ||||||
| chr3:141897217
|
C | T | 245 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(242): Show | 249 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(246): Show |
intron_variant | MODIFIER | c.110-6403C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141897217 | ||||||
| chr3:141897273
|
C | T | 1 | a0001c0001t0003g0298 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.110-6347C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141897273 | ||||||
| chr3:141897311
|
T | G | 15 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0186others(12): Show | 17 | NA18940.hp1 NA18944.hp2 NA18957.hp2 others(14): Show |
intron_variant | MODIFIER | c.110-6309T>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141897311 | ||||||
| chr3:141897356
|
T | C | 58 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(55): Show | 59 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.110-6264T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141897356 | ||||||
| chr3:141897535
|
G | T | 6 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0250others(3): Show | 8 | HG00544.hp2 HG02015.hp1 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.110-6085G>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141897535 | ||||||
| chr3:141897656
|
A | G | 3 | a0001c0001t0003g0310a0001c0001t0003g0311a0001c0001t0003g0313 | 3 | HG02647.hp2 HG02965.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.110-5964A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141897656 | ||||||
| chr3:141897706
|
T | A | 75 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0095others(72): Show | 77 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.110-5914T>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141897706 | ||||||
| chr3:141897709
|
T | C | 58 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(55): Show | 59 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.110-5911T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141897709 | ||||||
| chr3:141897774
|
A | G | 12 | a0001c0001t0001g0001a0001c0001t0001g0080a0001c0001t0001g0082others(9): Show | 13 | HG00738.hp2 HG01433.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.110-5846A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141897774 | ||||||
| chr3:141897837
|
G | A | 1 | a0001c0001t0002g0111 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.110-5783G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141897837 | ||||||
| chr3:141897930
|
G | A | 4 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0001g0321others(1): Show | 4 | HG01167.hp2 HG01978.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.110-5690G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141897930 | ||||||
| chr3:141897961
|
C | T | 1 | a0001c0001t0003g0011 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.110-5659C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141897961 | ||||||
| chr3:141897962
|
G | A | 58 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(55): Show | 59 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.110-5658G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141897962 | ||||||
| chr3:141898093
|
T | C | 1 | a0001c0001t0004g0365 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.110-5527T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141898093 | ||||||
| chr3:141898108
|
A | G | 2 | a0001c0002t0001g0305a0001c0002t0001g0306 | 2 | HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.110-5512A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141898108 | ||||||
| chr3:141898230
|
A | G | 1 | a0001c0001t0002g0394 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.110-5390A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141898230 | ||||||
| chr3:141898344
|
G | C | 2 | a0001c0001t0003g0017a0001c0001t0003g0053 | 2 | HG00099.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.110-5276G>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141898344 | ||||||
| chr3:141898607
|
A | G | 75 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0095others(72): Show | 77 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.110-5013A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141898607 | ||||||
| chr3:141899213
|
C | T | 1 | a0001c0001t0004g0378 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.110-4407C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141899213 | ||||||
| chr3:141899214
|
G | A | 1 | a0001c0001t0002g0185 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.110-4406G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141899214 | ||||||
| chr3:141899282
|
C | G | 15 | a0001c0001t0001g0095a0001c0001t0001g0107a0001c0001t0006g0092others(12): Show | 15 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.110-4338C>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141899282 | ||||||
| chr3:141899350
|
G | A | 2 | a0001c0001t0001g0152a0001c0001t0001g0222 | 2 | NA18989.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.110-4270G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141899350 | ||||||
| chr3:141899366
|
A | G | 14 | a0001c0001t0001g0095a0001c0001t0006g0092a0001c0001t0006g0093others(11): Show | 14 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.110-4254A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141899366 | ||||||
| chr3:141899612
|
G | A | 1 | a0001c0001t0003g0058 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.110-4008G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141899612 | ||||||
| chr3:141899699
|
G | A | 75 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0095others(72): Show | 77 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.110-3921G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141899699 | ||||||
| chr3:141899737
|
C | T | 58 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(55): Show | 59 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.110-3883C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141899737 | ||||||
| chr3:141899891
|
T | G | 75 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0095others(72): Show | 77 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.110-3729T>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141899891 | ||||||
| chr3:141899905
|
A | C | 1 | a0001c0001t0001g0287 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.110-3715A>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141899905 | ||||||
| chr3:141899991
|
G | A | 89 | a0001c0001t0001g0079a0001c0001t0001g0242a0001c0001t0001g0243others(86): Show | 90 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(87): Show |
intron_variant | MODIFIER | c.110-3629G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141899991 | ||||||
| chr3:141899996
|
A | C | 1 | a0001c0001t0001g0128 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.110-3624A>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141899996 | ||||||
| chr3:141900096
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.110-3524C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141900096 | ||||||
| chr3:141900125
|
T | G | 1 | a0001c0001t0004g0350 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.110-3495T>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141900125 | ||||||
| chr3:141900245
|
G | A | 58 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0244others(55): Show | 60 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.110-3375G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141900245 | ||||||
| chr3:141900313
|
C | T | 1 | a0001c0001t0001g0151 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.110-3307C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141900313 | ||||||
| chr3:141900370
|
A | G | 1 | a0001c0001t0002g0394 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.110-3250A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141900370 | ||||||
| chr3:141900383
|
G | A | 3 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0245 | 3 | HG03098.hp2 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.110-3237G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141900383 | ||||||
| chr3:141900433
|
C | T | 11 | a0001c0001t0001g0079a0001c0001t0001g0330a0001c0001t0001g0331others(8): Show | 11 | HG00735.hp2 HG01891.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.110-3187C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141900433 | ||||||
| chr3:141900710
|
G | A | 1 | a0001c0001t0001g0259 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.110-2910G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141900710 | ||||||
| chr3:141900714
|
G | A | 3 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0245 | 3 | HG03098.hp2 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.110-2906G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141900714 | ||||||
| chr3:141900861
|
C | G | 11 | a0001c0001t0001g0079a0001c0001t0001g0330a0001c0001t0001g0331others(8): Show | 11 | HG00735.hp2 HG01891.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.110-2759C>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141900861 | ||||||
| chr3:141900995
|
C | T | 14 | a0001c0001t0001g0095a0001c0001t0006g0092a0001c0001t0006g0093others(11): Show | 14 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.110-2625C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141900995 | ||||||
| chr3:141901020
|
T | C | 58 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(55): Show | 59 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.110-2600T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141901020 | ||||||
| chr3:141901070
|
A | C | 3 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0245 | 3 | HG03098.hp2 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.110-2550A>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141901070 | ||||||
| chr3:141901186
|
T | C | 3 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0245 | 3 | HG03098.hp2 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.110-2434T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141901186 | ||||||
| chr3:141901218
|
G | A | 1 | a0001c0001t0003g0012 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.110-2402G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141901218 | ||||||
| chr3:141901242
|
C | T | 1 | a0001c0001t0001g0246 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.110-2378C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141901242 | ||||||
| chr3:141901447
|
G | A | 3 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0245 | 3 | HG03098.hp2 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.110-2173G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141901447 | ||||||
| chr3:141901566
|
G | C | 1 | a0001c0001t0001g0122 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.110-2054G>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141901566 | ||||||
| chr3:141901691
|
ATATT | A | 58 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(55): Show | 59 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.110-1923_110-1920d others(6): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141901691 | |||||
| chr3:141901845
|
A | G | 5 | a0001c0001t0003g0015a0001c0001t0003g0027a0001c0001t0003g0039others(2): Show | 5 | HG01109.hp2 HG02896.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.110-1775A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141901845 | ||||||
| chr3:141902084
|
T | C | 3 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0245 | 3 | HG03098.hp2 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.110-1536T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141902084 | ||||||
| chr3:141902207
|
C | T | 1 | a0001c0001t0011g0231 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.110-1413C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141902207 | ||||||
| chr3:141902233
|
TG | T | 58 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(55): Show | 59 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.110-1380delG | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141902233 | |||||
| chr3:141902432
|
G | C | 12 | a0001c0001t0001g0079a0001c0001t0001g0330a0001c0001t0001g0331others(9): Show | 12 | HG00735.hp2 HG01891.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.110-1188G>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141902432 | ||||||
| chr3:141902516
|
A | G | 12 | a0001c0001t0003g0106a0001c0001t0003g0148a0001c0001t0003g0309others(9): Show | 12 | HG01891.hp2 HG02257.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.110-1104A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141902516 | ||||||
| chr3:141902724
|
G | A | 1 | a0001c0001t0001g0252 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.110-896G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141902724 | ||||||
| chr3:141902791
|
G | A | 12 | a0001c0001t0001g0001a0001c0001t0001g0080a0001c0001t0001g0082others(9): Show | 13 | HG00738.hp2 HG01433.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.110-829G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141902791 | ||||||
| chr3:141902835
|
G | C | 1 | a0001c0001t0002g0307 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.110-785G>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141902835 | ||||||
| chr3:141902868
|
T | C | 12 | a0001c0001t0001g0079a0001c0001t0001g0330a0001c0001t0001g0331others(9): Show | 12 | HG00735.hp2 HG01891.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.110-752T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141902868 | ||||||
| chr3:141902910
|
A | T | 4 | a0001c0001t0006g0092a0001c0001t0006g0098a0001c0001t0006g0099others(1): Show | 4 | HG02615.hp2 HG02809.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.110-710A>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141902910 | ||||||
| chr3:141902912
|
T | A | 1 | a0001c0001t0001g0132 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.110-708T>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141902912 | ||||||
| chr3:141902936
|
C | T | 2 | a0001c0001t0003g0302a0001c0001t0008g0303 | 2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.110-684C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141902936 | ||||||
| chr3:141902994
|
G | A | 2 | a0001c0002t0001g0305a0001c0002t0001g0306 | 2 | HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.110-626G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141902994 | ||||||
| chr3:141903034
|
A | G | 2 | a0001c0001t0001g0397a0001c0001t0001g0398 | 2 | NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.110-586A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141903034 | ||||||
| chr3:141903049
|
CAA | C | 4 | a0001c0001t0001g0079a0001c0001t0009g0076a0001c0001t0009g0077others(1): Show | 4 | HG00735.hp2 HG02145.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.110-569_110-568del others(2): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141903049 | |||||
| chr3:141903094
|
C | T | 14 | a0001c0001t0001g0001a0001c0001t0001g0080a0001c0001t0001g0082others(11): Show | 15 | HG00738.hp2 HG01109.hp2 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.110-526C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141903094 | ||||||
| chr3:141903121
|
G | T | 2 | a0001c0001t0003g0309a0001c0001t0003g0312 | 2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.110-499G>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141903121 | ||||||
| chr3:141903128
|
A | G | 1 | a0001c0001t0001g0107 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.110-492A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141903128 | ||||||
| chr3:141903136
|
G | A | 14 | a0001c0001t0003g0031a0001c0001t0003g0033a0001c0001t0003g0034others(11): Show | 14 | HG01081.hp1 HG01257.hp2 HG01928.hp2 others(11): Show |
intron_variant | MODIFIER | c.110-484G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141903136 | ||||||
| chr3:141903184
|
CTG | C | 3 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0245 | 3 | HG03098.hp2 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.110-433_110-432del others(2): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 141903184 | |||||
| chr3:141903196
|
C | T | 1 | a0001c0001t0002g0187 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.110-424C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141903196 | ||||||
| chr3:141903213
|
C | A | 68 | a0001c0001t0001g0024a0001c0001t0001g0032a0001c0001t0001g0043others(65): Show | 68 | HG00099.hp2 HG00733.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.110-407C>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141903213 | ||||||
| chr3:141903237
|
T | A | 242 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(239): Show | 246 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(243): Show |
intron_variant | MODIFIER | c.110-383T>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141903237 | ||||||
| chr3:141903455
|
T | C | 15 | a0001c0001t0001g0095a0001c0001t0002g0019a0001c0001t0006g0092others(12): Show | 15 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.110-165T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 1/6 | chr3 | 141903455 | ||||||
| chr3:141903782
|
T | G | 1 | a0001c0001t0001g0139 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.238+34T>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 2/6 | chr3 | 141903782 | ||||||
| chr3:141903853
|
G | A | 58 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(55): Show | 59 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.238+105G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 2/6 | chr3 | 141903853 | ||||||
| chr3:141903884
|
C | T | 1 | a0001c0001t0002g0329 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.238+136C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 2/6 | chr3 | 141903884 | ||||||
| chr3:141903907
|
G | C | 242 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(239): Show | 246 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(243): Show |
intron_variant | MODIFIER | c.238+159G>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 2/6 | chr3 | 141903907 | ||||||
| chr3:141903945
|
C | T | 6 | a0001c0001t0005g0014a0001c0001t0005g0021a0001c0001t0005g0029others(3): Show | 6 | NA18953.hp1 NA18962.hp2 NA18998.hp2 others(3): Show |
intron_variant | MODIFIER | c.238+197C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 2/6 | chr3 | 141903945 | ||||||
| chr3:141904004
|
G | A | 3 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0003g0041 | 3 | HG03041.hp1 HG03453.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.238+256G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 2/6 | chr3 | 141904004 | ||||||
| chr3:141904012
|
G | A | 1 | a0001c0001t0002g0394 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.238+264G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 2/6 | chr3 | 141904012 | ||||||
| chr3:141904069
|
G | A | 15 | a0001c0001t0003g0013a0001c0001t0003g0016a0001c0001t0003g0017others(12): Show | 15 | HG00099.hp2 HG00733.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.238+321G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 2/6 | chr3 | 141904069 | ||||||
| chr3:141904299
|
C | T | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0108others(103): Show | 109 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.238+551C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 2/6 | chr3 | 141904299 | ||||||
| chr3:141904300
|
G | A | 1 | a0001c0001t0001g0274 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.238+552G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 2/6 | chr3 | 141904300 | ||||||
| chr3:141904305
|
C | CT | 73 | a0001c0001t0001g0095a0001c0001t0002g0019a0001c0001t0004g0010others(70): Show | 74 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.238+568dupT | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 141904305 | |||||
| chr3:141904370
|
A | T | 15 | a0001c0001t0001g0095a0001c0001t0002g0019a0001c0001t0006g0092others(12): Show | 15 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.238+622A>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 2/6 | chr3 | 141904370 | ||||||
| chr3:141904404
|
C | T | 1 | a0001c0001t0003g0031 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.238+656C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 2/6 | chr3 | 141904404 | ||||||
| chr3:141904442
|
T | G | 2 | a0001c0001t0001g0397a0001c0001t0001g0398 | 2 | NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.238+694T>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 2/6 | chr3 | 141904442 | ||||||
| chr3:141904462
|
A | G | 172 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(169): Show | 176 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.238+714A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 2/6 | chr3 | 141904462 | ||||||
| chr3:141904512
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.238+764A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 2/6 | chr3 | 141904512 | ||||||
| chr3:141904530
|
T | A | 242 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(239): Show | 246 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(243): Show |
intron_variant | MODIFIER | c.238+782T>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 2/6 | chr3 | 141904530 | ||||||
| chr3:141904614
|
A | T | 98 | a0001c0001t0001g0024a0001c0001t0001g0032a0001c0001t0001g0043others(95): Show | 98 | HG00099.hp2 HG00733.hp1 HG00735.hp1 others(95): Show |
intron_variant | MODIFIER | c.238+866A>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 2/6 | chr3 | 141904614 | ||||||
| chr3:141904703
|
C | CT | 84 | a0001c0001t0001g0008a0001c0001t0001g0095a0001c0001t0001g0113others(81): Show | 85 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.238+978dupT | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 141904703 | |||||
| chr3:141904703
|
C | CTT | 6 | a0001c0001t0001g0009a0001c0001t0001g0248a0001c0001t0001g0262others(3): Show | 7 | HG01884.hp2 HG02015.hp1 HG02040.hp2 others(4): Show |
intron_variant | MODIFIER | c.238+977_238+978dup others(2): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 141904703 | |||||
| chr3:141904703
|
C | CTTT | 13 | a0001c0001t0001g0001a0001c0001t0001g0080a0001c0001t0001g0082others(10): Show | 14 | HG00738.hp2 HG01433.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.238+976_238+978dup others(3): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 141904703 | |||||
| chr3:141904703
|
C | CTTTT | 7 | a0001c0001t0001g0088a0001c0001t0002g0086a0001c0001t0004g0337others(4): Show | 7 | HG01517.hp1 HG02486.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.238+975_238+978dup others(4): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 141904703 | |||||
| chr3:141904703
|
C | CTTTTT | 37 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0338others(34): Show | 38 | HG00558.hp1 HG00673.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.238+974_238+978dup others(5): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 141904703 | |||||
| chr3:141904703
|
C | CTTTTTT | 14 | a0001c0001t0004g0339a0001c0001t0004g0346a0001c0001t0004g0361others(11): Show | 14 | HG00544.hp1 HG00642.hp2 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.238+973_238+978dup others(6): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 141904703 | |||||
| chr3:141904703
|
CT | C | 20 | a0001c0001t0001g0107a0001c0001t0001g0167a0001c0001t0002g0004others(17): Show | 21 | HG01257.hp1 HG01258.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.238+978delT | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 141904703 | |||||
| chr3:141904703
|
CTT | C | 59 | a0001c0001t0001g0024a0001c0001t0001g0032a0001c0001t0001g0043others(56): Show | 59 | HG00099.hp2 HG00733.hp1 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.238+977_238+978del others(2): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 141904703 | |||||
| chr3:141904957
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.238+1209C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 2/6 | chr3 | 141904957 | ||||||
| chr3:141905150
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.238+1402A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 2/6 | chr3 | 141905150 | ||||||
| chr3:141905391
|
G | A | 3 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0245 | 3 | HG03098.hp2 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.238+1643G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 2/6 | chr3 | 141905391 | ||||||
| chr3:141905529
|
C | G | 1 | a0001c0004t0001g0304 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.239-1638C>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 2/6 | chr3 | 141905529 | ||||||
| chr3:141905787
|
A | G | 72 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0095others(69): Show | 74 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.239-1380A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 2/6 | chr3 | 141905787 | ||||||
| chr3:141905797
|
A | AC | 68 | a0001c0001t0001g0024a0001c0001t0001g0032a0001c0001t0001g0043others(65): Show | 68 | HG00099.hp2 HG00733.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.239-1369dupC | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 141905797 | |||||
| chr3:141905889
|
C | T | 2 | a0001c0001t0003g0302a0001c0001t0008g0303 | 2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.239-1278C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 2/6 | chr3 | 141905889 | ||||||
| chr3:141905962
|
T | C | 1 | a0001c0001t0002g0214 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.239-1205T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 2/6 | chr3 | 141905962 | ||||||
| chr3:141906018
|
GTAATACA others(4): Show |
G | 1 | a0001c0001t0001g0279 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.239-1143_239-1133d others(13): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 141906018 | |||||
| chr3:141906020
|
AATAC | A | 56 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0203others(53): Show | 58 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.239-1143_239-1140d others(6): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 141906020 | |||||
| chr3:141906047
|
T | C | 2 | a0001c0001t0001g0261a0001c0001t0001g0272 | 2 | NA18943.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.239-1120T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 2/6 | chr3 | 141906047 | ||||||
| chr3:141906211
|
G | A | 2 | a0001c0001t0001g0151a0001c0001t0003g0148 | 2 | HG02717.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.239-956G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 2/6 | chr3 | 141906211 | ||||||
| chr3:141906236
|
A | G | 12 | a0001c0001t0002g0004a0001c0001t0002g0118a0001c0001t0002g0119others(9): Show | 13 | HG01070.hp1 HG01071.hp1 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.239-931A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 2/6 | chr3 | 141906236 | ||||||
| chr3:141906249
|
G | A | 2 | a0001c0001t0007g0308a0001c0001t0007g0314 | 2 | HG01891.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.239-918G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 2/6 | chr3 | 141906249 | ||||||
| chr3:141906273
|
A | G | 58 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(55): Show | 59 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.239-894A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 2/6 | chr3 | 141906273 | ||||||
| chr3:141906431
|
C | T | 55 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(52): Show | 56 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.239-736C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 2/6 | chr3 | 141906431 | ||||||
| chr3:141906577
|
T | G | 1 | a0001c0001t0001g0330 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.239-590T>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 2/6 | chr3 | 141906577 | ||||||
| chr3:141906594
|
T | G | 13 | a0001c0001t0003g0106a0001c0001t0003g0302a0001c0001t0003g0309others(10): Show | 13 | HG01891.hp2 HG02257.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.239-573T>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 2/6 | chr3 | 141906594 | ||||||
| chr3:141906664
|
A | G | 1 | a0001c0001t0001g0278 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.239-503A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 2/6 | chr3 | 141906664 | ||||||
| chr3:141906894
|
C | T | 1 | a0001c0001t0004g0386 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.239-273C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 2/6 | chr3 | 141906894 | ||||||
| chr3:141906895
|
A | G | 58 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(55): Show | 59 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.239-272A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 2/6 | chr3 | 141906895 | ||||||
| chr3:141907007
|
T | A | 3 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0245 | 3 | HG03098.hp2 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.239-160T>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 2/6 | chr3 | 141907007 | ||||||
| chr3:141907131
|
G | A | 1 | a0001c0001t0003g0042 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.239-36G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 2/6 | chr3 | 141907131 | ||||||
| chr3:141907144
|
C | A | 1 | a0001c0001t0001g0330 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.239-23C>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 2/6 | chr3 | 141907144 | ||||||
| chr3:141907149
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.239-18C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 2/6 | chr3 | 141907149 | ||||||
| chr3:141907157
|
G | C | 242 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(239): Show | 246 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(243): Show |
intron_variant | MODIFIER | c.239-10G>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 2/6 | chr3 | 141907157 | ||||||
| chr3:141907281
|
A | G | 58 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(55): Show | 59 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(56): Show |
splice_region_variant&intron_variant | LOW | c.346+7A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141907281 | ||||||
| chr3:141907314
|
T | C | 3 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0245 | 3 | HG03098.hp2 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.346+40T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141907314 | ||||||
| chr3:141907347
|
C | CGGTA | 70 | a0001c0001t0001g0024a0001c0001t0001g0032a0001c0001t0001g0043others(67): Show | 70 | HG00099.hp2 HG00733.hp1 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.346+75_346+78dupGT others(2): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 141907347 | |||||
| chr3:141907466
|
AC | A | 12 | a0001c0001t0001g0079a0001c0001t0001g0330a0001c0001t0001g0331others(9): Show | 12 | HG00735.hp2 HG01891.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.346+196delC | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 141907466 | |||||
| chr3:141907502
|
G | A | 59 | a0001c0001t0001g0221a0001c0001t0004g0010a0001c0001t0004g0336others(56): Show | 60 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.346+228G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141907502 | ||||||
| chr3:141907571
|
G | A | 6 | a0001c0001t0004g0340a0001c0001t0004g0376a0001c0001t0004g0378others(3): Show | 6 | HG00558.hp1 NA18612.hp1 NA18956.hp2 others(3): Show |
intron_variant | MODIFIER | c.346+297G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141907571 | ||||||
| chr3:141907595
|
T | G | 2 | a0001c0001t0003g0302a0001c0001t0008g0303 | 2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.346+321T>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141907595 | ||||||
| chr3:141907787
|
G | A | 1 | a0001c0001t0001g0297 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.346+513G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141907787 | ||||||
| chr3:141907791
|
CAG | C | 3 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0245 | 3 | HG03098.hp2 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.346+518_346+519del others(2): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141907791 | ||||||
| chr3:141907973
|
CT | C | 58 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(55): Show | 59 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.346+708delT | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 141907973 | |||||
| chr3:141908021
|
A | G | 1 | a0001c0001t0001g0125 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.346+747A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141908021 | ||||||
| chr3:141908068
|
C | CT | 82 | a0001c0001t0001g0001a0001c0001t0001g0080a0001c0001t0001g0082others(79): Show | 84 | HG00408.hp2 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.346+815dupT | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 141908068 | |||||
| chr3:141908068
|
C | CTT | 61 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0088others(58): Show | 63 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.346+814_346+815dup others(2): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 141908068 | |||||
| chr3:141908068
|
CT | C | 85 | a0001c0001t0001g0024a0001c0001t0001g0032a0001c0001t0001g0043others(82): Show | 85 | HG00099.hp2 HG00733.hp1 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.346+815delT | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 141908068 | |||||
| chr3:141908068
|
CTT | C | 15 | a0001c0001t0003g0037a0001c0001t0003g0106a0001c0001t0003g0309others(12): Show | 15 | HG01891.hp2 HG02129.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.346+814_346+815del others(2): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 141908068 | |||||
| chr3:141908089
|
T | A | 2 | a0001c0001t0003g0302a0001c0001t0008g0303 | 2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.346+815T>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141908089 | ||||||
| chr3:141908125
|
G | A | 1 | a0001c0001t0004g0370 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.346+851G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141908125 | ||||||
| chr3:141908231
|
C | T | 1 | a0001c0001t0002g0328 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.346+957C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141908231 | ||||||
| chr3:141908241
|
C | T | 57 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0203others(54): Show | 59 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.346+967C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141908241 | ||||||
| chr3:141908369
|
C | T | 12 | a0001c0001t0001g0079a0001c0001t0001g0330a0001c0001t0001g0331others(9): Show | 12 | HG00735.hp2 HG01891.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.346+1095C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141908369 | ||||||
| chr3:141908372
|
C | T | 1 | a0001c0001t0001g0330 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.346+1098C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141908372 | ||||||
| chr3:141908398
|
A | G | 3 | a0001c0001t0001g0270a0001c0001t0001g0273a0001c0001t0001g0290 | 3 | NA18612.hp2 NA18992.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.346+1124A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141908398 | ||||||
| chr3:141908522
|
C | A | 1 | a0001c0001t0003g0324 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.346+1248C>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141908522 | ||||||
| chr3:141908534
|
C | T | 1 | a0001c0001t0002g0162 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.346+1260C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141908534 | ||||||
| chr3:141908696
|
A | G | 68 | a0001c0001t0001g0024a0001c0001t0001g0032a0001c0001t0001g0043others(65): Show | 68 | HG00099.hp2 HG00733.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.346+1422A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141908696 | ||||||
| chr3:141908803
|
T | G | 58 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(55): Show | 59 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.346+1529T>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141908803 | ||||||
| chr3:141908947
|
G | A | 1 | a0001c0001t0004g0390 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.346+1673G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141908947 | ||||||
| chr3:141909018
|
C | A | 37 | a0001c0001t0001g0032a0001c0001t0003g0015a0001c0001t0003g0027others(34): Show | 37 | HG00735.hp1 HG01081.hp1 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.346+1744C>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141909018 | ||||||
| chr3:141909084
|
A | G | 2 | a0001c0001t0001g0397a0001c0001t0001g0398 | 2 | NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.346+1810A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141909084 | ||||||
| chr3:141909159
|
C | A | 57 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0203others(54): Show | 59 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.346+1885C>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141909159 | ||||||
| chr3:141909185
|
T | G | 1 | a0001c0001t0003g0313 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.346+1911T>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141909185 | ||||||
| chr3:141909216
|
G | A | 13 | a0001c0001t0001g0001a0001c0001t0001g0080a0001c0001t0001g0082others(10): Show | 14 | HG00738.hp2 HG01433.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.346+1942G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141909216 | ||||||
| chr3:141909283
|
C | G | 70 | a0001c0001t0001g0024a0001c0001t0001g0032a0001c0001t0001g0043others(67): Show | 70 | HG00099.hp2 HG00733.hp1 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.346+2009C>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141909283 | ||||||
| chr3:141909404
|
A | G | 12 | a0001c0001t0001g0001a0001c0001t0001g0080a0001c0001t0001g0082others(9): Show | 13 | HG00738.hp2 HG01433.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.346+2130A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141909404 | ||||||
| chr3:141909663
|
G | T | 1 | a0001c0001t0001g0183 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.346+2389G>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141909663 | ||||||
| chr3:141909884
|
C | A | 1 | a0001c0001t0003g0017 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.346+2610C>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141909884 | ||||||
| chr3:141909901
|
G | A | 67 | a0001c0001t0001g0024a0001c0001t0001g0032a0001c0001t0001g0043others(64): Show | 67 | HG00099.hp2 HG00733.hp1 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.346+2627G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141909901 | ||||||
| chr3:141910025
|
C | G | 2 | a0001c0001t0004g0385a0001c0001t0016g0384 | 2 | HG03927.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.346+2751C>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141910025 | ||||||
| chr3:141910091
|
C | T | 3 | a0001c0001t0001g0247a0001c0001t0001g0264a0001c0001t0001g0266 | 3 | NA18939.hp2 NA19012.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.346+2817C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141910091 | ||||||
| chr3:141910121
|
A | C | 9 | a0001c0001t0003g0055a0001c0001t0003g0058a0001c0001t0003g0060others(6): Show | 9 | HG00735.hp1 HG01099.hp2 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.346+2847A>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141910121 | ||||||
| chr3:141910128
|
C | T | 12 | a0001c0001t0001g0079a0001c0001t0001g0330a0001c0001t0001g0331others(9): Show | 12 | HG00735.hp2 HG01891.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.346+2854C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141910128 | ||||||
| chr3:141910775
|
G | GC | 241 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(238): Show | 247 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.347-2869dupC | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 141910775 | |||||
| chr3:141910775
|
G | GCC | 15 | a0001c0001t0001g0282a0001c0001t0001g0319a0001c0001t0001g0321others(12): Show | 15 | HG01167.hp2 HG01192.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.347-2870_347-2869d others(4): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 141910775 | |||||
| chr3:141910783
|
CT | C | 19 | a0001c0001t0001g0095a0001c0001t0001g0203a0001c0001t0001g0248others(16): Show | 19 | HG01109.hp2 HG01884.hp2 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.347-2861delT | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 141910783 | |||||
| chr3:141910784
|
T | C | 63 | a0001c0001t0001g0032a0001c0001t0001g0043a0001c0001t0001g0045others(60): Show | 63 | HG00099.hp2 HG00642.hp2 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.347-2868T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141910784 | ||||||
| chr3:141910921
|
C | T | 2 | a0001c0001t0003g0302a0001c0001t0008g0303 | 2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.347-2731C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141910921 | ||||||
| chr3:141910999
|
AT | A | 13 | a0001c0001t0001g0001a0001c0001t0001g0080a0001c0001t0001g0082others(10): Show | 14 | HG00738.hp2 HG01433.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.347-2643delT | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 141910999 | |||||
| chr3:141911135
|
A | G | 1 | a0001c0001t0001g0322 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.347-2517A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141911135 | ||||||
| chr3:141911184
|
T | C | 168 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(165): Show | 172 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.347-2468T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141911184 | ||||||
| chr3:141911210
|
G | C | 3 | a0001c0001t0002g0333a0001c0001t0002g0334a0001c0001t0002g0335 | 3 | HG01891.hp1 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.347-2442G>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141911210 | ||||||
| chr3:141911308
|
G | T | 1 | a0001c0001t0001g0271 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.347-2344G>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141911308 | ||||||
| chr3:141911442
|
T | C | 7 | a0001c0001t0001g0117a0001c0001t0002g0110a0001c0001t0002g0202others(4): Show | 7 | HG00438.hp1 HG01981.hp2 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.347-2210T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141911442 | ||||||
| chr3:141911492
|
C | CT | 26 | a0001c0001t0001g0079a0001c0001t0001g0183a0001c0001t0001g0331others(23): Show | 27 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.347-2145dupT | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 141911492 | |||||
| chr3:141911492
|
CT | C | 64 | a0001c0001t0001g0176a0001c0001t0004g0010a0001c0001t0004g0336others(61): Show | 65 | HG00544.hp1 HG00558.hp1 HG01069.hp2 others(62): Show |
intron_variant | MODIFIER | c.347-2145delT | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 141911492 | |||||
| chr3:141911559
|
T | G | 4 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0080others(1): Show | 4 | HG02451.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.347-2093T>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141911559 | ||||||
| chr3:141911597
|
C | T | 1 | a0001c0001t0001g0184 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.347-2055C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141911597 | ||||||
| chr3:141911639
|
C | T | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(189): Show | 197 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.347-2013C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141911639 | ||||||
| chr3:141911821
|
T | G | 19 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0129others(16): Show | 19 | HG00323.hp1 HG00558.hp2 HG00621.hp2 others(16): Show |
intron_variant | MODIFIER | c.347-1831T>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141911821 | ||||||
| chr3:141911838
|
C | T | 18 | a0001c0001t0001g0397a0001c0001t0001g0398a0001c0001t0002g0004others(15): Show | 19 | HG01070.hp1 HG01071.hp1 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.347-1814C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141911838 | ||||||
| chr3:141911880
|
A | G | 169 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(166): Show | 174 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.347-1772A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141911880 | ||||||
| chr3:141911976
|
G | C | 2 | a0001c0001t0006g0098a0001c0001t0006g0099 | 2 | HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.347-1676G>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141911976 | ||||||
| chr3:141911990
|
C | G | 20 | a0001c0001t0001g0079a0001c0001t0002g0004a0001c0001t0002g0118others(17): Show | 21 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.347-1662C>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141911990 | ||||||
| chr3:141912017
|
T | C | 1 | a0001c0001t0001g0331 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.347-1635T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141912017 | ||||||
| chr3:141912020
|
G | A | 1 | a0001c0001t0001g0278 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.347-1632G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141912020 | ||||||
| chr3:141912095
|
A | G | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(191): Show | 199 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.347-1557A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141912095 | ||||||
| chr3:141912096
|
C | G | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(191): Show | 199 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.347-1556C>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141912096 | ||||||
| chr3:141912201
|
AT | A | 352 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(349): Show | 359 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(356): Show |
intron_variant | MODIFIER | c.347-1444delT | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 141912201 | |||||
| chr3:141912208
|
T | C | 2 | a0001c0001t0003g0030a0001c0001t0003g0073 | 2 | HG03831.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.347-1444T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141912208 | ||||||
| chr3:141912220
|
A | G | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(189): Show | 197 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.347-1432A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141912220 | ||||||
| chr3:141912266
|
CTTATTTA others(5): Show |
C | 64 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(61): Show | 65 | HG00544.hp1 HG00558.hp1 HG01069.hp2 others(62): Show |
intron_variant | MODIFIER | c.347-1371_347-1360d others(14): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 141912266 | |||||
| chr3:141912309
|
G | C | 352 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(349): Show | 359 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(356): Show |
intron_variant | MODIFIER | c.347-1343G>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141912309 | ||||||
| chr3:141912314
|
G | A | 3 | a0001c0001t0003g0055a0001c0001t0003g0068a0001c0001t0003g0069 | 3 | HG01099.hp2 HG01167.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.347-1338G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141912314 | ||||||
| chr3:141912342
|
C | T | 3 | a0001c0001t0001g0232a0001c0001t0011g0178a0001c0001t0011g0231 | 3 | HG02559.hp2 HG02572.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.347-1310C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141912342 | ||||||
| chr3:141912426
|
T | A | 1 | a0001c0001t0003g0011 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.347-1226T>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141912426 | ||||||
| chr3:141912486
|
C | G | 64 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(61): Show | 65 | HG00544.hp1 HG00558.hp1 HG01069.hp2 others(62): Show |
intron_variant | MODIFIER | c.347-1166C>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141912486 | ||||||
| chr3:141912507
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.347-1145C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141912507 | ||||||
| chr3:141912634
|
A | G | 1 | a0001c0001t0003g0051 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.347-1018A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141912634 | ||||||
| chr3:141912636
|
G | A | 1 | a0001c0001t0002g0162 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.347-1016G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141912636 | ||||||
| chr3:141913389
|
A | G | 64 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(61): Show | 65 | HG00544.hp1 HG00558.hp1 HG01069.hp2 others(62): Show |
intron_variant | MODIFIER | c.347-263A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141913389 | ||||||
| chr3:141913391
|
G | T | 5 | a0001c0001t0001g0248a0001c0001t0002g0019a0001c0001t0002g0257others(2): Show | 5 | HG02040.hp2 HG02074.hp1 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.347-261G>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141913391 | ||||||
| chr3:141913955
|
G | T | 64 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(61): Show | 65 | HG00544.hp1 HG00558.hp1 HG01069.hp2 others(62): Show |
intron_variant | MODIFIER | c.531+119G>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 4/6 | chr3 | 141913955 | ||||||
| chr3:141913974
|
A | G | 64 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(61): Show | 65 | HG00544.hp1 HG00558.hp1 HG01069.hp2 others(62): Show |
intron_variant | MODIFIER | c.531+138A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 4/6 | chr3 | 141913974 | ||||||
| chr3:141913980
|
A | G | 64 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(61): Show | 65 | HG00544.hp1 HG00558.hp1 HG01069.hp2 others(62): Show |
intron_variant | MODIFIER | c.531+144A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 4/6 | chr3 | 141913980 | ||||||
| chr3:141914011
|
T | C | 1 | a0001c0001t0002g0211 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.531+175T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 4/6 | chr3 | 141914011 | ||||||
| chr3:141914018
|
C | CA | 63 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(60): Show | 64 | HG00544.hp1 HG00558.hp1 HG01069.hp2 others(61): Show |
intron_variant | MODIFIER | c.531+190dupA | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 141914018 | |||||
| chr3:141914380
|
G | A | 62 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(59): Show | 63 | HG00544.hp1 HG00558.hp1 HG01069.hp2 others(60): Show |
intron_variant | MODIFIER | c.531+544G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 4/6 | chr3 | 141914380 | ||||||
| chr3:141914396
|
T | C | 1 | a0001c0001t0014g0291 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.531+560T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 4/6 | chr3 | 141914396 | ||||||
| chr3:141914502
|
C | A | 5 | a0001c0001t0001g0248a0001c0001t0002g0019a0001c0001t0002g0257others(2): Show | 5 | HG02040.hp2 HG02074.hp1 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.531+666C>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 4/6 | chr3 | 141914502 | ||||||
| chr3:141914557
|
A | G | 1 | a0001c0001t0001g0217 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.531+721A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 4/6 | chr3 | 141914557 | ||||||
| chr3:141914891
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.531+1055G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 4/6 | chr3 | 141914891 | ||||||
| chr3:141915019
|
TAA | T | 163 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(160): Show | 168 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.532-950_532-949del others(2): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 4/6 | chr3 | 141915019 | ||||||
| chr3:141915214
|
G | A | 62 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(59): Show | 63 | HG00544.hp1 HG00558.hp1 HG01069.hp2 others(60): Show |
intron_variant | MODIFIER | c.532-756G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 4/6 | chr3 | 141915214 | ||||||
| chr3:141915240
|
ACACAGGA others(5): Show |
A | 1 | a0001c0001t0002g0207 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.532-729_532-718del others(12): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 4/6 | chr3 | 141915240 | ||||||
| chr3:141915409
|
A | G | 1 | a0001c0001t0004g0391 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.532-561A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 4/6 | chr3 | 141915409 | ||||||
| chr3:141915548
|
A | G | 1 | a0001c0001t0001g0142 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.532-422A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 4/6 | chr3 | 141915548 | ||||||
| chr3:141915631
|
T | G | 1 | a0001c0001t0004g0385 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.532-339T>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 4/6 | chr3 | 141915631 | ||||||
| chr3:141915639
|
T | C | 2 | a0001c0001t0002g0307a0001c0001t0007g0308 | 2 | HG01891.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.532-331T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 4/6 | chr3 | 141915639 | ||||||
| chr3:141915772
|
A | T | 1 | a0001c0001t0002g0207 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.532-198A>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 4/6 | chr3 | 141915772 | ||||||
| chr3:141915848
|
C | G | 16 | a0001c0001t0002g0004a0001c0001t0002g0081a0001c0001t0002g0118others(13): Show | 17 | HG01070.hp1 HG01071.hp1 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.532-122C>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 4/6 | chr3 | 141915848 | ||||||
| chr3:141916098
|
C | T | 3 | a0001c0001t0002g0004a0001c0003t0002g0160a0001c0003t0002g0161 | 4 | HG01257.hp1 HG01258.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.582+78C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141916098 | ||||||
| chr3:141916119
|
A | G | 1 | a0001c0001t0004g0371 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.582+99A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141916119 | ||||||
| chr3:141916362
|
C | T | 21 | a0001c0001t0002g0004a0001c0001t0002g0081a0001c0001t0002g0086others(18): Show | 22 | HG01070.hp1 HG01071.hp1 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.582+342C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141916362 | ||||||
| chr3:141916403
|
A | G | 1 | a0001c0001t0001g0270 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.582+383A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141916403 | ||||||
| chr3:141916433
|
T | A | 1 | a0001c0001t0005g0054 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.582+413T>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141916433 | ||||||
| chr3:141916513
|
A | G | 3 | a0001c0001t0001g0024a0001c0001t0001g0397a0001c0001t0001g0398 | 3 | HG02622.hp2 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.582+493A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141916513 | ||||||
| chr3:141916756
|
C | A | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(163): Show | 171 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.582+736C>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141916756 | ||||||
| chr3:141916870
|
C | CT | 22 | a0001c0001t0002g0004a0001c0001t0002g0081a0001c0001t0002g0086others(19): Show | 23 | HG01070.hp1 HG01071.hp1 HG01257.hp1 others(20): Show |
intron_variant | MODIFIER | c.582+859dupT | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 141916870 | |||||
| chr3:141916905
|
G | C | 14 | a0001c0001t0001g0024a0001c0001t0001g0397a0001c0001t0001g0398others(11): Show | 14 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.582+885G>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141916905 | ||||||
| chr3:141917012
|
G | A | 1 | a0001c0001t0002g0394 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.582+992G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141917012 | ||||||
| chr3:141917017
|
A | AT | 7 | a0001c0001t0001g0152a0001c0001t0001g0224a0001c0001t0001g0318others(4): Show | 7 | HG00741.hp2 HG01981.hp2 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.582+1015dupT | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 141917017 | |||||
| chr3:141917017
|
AT | A | 263 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(260): Show | 268 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(265): Show |
intron_variant | MODIFIER | c.582+1015delT | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 141917017 | |||||
| chr3:141917089
|
G | A | 72 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(69): Show | 72 | HG00099.hp2 HG00642.hp2 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.582+1069G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141917089 | ||||||
| chr3:141917114
|
A | G | 1 | a0001c0001t0002g0204 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.582+1094A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141917114 | ||||||
| chr3:141917121
|
G | A | 2 | a0001c0001t0003g0011a0001c0001t0003g0012 | 2 | HG02965.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.582+1101G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141917121 | ||||||
| chr3:141917142
|
C | T | 4 | a0001c0001t0008g0094a0001c0001t0008g0101a0001c0001t0008g0303others(1): Show | 4 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.582+1122C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141917142 | ||||||
| chr3:141917285
|
C | T | 3 | a0001c0001t0001g0108a0001c0001t0001g0153a0001c0001t0001g0224 | 3 | NA18941.hp2 NA18959.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.582+1265C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141917285 | ||||||
| chr3:141917342
|
C | T | 4 | a0001c0001t0002g0019a0001c0001t0002g0257a0001c0001t0002g0267others(1): Show | 4 | HG02074.hp1 HG02083.hp1 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.582+1322C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141917342 | ||||||
| chr3:141917407
|
C | T | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(183): Show | 191 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.582+1387C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141917407 | ||||||
| chr3:141917432
|
G | A | 3 | a0001c0001t0008g0094a0001c0001t0008g0101a0001c0001t0008g0303 | 3 | HG02451.hp1 HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.582+1412G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141917432 | ||||||
| chr3:141917518
|
A | C | 1 | a0001c0001t0001g0301 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.582+1498A>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141917518 | ||||||
| chr3:141917565
|
G | A | 2 | a0001c0001t0003g0011a0001c0001t0003g0012 | 2 | HG02965.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.582+1545G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141917565 | ||||||
| chr3:141917593
|
C | T | 4 | a0001c0001t0008g0094a0001c0001t0008g0101a0001c0001t0008g0303others(1): Show | 4 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.582+1573C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141917593 | ||||||
| chr3:141917688
|
A | G | 352 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(349): Show | 359 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(356): Show |
intron_variant | MODIFIER | c.582+1668A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141917688 | ||||||
| chr3:141917776
|
T | A | 64 | a0001c0001t0002g0394a0001c0001t0003g0058a0001c0001t0004g0010others(61): Show | 65 | HG00544.hp1 HG00558.hp1 HG01069.hp2 others(62): Show |
intron_variant | MODIFIER | c.582+1756T>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141917776 | ||||||
| chr3:141917777
|
T | A | 1 | a0001c0001t0006g0103 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.582+1757T>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141917777 | ||||||
| chr3:141917837
|
G | A | 17 | a0001c0001t0003g0013a0001c0001t0003g0016a0001c0001t0003g0017others(14): Show | 17 | HG00099.hp2 HG00642.hp2 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.582+1817G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141917837 | ||||||
| chr3:141917853
|
C | T | 1 | a0001c0001t0002g0394 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.582+1833C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141917853 | ||||||
| chr3:141917863
|
G | A | 2 | a0001c0001t0002g0162a0001c0001t0002g0241 | 2 | HG01515.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.582+1843G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141917863 | ||||||
| chr3:141917929
|
G | A | 1 | a0001c0001t0004g0345 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.582+1909G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141917929 | ||||||
| chr3:141918012
|
C | A | 72 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(69): Show | 72 | HG00099.hp2 HG00642.hp2 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.582+1992C>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141918012 | ||||||
| chr3:141918057
|
C | T | 1 | a0001c0001t0002g0394 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.582+2037C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141918057 | ||||||
| chr3:141918258
|
A | G | 1 | a0001c0001t0001g0287 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.582+2238A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141918258 | ||||||
| chr3:141918284
|
C | T | 2 | a0001c0001t0001g0152a0001c0001t0001g0222 | 2 | NA18989.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.582+2264C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141918284 | ||||||
| chr3:141918449
|
C | CTT | 63 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(60): Show | 64 | HG00544.hp1 HG00558.hp1 HG01069.hp2 others(61): Show |
intron_variant | MODIFIER | c.582+2441_582+2442d others(4): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 141918449 | |||||
| chr3:141918449
|
C | T | 1 | a0001c0001t0002g0207 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.582+2429C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141918449 | ||||||
| chr3:141918449
|
CT | C | 7 | a0001c0001t0001g0079a0001c0001t0001g0130a0001c0001t0001g0247others(4): Show | 7 | HG00735.hp2 HG01168.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.582+2442delT | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 141918449 | |||||
| chr3:141918588
|
G | C | 4 | a0001c0001t0002g0019a0001c0001t0002g0257a0001c0001t0002g0267others(1): Show | 4 | HG02074.hp1 HG02083.hp1 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.582+2568G>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141918588 | ||||||
| chr3:141918596
|
G | A | 283 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(280): Show | 289 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(286): Show |
intron_variant | MODIFIER | c.582+2576G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141918596 | ||||||
| chr3:141918684
|
T | C | 348 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(345): Show | 355 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(352): Show |
intron_variant | MODIFIER | c.582+2664T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141918684 | ||||||
| chr3:141918703
|
C | T | 1 | a0001c0001t0003g0072 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.582+2683C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141918703 | ||||||
| chr3:141918786
|
C | T | 2 | a0001c0001t0010g0197a0001c0001t0010g0198 | 2 | HG02155.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.582+2766C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141918786 | ||||||
| chr3:141918838
|
G | T | 1 | a0001c0001t0002g0394 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.582+2818G>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141918838 | ||||||
| chr3:141918913
|
G | A | 1 | a0001c0001t0001g0024 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.582+2893G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141918913 | ||||||
| chr3:141919025
|
G | A | 1 | a0001c0001t0001g0129 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.583-2952G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141919025 | ||||||
| chr3:141919062
|
T | C | 64 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(61): Show | 65 | HG00544.hp1 HG00558.hp1 HG01069.hp2 others(62): Show |
intron_variant | MODIFIER | c.583-2915T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141919062 | ||||||
| chr3:141919068
|
T | C | 18 | a0001c0001t0002g0004a0001c0001t0002g0081a0001c0001t0002g0086others(15): Show | 19 | HG01070.hp1 HG01071.hp1 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.583-2909T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141919068 | ||||||
| chr3:141919100
|
A | G | 1 | a0001c0001t0003g0040 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.583-2877A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141919100 | ||||||
| chr3:141919106
|
G | C | 1 | a0001c0001t0001g0226 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.583-2871G>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141919106 | ||||||
| chr3:141919275
|
C | CT | 38 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(35): Show | 38 | HG00099.hp2 HG00642.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.583-2691dupT | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 141919275 | |||||
| chr3:141919285
|
T | TC | 45 | a0001c0001t0002g0004a0001c0001t0002g0081a0001c0001t0002g0086others(42): Show | 46 | HG00735.hp1 HG01070.hp1 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.583-2692_583-2691i others(3): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141919285 | ||||||
| chr3:141919320
|
G | A | 2 | a0001c0001t0002g0081a0001c0001t0002g0086 | 2 | HG03225.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.583-2657G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141919320 | ||||||
| chr3:141919356
|
A | G | 1 | a0001c0001t0001g0255 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.583-2621A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141919356 | ||||||
| chr3:141919593
|
G | A | 1 | a0001c0001t0001g0180 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.583-2384G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141919593 | ||||||
| chr3:141919597
|
C | T | 3 | a0001c0001t0009g0076a0001c0001t0009g0077a0001c0001t0009g0078 | 3 | HG02145.hp1 HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.583-2380C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141919597 | ||||||
| chr3:141919671
|
G | A | 1 | a0001c0001t0003g0040 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.583-2306G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141919671 | ||||||
| chr3:141919832
|
G | T | 21 | a0001c0001t0002g0004a0001c0001t0002g0081a0001c0001t0002g0086others(18): Show | 22 | HG01070.hp1 HG01071.hp1 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.583-2145G>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141919832 | ||||||
| chr3:141919894
|
G | A | 4 | a0001c0001t0001g0150a0001c0001t0001g0251a0001c0001t0001g0252others(1): Show | 4 | NA18974.hp2 NA19064.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.583-2083G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141919894 | ||||||
| chr3:141919962
|
G | A | 1 | a0001c0001t0002g0111 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.583-2015G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141919962 | ||||||
| chr3:141920110
|
T | G | 352 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(349): Show | 359 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(356): Show |
intron_variant | MODIFIER | c.583-1867T>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141920110 | ||||||
| chr3:141920242
|
G | T | 1 | a0001c0001t0002g0394 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.583-1735G>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141920242 | ||||||
| chr3:141920263
|
T | A | 1 | a0001c0001t0002g0019 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.583-1714T>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141920263 | ||||||
| chr3:141920303
|
G | A | 1 | a0001c0001t0001g0274 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.583-1674G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141920303 | ||||||
| chr3:141920418
|
T | A | 2 | a0001c0001t0003g0028a0001c0001t0003g0044 | 2 | HG02056.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.583-1559T>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141920418 | ||||||
| chr3:141920420
|
A | T | 3 | a0001c0001t0001g0108a0001c0001t0001g0153a0001c0001t0001g0224 | 3 | NA18941.hp2 NA18959.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.583-1557A>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141920420 | ||||||
| chr3:141920452
|
G | A | 1 | a0001c0001t0003g0020 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.583-1525G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141920452 | ||||||
| chr3:141920526
|
C | CA | 64 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(61): Show | 65 | HG00544.hp1 HG00558.hp1 HG01069.hp2 others(62): Show |
intron_variant | MODIFIER | c.583-1443dupA | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 141920526 | |||||
| chr3:141920535
|
G | A | 64 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(61): Show | 65 | HG00544.hp1 HG00558.hp1 HG01069.hp2 others(62): Show |
intron_variant | MODIFIER | c.583-1442G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141920535 | ||||||
| chr3:141920611
|
G | A | 4 | a0001c0001t0002g0019a0001c0001t0002g0257a0001c0001t0002g0267others(1): Show | 4 | HG02074.hp1 HG02083.hp1 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.583-1366G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141920611 | ||||||
| chr3:141920725
|
T | C | 1 | a0001c0001t0003g0018 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.583-1252T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141920725 | ||||||
| chr3:141920855
|
C | G | 64 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(61): Show | 65 | HG00544.hp1 HG00558.hp1 HG01069.hp2 others(62): Show |
intron_variant | MODIFIER | c.583-1122C>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141920855 | ||||||
| chr3:141920869
|
C | T | 2 | a0001c0001t0011g0178a0001c0001t0011g0231 | 2 | HG02559.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.583-1108C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141920869 | ||||||
| chr3:141920895
|
C | G | 25 | a0001c0001t0001g0117a0001c0001t0002g0006a0001c0001t0002g0007others(22): Show | 27 | HG00438.hp1 HG01981.hp2 HG01993.hp1 others(24): Show |
intron_variant | MODIFIER | c.583-1082C>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141920895 | ||||||
| chr3:141920935
|
G | A | 1 | a0001c0001t0003g0018 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.583-1042G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141920935 | ||||||
| chr3:141921044
|
A | G | 64 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(61): Show | 65 | HG00544.hp1 HG00558.hp1 HG01069.hp2 others(62): Show |
intron_variant | MODIFIER | c.583-933A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141921044 | ||||||
| chr3:141921069
|
A | C | 1 | a0001c0001t0001g0168 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.583-908A>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141921069 | ||||||
| chr3:141921094
|
A | T | 1 | a0001c0001t0001g0125 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.583-883A>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141921094 | ||||||
| chr3:141921100
|
T | G | 1 | a0001c0001t0001g0125 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.583-877T>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141921100 | ||||||
| chr3:141921399
|
T | TA | 64 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(61): Show | 65 | HG00544.hp1 HG00558.hp1 HG01069.hp2 others(62): Show |
intron_variant | MODIFIER | c.583-577dupA | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 141921399 | |||||
| chr3:141921504
|
C | G | 1 | a0001c0001t0003g0091 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.583-473C>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141921504 | ||||||
| chr3:141921554
|
G | A | 161 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(158): Show | 166 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.583-423G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141921554 | ||||||
| chr3:141921720
|
C | T | 8 | a0001c0001t0003g0013a0001c0001t0003g0016a0001c0001t0003g0049others(5): Show | 8 | NA18951.hp1 NA18955.hp2 NA18956.hp1 others(5): Show |
intron_variant | MODIFIER | c.583-257C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141921720 | ||||||
| chr3:141921729
|
AAG | A | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(163): Show | 171 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.583-243_583-242del others(2): Show |
ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 141921729 | |||||
| chr3:141921789
|
A | T | 1 | a0001c0001t0001g0125 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.583-188A>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141921789 | ||||||
| chr3:141922123
|
G | A | 1 | a0001c0001t0002g0333 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.669+60G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 6/6 | chr3 | 141922123 | ||||||
| chr3:141922173
|
C | G | 184 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(181): Show | 189 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.669+110C>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 6/6 | chr3 | 141922173 | ||||||
| chr3:141922259
|
G | A | 10 | a0001c0001t0002g0004a0001c0001t0002g0118a0001c0001t0002g0119others(7): Show | 11 | HG01070.hp1 HG01071.hp1 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.669+196G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 6/6 | chr3 | 141922259 | ||||||
| chr3:141922374
|
C | T | 64 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(61): Show | 65 | HG00544.hp1 HG00558.hp1 HG01069.hp2 others(62): Show |
intron_variant | MODIFIER | c.669+311C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 6/6 | chr3 | 141922374 | ||||||
| chr3:141922526
|
G | T | 64 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(61): Show | 65 | HG00544.hp1 HG00558.hp1 HG01069.hp2 others(62): Show |
intron_variant | MODIFIER | c.669+463G>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 6/6 | chr3 | 141922526 | ||||||
| chr3:141922580
|
G | T | 1 | a0001c0001t0001g0154 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.669+517G>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 6/6 | chr3 | 141922580 | ||||||
| chr3:141922629
|
G | A | 1 | a0001c0001t0001g0271 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.669+566G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 6/6 | chr3 | 141922629 | ||||||
| chr3:141922696
|
A | G | 352 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(349): Show | 359 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(356): Show |
intron_variant | MODIFIER | c.669+633A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 6/6 | chr3 | 141922696 | ||||||
| chr3:141922722
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.669+659T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 6/6 | chr3 | 141922722 | ||||||
| chr3:141922781
|
C | A | 1 | a0001c0001t0002g0211 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.669+718C>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 6/6 | chr3 | 141922781 | ||||||
| chr3:141922840
|
C | T | 64 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(61): Show | 65 | HG00544.hp1 HG00558.hp1 HG01069.hp2 others(62): Show |
intron_variant | MODIFIER | c.669+777C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 6/6 | chr3 | 141922840 | ||||||
| chr3:141922858
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.669+795C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 6/6 | chr3 | 141922858 | ||||||
| chr3:141922872
|
A | G | 1 | a0001c0001t0004g0380 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.669+809A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 6/6 | chr3 | 141922872 | ||||||
| chr3:141922952
|
C | T | 21 | a0001c0001t0002g0004a0001c0001t0002g0081a0001c0001t0002g0086others(18): Show | 22 | HG01070.hp1 HG01071.hp1 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.669+889C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 6/6 | chr3 | 141922952 | ||||||
| chr3:141922971
|
A | G | 1 | a0001c0001t0010g0197 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.669+908A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 6/6 | chr3 | 141922971 | ||||||
| chr3:141922972
|
G | A | 1 | a0001c0001t0010g0197 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.669+909G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 6/6 | chr3 | 141922972 | ||||||
| chr3:141922999
|
C | T | 2 | a0001c0001t0006g0092a0001c0001t0006g0100 | 2 | HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.669+936C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 6/6 | chr3 | 141922999 | ||||||
| chr3:141923026
|
G | A | 4 | a0001c0001t0008g0094a0001c0001t0008g0101a0001c0001t0008g0303others(1): Show | 4 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.669+963G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 6/6 | chr3 | 141923026 | ||||||
| chr3:141923128
|
A | T | 64 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(61): Show | 65 | HG00544.hp1 HG00558.hp1 HG01069.hp2 others(62): Show |
intron_variant | MODIFIER | c.669+1065A>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 6/6 | chr3 | 141923128 | ||||||
| chr3:141923185
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.669+1122G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 6/6 | chr3 | 141923185 | ||||||
| chr3:141923277
|
CA | C | 269 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(266): Show | 276 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.669+1228delA | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 141923277 | |||||
| chr3:141923334
|
G | A | 64 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(61): Show | 65 | HG00544.hp1 HG00558.hp1 HG01069.hp2 others(62): Show |
intron_variant | MODIFIER | c.669+1271G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 6/6 | chr3 | 141923334 | ||||||
| chr3:141923389
|
C | G | 1 | a0001c0001t0004g0363 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.669+1326C>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 6/6 | chr3 | 141923389 | ||||||
| chr3:141923470
|
T | C | 64 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(61): Show | 65 | HG00544.hp1 HG00558.hp1 HG01069.hp2 others(62): Show |
intron_variant | MODIFIER | c.669+1407T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 6/6 | chr3 | 141923470 | ||||||
| chr3:141923503
|
T | A | 64 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(61): Show | 65 | HG00544.hp1 HG00558.hp1 HG01069.hp2 others(62): Show |
intron_variant | MODIFIER | c.669+1440T>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 6/6 | chr3 | 141923503 | ||||||
| chr3:141923643
|
A | T | 1 | a0001c0001t0002g0207 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.669+1580A>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 6/6 | chr3 | 141923643 | ||||||
| chr3:141923651
|
A | G | 6 | a0001c0001t0001g0024a0001c0001t0001g0397a0001c0001t0001g0398others(3): Show | 6 | HG02145.hp1 HG02622.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.669+1588A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 6/6 | chr3 | 141923651 | ||||||
| chr3:141923707
|
T | C | 1 | a0001c0001t0002g0394 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.669+1644T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 6/6 | chr3 | 141923707 | ||||||
| chr3:141923721
|
C | T | 64 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(61): Show | 65 | HG00544.hp1 HG00558.hp1 HG01069.hp2 others(62): Show |
intron_variant | MODIFIER | c.669+1658C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 6/6 | chr3 | 141923721 | ||||||
| chr3:141923759
|
G | A | 1 | a0001c0004t0001g0304 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.669+1696G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 6/6 | chr3 | 141923759 | ||||||
| chr3:141923808
|
T | G | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(183): Show | 191 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.670-1723T>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 6/6 | chr3 | 141923808 | ||||||
| chr3:141923939
|
C | G | 72 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(69): Show | 72 | HG00099.hp2 HG00642.hp2 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.670-1592C>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 6/6 | chr3 | 141923939 | ||||||
| chr3:141924023
|
A | G | 1 | a0001c0001t0001g0141 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.670-1508A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 6/6 | chr3 | 141924023 | ||||||
| chr3:141924024
|
T | C | 1 | a0001c0001t0002g0394 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.670-1507T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 6/6 | chr3 | 141924024 | ||||||
| chr3:141924056
|
C | T | 1 | a0001c0001t0001g0203 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.670-1475C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 6/6 | chr3 | 141924056 | ||||||
| chr3:141924072
|
G | T | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(279): Show | 288 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(285): Show |
intron_variant | MODIFIER | c.670-1459G>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 6/6 | chr3 | 141924072 | ||||||
| chr3:141924207
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.670-1324G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 6/6 | chr3 | 141924207 | ||||||
| chr3:141924305
|
T | C | 18 | a0001c0001t0002g0004a0001c0001t0002g0081a0001c0001t0002g0086others(15): Show | 19 | HG01070.hp1 HG01071.hp1 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.670-1226T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 6/6 | chr3 | 141924305 | ||||||
| chr3:141924339
|
CA | C | 321 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(318): Show | 328 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(325): Show |
intron_variant | MODIFIER | c.670-1175delA | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 141924339 | |||||
| chr3:141924377
|
G | A | 3 | a0001c0001t0001g0139a0001c0001t0001g0168a0001c0001t0001g0177 | 3 | HG02055.hp2 HG03579.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.670-1154G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 6/6 | chr3 | 141924377 | ||||||
| chr3:141924424
|
G | A | 23 | a0001c0001t0003g0028a0001c0001t0003g0030a0001c0001t0003g0031others(20): Show | 23 | HG00735.hp1 HG01081.hp1 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.670-1107G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 6/6 | chr3 | 141924424 | ||||||
| chr3:141924430
|
G | A | 3 | a0001c0001t0009g0076a0001c0001t0009g0077a0001c0001t0009g0078 | 3 | HG02145.hp1 HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.670-1101G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 6/6 | chr3 | 141924430 | ||||||
| chr3:141924445
|
C | G | 21 | a0001c0001t0002g0004a0001c0001t0002g0081a0001c0001t0002g0086others(18): Show | 22 | HG01070.hp1 HG01071.hp1 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.670-1086C>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 6/6 | chr3 | 141924445 | ||||||
| chr3:141924473
|
G | A | 1 | a0001c0001t0002g0162 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.670-1058G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 6/6 | chr3 | 141924473 | ||||||
| chr3:141924525
|
C | T | 1 | a0001c0001t0003g0072 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.670-1006C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 6/6 | chr3 | 141924525 | ||||||
| chr3:141924591
|
A | G | 1 | a0001c0001t0001g0261 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.670-940A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 6/6 | chr3 | 141924591 | ||||||
| chr3:141924792
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.670-739A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 6/6 | chr3 | 141924792 | ||||||
| chr3:141924813
|
C | T | 1 | a0001c0004t0001g0304 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.670-718C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 6/6 | chr3 | 141924813 | ||||||
| chr3:141924852
|
T | C | 351 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(348): Show | 358 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(355): Show |
intron_variant | MODIFIER | c.670-679T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 6/6 | chr3 | 141924852 | ||||||
| chr3:141924878
|
G | A | 1 | a0001c0001t0002g0185 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.670-653G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 6/6 | chr3 | 141924878 | ||||||
| chr3:141924903
|
G | A | 4 | a0001c0001t0002g0019a0001c0001t0002g0257a0001c0001t0002g0267others(1): Show | 4 | HG02074.hp1 HG02083.hp1 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.670-628G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 6/6 | chr3 | 141924903 | ||||||
| chr3:141925255
|
C | T | 64 | a0001c0001t0004g0010a0001c0001t0004g0336a0001c0001t0004g0337others(61): Show | 65 | HG00544.hp1 HG00558.hp1 HG01069.hp2 others(62): Show |
intron_variant | MODIFIER | c.670-276C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 6/6 | chr3 | 141925255 | ||||||
| chr3:141925276
|
G | A | 3 | a0001c0001t0008g0094a0001c0001t0008g0101a0001c0001t0008g0303 | 3 | HG02451.hp1 HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.670-255G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 6/6 | chr3 | 141925276 | ||||||
| chr3:141925333
|
T | C | 283 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(280): Show | 289 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(286): Show |
intron_variant | MODIFIER | c.670-198T>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 6/6 | chr3 | 141925333 | ||||||
| chr3:141925350
|
C | T | 72 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(69): Show | 72 | HG00099.hp2 HG00642.hp2 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.670-181C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 6/6 | chr3 | 141925350 | ||||||
| chr3:141925432
|
G | C | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(279): Show | 288 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(285): Show |
intron_variant | MODIFIER | c.670-99G>C | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 6/6 | chr3 | 141925432 | ||||||
| chr3:141925436
|
C | T | 1 | a0001c0001t0003g0063 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.670-95C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 6/6 | chr3 | 141925436 |