Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 837 | 403 | 89 | 62 | 192 | 14 | 44 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | ATGAC others(832): Show |
chr3 | 141871643 | 141931549 | ||
| a0001c0002 | 0/0 | 837 | 2 | 2 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | ATGAC others(832): Show |
chr3 | 141871643 | 141931549 | ||
| a0001c0003 | 0/0 | 837 | 2 | 0 | 0 | 0 | 2 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | ATGAC others(832): Show |
chr3 | 141871643 | 141931549 | ||
| a0001c0004 | 0/0 | 837 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | ATGAC others(832): Show |
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 | AGTCG others(1841): Show |
chr3 | 141871643 | 141931549 |
| a0001c0001t0002 | 1/0 | 1847 | 70 | 11 | 13 | 32 | 5 | 8 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | AGTCG others(1842): Show |
chr3 | 141871643 | 141931549 |
| a0001c0001t0003 | 0/0 | 1847 | 66 | 22 | 18 | 15 | 1 | 10 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | AGTCG others(1842): Show |
chr3 | 141871643 | 141931549 |
| a0001c0001t0004 | 0/0 | 1846 | 53 | 0 | 4 | 43 | 2 | 4 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | AGTCG others(1841): Show |
chr3 | 141871643 | 141931549 |
| a0001c0001t0005 | 0/0 | 1846 | 11 | 0 | 3 | 7 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | AGTCG others(1841): Show |
chr3 | 141871643 | 141931549 |
| a0001c0001t0006 | 0/0 | 1845 | 11 | 11 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | AGTCG others(1840): Show |
chr3 | 141871643 | 141931549 |
| a0001c0001t0007 | 0/0 | 1846 | 4 | 4 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | AGTCG others(1841): Show |
chr3 | 141871643 | 141931549 |
| a0001c0001t0008 | 0/0 | 1844 | 3 | 3 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | AGTCG others(1839): Show |
chr3 | 141871643 | 141931549 |
| a0001c0001t0009 | 0/0 | 1847 | 3 | 3 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | AGTCG others(1842): Show |
chr3 | 141871643 | 141931549 |
| a0001c0001t0010 | 0/0 | 1847 | 2 | 0 | 0 | 2 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | AGTCG others(1842): Show |
chr3 | 141871643 | 141931549 |
| a0001c0001t0011 | 0/0 | 1846 | 2 | 2 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | AGTCG others(1841): Show |
chr3 | 141871643 | 141931549 |
| a0001c0001t0012 | 0/0 | 1846 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | AGTCG others(1841): Show |
chr3 | 141871643 | 141931549 |
| a0001c0001t0013 | 0/0 | 1847 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | AGTCG others(1842): Show |
chr3 | 141871643 | 141931549 |
| a0001c0001t0014 | 0/0 | 1846 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | AGTCG others(1841): Show |
chr3 | 141871643 | 141931549 |
| a0001c0001t0015 | 0/0 | 1844 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | AGTCG others(1839): Show |
chr3 | 141871643 | 141931549 |
| a0001c0001t0016 | 0/0 | 1847 | 1 | 0 | 0 | 0 | 1 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | AGTCG others(1842): Show |
chr3 | 141871643 | 141931549 |
| a0001c0001t0017 | 0/0 | 1846 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | AGTCG others(1841): Show |
chr3 | 141871643 | 141931549 |
| a0001c0001t0018 | 0/0 | 1847 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | AGTCG others(1842): Show |
chr3 | 141871643 | 141931549 |
| a0001c0002t0001 | 0/0 | 1846 | 2 | 2 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | AGTCG others(1841): Show |
chr3 | 141871643 | 141931549 |
| a0001c0003t0002 | 0/0 | 1847 | 2 | 0 | 0 | 0 | 2 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | AGTCG others(1842): Show |
chr3 | 141871643 | 141931549 |
| a0001c0004t0001 | 0/0 | 1846 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | AGTCG others(1841): Show |
chr3 | 141871643 | 141931549 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0003 | 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 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0001g0086 | 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 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0123 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0164 | 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 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0249 | 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 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0277 | 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 | 1 | 0 | 0 | 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 | 0 | 1 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 1 | 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 | 1 | 0 | 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 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0389 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0391 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0392 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0393 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0001g0394 | 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 | 0 | 2 | 0 | 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 | 1 | 0 | 1 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0167 | 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 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0194 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0218 | 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 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0002g0332 | 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 |
| a0001c0001t0002g0390 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 1 | 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 | 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 |
| a0001c0001t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 |
| 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 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0308 | 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 |
| 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 |
| a0001c0001t0003g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0003g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0343 | 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 |
| a0001c0001t0004g0351 | 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 | 1 | 0 | 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 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0363 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0364 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0369 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0373 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0004g0381 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0004g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0004g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0005g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0005g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0005g0033 | 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 |
| a0001c0001t0005g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0005g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0005g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0005g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0005g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0005g0340 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0006g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0006g0095 | 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 |
| 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 |
| a0001c0001t0006g0101 | 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 |
| a0001c0001t0006g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0006g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0006g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0007g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0007g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0007g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0007g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0008g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0008g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0008g0301 | 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 |
| a0001c0001t0009g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0009g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0010g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0010g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0011g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0011g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0012g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0013g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0014g0289 | 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 |
| a0001c0001t0016g0380 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0017g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0001t0018g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0002t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0002t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0003t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0003t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| a0001c0004t0001g0302 | 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 | g0007 | EUR | GBR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0020 | EUR | GBR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0285 | EUR | FIN | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0146 | EUR | FIN | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0153 | EUR | FIN | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0192 | EUR | FIN | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | CHS | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00423 | hp1 | a0001 | c0001 | t0012 | g0257 | EAS | CHS | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | CHS | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | CHS | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00544 | hp1 | a0001 | c0001 | t0004 | g0357 | EAS | CHS | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00558 | hp1 | a0001 | c0001 | t0004 | g0369 | EAS | CHS | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | CHS | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | CHS | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | CHS | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0156 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00642 | hp2 | a0001 | c0001 | t0018 | g0358 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00673 | hp1 | a0001 | c0001 | t0017 | g0368 | EAS | CHS | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0241 | 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 | g0148 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0066 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0025 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0216 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0196 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01069 | hp2 | a0001 | c0001 | t0004 | g0012 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0120 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01070 | hp2 | a0001 | c0001 | t0005 | g0339 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0121 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0193 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0035 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0195 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0062 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0239 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0296 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0070 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0318 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0065 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0367 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0067 | AMR | PUR | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01256 | hp1 | a0001 | c0001 | t0005 | g0341 | AMR | CLM | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0071 | 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 | g0028 | AMR | CLM | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01258 | hp1 | a0001 | c0001 | t0005 | g0340 | 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 | g0144 | AMR | CLM | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0057 | AMR | CLM | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0063 | AMR | CLM | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0292 | 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 | g0092 | AMR | CLM | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01515 | hp1 | a0001 | c0003 | t0002 | g0169 | EUR | IBS | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0171 | EUR | IBS | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0243 | EUR | IBS | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01516 | hp2 | a0001 | c0001 | t0004 | g0364 | EUR | IBS | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01517 | hp1 | a0001 | c0001 | t0004 | g0363 | EUR | IBS | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01517 | hp2 | a0001 | c0003 | t0002 | g0168 | EUR | IBS | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0320 | AFR | ACB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01884 | hp2 | a0001 | c0001 | t0006 | g0099 | AFR | ACB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0333 | AFR | ACB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01891 | hp2 | a0001 | c0001 | t0007 | g0310 | AFR | ACB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0059 | AMR | PEL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0039 | AMR | PEL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0319 | AMR | PEL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01978 | hp2 | a0001 | c0001 | t0004 | g0388 | AMR | PEL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0041 | AMR | PEL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0209 | AMR | PEL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0207 | AMR | PEL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0151 | 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 | g0010 | EAS | KHV | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02015 | hp2 | a0001 | c0001 | t0004 | g0334 | EAS | KHV | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | KHV | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02040 | hp1 | a0001 | c0001 | t0004 | g0360 | EAS | KHV | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | KHV | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02055 | hp1 | a0001 | c0001 | t0006 | g0107 | AFR | ACB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0032 | EAS | KHV | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02071 | hp1 | a0001 | c0001 | t0004 | g0359 | EAS | KHV | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | KHV | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | KHV | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0064 | EAS | KHV | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02080 | hp1 | a0001 | c0001 | t0013 | g0152 | EAS | KHV | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02080 | hp2 | a0001 | c0001 | t0004 | g0379 | EAS | KHV | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | KHV | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02083 | hp2 | a0001 | c0001 | t0004 | g0385 | EAS | KHV | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0044 | EAS | KHV | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02132 | hp2 | a0001 | c0001 | t0004 | g0355 | EAS | KHV | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | KHV | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02135 | hp2 | a0001 | c0001 | t0004 | g0377 | EAS | KHV | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02145 | hp1 | a0001 | c0001 | t0009 | g0078 | AFR | ACB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0237 | AFR | ACB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0276 | AMR | PEL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0200 | AMR | PEL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CDX | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02155 | hp2 | a0001 | c0001 | t0010 | g0206 | EAS | CDX | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0327 | AFR | ACB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0108 | AFR | ACB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02258 | hp1 | a0001 | c0001 | t0006 | g0105 | AFR | ACB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0329 | AFR | ACB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02451 | hp1 | a0001 | c0001 | t0008 | g0096 | AFR | ACB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | KHV | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0300 | AFR | GWD | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0021 | SAS | PJL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0297 | SAS | PJL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02615 | hp2 | a0001 | c0001 | t0006 | g0094 | AFR | GWD | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02647 | hp1 | a0001 | c0001 | t0008 | g0301 | AFR | GWD | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0312 | AFR | GWD | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0275 | SAS | PJL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0331 | AFR | GWD | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0165 | AFR | GWD | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02723 | hp1 | a0001 | c0001 | t0011 | g0149 | AFR | GWD | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0311 | AFR | GWD | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0235 | SAS | PJL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02735 | hp2 | a0001 | c0001 | t0004 | g0336 | SAS | PJL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0323 | SAS | PJL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0077 | SAS | PJL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02809 | hp1 | a0001 | c0001 | t0006 | g0102 | AFR | GWD | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0027 | AFR | GWD | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0167 | AFR | GWD | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0308 | AFR | GWD | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0019 | AFR | GWD | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0130 | AFR | GWD | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0024 | AFR | GWD | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0131 | AFR | GWD | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0046 | AFR | ESN | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02922 | hp2 | a0001 | c0001 | t0006 | g0100 | AFR | ESN | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | ESN | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0306 | AFR | ESN | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0390 | AFR | ESN | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02970 | hp2 | a0001 | c0001 | t0007 | g0315 | AFR | ESN | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02976 | hp1 | a0001 | c0001 | t0006 | g0103 | AFR | ESN | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0060 | SAS | PJL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0023 | AFR | GWD | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03041 | hp2 | a0001 | c0001 | t0007 | g0050 | AFR | GWD | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | MSL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | MSL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | ESN | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03130 | hp2 | a0001 | c0001 | t0009 | g0079 | AFR | ESN | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03139 | hp1 | a0001 | c0001 | t0006 | g0101 | AFR | ESN | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | ESN | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0314 | AFR | ESN | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03195 | hp2 | a0001 | c0001 | t0006 | g0095 | AFR | ESN | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03209 | hp1 | a0001 | c0001 | t0008 | g0104 | AFR | MSL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | MSL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0083 | AFR | MSL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0014 | AFR | MSL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0272 | SAS | PJL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0330 | AFR | MSL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | MSL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0017 | AFR | MSL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03486 | hp2 | a0001 | c0001 | t0007 | g0313 | AFR | MSL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0058 | 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 | g0181 | SAS | PJL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0304 | AFR | ESN | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0244 | 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 | g0088 | AFR | GWD | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0328 | AFR | MSL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0316 | SAS | PJL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0211 | SAS | PJL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0295 | SAS | STU | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0238 | SAS | STU | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0072 | SAS | PJL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0166 | SAS | PJL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0162 | SAS | PJL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0075 | SAS | BEB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0248 | SAS | BEB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03834 | hp1 | a0001 | c0001 | t0004 | g0335 | SAS | BEB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03834 | hp2 | a0001 | c0001 | t0005 | g0029 | SAS | BEB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03927 | hp1 | a0001 | c0001 | t0004 | g0381 | SAS | BEB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0291 | SAS | BEB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | BEB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0074 | SAS | BEB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | STU | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | STU | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | BEB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0190 | SAS | BEB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | STU | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0322 | SAS | STU | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0218 | SAS | STU | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | STU | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | YRI | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0393 | AFR | YRI | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18612 | hp1 | a0001 | c0001 | t0004 | g0371 | EAS | CHB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | CHB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | CHB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | CHB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0394 | AFR | YRI | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0305 | AFR | YRI | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18941 | hp1 | a0001 | c0001 | t0004 | g0366 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18943 | hp1 | a0001 | c0001 | t0004 | g0361 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18944 | hp1 | a0001 | c0001 | t0014 | g0289 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18949 | hp1 | a0001 | c0001 | t0004 | g0384 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18952 | hp1 | a0001 | c0001 | t0004 | g0370 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18953 | hp1 | a0001 | c0001 | t0005 | g0061 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18956 | hp2 | a0001 | c0001 | t0004 | g0372 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18959 | hp1 | a0001 | c0001 | t0004 | g0346 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0110 | 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 | g0274 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18962 | hp2 | a0001 | c0001 | t0005 | g0033 | 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 | g0003 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18964 | hp1 | a0001 | c0001 | t0004 | g0375 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18966 | hp1 | a0001 | c0001 | t0004 | g0383 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0049 | 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 | g0378 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18970 | hp1 | a0001 | c0001 | t0004 | g0349 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0392 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18971 | hp2 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0326 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18972 | hp2 | a0001 | c0001 | t0004 | g0365 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18975 | hp1 | a0001 | c0001 | t0004 | g0353 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18977 | hp1 | a0001 | c0001 | t0004 | g0387 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18979 | hp2 | a0001 | c0001 | t0004 | g0347 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18984 | hp1 | a0001 | c0001 | t0004 | g0382 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18986 | hp2 | a0001 | c0001 | t0004 | g0342 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18987 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18988 | hp2 | a0001 | c0001 | t0004 | g0348 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0299 | 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 | g0374 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0125 | 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 | g0324 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18998 | hp1 | a0001 | c0001 | t0004 | g0376 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18998 | hp2 | a0001 | c0001 | t0005 | g0016 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0217 | 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 | g0337 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19003 | hp1 | a0001 | c0001 | t0004 | g0344 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0389 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19005 | hp1 | a0001 | c0001 | t0005 | g0042 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19007 | hp2 | a0001 | c0001 | t0004 | g0345 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19009 | hp1 | a0001 | c0001 | t0004 | g0373 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19010 | hp1 | a0001 | c0001 | t0004 | g0012 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19030 | hp1 | a0001 | c0001 | t0009 | g0080 | AFR | LWK | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0030 | AFR | LWK | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19043 | hp1 | a0001 | c0004 | t0001 | g0302 | 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 | g0294 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19056 | hp2 | a0001 | c0001 | t0004 | g0351 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19059 | hp1 | a0001 | c0001 | t0005 | g0036 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19059 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19060 | hp1 | a0001 | c0001 | t0004 | g0354 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19063 | hp1 | a0001 | c0001 | t0005 | g0043 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0073 | 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 | g0011 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19066 | hp2 | a0001 | c0001 | t0004 | g0352 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0253 | 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 | g0205 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19076 | hp2 | a0001 | c0001 | t0004 | g0343 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0391 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19082 | hp1 | a0001 | c0001 | t0004 | g0338 | 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 | g0208 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0258 | 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 | g0018 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19088 | hp1 | a0001 | c0001 | t0004 | g0350 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19089 | hp1 | a0001 | c0001 | t0005 | g0055 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19091 | hp1 | a0001 | c0001 | t0004 | g0386 | 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 | g0303 | AFR | YRI | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0332 | AFR | YRI | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0307 | AFR | ASW | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ASW | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0281 | EUR | TSI | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0317 | EUR | TSI | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA20805 | hp1 | a0001 | c0001 | t0016 | g0380 | EUR | TSI | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0198 | EUR | TSI | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0022 | SAS | GIH | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0034 | SAS | GIH | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01123 | hp1 | a0001 | c0001 | t0004 | g0362 | AMR | CLM | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0161 | 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 | g0090 | AFR | ACB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG02559 | hp2 | a0001 | c0001 | t0011 | g0228 | AFR | ACB | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0076 | AFR | MSL | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0093 | 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 | g0219 | AFR | USA | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA20300 | hp1 | a0001 | c0001 | t0006 | g0106 | AFR | USA | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | USA | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | LWK | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | LWK | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0123 | REF | REF | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0194 | REF | REF | ATP1B3_chr3_141871643_141931549 | ATP1B3 | chr3 | 141871643 | 141931549 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:141876685 | C | G | 4 | a0001c0001t0004 a0001c0001t0016 a0001c0001t0017 others(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 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0016 |
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 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0018 |
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 | a0001c0001t0008 a0001c0001t0015 |
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 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(8): Show |
257 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(254): 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 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0008 others(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 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:141876945 | C | G | 2 | a0001c0001t0001g0393 a0001c0001t0001g0394 |
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 | a0001c0001t0001g0038 a0001c0001t0001g0045 a0001c0001t0001g0047 others(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 | a0001c0001t0001g0391 a0001c0001t0001g0392 |
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 | a0001c0001t0001g0392 | 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 | a0001c0001t0001g0038 a0001c0001t0001g0045 a0001c0001t0001g0047 others(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 | a0001c0001t0001g0081 a0001c0001t0009g0078 a0001c0001t0009g0079 others(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 | a0001c0001t0002g0390 | 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 | a0001c0001t0001g0389 | 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 | 57 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(54): 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 | a0001c0001t0002g0390 | 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 | a0001c0001t0001g0081 a0001c0001t0001g0328 a0001c0001t0001g0329 others(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 | a0001c0001t0003g0013 a0001c0001t0003g0014 |
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 | a0001c0001t0001g0316 a0001c0001t0001g0317 a0001c0001t0001g0318 others(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 | a0001c0001t0001g0098 a0001c0001t0006g0094 a0001c0001t0006g0095 others(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 | a0001c0001t0002g0327 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0082 a0001c0001t0001g0084 others(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 | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(142): 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 | 70 | a0001c0001t0001g0297 a0001c0001t0001g0298 a0001c0001t0001g0299 others(67): 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 | a0001c0001t0002g0305 a0001c0001t0003g0306 a0001c0001t0003g0307 others(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 | a0001c0002t0001g0303 a0001c0002t0001g0304 |
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 | a0001c0001t0003g0073 | 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 | a0001c0001t0004g0386 | 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 | a0001c0001t0001g0244 a0001c0001t0001g0245 |
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 | a0001c0001t0001g0246 | 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 | 225 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(222): 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 | 225 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(222): 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 | 57 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(54): 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 | a0001c0001t0003g0300 a0001c0001t0008g0301 a0001c0004t0001g0302 |
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 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0247 |
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 | a0001c0002t0001g0303 a0001c0002t0001g0304 |
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 | a0001c0001t0003g0072 | 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 | 57 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(54): 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 | a0001c0001t0001g0002 a0001c0001t0001g0082 a0001c0001t0001g0084 others(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 | 57 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(54): 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 | a0001c0001t0001g0081 a0001c0001t0001g0328 a0001c0001t0001g0329 others(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 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0247 |
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 | a0001c0001t0001g0038 a0001c0001t0001g0045 a0001c0001t0001g0047 others(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 | a0001c0001t0004g0334 | 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 | 70 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(67): 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 | a0001c0001t0001g0292 | 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 | a0001c0001t0002g0243 | 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 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0247 |
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 | a0001c0001t0004g0386 | 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 | a0001c0001t0007g0315 | 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 | a0001c0001t0001g0081 a0001c0001t0001g0328 a0001c0001t0001g0329 others(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 | a0001c0001t0002g0327 | 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 | a0001c0001t0002g0305 a0001c0001t0003g0108 a0001c0001t0003g0300 others(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 | a0001c0001t0001g0081 a0001c0001t0001g0328 a0001c0001t0001g0329 others(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 | a0001c0001t0004g0385 | 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 |
52 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(49): 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 | a0001c0001t0004g0335 a0001c0001t0004g0336 a0001c0001t0004g0337 others(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 | a0001c0001t0009g0078 | 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 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0077 others(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 | a0001c0001t0001g0038 a0001c0001t0001g0045 a0001c0001t0001g0047 others(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 |
75 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(72): 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 | a0001c0001t0001g0081 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0001g0098 a0001c0001t0001g0247 a0001c0001t0004g0385 others(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 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0003g0296 others(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 | 24 | a0001c0001t0001g0109 a0001c0001t0004g0012 a0001c0001t0004g0337 others(21): 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 | a0001c0001t0001g0038 a0001c0001t0001g0045 a0001c0001t0001g0047 others(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 | a0001c0001t0002g0390 a0001c0001t0003g0014 a0001c0001t0003g0017 others(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 | a0001c0001t0001g0082 a0001c0001t0001g0110 a0001c0001t0001g0111 others(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 | 53 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(50): 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 | a0001c0001t0002g0327 | 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 | a0001c0001t0003g0108 | 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 | a0001c0001t0002g0113 | 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 | a0001c0001t0016g0380 | 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 | a0001c0001t0001g0038 a0001c0001t0001g0045 a0001c0001t0001g0047 others(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 | a0001c0001t0001g0290 | 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 | a0001c0004t0001g0302 | 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 | a0001c0001t0001g0098 a0001c0001t0001g0109 a0001c0001t0006g0094 others(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 | 57 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(54): 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 | a0001c0001t0001g0219 | 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 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(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 | a0001c0001t0009g0079 a0001c0001t0009g0080 |
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 | a0001c0001t0001g0081 a0001c0001t0001g0119 a0001c0001t0001g0221 others(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 | a0001c0001t0001g0038 a0001c0001t0001g0045 a0001c0001t0001g0047 others(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 | a0001c0001t0014g0289 | 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 | a0001c0001t0002g0305 a0001c0001t0003g0108 a0001c0001t0003g0306 others(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 | a0001c0001t0001g0109 | 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 | a0001c0001t0002g0390 | 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 | a0001c0001t0005g0016 | 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 | a0001c0001t0002g0113 | 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 | a0001c0001t0002g0120 a0001c0001t0002g0121 |
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 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0247 |
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 | a0001c0001t0001g0081 a0001c0001t0009g0078 a0001c0001t0009g0079 others(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 | a0001c0001t0003g0015 a0001c0001t0003g0018 a0001c0001t0003g0051 others(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 | 345 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(342): Show |
355 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(352): 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 | a0001c0001t0007g0050 | 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 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0247 |
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 | a0001c0001t0004g0011 a0001c0001t0004g0342 a0001c0001t0004g0365 |
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 | a0001c0001t0003g0296 | 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 | a0001c0001t0001g0109 | 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 | a0001c0001t0003g0070 a0001c0001t0003g0071 |
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 | a0001c0001t0001g0089 | 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 | a0001c0001t0002g0390 a0001c0001t0003g0296 |
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 | a0001c0001t0001g0038 a0001c0001t0001g0045 a0001c0001t0001g0047 others(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 | a0001c0001t0001g0288 | 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 | a0001c0001t0001g0109 | 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 | a0001c0001t0001g0109 | 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 | a0001c0001t0002g0305 a0001c0001t0003g0108 a0001c0001t0003g0306 others(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 | a0001c0001t0002g0305 | 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 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0014g0289 |
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 | a0001c0001t0001g0082 a0001c0001t0002g0083 |
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 | a0001c0001t0001g0122 | 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 | a0001c0001t0002g0088 | 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 | a0001c0001t0002g0305 a0001c0001t0003g0108 a0001c0001t0003g0306 others(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 | 57 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(54): 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 | a0001c0001t0003g0300 a0001c0001t0008g0301 a0001c0004t0001g0302 |
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 | 57 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(54): 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 | a0001c0002t0001g0303 a0001c0002t0001g0304 |
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 | a0001c0001t0001g0285 | 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 | 57 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(54): 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 | a0001c0001t0006g0094 a0001c0001t0006g0100 a0001c0001t0006g0101 others(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 | a0001c0001t0003g0017 | 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 | 57 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(54): 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 | 142 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(139): 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 | a0001c0001t0001g0098 a0001c0001t0001g0109 a0001c0001t0006g0094 others(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 | a0001c0001t0001g0284 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0082 a0001c0001t0001g0084 others(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 | a0001c0002t0001g0303 a0001c0002t0001g0304 |
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 | a0001c0001t0001g0081 a0001c0001t0001g0328 a0001c0001t0001g0329 others(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 | a0001c0001t0001g0098 a0001c0001t0006g0094 a0001c0001t0006g0095 others(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 | 72 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(69): 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 | 57 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(54): 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 | a0001c0001t0001g0188 | 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 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0247 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0048 others(70): Show |
75 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(72): 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 | a0001c0001t0001g0001 a0001c0001t0001g0118 a0001c0001t0001g0127 others(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 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0146 others(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 | a0001c0001t0001g0117 a0001c0001t0001g0180 a0001c0001t0001g0226 others(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 | a0001c0001t0002g0189 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0045 a0001c0001t0001g0086 others(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 | a0001c0001t0001g0047 a0001c0001t0001g0142 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0119 a0001c0001t0002g0005 a0001c0001t0002g0008 others(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 | a0001c0001t0001g0081 a0001c0001t0001g0151 a0001c0001t0001g0159 others(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 | a0001c0001t0001g0328 a0001c0001t0001g0329 a0001c0001t0002g0305 others(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 | a0001c0001t0003g0022 | 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 | a0001c0001t0001g0252 a0001c0001t0001g0255 a0001c0001t0003g0015 others(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 | a0001c0001t0002g0190 | 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 | a0001c0001t0002g0218 a0001c0001t0003g0077 a0001c0001t0004g0379 others(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 | a0001c0001t0002g0305 a0001c0001t0003g0108 a0001c0001t0003g0306 others(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 | a0001c0001t0001g0222 | 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 | a0001c0001t0001g0109 | 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 | a0001c0001t0003g0049 | 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 | a0001c0001t0001g0186 a0001c0001t0001g0187 |
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 | a0001c0001t0002g0390 a0001c0001t0003g0296 |
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 | a0001c0001t0002g0250 | 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 | a0001c0001t0001g0185 | 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 | a0001c0001t0003g0021 a0001c0001t0003g0077 |
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 | a0001c0001t0002g0331 a0001c0001t0002g0332 a0001c0001t0002g0333 |
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 | a0001c0001t0006g0094 a0001c0001t0006g0100 a0001c0001t0006g0101 others(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 | a0001c0001t0001g0098 a0001c0001t0001g0109 a0001c0001t0006g0094 others(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 | a0001c0001t0001g0124 | 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 | 225 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(222): 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 | a0001c0001t0001g0221 | 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 | a0001c0001t0003g0108 a0001c0001t0003g0306 a0001c0001t0003g0307 others(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 | 57 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(54): 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 | a0001c0001t0001g0328 | 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 | 57 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(54): 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 | 55 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(52): 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 | a0001c0001t0001g0329 a0001c0001t0001g0330 |
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 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0247 |
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 | 72 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(69): 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 | a0001c0001t0002g0331 a0001c0001t0002g0332 a0001c0001t0002g0333 |
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 | a0001c0001t0001g0184 | 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 | a0001c0001t0001g0081 | 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 | a0001c0001t0003g0020 | 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 | a0001c0001t0001g0219 | 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 | a0001c0001t0001g0183 | 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 | a0001c0001t0001g0284 | 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 | a0001c0001t0002g0390 a0001c0002t0001g0303 a0001c0002t0001g0304 |
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 | a0001c0001t0001g0182 | 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 | 57 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(54): 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 | a0001c0001t0003g0067 | 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 | a0001c0001t0003g0020 | 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 | a0001c0001t0002g0390 | 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 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 |
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 | a0001c0001t0003g0014 | 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 | 57 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(54): 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 | a0001c0001t0001g0038 a0001c0001t0001g0045 a0001c0001t0001g0047 others(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 | a0001c0001t0001g0316 a0001c0001t0001g0317 a0001c0001t0001g0318 others(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 | a0001c0001t0001g0098 a0001c0001t0006g0094 a0001c0001t0006g0095 others(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 | a0001c0001t0001g0290 | 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 | a0001c0001t0001g0282 a0001c0001t0001g0283 |
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 | 55 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(52): 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 | a0001c0001t0001g0098 a0001c0001t0001g0109 a0001c0001t0006g0094 others(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 | a0001c0001t0001g0038 a0001c0001t0001g0045 a0001c0001t0001g0047 others(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 | a0001c0001t0001g0249 | 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 | a0001c0001t0001g0281 | 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 | a0001c0001t0001g0081 a0001c0001t0001g0328 a0001c0001t0001g0329 others(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 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(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 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0247 |
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 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0125 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(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 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0002g0004 others(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 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0174 others(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 | a0001c0001t0003g0058 a0001c0001t0003g0108 a0001c0001t0003g0306 others(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 | a0001c0001t0001g0038 a0001c0001t0003g0032 a0001c0001t0003g0034 others(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 | a0001c0001t0002g0327 | 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 | a0001c0001t0001g0329 a0001c0001t0001g0330 a0001c0001t0002g0331 others(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 | 4 | a0001c0001t0004g0012 a0001c0001t0004g0335 a0001c0001t0004g0347 others(1): 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 | a0001c0001t0002g0332 a0001c0001t0002g0333 a0001c0001t0004g0338 others(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 | a0001c0001t0004g0011 a0001c0001t0004g0334 a0001c0001t0004g0342 others(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 | a0001c0001t0001g0048 a0001c0001t0001g0081 a0001c0001t0001g0328 others(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 | a0001c0001t0002g0390 | 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 | a0001c0001t0001g0247 a0001c0001t0003g0296 a0001c0001t0004g0343 others(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 | 80 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0048 others(77): 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 | a0001c0001t0003g0300 a0001c0001t0008g0301 a0001c0004t0001g0302 |
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 | 119 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0048 others(116): 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 | a0001c0001t0001g0009 a0001c0001t0001g0246 a0001c0001t0001g0252 others(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 | a0001c0001t0001g0288 a0001c0001t0002g0217 a0001c0001t0002g0242 |
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 | a0001c0001t0001g0098 a0001c0001t0001g0393 a0001c0001t0001g0394 others(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 | a0001c0001t0006g0094 a0001c0001t0006g0100 a0001c0001t0006g0101 others(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 | 47 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(44): 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 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0327 others(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 | 14 | a0001c0001t0001g0009 a0001c0001t0001g0246 a0001c0001t0001g0252 others(11): 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 | a0001c0001t0001g0081 a0001c0001t0002g0130 a0001c0001t0002g0131 |
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 | a0001c0001t0001g0129 a0001c0001t0001g0329 a0001c0001t0001g0330 others(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 | a0001c0001t0001g0122 a0001c0001t0001g0138 a0001c0001t0001g0139 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0135 a0001c0001t0001g0136 others(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 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0132 others(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 | a0001c0001t0004g0385 | 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 | 69 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0114 others(66): 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 | a0001c0001t0001g0109 a0001c0001t0001g0127 a0001c0001t0001g0128 others(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 | a0001c0001t0001g0115 a0001c0001t0001g0186 a0001c0001t0001g0187 others(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 | a0001c0001t0002g0031 | 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 | a0001c0001t0003g0021 a0001c0001t0003g0030 a0001c0001t0003g0077 |
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 | a0001c0001t0001g0098 a0001c0001t0001g0393 a0001c0001t0001g0394 others(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 | 132 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0038 others(129): 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 | a0001c0001t0006g0094 a0001c0001t0006g0095 a0001c0001t0006g0100 others(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 | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(153): 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 | a0001c0001t0006g0103 | 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 | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(154): 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 | a0001c0001t0001g0038 a0001c0001t0001g0045 a0001c0001t0001g0047 others(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 | a0001c0001t0001g0038 a0001c0001t0001g0045 a0001c0001t0001g0047 others(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 | a0001c0001t0001g0038 a0001c0001t0001g0048 a0001c0001t0001g0098 others(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 | a0001c0001t0001g0048 a0001c0001t0002g0031 a0001c0001t0003g0021 others(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 | a0001c0001t0001g0048 a0001c0001t0002g0031 a0001c0001t0003g0021 others(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 | a0001c0001t0002g0031 a0001c0001t0003g0021 a0001c0001t0003g0030 others(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 | a0001c0001t0002g0031 a0001c0001t0003g0021 a0001c0001t0003g0030 others(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 | a0001c0001t0012g0257 | 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 | 58 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(55): 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 | a0001c0001t0001g0393 a0001c0001t0001g0394 a0001c0001t0002g0390 |
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 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0247 |
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 | 225 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(222): 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 | a0001c0001t0003g0027 | 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 | 57 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(54): 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 | a0001c0001t0001g0126 a0001c0001t0001g0144 a0001c0001t0001g0157 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0082 a0001c0001t0001g0085 others(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 | a0001c0001t0001g0038 a0001c0001t0001g0045 a0001c0001t0001g0047 others(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 | 74 | a0001c0001t0001g0328 a0001c0001t0001g0329 a0001c0001t0001g0330 others(71): 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 | a0001c0001t0001g0098 a0001c0001t0006g0095 a0001c0001t0006g0097 others(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 | a0001c0001t0006g0094 a0001c0001t0006g0099 a0001c0001t0006g0100 others(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 | 53 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(50): 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 | a0001c0001t0001g0145 | 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 | a0001c0001t0001g0038 a0001c0001t0001g0045 a0001c0001t0001g0047 others(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 | a0001c0001t0001g0109 a0001c0001t0003g0296 |
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 | a0001c0001t0001g0258 | 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 | a0001c0001t0004g0011 a0001c0001t0004g0342 a0001c0001t0004g0349 others(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 | a0001c0001t0002g0305 a0001c0001t0003g0108 a0001c0001t0003g0300 others(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 | a0001c0001t0002g0162 | 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 | a0001c0001t0001g0155 a0001c0001t0001g0164 a0001c0001t0001g0208 others(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 | a0001c0001t0002g0113 a0001c0001t0002g0156 a0001c0001t0002g0191 others(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 | 20 | a0001c0001t0001g0118 a0001c0001t0001g0122 a0001c0001t0001g0137 others(17): 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 | a0001c0001t0001g0003 a0001c0001t0001g0086 a0001c0001t0001g0090 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(37): Show |
41 | HG00280.hp2 HG00639.hp1 HG00733.hp2 others(38): 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 | a0001c0001t0001g0082 a0001c0001t0001g0110 a0001c0001t0001g0393 others(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 | a0001c0001t0001g0047 a0001c0001t0001g0087 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0038 a0001c0001t0001g0045 a0001c0001t0001g0048 others(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 | 16 | a0001c0001t0001g0009 a0001c0001t0001g0254 a0001c0001t0001g0255 others(13): 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 | 67 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0248 others(64): 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 | 51 | a0001c0001t0001g0249 a0001c0001t0001g0260 a0001c0001t0001g0261 others(48): 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 | a0001c0001t0001g0081 a0001c0001t0001g0328 a0001c0001t0001g0329 others(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 | a0001c0001t0009g0078 a0001c0001t0009g0079 a0001c0001t0009g0080 |
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 | a0001c0001t0002g0204 | 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 | a0001c0001t0003g0059 | 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 | a0001c0001t0001g0259 a0001c0001t0003g0296 |
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 | a0001c0001t0002g0390 | 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 | a0001c0001t0001g0158 a0001c0001t0002g0162 a0001c0001t0002g0323 |
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 | a0001c0001t0001g0245 a0001c0001t0001g0247 |
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 | a0001c0001t0001g0244 a0001c0002t0001g0303 |
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 | a0001c0002t0001g0304 | 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 | a0001c0001t0003g0017 a0001c0001t0015g0026 |
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 | a0001c0001t0001g0047 a0001c0001t0002g0031 a0001c0001t0003g0025 others(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 | a0001c0001t0001g0038 a0001c0001t0001g0045 a0001c0001t0001g0048 others(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 | a0001c0001t0003g0059 | 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 | a0001c0001t0002g0305 a0001c0001t0003g0108 a0001c0001t0003g0300 others(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 | a0001c0001t0002g0293 | 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 | a0001c0001t0002g0293 | 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 | a0001c0001t0001g0081 a0001c0001t0001g0328 a0001c0001t0001g0329 others(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 | a0001c0002t0001g0303 a0001c0002t0001g0304 |
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 | 57 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(54): 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 | 57 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(54): 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 | a0001c0001t0001g0188 | 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 | a0001c0001t0004g0372 | 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 | a0001c0001t0002g0390 a0001c0001t0003g0296 |
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 | 142 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(139): 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 | 72 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(69): 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 | a0001c0001t0002g0293 | 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 | a0001c0001t0003g0093 | 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 | a0001c0001t0001g0038 a0001c0001t0001g0045 a0001c0001t0001g0047 others(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 | 225 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(222): 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 | 57 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(54): 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 | 57 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(54): 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 | a0001c0001t0001g0393 a0001c0001t0001g0394 |
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 | 55 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(52): 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 | a0001c0001t0001g0002 a0001c0001t0001g0082 a0001c0001t0001g0084 others(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 | 240 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(237): 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 | a0001c0001t0001g0287 | 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 | a0001c0001t0004g0362 | 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 | a0001c0001t0003g0049 | 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0221 | 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 | a0001c0001t0001g0262 | 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 | a0001c0001t0001g0262 | 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 | a0001c0001t0001g0262 | 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 | a0001c0001t0003g0074 | 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 | a0001c0001t0003g0039 | 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 | a0001c0001t0001g0284 | 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 | 57 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(54): 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 | a0001c0001t0001g0081 a0001c0001t0001g0328 a0001c0001t0001g0329 others(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 | a0001c0001t0001g0114 a0001c0001t0001g0126 a0001c0001t0001g0145 others(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 | 43 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(40): 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 | a0001c0001t0001g0252 a0001c0001t0001g0263 a0001c0001t0001g0264 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0048 a0001c0001t0001g0081 others(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 | a0001c0001t0001g0038 a0001c0001t0001g0045 a0001c0001t0001g0047 others(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 | a0001c0001t0001g0244 a0001c0001t0001g0247 a0001c0001t0001g0330 others(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 | 52 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(49): 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 | a0001c0001t0003g0021 a0001c0001t0003g0077 |
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 | a0001c0001t0002g0210 | 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 | 57 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(54): 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 | a0001c0001t0003g0296 | 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 | 240 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(237): 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 | a0001c0001t0002g0004 a0001c0003t0002g0168 a0001c0003t0002g0169 |
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 | a0001c0001t0001g0393 a0001c0001t0001g0394 |
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 | a0001c0001t0012g0257 | 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 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0247 |
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 | 57 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(54): 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 | 57 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(54): 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 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0247 |
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 | 225 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(222): 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 | a0001c0001t0002g0305 a0001c0001t0003g0108 a0001c0001t0003g0300 others(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 | a0001c0001t0001g0182 a0001c0001t0001g0233 |
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 | 57 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(54): 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 | a0001c0001t0003g0040 | 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 | a0001c0001t0002g0305 | 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 | a0001c0001t0001g0393 a0001c0001t0001g0394 |
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 | a0001c0001t0001g0155 a0001c0001t0001g0222 a0001c0001t0001g0232 |
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 | 240 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(237): 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 | a0001c0001t0002g0305 a0001c0001t0003g0108 a0001c0001t0003g0300 others(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 | 53 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(50): 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 | a0001c0001t0003g0019 | 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 | 74 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(71): 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 | a0001c0001t0003g0300 a0001c0001t0008g0301 a0001c0004t0001g0302 |
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 | a0001c0001t0001g0145 | 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 | a0001c0001t0003g0296 | 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 | a0001c0001t0001g0109 | 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 | 55 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(52): 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 | a0001c0001t0001g0254 a0001c0001t0001g0263 |
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 | 241 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(238): 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 | a0001c0001t0001g0098 a0001c0001t0001g0109 a0001c0001t0001g0188 others(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 | a0001c0001t0001g0119 a0001c0001t0001g0129 a0001c0001t0001g0135 others(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 | 55 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(52): 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 | a0001c0001t0005g0339 | 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 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0014g0289 |
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 | a0001c0001t0001g0038 a0001c0001t0001g0045 a0001c0001t0001g0047 others(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 | a0001c0001t0001g0329 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0085 others(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 | a0001c0001t0001g0038 a0001c0001t0001g0045 a0001c0001t0001g0047 others(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 | 57 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(54): 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 | a0001c0001t0001g0273 a0001c0001t0001g0279 a0001c0001t0001g0288 others(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 | a0001c0001t0002g0166 a0001c0001t0002g0171 a0001c0001t0002g0243 |
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 | a0001c0001t0001g0160 a0001c0001t0001g0295 a0001c0001t0002g0156 |
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 | a0001c0001t0001g0098 a0001c0001t0006g0094 a0001c0001t0006g0095 others(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 | a0001c0001t0001g0081 a0001c0001t0001g0328 a0001c0001t0001g0329 others(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 | a0001c0001t0001g0038 a0001c0001t0001g0045 a0001c0001t0001g0047 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0081 a0001c0001t0001g0084 others(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 | a0001c0001t0002g0305 a0001c0001t0003g0108 a0001c0001t0003g0306 others(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 | a0001c0001t0001g0082 a0001c0001t0002g0083 a0001c0001t0002g0088 |
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 | a0001c0001t0001g0038 a0001c0001t0001g0045 a0001c0001t0001g0047 others(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 | a0001c0001t0001g0275 | 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 | a0001c0001t0003g0300 | 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 | a0001c0001t0003g0072 | 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 | 55 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(52): 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 | a0001c0001t0002g0390 | 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 | 241 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(238): 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 | a0001c0001t0003g0296 | 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 | a0001c0001t0002g0005 a0001c0001t0002g0008 a0001c0001t0002g0189 others(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 | 57 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(54): 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 | 4 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0277 others(1): 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 | a0001c0001t0003g0306 a0001c0001t0003g0307 a0001c0001t0003g0312 |
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 | 72 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(69): 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 | 57 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(54): 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 | a0001c0001t0001g0002 a0001c0001t0001g0082 a0001c0001t0001g0084 others(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 | a0001c0001t0002g0113 | 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 | a0001c0001t0001g0316 a0001c0001t0001g0317 a0001c0001t0001g0318 others(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 | a0001c0001t0003g0013 | 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 | 57 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(54): 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 | a0001c0001t0004g0345 | 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 | a0001c0002t0001g0303 a0001c0002t0001g0304 |
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 | a0001c0001t0002g0390 | 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 | a0001c0001t0003g0020 a0001c0001t0003g0057 |
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 | 72 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(69): 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 | a0001c0001t0004g0371 | 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 | a0001c0001t0002g0192 | 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 | a0001c0001t0001g0098 a0001c0001t0001g0109 a0001c0001t0006g0094 others(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 | a0001c0001t0001g0125 a0001c0001t0001g0225 |
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 | a0001c0001t0001g0098 a0001c0001t0006g0094 a0001c0001t0006g0095 others(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 | a0001c0001t0003g0060 | 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 | 72 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(69): 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 | 57 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(54): 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 | 72 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(69): 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 | a0001c0001t0001g0285 | 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 | 88 | a0001c0001t0001g0081 a0001c0001t0001g0244 a0001c0001t0001g0245 others(85): 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 | a0001c0001t0001g0181 | 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 | a0001c0001t0001g0232 | 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 | a0001c0001t0004g0352 | 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 | 55 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(52): 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 | a0001c0001t0001g0184 | 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 | a0001c0001t0002g0390 | 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 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0247 |
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 | a0001c0001t0001g0081 a0001c0001t0001g0328 a0001c0001t0001g0329 others(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 | a0001c0001t0001g0254 | 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 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0247 |
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 | a0001c0001t0001g0081 a0001c0001t0001g0328 a0001c0001t0001g0329 others(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 | a0001c0001t0001g0098 a0001c0001t0006g0094 a0001c0001t0006g0095 others(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 | 57 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(54): 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 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0247 |
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 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0247 |
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 | a0001c0001t0003g0014 | 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 | a0001c0001t0001g0248 | 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 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0247 |
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 | a0001c0001t0001g0146 | 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 | 57 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(54): 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 | a0001c0001t0003g0017 a0001c0001t0003g0024 a0001c0001t0003g0046 others(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 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0247 |
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 | a0001c0001t0011g0228 | 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 | 57 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(54): 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 | a0001c0001t0001g0081 a0001c0001t0001g0328 a0001c0001t0001g0329 others(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 | a0001c0001t0003g0108 a0001c0001t0003g0165 a0001c0001t0003g0306 others(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 | a0001c0001t0001g0279 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0082 a0001c0001t0001g0084 others(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 | a0001c0001t0002g0305 | 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 | a0001c0001t0001g0081 a0001c0001t0001g0328 a0001c0001t0001g0329 others(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 | a0001c0001t0006g0094 a0001c0001t0006g0100 a0001c0001t0006g0101 others(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 | a0001c0001t0001g0128 | 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 | a0001c0001t0003g0300 a0001c0001t0008g0301 |
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 | a0001c0002t0001g0303 a0001c0002t0001g0304 |
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 | a0001c0001t0001g0393 a0001c0001t0001g0394 |
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 | a0001c0001t0001g0081 a0001c0001t0009g0078 a0001c0001t0009g0079 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0082 a0001c0001t0001g0084 others(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 | a0001c0001t0003g0308 a0001c0001t0003g0309 |
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 | a0001c0001t0001g0109 | 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 | a0001c0001t0003g0028 a0001c0001t0003g0035 a0001c0001t0003g0039 others(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 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0247 |
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 | a0001c0001t0002g0195 | 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 | a0001c0001t0001g0038 a0001c0001t0001g0045 a0001c0001t0001g0047 others(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 | 238 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(235): 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 | a0001c0001t0001g0098 a0001c0001t0002g0031 a0001c0001t0006g0094 others(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 | 57 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(54): 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 | a0001c0001t0002g0327 | 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 | 238 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(235): 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 | a0001c0001t0005g0016 a0001c0001t0005g0033 a0001c0001t0005g0036 others(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 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0003g0023 |
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 | a0001c0001t0002g0390 | 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 | a0001c0001t0003g0015 a0001c0001t0003g0018 a0001c0001t0003g0020 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0110 a0001c0001t0001g0111 others(103): Show |
108 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(105): 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 | a0001c0001t0001g0281 | 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 | 72 | a0001c0001t0001g0098 a0001c0001t0002g0031 a0001c0001t0004g0011 others(69): 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 | a0001c0001t0001g0098 a0001c0001t0002g0031 a0001c0001t0006g0094 others(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 | a0001c0001t0003g0035 | 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 | a0001c0001t0001g0393 a0001c0001t0001g0394 |
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 | 168 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(165): 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 | a0001c0001t0001g0081 | 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 | 238 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(235): 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 | a0001c0001t0001g0038 a0001c0001t0001g0045 a0001c0001t0001g0047 others(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 | 81 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0098 others(78): 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 | a0001c0001t0001g0010 a0001c0001t0001g0251 a0001c0001t0001g0265 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0082 a0001c0001t0001g0084 others(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 | a0001c0001t0001g0090 a0001c0001t0002g0088 a0001c0001t0004g0336 others(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 | 36 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(33): 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 | a0001c0001t0004g0337 a0001c0001t0004g0346 a0001c0001t0004g0355 others(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 | a0001c0001t0001g0109 a0001c0001t0001g0150 a0001c0001t0002g0004 others(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 | a0001c0001t0001g0038 a0001c0001t0001g0045 a0001c0001t0001g0047 others(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 | a0001c0001t0001g0224 | 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 | a0001c0001t0001g0081 | 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 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0247 |
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 | a0001c0004t0001g0302 | 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 | 69 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(66): 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 | a0001c0001t0001g0038 a0001c0001t0001g0045 a0001c0001t0001g0047 others(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 | a0001c0001t0003g0300 a0001c0001t0008g0301 |
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 | a0001c0001t0002g0215 | 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 | a0001c0001t0001g0275 | 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 | 53 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(50): 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 | a0001c0001t0001g0256 a0001c0001t0001g0274 |
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 | a0001c0001t0001g0184 a0001c0001t0003g0165 |
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 | a0001c0001t0002g0004 a0001c0001t0002g0120 a0001c0001t0002g0121 others(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 | a0001c0001t0007g0310 a0001c0001t0007g0313 |
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 | 57 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(54): 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 | 54 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(51): 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 | a0001c0001t0001g0328 | 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 | a0001c0001t0003g0108 a0001c0001t0003g0300 a0001c0001t0003g0306 others(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 | a0001c0001t0001g0264 | 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 | a0001c0001t0004g0383 | 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 | 57 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(54): 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 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0247 |
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 | a0001c0001t0003g0025 | 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 | a0001c0001t0001g0328 | 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 | a0001c0001t0001g0272 | 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 | 238 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(235): 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 | 57 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(54): 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 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0247 |
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 | a0001c0001t0001g0038 a0001c0001t0001g0045 a0001c0001t0001g0047 others(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 | a0001c0001t0001g0081 a0001c0001t0001g0328 a0001c0001t0001g0329 others(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 | 58 | a0001c0001t0001g0224 a0001c0001t0004g0011 a0001c0001t0004g0012 others(55): 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 | a0001c0001t0004g0338 a0001c0001t0004g0369 a0001c0001t0004g0371 others(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 | a0001c0001t0003g0300 a0001c0001t0008g0301 |
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 | a0001c0001t0001g0295 | 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 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0247 |
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 | 57 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(54): 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 | a0001c0001t0001g0153 | 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 | 81 | a0001c0001t0001g0002 a0001c0001t0001g0082 a0001c0001t0001g0084 others(78): 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 | 58 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(55): 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 | a0001c0001t0001g0038 a0001c0001t0001g0045 a0001c0001t0001g0047 others(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 | a0001c0001t0003g0044 a0001c0001t0003g0108 a0001c0001t0003g0306 others(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 | a0001c0001t0003g0300 a0001c0001t0008g0301 |
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 | a0001c0001t0004g0379 | 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 | a0001c0001t0002g0326 | 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 | 54 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(51): 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 | a0001c0001t0001g0081 a0001c0001t0001g0328 a0001c0001t0001g0329 others(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 | a0001c0001t0001g0328 | 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 | a0001c0001t0001g0271 a0001c0001t0001g0280 a0001c0001t0001g0288 |
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 | a0001c0001t0003g0322 | 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 | a0001c0001t0002g0171 | 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 | a0001c0001t0001g0038 a0001c0001t0001g0045 a0001c0001t0001g0047 others(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 | 57 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(54): 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 | a0001c0001t0004g0386 | 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 | a0001c0001t0001g0038 a0001c0001t0003g0017 a0001c0001t0003g0024 others(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 | a0001c0001t0001g0393 a0001c0001t0001g0394 |
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 | 54 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(51): 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 | a0001c0001t0003g0312 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0082 a0001c0001t0001g0084 others(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 | a0001c0001t0001g0038 a0001c0001t0001g0045 a0001c0001t0001g0047 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0082 a0001c0001t0001g0084 others(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 | a0001c0001t0001g0174 | 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 | a0001c0001t0003g0020 | 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 | a0001c0001t0001g0038 a0001c0001t0001g0045 a0001c0001t0001g0047 others(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 | a0001c0001t0004g0381 a0001c0001t0016g0380 |
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 | a0001c0001t0001g0249 a0001c0001t0001g0261 a0001c0001t0001g0266 |
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 | a0001c0001t0003g0058 a0001c0001t0003g0060 a0001c0001t0003g0062 others(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 | a0001c0001t0001g0081 a0001c0001t0001g0328 a0001c0001t0001g0329 others(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 | 238 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(235): Show |
246 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(243): 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 | a0001c0001t0001g0267 a0001c0001t0001g0317 a0001c0001t0001g0318 others(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 | a0001c0001t0001g0098 a0001c0001t0001g0208 a0001c0001t0001g0265 others(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 | a0001c0001t0001g0038 a0001c0001t0001g0045 a0001c0001t0001g0047 others(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 | a0001c0001t0003g0300 a0001c0001t0008g0301 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0082 a0001c0001t0001g0084 others(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 | a0001c0001t0001g0319 | 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 | 165 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(162): Show |
171 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(168): 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 | a0001c0001t0002g0331 a0001c0001t0002g0332 a0001c0001t0002g0333 |
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 | a0001c0001t0001g0272 | 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 | a0001c0001t0001g0119 a0001c0001t0002g0112 a0001c0001t0002g0190 others(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 | a0001c0001t0001g0081 a0001c0001t0001g0174 a0001c0001t0001g0329 others(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 | 63 | a0001c0001t0001g0187 a0001c0001t0004g0011 a0001c0001t0004g0012 others(60): 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 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0082 others(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 | a0001c0001t0001g0188 | 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 | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(186): Show |
196 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(193): 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 | a0001c0001t0001g0124 a0001c0001t0001g0128 a0001c0001t0001g0129 others(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 | a0001c0001t0001g0393 a0001c0001t0001g0394 a0001c0001t0002g0004 others(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 | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(163): Show |
173 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(170): 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 | a0001c0001t0006g0100 a0001c0001t0006g0101 |
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 | a0001c0001t0001g0081 a0001c0001t0002g0004 a0001c0001t0002g0120 others(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 | a0001c0001t0001g0330 | 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 | a0001c0001t0001g0264 | 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 | 191 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(188): Show |
198 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.347-1557A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141912095 | |||||||
| chr3:141912096 | C | G | 191 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(188): Show |
198 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.347-1556C>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 3/6 | chr3 | 141912096 | |||||||
| chr3:141912201 | AT | A | 348 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(345): Show |
358 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(355): 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 | a0001c0001t0003g0034 a0001c0001t0003g0075 |
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 | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(186): Show |
196 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(193): 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 | 63 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(60): 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 | 348 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(345): Show |
358 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(355): 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 | a0001c0001t0003g0062 a0001c0001t0003g0070 a0001c0001t0003g0071 |
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 | a0001c0001t0001g0229 a0001c0001t0011g0149 a0001c0001t0011g0228 |
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 | a0001c0001t0003g0013 | 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 | 63 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(60): 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 | a0001c0001t0001g0081 | 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 | a0001c0001t0003g0053 | 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 | a0001c0001t0002g0171 | 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 | 63 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(60): 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 | a0001c0001t0001g0265 a0001c0001t0002g0031 a0001c0001t0002g0250 others(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 | 63 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(60): 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 | 63 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(60): 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 | 63 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(60): 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 | a0001c0001t0002g0210 | 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 | 62 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(59): 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 | 61 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(58): 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 | a0001c0001t0014g0289 | 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 | a0001c0001t0001g0265 a0001c0001t0002g0031 a0001c0001t0002g0250 others(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 | a0001c0001t0001g0219 | 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 | a0001c0001t0001g0224 | 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 | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(157): Show |
167 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(164): 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 | 61 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(58): 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 | a0001c0001t0002g0203 | 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 | a0001c0001t0004g0387 | 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 | a0001c0001t0001g0155 | 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 | a0001c0001t0004g0381 | 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 | a0001c0001t0002g0305 a0001c0001t0007g0310 |
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 | a0001c0001t0002g0203 | 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 | a0001c0001t0002g0004 a0001c0001t0002g0083 a0001c0001t0002g0120 others(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 | a0001c0001t0002g0004 a0001c0003t0002g0168 a0001c0003t0002g0169 |
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 | a0001c0001t0004g0366 | 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 | a0001c0001t0002g0004 a0001c0001t0002g0083 a0001c0001t0002g0088 others(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 | a0001c0001t0001g0271 | 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 | a0001c0001t0005g0055 | 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 | a0001c0001t0001g0048 a0001c0001t0001g0393 a0001c0001t0001g0394 |
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 | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(160): Show |
170 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(167): 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 | a0001c0001t0002g0004 a0001c0001t0002g0083 a0001c0001t0002g0088 others(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 | a0001c0001t0001g0048 a0001c0001t0001g0393 a0001c0001t0001g0394 others(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 | a0001c0001t0002g0390 | 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 | a0001c0001t0001g0125 a0001c0001t0001g0223 a0001c0001t0001g0316 others(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 | 259 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(256): 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 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(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 | a0001c0001t0002g0199 | 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 | a0001c0001t0003g0013 a0001c0001t0003g0014 |
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 | a0001c0001t0008g0096 a0001c0001t0008g0104 a0001c0001t0008g0301 others(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 | a0001c0001t0001g0110 a0001c0001t0001g0132 a0001c0001t0001g0223 |
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 | a0001c0001t0002g0031 a0001c0001t0002g0250 a0001c0001t0002g0270 others(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 | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(180): Show |
190 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(187): 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 | a0001c0001t0008g0096 a0001c0001t0008g0104 a0001c0001t0008g0301 |
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 | a0001c0001t0001g0297 | 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 | a0001c0001t0003g0013 a0001c0001t0003g0014 |
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 | a0001c0001t0008g0096 a0001c0001t0008g0104 a0001c0001t0008g0301 others(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 | 348 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(345): Show |
358 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(355): Show |
intron_variant | MODIFIER | c.582+1668A>G | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141917688 | |||||||
| chr3:141917776 | T | A | 63 | a0001c0001t0002g0390 a0001c0001t0003g0060 a0001c0001t0004g0011 others(60): 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 | a0001c0001t0006g0105 | 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 | a0001c0001t0003g0015 a0001c0001t0003g0018 a0001c0001t0003g0020 others(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 | a0001c0001t0002g0390 | 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 | a0001c0001t0002g0171 a0001c0001t0002g0243 |
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 | a0001c0001t0004g0360 | 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 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(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 | a0001c0001t0002g0390 | 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 | a0001c0001t0001g0285 | 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 | a0001c0001t0001g0125 a0001c0001t0001g0225 |
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 | 62 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(59): 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 | a0001c0001t0002g0203 | 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 | a0001c0001t0001g0081 a0001c0001t0001g0124 a0001c0001t0001g0249 others(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 | a0001c0001t0002g0031 a0001c0001t0002g0250 a0001c0001t0002g0270 others(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 | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(277): Show |
288 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(285): Show |
intron_variant | MODIFIER | c.582+2576G>A | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 5/6 | chr3 | 141918596 | |||||||
| chr3:141918684 | T | C | 344 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(341): Show |
354 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(351): 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 | a0001c0001t0003g0074 | 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 | a0001c0001t0010g0205 a0001c0001t0010g0206 |
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 | a0001c0001t0002g0390 | 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 | a0001c0001t0001g0048 | 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 | a0001c0001t0001g0185 | 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 | 63 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(60): 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 | a0001c0001t0002g0004 a0001c0001t0002g0083 a0001c0001t0002g0088 others(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 | a0001c0001t0003g0049 | 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 | a0001c0001t0001g0230 | 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 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(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 | a0001c0001t0002g0004 a0001c0001t0002g0083 a0001c0001t0002g0088 others(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 | a0001c0001t0002g0083 a0001c0001t0002g0088 |
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 | a0001c0001t0001g0278 | 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 | a0001c0001t0001g0183 | 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 | a0001c0001t0009g0078 a0001c0001t0009g0079 a0001c0001t0009g0080 |
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 | a0001c0001t0003g0049 | 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 | a0001c0001t0002g0004 a0001c0001t0002g0083 a0001c0001t0002g0088 others(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 | a0001c0001t0001g0182 a0001c0001t0001g0273 a0001c0001t0001g0279 others(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 | a0001c0001t0002g0113 | 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 | 348 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(345): Show |
358 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(355): 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 | a0001c0001t0002g0390 | 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 | a0001c0001t0002g0031 | 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 | a0001c0001t0001g0281 | 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 | a0001c0001t0003g0032 a0001c0001t0003g0037 |
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 | a0001c0001t0001g0110 a0001c0001t0001g0132 a0001c0001t0001g0223 |
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 | a0001c0001t0003g0027 | 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 | 63 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(60): 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 | 63 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(60): 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 | a0001c0001t0002g0031 a0001c0001t0002g0250 a0001c0001t0002g0270 others(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 | a0001c0001t0003g0019 | 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 | 63 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(60): 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 | a0001c0001t0011g0149 a0001c0001t0011g0228 |
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 | a0001c0001t0001g0119 a0001c0001t0002g0005 a0001c0001t0002g0008 others(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 | a0001c0001t0003g0019 | 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 | 63 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(60): 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 | a0001c0001t0001g0145 | 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 | a0001c0001t0001g0153 | 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 | a0001c0001t0001g0153 | 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 | 63 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(60): 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 | a0001c0001t0003g0093 | 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 | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(155): Show |
165 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(162): 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 | a0001c0001t0003g0015 a0001c0001t0003g0018 a0001c0001t0003g0051 others(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 | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(160): Show |
170 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(167): 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 | a0001c0001t0001g0153 | 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 | a0001c0001t0002g0332 | 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 | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
188 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(185): 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 | a0001c0001t0002g0004 a0001c0001t0002g0120 a0001c0001t0002g0121 others(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 | 63 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(60): 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 | 63 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(60): 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 | a0001c0001t0001g0143 | 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 | a0001c0001t0001g0272 | 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 | 348 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(345): Show |
358 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(355): 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 | a0001c0001t0001g0081 | 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 | a0001c0001t0002g0210 | 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 | 63 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(60): 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 | a0001c0001t0001g0082 | 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 | a0001c0001t0004g0374 | 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 | a0001c0001t0002g0004 a0001c0001t0002g0083 a0001c0001t0002g0088 others(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 | a0001c0001t0010g0205 | 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 | a0001c0001t0010g0205 | 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 | a0001c0001t0006g0094 a0001c0001t0006g0102 |
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 | a0001c0001t0008g0096 a0001c0001t0008g0104 a0001c0001t0008g0301 others(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 | 63 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(60): 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 | a0001c0001t0001g0161 | 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 | 265 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(262): Show |
275 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(272): 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 | 63 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(60): 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 | a0001c0001t0004g0347 | 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 | 63 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(60): 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 | 63 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(60): 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 | a0001c0001t0002g0203 | 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 | a0001c0001t0001g0048 a0001c0001t0001g0393 a0001c0001t0001g0394 others(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 | a0001c0001t0002g0390 | 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 | 63 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(60): 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 | a0001c0004t0001g0302 | 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 | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(180): Show |
190 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(187): 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 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(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 | a0001c0001t0001g0147 | 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 | a0001c0001t0002g0390 | 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 | a0001c0001t0001g0208 | 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 | 279 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(276): Show |
287 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(284): 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 | a0001c0001t0001g0081 | 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 | a0001c0001t0002g0004 a0001c0001t0002g0083 a0001c0001t0002g0088 others(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 | 317 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(314): Show |
327 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(324): 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 | a0001c0001t0001g0139 a0001c0001t0001g0142 a0001c0001t0001g0145 |
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 | a0001c0001t0003g0028 a0001c0001t0003g0032 a0001c0001t0003g0034 others(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 | a0001c0001t0009g0078 a0001c0001t0009g0079 a0001c0001t0009g0080 |
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 | a0001c0001t0002g0004 a0001c0001t0002g0083 a0001c0001t0002g0088 others(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 | a0001c0001t0002g0171 | 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 | a0001c0001t0003g0074 | 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 | a0001c0001t0001g0256 | 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 | a0001c0001t0001g0159 | 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 | a0001c0004t0001g0302 | 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 | 347 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(344): Show |
357 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(354): 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 | a0001c0001t0002g0192 | 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 | a0001c0001t0002g0031 a0001c0001t0002g0250 a0001c0001t0002g0270 others(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 | 63 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0334 others(60): 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 | a0001c0001t0008g0096 a0001c0001t0008g0104 a0001c0001t0008g0301 |
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 | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(277): Show |
288 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(285): 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 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(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 | 279 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(276): Show |
287 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(284): 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 | a0001c0001t0003g0066 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.670-95C>T | ATP1B3 | ENSG00000069849.11 | transcript | ENST00000286371.8 | protein_coding | 6/6 | chr3 | 141925436 |