Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 492 |
| ensemblid | ENSG00000067842.19 |
| hgncid | 816 |
| symbol | ATP2B3 |
| name | ATPase plasma membrane Ca2+ transporting 3 |
| refseq_nuc | NM_001001344.3 |
| refseq_prot | NP_001001344.1 |
| ensembl_nuc | ENST00000263519.5 |
| ensembl_prot | ENSP00000263519.4 |
| mane_status | MANE Select |
| chr | chrX |
| start | 153517642 |
| end | 153582929 |
| strand | + |
| ver | v1.2 |
| region | chrX:153517642-153582929 |
| region5000 | chrX:153512642-153587929 |
| regionname0 | ATP2B3_chrX_153517642_153582929 |
| regionname5000 | ATP2B3_chrX_153512642_153587929 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1220 | 264 | 75 | 44 | 106 | 7 | 30 | 79 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | MGDMA others(1215): Show |
chrX | 153512642 | 153587929 |
| a0002 | 0/0 | 1220 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | MGDMA others(1215): Show |
chrX | 153512642 | 153587929 |
| a0003 | 0/0 | 1220 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | MGDMA others(1215): Show |
chrX | 153512642 | 153587929 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 3660 | 121 | 49 | 16 | 36 | 5 | 15 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | ATGGG others(3655): Show |
chrX | 153512642 | 153587929 | ||
| a0001c0002 | 0/1 | 3660 | 113 | 5 | 25 | 67 | 1 | 14 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | ATGGG others(3655): Show |
chrX | 153512642 | 153587929 | ||
| a0001c0003 | 0/0 | 3660 | 12 | 10 | 2 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | ATGGG others(3655): Show |
chrX | 153512642 | 153587929 | ||
| a0001c0004 | 1/0 | 3660 | 4 | 2 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | ATGGG others(3655): Show |
chrX | 153512642 | 153587929 | ||
| a0001c0005 | 0/0 | 3660 | 2 | 2 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | ATGGG others(3655): Show |
chrX | 153512642 | 153587929 | ||
| a0001c0007 | 0/0 | 3660 | 2 | 0 | 0 | 2 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | ATGGG others(3655): Show |
chrX | 153512642 | 153587929 | ||
| a0001c0008 | 0/0 | 3660 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | ATGGG others(3655): Show |
chrX | 153512642 | 153587929 | ||
| a0001c0010 | 0/0 | 3660 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | ATGGG others(3655): Show |
chrX | 153512642 | 153587929 | ||
| a0001c0011 | 0/0 | 3660 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | ATGGG others(3655): Show |
chrX | 153512642 | 153587929 | ||
| a0001c0012 | 0/0 | 3660 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | ATGGG others(3655): Show |
chrX | 153512642 | 153587929 | ||
| a0001c0013 | 0/0 | 3660 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | ATGGG others(3655): Show |
chrX | 153512642 | 153587929 | ||
| a0001c0014 | 0/0 | 3660 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | ATGGG others(3655): Show |
chrX | 153512642 | 153587929 | ||
| a0001c0015 | 0/0 | 3660 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | ATGGG others(3655): Show |
chrX | 153512642 | 153587929 | ||
| a0001c0016 | 0/0 | 3660 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | ATGGG others(3655): Show |
chrX | 153512642 | 153587929 | ||
| a0001c0017 | 0/0 | 3660 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | ATGGG others(3655): Show |
chrX | 153512642 | 153587929 | ||
| a0001c0018 | 0/0 | 3660 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | ATGGG others(3655): Show |
chrX | 153512642 | 153587929 | ||
| a0002c0006 | 0/0 | 3660 | 2 | 0 | 0 | 2 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | ATGGG others(3655): Show |
chrX | 153512642 | 153587929 | ||
| a0003c0009 | 0/0 | 3660 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | ATGGG others(3655): Show |
chrX | 153512642 | 153587929 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6776 | 57 | 22 | 8 | 14 | 4 | 9 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6771): Show |
chrX | 153512642 | 153587929 |
| a0001c0001t0002 | 0/0 | 6774 | 8 | 3 | 1 | 2 | 1 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6769): Show |
chrX | 153512642 | 153587929 |
| a0001c0001t0003 | 0/0 | 6777 | 5 | 1 | 3 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6772): Show |
chrX | 153512642 | 153587929 |
| a0001c0001t0004 | 0/0 | 6774 | 9 | 0 | 0 | 9 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6769): Show |
chrX | 153512642 | 153587929 |
| a0001c0001t0005 | 0/0 | 6775 | 7 | 5 | 0 | 1 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6770): Show |
chrX | 153512642 | 153587929 |
| a0001c0001t0006 | 0/0 | 6775 | 5 | 0 | 2 | 3 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6770): Show |
chrX | 153512642 | 153587929 |
| a0001c0001t0007 | 0/0 | 6776 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6771): Show |
chrX | 153512642 | 153587929 |
| a0001c0001t0008 | 0/0 | 6777 | 4 | 4 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6772): Show |
chrX | 153512642 | 153587929 |
| a0001c0001t0009 | 0/0 | 6774 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6769): Show |
chrX | 153512642 | 153587929 |
| a0001c0001t0010 | 0/0 | 6777 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6772): Show |
chrX | 153512642 | 153587929 |
| a0001c0001t0011 | 0/0 | 6776 | 3 | 3 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6771): Show |
chrX | 153512642 | 153587929 |
| a0001c0001t0012 | 0/0 | 6775 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6770): Show |
chrX | 153512642 | 153587929 |
| a0001c0001t0014 | 0/0 | 6776 | 2 | 1 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6771): Show |
chrX | 153512642 | 153587929 |
| a0001c0001t0015 | 0/0 | 6776 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6771): Show |
chrX | 153512642 | 153587929 |
| a0001c0001t0016 | 0/0 | 6775 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6770): Show |
chrX | 153512642 | 153587929 |
| a0001c0001t0017 | 0/0 | 6778 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6773): Show |
chrX | 153512642 | 153587929 |
| a0001c0001t0019 | 0/0 | 6776 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6771): Show |
chrX | 153512642 | 153587929 |
| a0001c0001t0020 | 0/0 | 6774 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6769): Show |
chrX | 153512642 | 153587929 |
| a0001c0001t0021 | 0/0 | 6774 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6769): Show |
chrX | 153512642 | 153587929 |
| a0001c0001t0022 | 0/0 | 6778 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6773): Show |
chrX | 153512642 | 153587929 |
| a0001c0001t0028 | 0/0 | 6775 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6770): Show |
chrX | 153512642 | 153587929 |
| a0001c0001t0031 | 0/0 | 6776 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6771): Show |
chrX | 153512642 | 153587929 |
| a0001c0001t0032 | 0/0 | 6775 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6770): Show |
chrX | 153512642 | 153587929 |
| a0001c0001t0036 | 0/0 | 6775 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6770): Show |
chrX | 153512642 | 153587929 |
| a0001c0001t0037 | 0/0 | 6776 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6771): Show |
chrX | 153512642 | 153587929 |
| a0001c0001t0039 | 0/0 | 6775 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6770): Show |
chrX | 153512642 | 153587929 |
| a0001c0001t0042 | 0/0 | 6774 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6769): Show |
chrX | 153512642 | 153587929 |
| a0001c0001t0043 | 0/0 | 6775 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6770): Show |
chrX | 153512642 | 153587929 |
| a0001c0001t0044 | 0/0 | 6775 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6770): Show |
chrX | 153512642 | 153587929 |
| a0001c0001t0046 | 0/0 | 6776 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6771): Show |
chrX | 153512642 | 153587929 |
| a0001c0002t0001 | 0/1 | 6776 | 62 | 3 | 14 | 37 | 1 | 6 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6771): Show |
chrX | 153512642 | 153587929 |
| a0001c0002t0002 | 0/0 | 6774 | 26 | 0 | 6 | 13 | 0 | 7 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6769): Show |
chrX | 153512642 | 153587929 |
| a0001c0002t0003 | 0/0 | 6777 | 6 | 0 | 2 | 3 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6772): Show |
chrX | 153512642 | 153587929 |
| a0001c0002t0006 | 0/0 | 6775 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6770): Show |
chrX | 153512642 | 153587929 |
| a0001c0002t0010 | 0/0 | 6777 | 2 | 0 | 0 | 2 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6772): Show |
chrX | 153512642 | 153587929 |
| a0001c0002t0012 | 0/0 | 6775 | 2 | 0 | 0 | 2 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6770): Show |
chrX | 153512642 | 153587929 |
| a0001c0002t0013 | 0/0 | 6776 | 3 | 0 | 0 | 3 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6771): Show |
chrX | 153512642 | 153587929 |
| a0001c0002t0014 | 0/0 | 6776 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6771): Show |
chrX | 153512642 | 153587929 |
| a0001c0002t0015 | 0/0 | 6776 | 2 | 0 | 1 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6771): Show |
chrX | 153512642 | 153587929 |
| a0001c0002t0017 | 0/0 | 6778 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6773): Show |
chrX | 153512642 | 153587929 |
| a0001c0002t0018 | 0/0 | 6776 | 2 | 0 | 2 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6771): Show |
chrX | 153512642 | 153587929 |
| a0001c0002t0019 | 0/0 | 6776 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6771): Show |
chrX | 153512642 | 153587929 |
| a0001c0002t0030 | 0/0 | 6774 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6769): Show |
chrX | 153512642 | 153587929 |
| a0001c0002t0034 | 0/0 | 6777 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6772): Show |
chrX | 153512642 | 153587929 |
| a0001c0002t0035 | 0/0 | 6775 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6770): Show |
chrX | 153512642 | 153587929 |
| a0001c0002t0038 | 0/0 | 6777 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6772): Show |
chrX | 153512642 | 153587929 |
| a0001c0003t0001 | 0/0 | 6776 | 2 | 2 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6771): Show |
chrX | 153512642 | 153587929 |
| a0001c0003t0002 | 0/0 | 6774 | 4 | 2 | 2 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6769): Show |
chrX | 153512642 | 153587929 |
| a0001c0003t0007 | 0/0 | 6776 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6771): Show |
chrX | 153512642 | 153587929 |
| a0001c0003t0024 | 0/0 | 6776 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6771): Show |
chrX | 153512642 | 153587929 |
| a0001c0003t0027 | 0/0 | 6775 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6770): Show |
chrX | 153512642 | 153587929 |
| a0001c0003t0033 | 0/0 | 6776 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6771): Show |
chrX | 153512642 | 153587929 |
| a0001c0003t0040 | 0/0 | 6775 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6770): Show |
chrX | 153512642 | 153587929 |
| a0001c0003t0045 | 0/0 | 6776 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6771): Show |
chrX | 153512642 | 153587929 |
| a0001c0004t0007 | 0/0 | 6776 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6771): Show |
chrX | 153512642 | 153587929 |
| a0001c0004t0009 | 0/0 | 6774 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6769): Show |
chrX | 153512642 | 153587929 |
| a0001c0004t0016 | 0/0 | 6775 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6770): Show |
chrX | 153512642 | 153587929 |
| a0001c0004t0029 | 1/0 | 6774 | 1 | 0 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6769): Show |
chrX | 153512642 | 153587929 |
| a0001c0005t0007 | 0/0 | 6776 | 2 | 2 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6771): Show |
chrX | 153512642 | 153587929 |
| a0001c0007t0001 | 0/0 | 6776 | 2 | 0 | 0 | 2 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6771): Show |
chrX | 153512642 | 153587929 |
| a0001c0008t0026 | 0/0 | 6774 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6769): Show |
chrX | 153512642 | 153587929 |
| a0001c0010t0005 | 0/0 | 6775 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6770): Show |
chrX | 153512642 | 153587929 |
| a0001c0011t0023 | 0/0 | 6777 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6772): Show |
chrX | 153512642 | 153587929 |
| a0001c0012t0001 | 0/0 | 6776 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6771): Show |
chrX | 153512642 | 153587929 |
| a0001c0013t0002 | 0/0 | 6774 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6769): Show |
chrX | 153512642 | 153587929 |
| a0001c0014t0041 | 0/0 | 6774 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6769): Show |
chrX | 153512642 | 153587929 |
| a0001c0015t0009 | 0/0 | 6774 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6769): Show |
chrX | 153512642 | 153587929 |
| a0001c0016t0020 | 0/0 | 6774 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6769): Show |
chrX | 153512642 | 153587929 |
| a0001c0017t0025 | 0/0 | 6776 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6771): Show |
chrX | 153512642 | 153587929 |
| a0001c0018t0001 | 0/0 | 6776 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6771): Show |
chrX | 153512642 | 153587929 |
| a0002c0006t0001 | 0/0 | 6776 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6771): Show |
chrX | 153512642 | 153587929 |
| a0002c0006t0003 | 0/0 | 6777 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6772): Show |
chrX | 153512642 | 153587929 |
| a0003c0009t0005 | 0/0 | 6775 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | AGAGC others(6770): Show |
chrX | 153512642 | 153587929 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0001g0003 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0002g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0003g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0004g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0004g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0004g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0004g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0004g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0004g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0004g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0004g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0005g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0005g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0005g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0005g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0005g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0005g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0005g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0006g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0006g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0006g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0006g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0007g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0008g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0008g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0008g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0009g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0010g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0011g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0011g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0011g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0012g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0014g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0014g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0015g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0016g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0017g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0019g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0020g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0021g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0022g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0028g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0031g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0032g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0036g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0037g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0039g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0042g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0043g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0044g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0001t0046g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0001g0001 | 0/0 | 7 | 0 | 2 | 5 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0001g0014 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0001g0172 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0002g0005 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0002g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0003g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0003g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0003g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0003g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0006g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0010g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0010g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0012g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0012g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0013g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0013g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0013g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0014g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0015g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0015g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0017g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0018g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0018g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0019g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0030g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0034g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0035g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0002t0038g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0003t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0003t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0003t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0003t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0003t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0003t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0003t0007g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0003t0024g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0003t0027g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0003t0033g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0003t0040g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0003t0045g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0004t0007g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0004t0009g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0004t0016g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0004t0029g0197 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0005t0007g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0007t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0007t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0008t0026g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0010t0005g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0011t0023g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0012t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0013t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0014t0041g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0015t0009g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0016t0020g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0017t0025g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0001c0018t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0002c0006t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0002c0006t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| a0003c0009t0005g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0044 | EUR | GBR | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG00280 | hp1 | a0001 | c0014 | t0041 | g0046 | EUR | FIN | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | CHS | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG00408 | hp2 | a0001 | c0001 | t0006 | g0010 | EAS | CHS | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG00423 | hp2 | a0001 | c0002 | t0002 | g0183 | EAS | CHS | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG00544 | hp1 | a0001 | c0002 | t0002 | g0186 | EAS | CHS | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG00544 | hp2 | a0001 | c0001 | t0010 | g0008 | EAS | CHS | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0107 | EAS | CHS | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0120 | EAS | CHS | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | CHS | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | CHS | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG00639 | hp1 | a0001 | c0002 | t0002 | g0167 | AMR | PUR | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG00639 | hp2 | a0001 | c0002 | t0018 | g0193 | AMR | PUR | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG00642 | hp1 | a0001 | c0001 | t0009 | g0228 | AMR | PUR | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | CHS | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG00735 | hp1 | a0001 | c0002 | t0003 | g0131 | AMR | PUR | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0204 | AMR | PUR | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0173 | AMR | PUR | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG00741 | hp1 | a0001 | c0001 | t0039 | g0234 | AMR | PUR | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG00741 | hp2 | a0001 | c0002 | t0003 | g0122 | AMR | PUR | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0143 | AMR | PUR | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0155 | AMR | PUR | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0059 | AMR | PUR | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0136 | AMR | PUR | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0154 | AMR | PUR | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG01243 | hp1 | a0001 | c0004 | t0016 | g0217 | AMR | PUR | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | CLM | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG01256 | hp1 | a0001 | c0002 | t0018 | g0128 | AMR | CLM | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0130 | AMR | CLM | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0065 | AMR | CLM | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0095 | AMR | CLM | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG01346 | hp2 | a0001 | c0002 | t0002 | g0005 | AMR | CLM | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG01361 | hp1 | a0001 | c0002 | t0002 | g0145 | AMR | CLM | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG01361 | hp2 | a0001 | c0003 | t0002 | g0032 | AMR | CLM | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG01433 | hp1 | a0001 | c0002 | t0015 | g0015 | AMR | CLM | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0111 | EUR | IBS | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0113 | EUR | IBS | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0195 | EUR | IBS | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0072 | AFR | ACB | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG01884 | hp2 | a0001 | c0001 | t0007 | g0229 | AFR | ACB | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | PEL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG01934 | hp1 | a0001 | c0003 | t0002 | g0203 | AMR | PEL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG01943 | hp1 | a0001 | c0001 | t0006 | g0010 | AMR | PEL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0045 | AMR | PEL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG01975 | hp1 | a0001 | c0001 | t0006 | g0066 | AMR | PEL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0168 | AMR | PEL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG01981 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | PEL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0142 | AMR | PEL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02004 | hp1 | a0001 | c0002 | t0002 | g0015 | AMR | PEL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0133 | AMR | PEL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0108 | EAS | KHV | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0208 | EAS | KHV | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02055 | hp1 | a0001 | c0010 | t0005 | g0091 | AFR | ACB | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02056 | hp1 | a0002 | c0006 | t0001 | g0147 | EAS | KHV | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0182 | EAS | KHV | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02074 | hp1 | a0001 | c0002 | t0002 | g0050 | EAS | KHV | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02080 | hp1 | a0001 | c0001 | t0015 | g0056 | EAS | KHV | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02080 | hp2 | a0002 | c0006 | t0003 | g0139 | EAS | KHV | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02083 | hp1 | a0001 | c0002 | t0002 | g0188 | EAS | KHV | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | KHV | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0138 | EAS | KHV | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02135 | hp1 | a0001 | c0001 | t0031 | g0002 | EAS | KHV | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02145 | hp1 | a0001 | c0001 | t0016 | g0219 | AFR | ACB | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0207 | EAS | CDX | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | CDX | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02257 | hp1 | a0001 | c0001 | t0046 | g0079 | AFR | ACB | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02257 | hp2 | a0001 | c0003 | t0007 | g0223 | AFR | ACB | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0036 | AFR | ACB | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02280 | hp1 | a0001 | c0004 | t0007 | g0218 | AFR | ACB | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02280 | hp2 | a0001 | c0001 | t0008 | g0017 | AFR | ACB | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02451 | hp1 | a0001 | c0003 | t0040 | g0090 | AFR | ACB | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02451 | hp2 | a0001 | c0001 | t0042 | g0078 | AFR | ACB | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0126 | SAS | PJL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02615 | hp1 | a0001 | c0016 | t0020 | g0070 | AFR | GWD | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02622 | hp1 | a0001 | c0001 | t0017 | g0177 | AFR | GWD | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02622 | hp2 | a0001 | c0001 | t0008 | g0025 | AFR | GWD | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02630 | hp2 | a0001 | c0001 | t0011 | g0038 | AFR | GWD | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0134 | SAS | PJL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0146 | SAS | PJL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02717 | hp1 | a0001 | c0001 | t0011 | g0037 | AFR | GWD | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0094 | AFR | GWD | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02809 | hp1 | a0001 | c0011 | t0023 | g0224 | AFR | GWD | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02809 | hp2 | a0001 | c0004 | t0009 | g0231 | AFR | GWD | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02818 | hp1 | a0001 | c0001 | t0020 | g0199 | AFR | GWD | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02886 | hp2 | a0001 | c0003 | t0033 | g0030 | AFR | GWD | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02896 | hp2 | a0001 | c0001 | t0005 | g0088 | AFR | GWD | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02922 | hp1 | a0001 | c0001 | t0044 | g0021 | AFR | ESN | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ESN | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02970 | hp1 | a0001 | c0003 | t0027 | g0227 | AFR | ESN | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02976 | hp1 | a0001 | c0003 | t0024 | g0230 | AFR | ESN | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02976 | hp2 | a0001 | c0008 | t0026 | g0220 | AFR | ESN | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG03041 | hp2 | a0003 | c0009 | t0005 | g0076 | AFR | GWD | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0157 | AFR | MSL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG03195 | hp2 | a0001 | c0012 | t0001 | g0148 | AFR | ESN | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG03225 | hp1 | a0001 | c0001 | t0011 | g0039 | AFR | MSL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0099 | SAS | PJL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG03453 | hp1 | a0001 | c0005 | t0007 | g0020 | AFR | MSL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG03453 | hp2 | a0001 | c0001 | t0021 | g0222 | AFR | MSL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG03486 | hp1 | a0001 | c0002 | t0017 | g0071 | AFR | MSL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG03486 | hp2 | a0001 | c0003 | t0045 | g0092 | AFR | MSL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG03491 | hp1 | a0001 | c0002 | t0003 | g0016 | SAS | PJL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG03491 | hp2 | a0001 | c0002 | t0002 | g0178 | SAS | PJL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0016 | SAS | PJL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0175 | AFR | ESN | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG03516 | hp2 | a0001 | c0003 | t0001 | g0035 | AFR | ESN | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG03540 | hp1 | a0001 | c0003 | t0002 | g0033 | AFR | GWD | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0233 | AFR | GWD | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | MSL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG03654 | hp1 | a0001 | c0001 | t0037 | g0052 | SAS | PJL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG03688 | hp1 | a0001 | c0002 | t0002 | g0041 | SAS | STU | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG03831 | hp1 | a0001 | c0013 | t0002 | g0180 | SAS | BEB | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG03831 | hp2 | a0001 | c0002 | t0002 | g0192 | SAS | BEB | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG03834 | hp1 | a0001 | c0002 | t0002 | g0042 | SAS | BEB | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG03834 | hp2 | a0001 | c0001 | t0005 | g0087 | SAS | BEB | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG03927 | hp1 | a0001 | c0001 | t0014 | g0086 | SAS | BEB | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | BEB | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | BEB | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG04115 | hp1 | a0001 | c0001 | t0012 | g0048 | SAS | STU | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | BEB | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0057 | SAS | BEB | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG04199 | hp1 | a0001 | c0002 | t0002 | g0179 | SAS | STU | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0082 | SAS | STU | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG04228 | hp1 | a0001 | c0002 | t0002 | g0181 | SAS | STU | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA18522 | hp1 | a0001 | c0003 | t0001 | g0034 | AFR | YRI | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA18612 | hp1 | a0001 | c0001 | t0004 | g0119 | EAS | CHB | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | CHB | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA18906 | hp1 | a0001 | c0005 | t0007 | g0020 | AFR | YRI | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | YRI | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA18939 | hp1 | a0001 | c0001 | t0004 | g0209 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA18939 | hp2 | a0001 | c0002 | t0014 | g0191 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA18940 | hp1 | a0001 | c0001 | t0006 | g0069 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA18943 | hp1 | a0001 | c0002 | t0003 | g0150 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA18944 | hp1 | a0001 | c0007 | t0001 | g0062 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA18945 | hp1 | a0001 | c0001 | t0004 | g0018 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA18948 | hp1 | a0001 | c0002 | t0013 | g0083 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0129 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA18950 | hp2 | a0001 | c0002 | t0015 | g0165 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA18951 | hp1 | a0001 | c0001 | t0004 | g0018 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA18951 | hp2 | a0001 | c0001 | t0006 | g0053 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA18952 | hp1 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA18957 | hp1 | a0001 | c0002 | t0002 | g0166 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA18960 | hp1 | a0001 | c0002 | t0012 | g0097 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA18961 | hp1 | a0001 | c0002 | t0010 | g0093 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA18965 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA18966 | hp1 | a0001 | c0018 | t0001 | g0174 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA18971 | hp1 | a0001 | c0001 | t0004 | g0213 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA18975 | hp1 | a0001 | c0001 | t0032 | g0206 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA18977 | hp1 | a0001 | c0002 | t0002 | g0190 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0151 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA18983 | hp1 | a0001 | c0001 | t0004 | g0211 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA18984 | hp1 | a0001 | c0001 | t0004 | g0212 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA18985 | hp1 | a0001 | c0001 | t0019 | g0064 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA18986 | hp1 | a0001 | c0001 | t0005 | g0127 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA18989 | hp1 | a0001 | c0002 | t0001 | g0164 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA18990 | hp1 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA18994 | hp1 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA18998 | hp1 | a0001 | c0002 | t0013 | g0084 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA19000 | hp1 | a0001 | c0002 | t0010 | g0141 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA19003 | hp1 | a0001 | c0002 | t0002 | g0184 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA19003 | hp2 | a0001 | c0002 | t0001 | g0152 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA19004 | hp1 | a0001 | c0002 | t0002 | g0185 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA19005 | hp1 | a0001 | c0002 | t0013 | g0085 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA19010 | hp1 | a0001 | c0002 | t0034 | g0067 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0137 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA19011 | hp1 | a0001 | c0001 | t0004 | g0216 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA19011 | hp2 | a0001 | c0002 | t0012 | g0171 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA19030 | hp1 | a0001 | c0003 | t0002 | g0080 | AFR | LWK | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0022 | AFR | LWK | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA19043 | hp1 | a0001 | c0017 | t0025 | g0226 | AFR | LWK | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA19056 | hp1 | a0001 | c0002 | t0003 | g0135 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA19057 | hp2 | a0001 | c0001 | t0043 | g0098 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA19063 | hp1 | a0001 | c0002 | t0002 | g0089 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0176 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA19065 | hp2 | a0001 | c0001 | t0004 | g0215 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA19067 | hp1 | a0001 | c0002 | t0038 | g0153 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA19068 | hp1 | a0001 | c0002 | t0006 | g0012 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA19070 | hp1 | a0001 | c0002 | t0002 | g0187 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA19075 | hp1 | a0001 | c0002 | t0001 | g0170 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA19079 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA19080 | hp1 | a0001 | c0007 | t0001 | g0043 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA19080 | hp2 | a0001 | c0002 | t0002 | g0169 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA19082 | hp1 | a0001 | c0001 | t0036 | g0214 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA19083 | hp1 | a0001 | c0002 | t0019 | g0144 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA19084 | hp2 | a0001 | c0002 | t0030 | g0081 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0140 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0149 | EAS | JPT | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA20129 | hp1 | a0001 | c0001 | t0005 | g0201 | AFR | ASW | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA20129 | hp2 | a0001 | c0001 | t0008 | g0017 | AFR | ASW | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0061 | EUR | TSI | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0194 | EUR | TSI | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0014 | SAS | GIH | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | CLM | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG01123 | hp2 | a0001 | c0002 | t0002 | g0189 | AMR | CLM | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02109 | hp1 | a0001 | c0001 | t0014 | g0161 | AFR | ACB | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02109 | hp2 | a0001 | c0015 | t0009 | g0221 | AFR | ACB | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02486 | hp1 | a0001 | c0001 | t0028 | g0232 | AFR | ACB | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02559 | hp1 | a0001 | c0002 | t0035 | g0060 | AFR | ACB | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0159 | AFR | MSL | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG06807 | hp1 | a0001 | c0001 | t0005 | g0158 | AFR | USA | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | USA | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | USA | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | USA | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA21309 | hp1 | a0001 | c0001 | t0022 | g0225 | AFR | LWK | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| NA21309 | hp2 | a0001 | c0001 | t0008 | g0160 | AFR | LWK | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0172 | REF | REF | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| homoSapiens | grch38p0 | a0001 | c0004 | t0029 | g0197 | REF | REF | ATP2B3_chrX_153512642_153587929 | ATP2B3 | chrX | 153512642 | 153587929 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:153541825 | G | A | 1 | a0003 | 1 | HG03041.hp2 | missense_variant | MODERATE | c.563G>A | p.Arg188Gln | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 5/22 | 1043/6774 | 563/3663 | 188/1220 | chrX | 153541825 | |||
| chrX:153550226 | G | A | 1 | a0002 | 2 | HG02056.hp1 HG02080.hp2 |
missense_variant | MODERATE | c.1763G>A | p.Arg588His | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/22 | 2243/6774 | 1763/3663 | 588/1220 | chrX | 153550226 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:153536406 | C | T | 1 | a0001c0018 | 1 | NA18966.hp1 | synonymous_variant | LOW | c.159C>T | p.Tyr53Tyr | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/22 | 639/6774 | 159/3663 | 53/1220 | chrX | 153536406 | |||
| chrX:153541480 | C | A | 1 | a0001c0008 | 1 | HG02976.hp2 | synonymous_variant | LOW | c.330C>A | p.Thr110Thr | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 4/22 | 810/6774 | 330/3663 | 110/1220 | chrX | 153541480 | |||
| chrX:153541892 | G | A | 1 | a0001c0010 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.630G>A | p.Ala210Ala | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 5/22 | 1110/6774 | 630/3663 | 210/1220 | chrX | 153541892 | |||
| chrX:153543083 | C | T | 1 | a0001c0017 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.831C>T | p.Thr277Thr | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/22 | 1311/6774 | 831/3663 | 277/1220 | chrX | 153543083 | |||
| chrX:153548740 | G | A | 1 | a0001c0005 | 2 | HG03453.hp1 NA18906.hp1 |
synonymous_variant | LOW | c.1224G>A | p.Pro408Pro | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 10/22 | 1704/6774 | 1224/3663 | 408/1220 | chrX | 153548740 | |||
| chrX:153548809 | G | A | 2 | a0001c0008 a0001c0011 |
2 | HG02809.hp1 HG02976.hp2 |
synonymous_variant | LOW | c.1293G>A | p.Glu431Glu | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 10/22 | 1773/6774 | 1293/3663 | 431/1220 | chrX | 153548809 | |||
| chrX:153549631 | A | G | 17 | a0001c0001 a0001c0002 a0001c0003 others(14): Show |
262 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(259): Show |
synonymous_variant | LOW | c.1473A>G | p.Gly491Gly | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 11/22 | 1953/6774 | 1473/3663 | 491/1220 | chrX | 153549631 | |||
| chrX:153550098 | C | T | 2 | a0001c0015 a0001c0016 |
2 | HG02109.hp2 HG02615.hp1 |
synonymous_variant | LOW | c.1635C>T | p.Cys545Cys | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/22 | 2115/6774 | 1635/3663 | 545/1220 | chrX | 153550098 | |||
| chrX:153556123 | G | A | 1 | a0001c0015 | 1 | HG02109.hp2 | synonymous_variant | LOW | c.2133G>A | p.Thr711Thr | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 14/22 | 2613/6774 | 2133/3663 | 711/1220 | chrX | 153556123 | |||
| chrX:153558270 | G | C | 5 | a0001c0002 a0001c0012 a0001c0013 others(2): Show |
117 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(114): Show |
synonymous_variant | LOW | c.2592G>C | p.Val864Val | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 17/22 | 3072/6774 | 2592/3663 | 864/1220 | chrX | 153558270 | |||
| chrX:153558273 | C | T | 1 | a0001c0013 | 1 | HG03831.hp1 | synonymous_variant | LOW | c.2595C>T | p.Ile865Ile | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 17/22 | 3075/6774 | 2595/3663 | 865/1220 | chrX | 153558273 | |||
| chrX:153560878 | C | T | 1 | a0001c0012 | 1 | HG03195.hp2 | synonymous_variant | LOW | c.3042C>T | p.Phe1014Phe | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 19/22 | 3522/6774 | 3042/3663 | 1014/1220 | chrX | 153560878 | |||
| chrX:153565037 | T | C | 5 | a0001c0003 a0001c0008 a0001c0010 others(2): Show |
16 | HG01361.hp2 HG01934.hp1 HG02055.hp1 others(13): Show |
synonymous_variant | LOW | c.3276T>C | p.His1092His | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/22 | 3756/6774 | 3276/3663 | 1092/1220 | chrX | 153565037 | |||
| chrX:153580007 | G | A | 1 | a0001c0014 | 1 | HG00280.hp1 | synonymous_variant | LOW | c.3372G>A | p.Ser1124Ser | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 3852/6774 | 3372/3663 | 1124/1220 | chrX | 153580007 | |||
| chrX:153580106 | G | A | 1 | a0001c0007 | 2 | NA18944.hp1 NA19080.hp1 |
synonymous_variant | LOW | c.3471G>A | p.Pro1157Pro | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 3951/6774 | 3471/3663 | 1157/1220 | chrX | 153580106 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:153517683 | C | G | 55 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(52): Show |
247 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(244): Show |
5_prime_UTR_variant | MODIFIER | c.-439C>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 1/22 | 18565 | chrX | 153517683 | ||||||
| chrX:153517722 | C | T | 55 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(52): Show |
247 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(244): Show |
5_prime_UTR_variant | MODIFIER | c.-400C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 1/22 | 18526 | chrX | 153517722 | ||||||
| chrX:153518435 | C | A | 1 | a0001c0002t0030 | 1 | NA19084.hp2 | 5_prime_UTR_variant | MODIFIER | c.-243C>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/22 | 17813 | chrX | 153518435 | ||||||
| chrX:153518436 | G | A | 17 | a0001c0001t0007 a0001c0001t0009 a0001c0001t0016 others(14): Show |
18 | HG00642.hp1 HG01243.hp1 HG01884.hp2 others(15): Show |
5_prime_UTR_variant | MODIFIER | c.-242G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/22 | 17812 | chrX | 153518436 | ||||||
| chrX:153580328 | G | A | 1 | a0001c0001t0021 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*30G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 30 | chrX | 153580328 | ||||||
| chrX:153580405 | G | A | 1 | a0001c0001t0031 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*107G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 107 | chrX | 153580405 | ||||||
| chrX:153580728 | A | T | 2 | a0001c0001t0046 a0001c0003t0045 |
2 | HG02257.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*430A>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 430 | chrX | 153580728 | ||||||
| chrX:153580781 | C | CA | 37 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(34): Show |
186 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(183): Show |
3_prime_UTR_variant | MODIFIER | c.*498dupA | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 499 | INFO_REALIGN_3_PRIME | chrX | 153580781 | |||||
| chrX:153580781 | C | CAA | 6 | a0001c0001t0010 a0001c0001t0017 a0001c0001t0022 others(3): Show |
7 | HG00544.hp2 HG02622.hp1 HG03486.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*497_*498dupAA | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 499 | INFO_REALIGN_3_PRIME | chrX | 153580781 | |||||
| chrX:153580851 | C | T | 2 | a0001c0002t0013 a0001c0002t0038 |
4 | NA18948.hp1 NA18998.hp1 NA19005.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*553C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 553 | chrX | 153580851 | ||||||
| chrX:153580965 | G | A | 1 | a0001c0008t0026 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*667G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 667 | chrX | 153580965 | ||||||
| chrX:153581083 | T | A | 1 | a0001c0001t0039 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*785T>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 785 | chrX | 153581083 | ||||||
| chrX:153581084 | G | GT | 5 | a0001c0001t0015 a0001c0001t0028 a0001c0001t0043 others(2): Show |
6 | HG01433.hp1 HG02080.hp1 HG02486.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*801dupT | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 802 | INFO_REALIGN_3_PRIME | chrX | 153581084 | |||||
| chrX:153581084 | GT | G | 3 | a0001c0001t0004 a0001c0001t0032 a0001c0002t0035 |
11 | HG02559.hp1 NA18612.hp1 NA18939.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*801delT | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 801 | INFO_REALIGN_3_PRIME | chrX | 153581084 | |||||
| chrX:153581086 | T | TG | 42 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(39): Show |
186 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(183): Show |
3_prime_UTR_variant | MODIFIER | c.*788_*789insG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 789 | chrX | 153581086 | ||||||
| chrX:153581166 | A | G | 2 | a0001c0001t0020 a0001c0016t0020 |
2 | HG02615.hp1 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*868A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 868 | chrX | 153581166 | ||||||
| chrX:153581173 | G | A | 1 | a0001c0003t0033 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*875G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 875 | chrX | 153581173 | ||||||
| chrX:153581220 | G | A | 1 | a0001c0003t0045 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*922G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 922 | chrX | 153581220 | ||||||
| chrX:153581304 | G | T | 4 | a0001c0001t0028 a0001c0001t0042 a0001c0001t0044 others(1): Show |
4 | HG02451.hp2 HG02486.hp1 HG02922.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1006G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 1006 | chrX | 153581304 | ||||||
| chrX:153581470 | T | C | 1 | a0001c0001t0011 | 3 | HG02630.hp2 HG02717.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1172T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 1172 | chrX | 153581470 | ||||||
| chrX:153581614 | G | T | 1 | a0001c0002t0018 | 2 | HG00639.hp2 HG01256.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1316G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 1316 | chrX | 153581614 | ||||||
| chrX:153581672 | G | C | 2 | a0001c0001t0011 a0001c0003t0045 |
4 | HG02630.hp2 HG02717.hp1 HG03225.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1374G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 1374 | chrX | 153581672 | ||||||
| chrX:153581779 | C | A | 1 | a0001c0014t0041 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1481C>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 1481 | chrX | 153581779 | ||||||
| chrX:153581833 | T | C | 50 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(47): Show |
203 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(200): Show |
3_prime_UTR_variant | MODIFIER | c.*1535T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 1535 | chrX | 153581833 | ||||||
| chrX:153581843 | G | C | 51 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(48): Show |
204 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(201): Show |
3_prime_UTR_variant | MODIFIER | c.*1545G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 1545 | chrX | 153581843 | ||||||
| chrX:153582005 | G | A | 4 | a0001c0001t0004 a0001c0001t0032 a0001c0001t0036 others(1): Show |
12 | HG02559.hp1 NA18612.hp1 NA18939.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1707G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 1707 | chrX | 153582005 | ||||||
| chrX:153582030 | T | G | 51 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(48): Show |
204 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(201): Show |
3_prime_UTR_variant | MODIFIER | c.*1732T>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 1732 | chrX | 153582030 | ||||||
| chrX:153582076 | C | T | 1 | a0001c0017t0025 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1778C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 1778 | chrX | 153582076 | ||||||
| chrX:153582095 | G | T | 1 | a0001c0001t0039 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1797G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 1797 | chrX | 153582095 | ||||||
| chrX:153582253 | A | G | 1 | a0001c0001t0021 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1955A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 1955 | chrX | 153582253 | ||||||
| chrX:153582432 | G | A | 1 | a0001c0002t0034 | 1 | NA19010.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2134G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 2134 | chrX | 153582432 | ||||||
| chrX:153582540 | C | T | 1 | a0001c0003t0024 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2242C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 2242 | chrX | 153582540 | ||||||
| chrX:153582628 | C | CG | 14 | a0001c0001t0003 a0001c0001t0014 a0001c0001t0015 others(11): Show |
25 | HG00735.hp1 HG00735.hp2 HG00741.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*2334dupG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 2335 | INFO_REALIGN_3_PRIME | chrX | 153582628 | |||||
| chrX:153582899 | T | TA | 4 | a0001c0001t0008 a0001c0001t0017 a0001c0001t0022 others(1): Show |
7 | HG02280.hp2 HG02622.hp1 HG02622.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2610dupA | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 2611 | INFO_REALIGN_3_PRIME | chrX | 153582899 | |||||
| chrX:153582904 | A | C | 1 | a0001c0008t0026 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2606A>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 22/22 | 2606 | chrX | 153582904 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:153517893 | C | T | 3 | a0001c0001t0001g0235 a0001c0001t0039g0234 a0001c0002t0001g0233 |
3 | HG00609.hp1 HG00741.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-247+18C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 1/21 | chrX | 153517893 | |||||||
| chrX:153517935 | CA | C | 17 | a0001c0001t0007g0229 a0001c0001t0009g0228 a0001c0001t0016g0219 others(14): Show |
18 | HG00642.hp1 HG01243.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.-247+62delA | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chrX | 153517935 | ||||||
| chrX:153517982 | G | A | 1 | a0001c0001t0044g0021 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-247+107G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 1/21 | chrX | 153517982 | |||||||
| chrX:153518278 | C | A | 21 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(18): Show |
26 | HG01109.hp1 HG01361.hp2 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.-246-154C>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 1/21 | chrX | 153518278 | |||||||
| chrX:153518304 | C | T | 2 | a0001c0001t0011g0038 a0001c0001t0011g0039 |
2 | HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-246-128C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 1/21 | chrX | 153518304 | |||||||
| chrX:153518556 | G | C | 17 | a0001c0001t0007g0229 a0001c0001t0009g0228 a0001c0001t0016g0219 others(14): Show |
18 | HG00642.hp1 HG01243.hp1 HG01884.hp2 others(15): Show |
splice_region_variant&intron_variant | LOW | c.-127+5G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153518556 | |||||||
| chrX:153518995 | G | A | 2 | a0001c0001t0001g0040 a0001c0002t0002g0041 |
2 | HG02735.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.-127+444G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153518995 | |||||||
| chrX:153519070 | C | T | 13 | a0001c0001t0001g0210 a0001c0001t0004g0018 a0001c0001t0004g0209 others(10): Show |
15 | HG02040.hp1 HG02129.hp1 HG02165.hp1 others(12): Show |
intron_variant | MODIFIER | c.-127+519C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153519070 | |||||||
| chrX:153519397 | C | T | 1 | a0001c0001t0011g0037 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-127+846C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153519397 | |||||||
| chrX:153519502 | G | A | 3 | a0001c0001t0016g0219 a0001c0004t0007g0218 a0001c0004t0016g0217 |
3 | HG01243.hp1 HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.-127+951G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153519502 | |||||||
| chrX:153519696 | G | A | 3 | a0001c0001t0001g0040 a0001c0002t0002g0041 a0001c0002t0002g0042 |
3 | HG02735.hp1 HG03688.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-127+1145G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153519696 | |||||||
| chrX:153519804 | G | T | 1 | a0001c0001t0001g0205 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-127+1253G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153519804 | |||||||
| chrX:153519853 | G | A | 219 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(216): Show |
241 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.-127+1302G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153519853 | |||||||
| chrX:153519861 | G | A | 1 | a0001c0007t0001g0043 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-127+1310G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153519861 | |||||||
| chrX:153519886 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-127+1335G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153519886 | |||||||
| chrX:153519950 | G | A | 80 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(77): Show |
90 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.-127+1399G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153519950 | |||||||
| chrX:153519962 | G | T | 4 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(1): Show |
4 | HG00639.hp2 HG01516.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.-127+1411G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153519962 | |||||||
| chrX:153520108 | C | T | 1 | a0001c0001t0028g0232 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-127+1557C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153520108 | |||||||
| chrX:153520138 | G | C | 2 | a0001c0001t0022g0225 a0001c0011t0023g0224 |
2 | HG02809.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-127+1587G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153520138 | |||||||
| chrX:153520218 | G | A | 4 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(1): Show |
4 | HG00639.hp2 HG01516.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.-127+1667G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153520218 | |||||||
| chrX:153520232 | A | G | 20 | a0001c0001t0001g0040 a0001c0001t0017g0177 a0001c0002t0001g0182 others(17): Show |
22 | HG00423.hp2 HG00544.hp1 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.-127+1681A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153520232 | |||||||
| chrX:153520369 | C | T | 8 | a0001c0001t0001g0198 a0001c0001t0001g0200 a0001c0001t0001g0202 others(5): Show |
9 | HG00735.hp2 HG01934.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-127+1818C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153520369 | |||||||
| chrX:153520459 | T | A | 1 | a0001c0002t0030g0081 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-127+1908T>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153520459 | |||||||
| chrX:153520830 | T | C | 2 | a0001c0001t0022g0225 a0001c0011t0023g0224 |
2 | HG02809.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-127+2279T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153520830 | |||||||
| chrX:153520864 | C | T | 1 | a0001c0002t0001g0176 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-127+2313C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153520864 | |||||||
| chrX:153520880 | G | C | 1 | a0001c0001t0001g0198 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-127+2329G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153520880 | |||||||
| chrX:153520917 | G | A | 1 | a0001c0002t0001g0082 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-127+2366G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153520917 | |||||||
| chrX:153521203 | A | G | 218 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(215): Show |
241 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.-127+2652A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153521203 | |||||||
| chrX:153521247 | G | A | 3 | a0001c0002t0013g0083 a0001c0002t0013g0084 a0001c0002t0013g0085 |
3 | NA18948.hp1 NA18998.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.-127+2696G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153521247 | |||||||
| chrX:153521337 | G | A | 2 | a0001c0001t0005g0087 a0001c0001t0014g0086 |
2 | HG03834.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.-127+2786G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153521337 | |||||||
| chrX:153521404 | T | C | 1 | a0001c0001t0020g0199 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-127+2853T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153521404 | |||||||
| chrX:153521715 | A | G | 219 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(216): Show |
242 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.-127+3164A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153521715 | |||||||
| chrX:153521802 | G | A | 53 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(50): Show |
61 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.-127+3251G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153521802 | |||||||
| chrX:153521925 | G | A | 1 | a0001c0001t0005g0088 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-127+3374G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153521925 | |||||||
| chrX:153521928 | C | A | 1 | a0001c0016t0020g0070 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-127+3377C>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153521928 | |||||||
| chrX:153522028 | G | A | 7 | a0001c0001t0001g0198 a0001c0001t0001g0200 a0001c0001t0001g0202 others(4): Show |
8 | HG01934.hp1 HG02280.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.-127+3477G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153522028 | |||||||
| chrX:153522380 | C | A | 18 | a0001c0001t0001g0198 a0001c0001t0001g0200 a0001c0001t0001g0202 others(15): Show |
19 | HG00642.hp1 HG01243.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.-127+3829C>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153522380 | |||||||
| chrX:153522381 | G | A | 2 | a0001c0001t0011g0038 a0001c0001t0011g0039 |
2 | HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-127+3830G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153522381 | |||||||
| chrX:153522412 | G | A | 53 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(50): Show |
61 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.-127+3861G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153522412 | |||||||
| chrX:153522569 | G | A | 1 | a0001c0004t0016g0217 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-127+4018G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153522569 | |||||||
| chrX:153522895 | GT | G | 230 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(227): Show |
254 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.-127+4357delT | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153522895 | ||||||
| chrX:153523212 | A | C | 3 | a0001c0001t0042g0078 a0001c0001t0046g0079 a0001c0003t0002g0080 |
3 | HG02257.hp1 HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-127+4661A>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153523212 | |||||||
| chrX:153523273 | G | C | 20 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(17): Show |
22 | HG01884.hp1 HG02040.hp1 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.-127+4722G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153523273 | |||||||
| chrX:153523294 | G | A | 1 | a0001c0001t0017g0177 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-127+4743G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153523294 | |||||||
| chrX:153523295 | C | A | 1 | a0001c0001t0017g0177 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-127+4744C>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153523295 | |||||||
| chrX:153523299 | C | G | 4 | a0001c0001t0003g0204 a0001c0001t0008g0017 a0001c0001t0020g0199 others(1): Show |
5 | HG00735.hp2 HG01934.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-127+4748C>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153523299 | |||||||
| chrX:153523352 | C | T | 1 | a0001c0001t0011g0039 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-127+4801C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153523352 | |||||||
| chrX:153523433 | C | G | 4 | a0001c0001t0011g0037 a0001c0001t0011g0038 a0001c0001t0011g0039 others(1): Show |
4 | HG02486.hp1 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-127+4882C>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153523433 | |||||||
| chrX:153523709 | TTTC | T | 70 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(67): Show |
80 | HG00280.hp1 HG00544.hp2 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.-127+5159_-127+516 others(7): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153523709 | |||||||
| chrX:153523710 | TTC | T | 19 | a0001c0001t0002g0068 a0001c0001t0004g0216 a0001c0001t0006g0010 others(16): Show |
20 | HG00408.hp2 HG01192.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.-127+5160_-127+516 others(6): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153523710 | |||||||
| chrX:153523711 | TC | T | 125 | a0001c0001t0001g0040 a0001c0001t0001g0044 a0001c0001t0001g0102 others(122): Show |
135 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.-127+5163delC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153523711 | ||||||
| chrX:153523712 | C | T | 28 | a0001c0001t0001g0104 a0001c0001t0001g0110 a0001c0001t0001g0112 others(25): Show |
30 | HG00408.hp1 HG00544.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.-127+5161C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153523712 | |||||||
| chrX:153523759 | G | A | 21 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(18): Show |
23 | HG01884.hp1 HG02040.hp1 HG02129.hp1 others(20): Show |
intron_variant | MODIFIER | c.-127+5208G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153523759 | |||||||
| chrX:153523850 | C | A | 3 | a0001c0001t0044g0021 a0001c0003t0040g0090 a0001c0010t0005g0091 |
3 | HG02055.hp1 HG02451.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-127+5299C>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153523850 | |||||||
| chrX:153523857 | G | A | 2 | a0001c0001t0021g0222 a0001c0015t0009g0221 |
2 | HG02109.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-127+5306G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153523857 | |||||||
| chrX:153524066 | A | G | 4 | a0001c0001t0016g0219 a0001c0004t0007g0218 a0001c0004t0009g0231 others(1): Show |
4 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.-127+5515A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153524066 | |||||||
| chrX:153524091 | AT | A | 99 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(96): Show |
106 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.-127+5551delT | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153524091 | ||||||
| chrX:153524091 | ATT | A | 18 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(15): Show |
23 | HG00609.hp1 HG00741.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.-127+5550_-127+555 others(6): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153524091 | ||||||
| chrX:153524238 | C | CTG | 12 | a0001c0001t0001g0235 a0001c0001t0003g0204 a0001c0001t0019g0064 others(9): Show |
12 | HG00609.hp1 HG00735.hp2 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.-127+5707_-127+570 others(6): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153524238 | ||||||
| chrX:153524238 | CTG | C | 7 | a0001c0001t0001g0198 a0001c0001t0001g0200 a0001c0001t0001g0202 others(4): Show |
8 | HG01934.hp1 HG02280.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.-127+5707_-127+570 others(6): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153524238 | ||||||
| chrX:153524291 | C | T | 9 | a0001c0001t0007g0229 a0001c0001t0009g0228 a0001c0001t0016g0219 others(6): Show |
9 | HG00642.hp1 HG01243.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.-127+5740C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153524291 | |||||||
| chrX:153524370 | C | T | 1 | a0001c0003t0045g0092 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-127+5819C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153524370 | |||||||
| chrX:153524378 | C | A | 1 | a0001c0015t0009g0221 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-127+5827C>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153524378 | |||||||
| chrX:153524395 | C | T | 1 | a0001c0005t0007g0020 | 2 | HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-127+5844C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153524395 | |||||||
| chrX:153524536 | A | G | 1 | a0001c0002t0002g0192 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-127+5985A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153524536 | |||||||
| chrX:153524729 | G | C | 130 | a0001c0001t0001g0040 a0001c0001t0001g0044 a0001c0001t0001g0102 others(127): Show |
142 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.-127+6178G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153524729 | |||||||
| chrX:153524734 | G | A | 1 | a0001c0015t0009g0221 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-127+6183G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153524734 | |||||||
| chrX:153525287 | C | T | 1 | a0001c0002t0002g0169 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-127+6736C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153525287 | |||||||
| chrX:153525306 | G | A | 128 | a0001c0001t0001g0040 a0001c0001t0001g0044 a0001c0001t0001g0102 others(125): Show |
140 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.-127+6755G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153525306 | |||||||
| chrX:153525325 | C | A | 5 | a0001c0001t0001g0235 a0001c0001t0039g0234 a0001c0002t0001g0233 others(2): Show |
5 | HG00609.hp1 HG00741.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-127+6774C>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153525325 | |||||||
| chrX:153525348 | G | T | 1 | a0001c0015t0009g0221 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-127+6797G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153525348 | |||||||
| chrX:153525444 | A | G | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(234): Show |
261 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(258): Show |
intron_variant | MODIFIER | c.-127+6893A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153525444 | |||||||
| chrX:153525525 | G | A | 20 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(17): Show |
20 | HG00609.hp1 HG00639.hp2 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.-127+6974G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153525525 | |||||||
| chrX:153525551 | G | A | 9 | a0001c0001t0007g0229 a0001c0001t0009g0228 a0001c0001t0011g0037 others(6): Show |
9 | HG00642.hp1 HG01884.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-127+7000G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153525551 | |||||||
| chrX:153525556 | C | A | 3 | a0001c0001t0044g0021 a0001c0003t0040g0090 a0001c0010t0005g0091 |
3 | HG02055.hp1 HG02451.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-127+7005C>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153525556 | |||||||
| chrX:153525563 | A | G | 25 | a0001c0001t0001g0040 a0001c0002t0001g0168 a0001c0002t0001g0182 others(22): Show |
27 | HG00423.hp2 HG00544.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.-127+7012A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153525563 | |||||||
| chrX:153525754 | C | T | 1 | a0001c0003t0002g0203 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-127+7203C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153525754 | |||||||
| chrX:153525802 | C | T | 13 | a0001c0001t0001g0210 a0001c0001t0004g0018 a0001c0001t0004g0209 others(10): Show |
15 | HG02040.hp1 HG02129.hp1 HG02165.hp1 others(12): Show |
intron_variant | MODIFIER | c.-127+7251C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153525802 | |||||||
| chrX:153525884 | G | A | 56 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(53): Show |
65 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.-127+7333G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153525884 | |||||||
| chrX:153525963 | T | C | 67 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(64): Show |
77 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.-127+7412T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153525963 | |||||||
| chrX:153526075 | G | A | 31 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(28): Show |
34 | HG00735.hp2 HG01361.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.-127+7524G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153526075 | |||||||
| chrX:153526128 | G | A | 102 | a0001c0001t0001g0044 a0001c0001t0001g0102 a0001c0001t0001g0103 others(99): Show |
112 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.-127+7577G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153526128 | |||||||
| chrX:153526132 | G | C | 1 | a0001c0001t0044g0021 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-127+7581G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153526132 | |||||||
| chrX:153526212 | G | C | 130 | a0001c0001t0001g0040 a0001c0001t0001g0044 a0001c0001t0001g0102 others(127): Show |
142 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.-127+7661G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153526212 | |||||||
| chrX:153526271 | A | G | 4 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(1): Show |
4 | HG00639.hp2 HG01516.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.-127+7720A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153526271 | |||||||
| chrX:153526430 | G | A | 1 | a0001c0001t0011g0037 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-127+7879G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153526430 | |||||||
| chrX:153526473 | G | T | 6 | a0001c0001t0007g0229 a0001c0001t0009g0228 a0001c0001t0042g0078 others(3): Show |
6 | HG00642.hp1 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.-127+7922G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153526473 | |||||||
| chrX:153526799 | T | C | 5 | a0001c0001t0022g0225 a0001c0001t0044g0021 a0001c0003t0040g0090 others(2): Show |
5 | HG02055.hp1 HG02451.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-127+8248T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153526799 | |||||||
| chrX:153526908 | G | C | 4 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(1): Show |
4 | HG00639.hp2 HG01516.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.-127+8357G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153526908 | |||||||
| chrX:153526969 | G | A | 26 | a0001c0001t0001g0040 a0001c0001t0017g0177 a0001c0002t0001g0168 others(23): Show |
28 | HG00423.hp2 HG00544.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.-127+8418G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153526969 | |||||||
| chrX:153527066 | G | A | 1 | a0001c0001t0032g0206 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-127+8515G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153527066 | |||||||
| chrX:153527111 | G | A | 6 | a0001c0001t0007g0229 a0001c0001t0009g0228 a0001c0001t0042g0078 others(3): Show |
6 | HG00642.hp1 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.-127+8560G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153527111 | |||||||
| chrX:153527128 | A | G | 1 | a0001c0001t0044g0021 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-127+8577A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153527128 | |||||||
| chrX:153527388 | G | C | 5 | a0001c0001t0001g0235 a0001c0001t0039g0234 a0001c0002t0001g0233 others(2): Show |
5 | HG00609.hp1 HG00741.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-126-8734G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153527388 | |||||||
| chrX:153527453 | T | A | 20 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(17): Show |
20 | HG00609.hp1 HG00639.hp2 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.-126-8669T>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153527453 | |||||||
| chrX:153527463 | G | A | 23 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0210 others(20): Show |
25 | HG01361.hp2 HG01884.hp1 HG02040.hp1 others(22): Show |
intron_variant | MODIFIER | c.-126-8659G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153527463 | |||||||
| chrX:153527466 | C | T | 23 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0210 others(20): Show |
25 | HG01361.hp2 HG01884.hp1 HG02040.hp1 others(22): Show |
intron_variant | MODIFIER | c.-126-8656C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153527466 | |||||||
| chrX:153527522 | C | T | 129 | a0001c0001t0001g0040 a0001c0001t0001g0044 a0001c0001t0001g0102 others(126): Show |
141 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.-126-8600C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153527522 | |||||||
| chrX:153527604 | A | T | 2 | a0001c0001t0022g0225 a0001c0011t0023g0224 |
2 | HG02809.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-126-8518A>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153527604 | |||||||
| chrX:153527640 | C | A | 2 | a0001c0001t0022g0225 a0001c0011t0023g0224 |
2 | HG02809.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-126-8482C>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153527640 | |||||||
| chrX:153527691 | G | A | 1 | a0001c0017t0025g0226 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-126-8431G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153527691 | |||||||
| chrX:153527823 | T | G | 1 | a0001c0002t0001g0065 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-126-8299T>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153527823 | |||||||
| chrX:153527997 | C | T | 5 | a0001c0001t0001g0235 a0001c0001t0039g0234 a0001c0002t0001g0233 others(2): Show |
5 | HG00609.hp1 HG00741.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-126-8125C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153527997 | |||||||
| chrX:153528100 | G | T | 1 | a0001c0001t0001g0031 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-126-8022G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153528100 | |||||||
| chrX:153528126 | A | T | 1 | a0001c0002t0001g0164 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-126-7996A>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153528126 | |||||||
| chrX:153528309 | T | G | 9 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(6): Show |
9 | HG00609.hp1 HG00639.hp2 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.-126-7813T>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153528309 | |||||||
| chrX:153528510 | G | T | 2 | a0001c0001t0022g0225 a0001c0011t0023g0224 |
2 | HG02809.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-126-7612G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153528510 | |||||||
| chrX:153528617 | G | T | 129 | a0001c0001t0001g0040 a0001c0001t0001g0044 a0001c0001t0001g0102 others(126): Show |
141 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.-126-7505G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153528617 | |||||||
| chrX:153528629 | T | C | 9 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(6): Show |
9 | HG00609.hp1 HG00639.hp2 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.-126-7493T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153528629 | |||||||
| chrX:153528721 | T | A | 2 | a0001c0008t0026g0220 a0001c0017t0025g0226 |
2 | HG02976.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-126-7401T>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153528721 | |||||||
| chrX:153529004 | G | A | 2 | a0001c0001t0005g0087 a0001c0001t0014g0086 |
2 | HG03834.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.-126-7118G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153529004 | |||||||
| chrX:153529475 | G | A | 104 | a0001c0001t0001g0040 a0001c0001t0001g0044 a0001c0001t0001g0102 others(101): Show |
114 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.-126-6647G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153529475 | |||||||
| chrX:153529557 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-126-6565G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153529557 | |||||||
| chrX:153529598 | T | G | 1 | a0001c0001t0003g0045 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-126-6524T>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153529598 | |||||||
| chrX:153529623 | G | A | 1 | a0001c0005t0007g0020 | 2 | HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-126-6499G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153529623 | |||||||
| chrX:153529723 | G | C | 2 | a0001c0001t0002g0023 a0001c0002t0018g0128 |
2 | HG01256.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-126-6399G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153529723 | |||||||
| chrX:153529744 | C | A | 1 | a0001c0001t0001g0031 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-126-6378C>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153529744 | |||||||
| chrX:153530123 | A | G | 1 | a0001c0005t0007g0020 | 2 | HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-126-5999A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153530123 | |||||||
| chrX:153530124 | G | A | 2 | a0001c0002t0001g0094 a0001c0002t0001g0173 |
2 | HG00738.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-126-5998G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153530124 | |||||||
| chrX:153530393 | G | C | 2 | a0001c0002t0001g0094 a0001c0002t0001g0095 |
2 | HG01346.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-126-5729G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153530393 | |||||||
| chrX:153530650 | G | A | 2 | a0001c0002t0001g0096 a0001c0002t0012g0097 |
2 | NA18960.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.-126-5472G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153530650 | |||||||
| chrX:153530817 | G | T | 2 | a0001c0001t0001g0162 a0001c0001t0001g0163 |
2 | HG00423.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.-126-5305G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153530817 | |||||||
| chrX:153530818 | G | T | 3 | a0001c0001t0001g0194 a0001c0001t0001g0196 a0001c0002t0018g0193 |
3 | HG00639.hp2 HG03239.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-126-5304G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153530818 | |||||||
| chrX:153530938 | G | A | 5 | a0001c0001t0009g0228 a0001c0001t0042g0078 a0001c0001t0046g0079 others(2): Show |
5 | HG00642.hp1 HG02257.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-126-5184G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153530938 | |||||||
| chrX:153530939 | A | T | 1 | a0001c0001t0001g0075 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-126-5183A>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153530939 | |||||||
| chrX:153531057 | A | C | 1 | a0001c0001t0006g0069 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-126-5065A>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153531057 | |||||||
| chrX:153531069 | G | A | 5 | a0001c0001t0011g0037 a0001c0001t0011g0038 a0001c0001t0011g0039 others(2): Show |
5 | HG02615.hp1 HG02630.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-126-5053G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153531069 | |||||||
| chrX:153531264 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-126-4858C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153531264 | |||||||
| chrX:153531442 | G | A | 1 | a0001c0013t0002g0180 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-126-4680G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153531442 | |||||||
| chrX:153531457 | G | A | 1 | a0001c0002t0001g0207 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-126-4665G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153531457 | |||||||
| chrX:153531512 | G | A | 1 | a0001c0017t0025g0226 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-126-4610G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153531512 | |||||||
| chrX:153531636 | C | T | 1 | a0001c0005t0007g0020 | 2 | HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-126-4486C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153531636 | |||||||
| chrX:153531654 | T | C | 1 | a0001c0014t0041g0046 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-126-4468T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153531654 | |||||||
| chrX:153531818 | G | T | 29 | a0001c0001t0001g0077 a0001c0001t0001g0202 a0001c0001t0001g0210 others(26): Show |
32 | HG00642.hp1 HG01934.hp1 HG02040.hp1 others(29): Show |
intron_variant | MODIFIER | c.-126-4304G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153531818 | |||||||
| chrX:153531854 | A | T | 2 | a0001c0015t0009g0221 a0001c0017t0025g0226 |
2 | HG02109.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-126-4268A>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153531854 | |||||||
| chrX:153531858 | C | G | 232 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(229): Show |
256 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(253): Show |
intron_variant | MODIFIER | c.-126-4264C>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153531858 | |||||||
| chrX:153531873 | G | A | 3 | a0001c0001t0001g0194 a0001c0001t0001g0196 a0001c0002t0018g0193 |
3 | HG00639.hp2 HG03239.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-126-4249G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153531873 | |||||||
| chrX:153532217 | C | T | 1 | a0001c0002t0014g0191 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-126-3905C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153532217 | |||||||
| chrX:153532244 | G | A | 51 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(48): Show |
59 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.-126-3878G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153532244 | |||||||
| chrX:153532408 | G | A | 1 | a0001c0002t0001g0099 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-126-3714G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153532408 | |||||||
| chrX:153532414 | G | A | 5 | a0001c0001t0009g0228 a0001c0001t0042g0078 a0001c0001t0046g0079 others(2): Show |
5 | HG00642.hp1 HG02257.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-126-3708G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153532414 | |||||||
| chrX:153532479 | C | G | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(234): Show |
261 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(258): Show |
intron_variant | MODIFIER | c.-126-3643C>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153532479 | |||||||
| chrX:153532621 | G | A | 117 | a0001c0001t0001g0040 a0001c0001t0001g0044 a0001c0001t0001g0102 others(114): Show |
129 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.-126-3501G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153532621 | |||||||
| chrX:153532720 | G | C | 1 | a0001c0016t0020g0070 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-126-3402G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153532720 | |||||||
| chrX:153532876 | C | G | 1 | a0001c0001t0001g0195 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-126-3246C>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153532876 | |||||||
| chrX:153532878 | G | A | 10 | a0001c0002t0001g0182 a0001c0002t0002g0089 a0001c0002t0002g0166 others(7): Show |
10 | HG00423.hp2 HG02071.hp1 HG03831.hp1 others(7): Show |
intron_variant | MODIFIER | c.-126-3244G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153532878 | |||||||
| chrX:153532890 | A | G | 2 | a0001c0015t0009g0221 a0001c0017t0025g0226 |
2 | HG02109.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-126-3232A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153532890 | |||||||
| chrX:153532946 | G | C | 1 | a0001c0001t0002g0047 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-126-3176G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153532946 | |||||||
| chrX:153533275 | C | T | 1 | a0001c0001t0001g0063 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-126-2847C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153533275 | |||||||
| chrX:153533294 | G | A | 6 | a0001c0001t0001g0235 a0001c0001t0005g0087 a0001c0001t0014g0086 others(3): Show |
6 | HG00609.hp1 HG00741.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-126-2828G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153533294 | |||||||
| chrX:153533408 | G | A | 1 | a0001c0002t0001g0096 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-126-2714G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153533408 | |||||||
| chrX:153533472 | A | G | 5 | a0001c0001t0011g0037 a0001c0001t0011g0038 a0001c0001t0011g0039 others(2): Show |
5 | HG02615.hp1 HG02630.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-126-2650A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153533472 | |||||||
| chrX:153533522 | G | A | 5 | a0001c0001t0009g0228 a0001c0001t0042g0078 a0001c0001t0046g0079 others(2): Show |
5 | HG00642.hp1 HG02257.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-126-2600G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153533522 | |||||||
| chrX:153533668 | A | G | 20 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0156 others(17): Show |
20 | HG01361.hp2 HG01884.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.-126-2454A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153533668 | |||||||
| chrX:153533669 | G | C | 116 | a0001c0001t0001g0040 a0001c0001t0001g0044 a0001c0001t0001g0102 others(113): Show |
128 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.-126-2453G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153533669 | |||||||
| chrX:153533838 | C | T | 1 | a0001c0013t0002g0180 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-126-2284C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153533838 | |||||||
| chrX:153534167 | G | A | 1 | a0001c0002t0013g0083 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-126-1955G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153534167 | |||||||
| chrX:153534199 | AG | A | 13 | a0001c0001t0001g0210 a0001c0001t0004g0018 a0001c0001t0004g0209 others(10): Show |
15 | HG02040.hp1 HG02129.hp1 HG02165.hp1 others(12): Show |
intron_variant | MODIFIER | c.-126-1919delG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153534199 | ||||||
| chrX:153534298 | G | A | 7 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(4): Show |
7 | HG00423.hp1 HG00558.hp2 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.-126-1824G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153534298 | |||||||
| chrX:153534332 | C | T | 2 | a0001c0001t0005g0087 a0001c0001t0014g0086 |
2 | HG03834.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.-126-1790C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153534332 | |||||||
| chrX:153534451 | T | C | 2 | a0001c0001t0022g0225 a0001c0011t0023g0224 |
2 | HG02809.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-126-1671T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153534451 | |||||||
| chrX:153534460 | CA | C | 96 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(93): Show |
105 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.-126-1660delA | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chrX | 153534460 | ||||||
| chrX:153534471 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-126-1651C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153534471 | |||||||
| chrX:153534526 | C | T | 2 | a0001c0007t0001g0043 a0001c0007t0001g0062 |
2 | NA18944.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.-126-1596C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153534526 | |||||||
| chrX:153534695 | C | T | 1 | a0001c0002t0001g0155 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-126-1427C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153534695 | |||||||
| chrX:153534985 | T | G | 231 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(228): Show |
255 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.-126-1137T>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153534985 | |||||||
| chrX:153535050 | A | G | 9 | a0001c0001t0009g0228 a0001c0001t0021g0222 a0001c0001t0042g0078 others(6): Show |
9 | HG00642.hp1 HG02109.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-126-1072A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153535050 | |||||||
| chrX:153535178 | G | T | 3 | a0001c0001t0001g0194 a0001c0001t0001g0196 a0001c0002t0018g0193 |
3 | HG00639.hp2 HG03239.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-126-944G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153535178 | |||||||
| chrX:153535372 | A | G | 229 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(226): Show |
253 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.-126-750A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153535372 | |||||||
| chrX:153535544 | C | T | 114 | a0001c0001t0001g0040 a0001c0001t0001g0044 a0001c0001t0001g0102 others(111): Show |
126 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.-126-578C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153535544 | |||||||
| chrX:153535562 | C | T | 1 | a0001c0001t0022g0225 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-126-560C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153535562 | |||||||
| chrX:153535602 | G | A | 2 | a0001c0005t0007g0020 a0001c0008t0026g0220 |
3 | HG02976.hp2 HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-126-520G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153535602 | |||||||
| chrX:153535842 | A | G | 231 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(228): Show |
255 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.-126-280A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153535842 | |||||||
| chrX:153535887 | C | A | 3 | a0001c0001t0001g0063 a0001c0001t0001g0156 a0003c0009t0005g0076 |
3 | HG02559.hp2 HG03041.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.-126-235C>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 2/21 | chrX | 153535887 | |||||||
| chrX:153536534 | C | T | 1 | a0001c0001t0022g0225 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.208+79C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153536534 | |||||||
| chrX:153536549 | T | C | 1 | a0001c0001t0022g0225 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.208+94T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153536549 | |||||||
| chrX:153536685 | G | A | 2 | a0001c0002t0002g0178 a0001c0002t0002g0179 |
2 | HG03491.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.208+230G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153536685 | |||||||
| chrX:153536897 | C | G | 1 | a0003c0009t0005g0076 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.208+442C>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153536897 | |||||||
| chrX:153536986 | G | A | 72 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(69): Show |
80 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.208+531G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153536986 | |||||||
| chrX:153536986 | G | T | 5 | a0001c0001t0009g0228 a0001c0001t0017g0177 a0001c0003t0002g0080 others(2): Show |
5 | HG00642.hp1 HG02109.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.208+531G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153536986 | |||||||
| chrX:153537128 | G | A | 2 | a0001c0002t0001g0011 a0001c0002t0001g0106 |
3 | HG00673.hp1 NA19066.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.208+673G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153537128 | |||||||
| chrX:153537274 | G | A | 1 | a0001c0002t0001g0107 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.208+819G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153537274 | |||||||
| chrX:153537487 | G | A | 1 | a0001c0001t0012g0048 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.208+1032G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153537487 | |||||||
| chrX:153537587 | C | T | 1 | a0001c0005t0007g0020 | 2 | HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.208+1132C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153537587 | |||||||
| chrX:153537642 | G | A | 1 | a0001c0008t0026g0220 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.208+1187G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153537642 | |||||||
| chrX:153537678 | A | C | 1 | a0001c0001t0005g0087 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.208+1223A>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153537678 | |||||||
| chrX:153537831 | G | A | 1 | a0001c0008t0026g0220 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.208+1376G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153537831 | |||||||
| chrX:153538096 | G | A | 4 | a0001c0001t0003g0204 a0001c0001t0008g0017 a0001c0001t0020g0199 others(1): Show |
5 | HG00735.hp2 HG01934.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.208+1641G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153538096 | |||||||
| chrX:153538136 | G | A | 11 | a0001c0001t0011g0037 a0001c0001t0011g0038 a0001c0001t0011g0039 others(8): Show |
11 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.208+1681G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153538136 | |||||||
| chrX:153538396 | T | C | 1 | a0001c0001t0044g0021 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.208+1941T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153538396 | |||||||
| chrX:153538414 | G | A | 1 | a0001c0008t0026g0220 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.208+1959G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153538414 | |||||||
| chrX:153538502 | C | T | 2 | a0001c0001t0021g0222 a0003c0009t0005g0076 |
2 | HG03041.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.208+2047C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153538502 | |||||||
| chrX:153538593 | C | T | 1 | a0001c0002t0001g0154 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.208+2138C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153538593 | |||||||
| chrX:153538786 | C | G | 1 | a0001c0001t0005g0036 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.208+2331C>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153538786 | |||||||
| chrX:153538814 | G | A | 1 | a0001c0001t0022g0225 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.208+2359G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153538814 | |||||||
| chrX:153538908 | G | A | 30 | a0001c0001t0001g0077 a0001c0001t0001g0194 a0001c0001t0001g0196 others(27): Show |
34 | HG00639.hp2 HG00735.hp2 HG01934.hp1 others(31): Show |
intron_variant | MODIFIER | c.209-2451G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153538908 | |||||||
| chrX:153538960 | C | G | 1 | a0001c0002t0001g0233 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.209-2399C>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153538960 | |||||||
| chrX:153539191 | G | A | 1 | a0001c0002t0001g0108 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.209-2168G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153539191 | |||||||
| chrX:153539293 | C | T | 6 | a0001c0001t0001g0235 a0001c0001t0005g0087 a0001c0001t0014g0086 others(3): Show |
6 | HG00609.hp1 HG00741.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.209-2066C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153539293 | |||||||
| chrX:153539360 | T | C | 1 | a0001c0002t0002g0185 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.209-1999T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153539360 | |||||||
| chrX:153539594 | C | G | 1 | a0001c0002t0038g0153 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.209-1765C>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153539594 | |||||||
| chrX:153539624 | C | T | 136 | a0001c0001t0001g0040 a0001c0001t0001g0044 a0001c0001t0001g0073 others(133): Show |
148 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.209-1735C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153539624 | |||||||
| chrX:153539684 | T | C | 72 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(69): Show |
80 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.209-1675T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153539684 | |||||||
| chrX:153539737 | C | T | 19 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0105 others(16): Show |
19 | HG01361.hp2 HG01884.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.209-1622C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153539737 | |||||||
| chrX:153539812 | G | A | 1 | a0001c0003t0027g0227 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.209-1547G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153539812 | |||||||
| chrX:153539823 | G | A | 26 | a0001c0001t0001g0077 a0001c0001t0001g0202 a0001c0001t0001g0210 others(23): Show |
30 | HG00735.hp2 HG01934.hp1 HG02040.hp1 others(27): Show |
intron_variant | MODIFIER | c.209-1536G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153539823 | |||||||
| chrX:153539902 | A | G | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(234): Show |
261 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(258): Show |
intron_variant | MODIFIER | c.209-1457A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153539902 | |||||||
| chrX:153540004 | A | C | 1 | a0001c0001t0002g0068 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.209-1355A>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153540004 | |||||||
| chrX:153540286 | A | T | 1 | a0001c0008t0026g0220 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.209-1073A>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153540286 | |||||||
| chrX:153540431 | C | T | 2 | a0001c0001t0001g0194 a0001c0001t0001g0196 |
2 | HG03239.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.209-928C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153540431 | |||||||
| chrX:153540539 | G | T | 1 | a0001c0002t0002g0192 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.209-820G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153540539 | |||||||
| chrX:153540687 | G | A | 1 | a0001c0008t0026g0220 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.209-672G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153540687 | |||||||
| chrX:153540994 | TCC | T | 4 | a0001c0001t0016g0219 a0001c0004t0007g0218 a0001c0004t0009g0231 others(1): Show |
4 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.209-362_209-361del others(2): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chrX | 153540994 | ||||||
| chrX:153541111 | G | A | 1 | a0001c0002t0002g0169 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.209-248G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153541111 | |||||||
| chrX:153541155 | G | A | 1 | a0001c0001t0022g0225 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.209-204G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153541155 | |||||||
| chrX:153541170 | C | T | 21 | a0001c0001t0001g0077 a0001c0001t0001g0202 a0001c0001t0001g0210 others(18): Show |
24 | HG00735.hp2 HG01934.hp1 HG02129.hp1 others(21): Show |
intron_variant | MODIFIER | c.209-189C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153541170 | |||||||
| chrX:153541236 | G | A | 1 | a0001c0008t0026g0220 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.209-123G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 3/21 | chrX | 153541236 | |||||||
| chrX:153541576 | G | A | 13 | a0001c0001t0001g0156 a0001c0001t0001g0198 a0001c0001t0001g0200 others(10): Show |
13 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.406+20G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 4/21 | chrX | 153541576 | |||||||
| chrX:153541663 | G | A | 2 | a0001c0008t0026g0220 a0003c0009t0005g0076 |
2 | HG02976.hp2 HG03041.hp2 |
splice_region_variant&intron_variant | LOW | c.407-6G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 4/21 | chrX | 153541663 | |||||||
| chrX:153541967 | G | A | 120 | a0001c0001t0001g0040 a0001c0001t0001g0044 a0001c0001t0001g0102 others(117): Show |
132 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.664+41G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 5/21 | chrX | 153541967 | |||||||
| chrX:153542046 | CCTT | C | 164 | a0001c0001t0001g0040 a0001c0001t0001g0044 a0001c0001t0001g0077 others(161): Show |
180 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(177): Show |
intron_variant | MODIFIER | c.664+121_664+123del others(3): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 5/21 | chrX | 153542046 | |||||||
| chrX:153542049 | TAGGAGGC others(64): Show |
T | 77 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(74): Show |
85 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.664+124_664+194del others(71): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 5/21 | chrX | 153542049 | |||||||
| chrX:153542072 | T | G | 1 | a0001c0002t0001g0109 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.664+146T>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 5/21 | chrX | 153542072 | |||||||
| chrX:153542099 | G | T | 1 | a0001c0002t0001g0164 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.664+173G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 5/21 | chrX | 153542099 | |||||||
| chrX:153542168 | TC | T | 155 | a0001c0001t0001g0040 a0001c0001t0001g0044 a0001c0001t0001g0077 others(152): Show |
171 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(168): Show |
intron_variant | MODIFIER | c.665-149delC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chrX | 153542168 | ||||||
| chrX:153542207 | A | G | 230 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(227): Show |
254 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.665-116A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 5/21 | chrX | 153542207 | |||||||
| chrX:153542262 | T | C | 8 | a0001c0001t0011g0037 a0001c0001t0011g0038 a0001c0001t0011g0039 others(5): Show |
8 | HG02257.hp1 HG02451.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.665-61T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 5/21 | chrX | 153542262 | |||||||
| chrX:153542465 | G | C | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(234): Show |
261 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(258): Show |
intron_variant | MODIFIER | c.790+17G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 6/21 | chrX | 153542465 | |||||||
| chrX:153542488 | G | A | 3 | a0001c0001t0005g0088 a0001c0001t0005g0157 a0001c0017t0025g0226 |
3 | HG02896.hp2 HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.790+40G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 6/21 | chrX | 153542488 | |||||||
| chrX:153542662 | G | A | 233 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(230): Show |
257 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(254): Show |
intron_variant | MODIFIER | c.790+214G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 6/21 | chrX | 153542662 | |||||||
| chrX:153542683 | A | G | 1 | a0001c0003t0024g0230 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.790+235A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 6/21 | chrX | 153542683 | |||||||
| chrX:153542761 | T | A | 23 | a0001c0001t0001g0077 a0001c0001t0001g0202 a0001c0001t0001g0210 others(20): Show |
27 | HG00735.hp2 HG01934.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.791-282T>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 6/21 | chrX | 153542761 | |||||||
| chrX:153542884 | G | A | 2 | a0001c0001t0011g0037 a0001c0011t0023g0224 |
2 | HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.791-159G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 6/21 | chrX | 153542884 | |||||||
| chrX:153543244 | G | A | 1 | a0001c0001t0002g0175 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.916+76G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | chrX | 153543244 | |||||||
| chrX:153543421 | C | T | 1 | a0001c0008t0026g0220 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.916+253C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | chrX | 153543421 | |||||||
| chrX:153543490 | C | T | 23 | a0001c0001t0001g0077 a0001c0001t0001g0202 a0001c0001t0001g0210 others(20): Show |
27 | HG00735.hp2 HG01934.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.916+322C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | chrX | 153543490 | |||||||
| chrX:153543607 | A | C | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(234): Show |
261 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(258): Show |
intron_variant | MODIFIER | c.916+439A>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | chrX | 153543607 | |||||||
| chrX:153543677 | G | A | 1 | a0001c0001t0004g0209 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.916+509G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | chrX | 153543677 | |||||||
| chrX:153543745 | T | G | 25 | a0001c0001t0001g0077 a0001c0001t0001g0202 a0001c0001t0001g0210 others(22): Show |
29 | HG00642.hp1 HG00735.hp2 HG01934.hp1 others(26): Show |
intron_variant | MODIFIER | c.916+577T>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | chrX | 153543745 | |||||||
| chrX:153543776 | T | C | 236 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(233): Show |
260 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(257): Show |
intron_variant | MODIFIER | c.916+608T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | chrX | 153543776 | |||||||
| chrX:153543852 | C | T | 1 | a0001c0001t0007g0229 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.916+684C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | chrX | 153543852 | |||||||
| chrX:153544169 | G | T | 1 | a0001c0002t0001g0164 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.916+1001G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | chrX | 153544169 | |||||||
| chrX:153544284 | T | C | 8 | a0001c0001t0001g0194 a0001c0001t0001g0196 a0001c0001t0001g0235 others(5): Show |
8 | HG00609.hp1 HG00741.hp1 HG03239.hp2 others(5): Show |
intron_variant | MODIFIER | c.916+1116T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | chrX | 153544284 | |||||||
| chrX:153544378 | C | T | 2 | a0001c0001t0028g0232 a0001c0010t0005g0091 |
2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.916+1210C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | chrX | 153544378 | |||||||
| chrX:153544564 | G | A | 6 | a0001c0001t0001g0235 a0001c0001t0005g0087 a0001c0001t0014g0086 others(3): Show |
6 | HG00609.hp1 HG00741.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.916+1396G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | chrX | 153544564 | |||||||
| chrX:153544787 | C | G | 1 | a0001c0001t0004g0215 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.917-1301C>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | chrX | 153544787 | |||||||
| chrX:153544814 | G | A | 1 | a0001c0001t0001g0049 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.917-1274G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | chrX | 153544814 | |||||||
| chrX:153544850 | C | T | 19 | a0001c0001t0001g0077 a0001c0001t0001g0202 a0001c0001t0001g0210 others(16): Show |
22 | HG00642.hp1 HG01934.hp1 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.917-1238C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | chrX | 153544850 | |||||||
| chrX:153544994 | G | A | 27 | a0001c0001t0001g0077 a0001c0001t0001g0202 a0001c0001t0001g0210 others(24): Show |
30 | HG00609.hp1 HG00642.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.917-1094G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | chrX | 153544994 | |||||||
| chrX:153545066 | A | G | 1 | a0001c0012t0001g0148 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.917-1022A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | chrX | 153545066 | |||||||
| chrX:153545092 | CG | C | 162 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0024 others(159): Show |
181 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.917-986delG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chrX | 153545092 | ||||||
| chrX:153545096 | G | T | 1 | a0001c0001t0014g0161 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.917-992G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | chrX | 153545096 | |||||||
| chrX:153545127 | G | A | 1 | a0001c0002t0002g0186 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.917-961G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | chrX | 153545127 | |||||||
| chrX:153545347 | T | A | 1 | a0001c0001t0022g0225 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.917-741T>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | chrX | 153545347 | |||||||
| chrX:153545363 | C | T | 1 | a0001c0016t0020g0070 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.917-725C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | chrX | 153545363 | |||||||
| chrX:153545499 | C | T | 5 | a0001c0001t0011g0038 a0001c0001t0011g0039 a0001c0001t0042g0078 others(2): Show |
5 | HG02257.hp1 HG02451.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.917-589C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | chrX | 153545499 | |||||||
| chrX:153545500 | G | A | 1 | a0001c0017t0025g0226 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.917-588G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | chrX | 153545500 | |||||||
| chrX:153545599 | A | T | 1 | a0001c0001t0001g0202 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.917-489A>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | chrX | 153545599 | |||||||
| chrX:153545628 | C | T | 21 | a0001c0001t0001g0077 a0001c0001t0001g0202 a0001c0001t0001g0210 others(18): Show |
24 | HG00642.hp1 HG00735.hp2 HG01934.hp1 others(21): Show |
intron_variant | MODIFIER | c.917-460C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | chrX | 153545628 | |||||||
| chrX:153545747 | G | A | 17 | a0001c0001t0001g0156 a0001c0001t0001g0198 a0001c0001t0001g0200 others(14): Show |
17 | HG00609.hp1 HG00741.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.917-341G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | chrX | 153545747 | |||||||
| chrX:153545765 | G | A | 2 | a0001c0001t0020g0199 a0001c0005t0007g0020 |
3 | HG02818.hp1 HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.917-323G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | chrX | 153545765 | |||||||
| chrX:153545773 | T | C | 1 | a0001c0005t0007g0020 | 2 | HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.917-315T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | chrX | 153545773 | |||||||
| chrX:153546029 | C | T | 2 | a0001c0003t0001g0034 a0001c0017t0025g0226 |
2 | NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.917-59C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 7/21 | chrX | 153546029 | |||||||
| chrX:153546226 | G | T | 1 | a0001c0005t0007g0020 | 2 | HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.958+97G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 8/21 | chrX | 153546226 | |||||||
| chrX:153546414 | C | T | 1 | a0001c0002t0001g0176 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.958+285C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 8/21 | chrX | 153546414 | |||||||
| chrX:153546430 | T | C | 29 | a0001c0001t0001g0194 a0001c0001t0001g0196 a0001c0002t0001g0100 others(26): Show |
31 | HG00423.hp2 HG00544.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.958+301T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 8/21 | chrX | 153546430 | |||||||
| chrX:153546716 | C | G | 22 | a0001c0001t0001g0077 a0001c0001t0001g0202 a0001c0001t0001g0210 others(19): Show |
25 | HG00642.hp1 HG00735.hp2 HG01934.hp1 others(22): Show |
intron_variant | MODIFIER | c.958+587C>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 8/21 | chrX | 153546716 | |||||||
| chrX:153546814 | G | A | 2 | a0001c0001t0011g0037 a0001c0011t0023g0224 |
2 | HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.958+685G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 8/21 | chrX | 153546814 | |||||||
| chrX:153546929 | G | T | 1 | a0001c0015t0009g0221 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.958+800G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 8/21 | chrX | 153546929 | |||||||
| chrX:153547333 | G | A | 1 | a0001c0008t0026g0220 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.959-502G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 8/21 | chrX | 153547333 | |||||||
| chrX:153547496 | C | T | 1 | a0001c0001t0001g0194 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.959-339C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 8/21 | chrX | 153547496 | |||||||
| chrX:153548017 | T | G | 5 | a0001c0001t0001g0073 a0001c0003t0001g0034 a0001c0003t0001g0035 others(2): Show |
5 | HG01361.hp2 HG02647.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1123+18T>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 9/21 | chrX | 153548017 | |||||||
| chrX:153548057 | G | C | 8 | a0001c0001t0011g0037 a0001c0001t0011g0038 a0001c0001t0011g0039 others(5): Show |
8 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1123+58G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 9/21 | chrX | 153548057 | |||||||
| chrX:153548165 | G | A | 2 | a0001c0008t0026g0220 a0001c0011t0023g0224 |
2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1123+166G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 9/21 | chrX | 153548165 | |||||||
| chrX:153548281 | CT | C | 63 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(60): Show |
68 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.1123+283delT | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 9/21 | chrX | 153548281 | |||||||
| chrX:153548288 | C | A | 19 | a0001c0001t0002g0175 a0001c0001t0005g0087 a0001c0001t0011g0037 others(16): Show |
19 | HG00741.hp1 HG01243.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1123+289C>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 9/21 | chrX | 153548288 | |||||||
| chrX:153548915 | T | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(91): Show |
107 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.1338+61T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 10/21 | chrX | 153548915 | |||||||
| chrX:153549012 | TCTGTCAG others(4): Show |
T | 1 | a0001c0001t0036g0214 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1338+159_1338+169d others(13): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 10/21 | chrX | 153549012 | |||||||
| chrX:153549299 | G | A | 1 | a0001c0002t0001g0095 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1339-198G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 10/21 | chrX | 153549299 | |||||||
| chrX:153549305 | A | G | 23 | a0001c0001t0001g0024 a0001c0001t0001g0040 a0001c0001t0001g0077 others(20): Show |
23 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.1339-192A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 10/21 | chrX | 153549305 | |||||||
| chrX:153549418 | C | T | 3 | a0001c0001t0022g0225 a0001c0008t0026g0220 a0001c0011t0023g0224 |
3 | HG02809.hp1 HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1339-79C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 10/21 | chrX | 153549418 | |||||||
| chrX:153549964 | G | C | 5 | a0001c0001t0011g0037 a0001c0001t0011g0038 a0001c0001t0011g0039 others(2): Show |
5 | HG02257.hp1 HG02451.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1582-81G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 11/21 | chrX | 153549964 | |||||||
| chrX:153550343 | G | A | 9 | a0001c0001t0001g0121 a0001c0001t0001g0202 a0001c0001t0002g0175 others(6): Show |
9 | HG00741.hp1 HG02486.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1823+57G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153550343 | |||||||
| chrX:153550417 | G | A | 1 | a0001c0001t0022g0225 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1823+131G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153550417 | |||||||
| chrX:153550426 | A | G | 1 | a0001c0001t0022g0225 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1823+140A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153550426 | |||||||
| chrX:153550428 | C | T | 106 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0005g0127 others(103): Show |
119 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.1823+142C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153550428 | |||||||
| chrX:153550581 | C | G | 11 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0121 others(8): Show |
11 | HG00741.hp1 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1823+295C>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153550581 | |||||||
| chrX:153550645 | T | C | 187 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(184): Show |
203 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.1823+359T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153550645 | |||||||
| chrX:153550669 | T | TTTTTG | 4 | a0001c0001t0001g0210 a0001c0001t0004g0209 a0001c0001t0032g0206 others(1): Show |
4 | NA18939.hp1 NA18975.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.1823+398_1823+402d others(7): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chrX | 153550669 | ||||||
| chrX:153550748 | C | T | 68 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(65): Show |
71 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.1823+462C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153550748 | |||||||
| chrX:153550761 | G | A | 106 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0005g0127 others(103): Show |
119 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.1823+475G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153550761 | |||||||
| chrX:153550835 | G | A | 4 | a0001c0001t0001g0008 a0001c0001t0002g0051 a0001c0001t0002g0068 others(1): Show |
4 | HG00544.hp2 NA18979.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.1823+549G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153550835 | |||||||
| chrX:153550989 | G | A | 106 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0005g0127 others(103): Show |
119 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.1823+703G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153550989 | |||||||
| chrX:153551006 | TC | T | 8 | a0001c0001t0001g0040 a0001c0001t0001g0194 a0001c0001t0001g0196 others(5): Show |
8 | HG02257.hp2 HG02735.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1823+721delC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153551006 | |||||||
| chrX:153551008 | G | A | 2 | a0001c0002t0001g0108 a0001c0002t0001g0208 |
2 | HG02015.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.1823+722G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153551008 | |||||||
| chrX:153551125 | C | T | 106 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0005g0127 others(103): Show |
119 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.1823+839C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153551125 | |||||||
| chrX:153551128 | G | A | 106 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0005g0127 others(103): Show |
119 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.1823+842G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153551128 | |||||||
| chrX:153551143 | G | C | 2 | a0001c0003t0007g0223 a0001c0003t0033g0030 |
2 | HG02257.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1823+857G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153551143 | |||||||
| chrX:153551164 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1823+878G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153551164 | |||||||
| chrX:153551212 | C | G | 11 | a0001c0001t0001g0121 a0001c0001t0001g0202 a0001c0001t0002g0175 others(8): Show |
11 | HG00741.hp1 HG02109.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1823+926C>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153551212 | |||||||
| chrX:153551395 | G | T | 1 | a0001c0002t0002g0146 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1823+1109G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153551395 | |||||||
| chrX:153551506 | A | G | 2 | a0001c0002t0013g0084 a0001c0002t0013g0085 |
2 | NA18998.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.1823+1220A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153551506 | |||||||
| chrX:153551573 | C | T | 11 | a0001c0001t0001g0210 a0001c0001t0004g0018 a0001c0001t0004g0119 others(8): Show |
12 | NA18612.hp1 NA18939.hp1 NA18945.hp1 others(9): Show |
intron_variant | MODIFIER | c.1823+1287C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153551573 | |||||||
| chrX:153551574 | G | A | 2 | a0001c0003t0002g0080 a0003c0009t0005g0076 |
2 | HG03041.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1823+1288G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153551574 | |||||||
| chrX:153551601 | GCTTAGAG others(14): Show |
G | 1 | a0001c0001t0044g0021 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1823+1339_1823+135 others(25): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chrX | 153551601 | ||||||
| chrX:153551699 | C | T | 231 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(228): Show |
254 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.1824-1336C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153551699 | |||||||
| chrX:153551732 | G | T | 4 | a0001c0002t0002g0089 a0001c0002t0002g0166 a0001c0002t0015g0165 others(1): Show |
4 | NA18950.hp2 NA18957.hp1 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.1824-1303G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153551732 | |||||||
| chrX:153551804 | C | T | 2 | a0001c0002t0001g0072 a0001c0002t0017g0071 |
2 | HG01884.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1824-1231C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153551804 | |||||||
| chrX:153551832 | C | G | 1 | a0001c0001t0004g0213 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1824-1203C>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153551832 | |||||||
| chrX:153551892 | C | G | 1 | a0001c0002t0002g0042 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1824-1143C>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153551892 | |||||||
| chrX:153551893 | T | G | 1 | a0001c0002t0002g0042 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1824-1142T>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153551893 | |||||||
| chrX:153551894 | G | T | 1 | a0001c0002t0002g0042 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1824-1141G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153551894 | |||||||
| chrX:153551895 | C | G | 1 | a0001c0002t0002g0042 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1824-1140C>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153551895 | |||||||
| chrX:153551897 | G | A | 1 | a0001c0001t0021g0222 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1824-1138G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153551897 | |||||||
| chrX:153551932 | C | G | 1 | a0001c0001t0028g0232 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1824-1103C>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153551932 | |||||||
| chrX:153552014 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1824-1021G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153552014 | |||||||
| chrX:153552113 | G | A | 236 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(233): Show |
259 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.1824-922G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153552113 | |||||||
| chrX:153552114 | C | A | 236 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(233): Show |
259 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.1824-921C>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153552114 | |||||||
| chrX:153552172 | C | T | 1 | a0001c0002t0002g0167 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1824-863C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153552172 | |||||||
| chrX:153552205 | T | G | 1 | a0001c0001t0001g0105 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1824-830T>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153552205 | |||||||
| chrX:153552281 | C | T | 4 | a0001c0003t0001g0034 a0001c0003t0001g0035 a0001c0003t0002g0032 others(1): Show |
4 | HG01361.hp2 HG03516.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1824-754C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153552281 | |||||||
| chrX:153552309 | T | C | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(234): Show |
260 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(257): Show |
intron_variant | MODIFIER | c.1824-726T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153552309 | |||||||
| chrX:153552333 | T | G | 4 | a0001c0003t0001g0034 a0001c0003t0001g0035 a0001c0003t0002g0032 others(1): Show |
4 | HG01361.hp2 HG03516.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1824-702T>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153552333 | |||||||
| chrX:153552536 | G | A | 1 | a0001c0001t0039g0234 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1824-499G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153552536 | |||||||
| chrX:153552581 | C | T | 1 | a0001c0001t0002g0023 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1824-454C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153552581 | |||||||
| chrX:153552662 | G | A | 1 | a0001c0015t0009g0221 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1824-373G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153552662 | |||||||
| chrX:153552679 | T | C | 4 | a0001c0003t0001g0034 a0001c0003t0001g0035 a0001c0003t0002g0032 others(1): Show |
4 | HG01361.hp2 HG03516.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1824-356T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153552679 | |||||||
| chrX:153552721 | G | C | 1 | a0001c0001t0021g0222 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1824-314G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153552721 | |||||||
| chrX:153552857 | C | A | 1 | a0001c0001t0022g0225 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1824-178C>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153552857 | |||||||
| chrX:153552977 | G | A | 105 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0005g0127 others(102): Show |
118 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.1824-58G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 12/21 | chrX | 153552977 | |||||||
| chrX:153553432 | G | T | 175 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(172): Show |
191 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.2058+163G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/21 | chrX | 153553432 | |||||||
| chrX:153553523 | G | A | 7 | a0001c0001t0001g0121 a0001c0001t0002g0175 a0001c0001t0005g0087 others(4): Show |
7 | HG00741.hp1 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2058+254G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/21 | chrX | 153553523 | |||||||
| chrX:153553655 | C | G | 109 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0005g0127 others(106): Show |
122 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.2058+386C>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/21 | chrX | 153553655 | |||||||
| chrX:153553658 | C | T | 231 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(228): Show |
254 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.2058+389C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/21 | chrX | 153553658 | |||||||
| chrX:153553778 | G | A | 2 | a0001c0002t0001g0059 a0001c0002t0003g0122 |
2 | HG00741.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.2058+509G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/21 | chrX | 153553778 | |||||||
| chrX:153553779 | C | T | 1 | a0001c0001t0005g0036 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2058+510C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/21 | chrX | 153553779 | |||||||
| chrX:153553780 | G | A | 2 | a0001c0003t0002g0080 a0003c0009t0005g0076 |
2 | HG03041.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2058+511G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/21 | chrX | 153553780 | |||||||
| chrX:153553792 | A | G | 1 | a0001c0002t0002g0145 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2058+523A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/21 | chrX | 153553792 | |||||||
| chrX:153553816 | T | G | 1 | a0001c0001t0039g0234 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2058+547T>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/21 | chrX | 153553816 | |||||||
| chrX:153553891 | G | A | 2 | a0001c0001t0005g0088 a0001c0001t0005g0157 |
2 | HG02896.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2058+622G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/21 | chrX | 153553891 | |||||||
| chrX:153554103 | C | T | 1 | a0001c0001t0020g0199 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2058+834C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/21 | chrX | 153554103 | |||||||
| chrX:153554136 | C | T | 2 | a0001c0003t0002g0080 a0003c0009t0005g0076 |
2 | HG03041.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2058+867C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/21 | chrX | 153554136 | |||||||
| chrX:153554214 | C | A | 1 | a0001c0017t0025g0226 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2058+945C>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/21 | chrX | 153554214 | |||||||
| chrX:153554487 | G | T | 231 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(228): Show |
254 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.2058+1218G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/21 | chrX | 153554487 | |||||||
| chrX:153554517 | G | C | 9 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(6): Show |
14 | HG01109.hp1 HG02258.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.2058+1248G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/21 | chrX | 153554517 | |||||||
| chrX:153554847 | C | T | 103 | a0001c0001t0005g0127 a0001c0001t0020g0199 a0001c0002t0001g0001 others(100): Show |
116 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.2059-1202C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/21 | chrX | 153554847 | |||||||
| chrX:153554904 | CA | C | 12 | a0001c0001t0021g0222 a0001c0001t0022g0225 a0001c0003t0001g0034 others(9): Show |
13 | HG01243.hp1 HG01361.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.2059-1144delA | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/21 | chrX | 153554904 | |||||||
| chrX:153554939 | G | A | 1 | a0001c0001t0028g0232 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2059-1110G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/21 | chrX | 153554939 | |||||||
| chrX:153555118 | T | G | 11 | a0001c0001t0001g0121 a0001c0001t0001g0202 a0001c0001t0002g0175 others(8): Show |
11 | HG00741.hp1 HG02486.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.2059-931T>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/21 | chrX | 153555118 | |||||||
| chrX:153555705 | G | A | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(234): Show |
261 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(258): Show |
intron_variant | MODIFIER | c.2059-344G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/21 | chrX | 153555705 | |||||||
| chrX:153555792 | A | ATGCAACA others(4): Show |
2 | a0001c0003t0002g0080 a0003c0009t0005g0076 |
2 | HG03041.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2059-254_2059-253i others(13): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chrX | 153555792 | ||||||
| chrX:153555807 | A | G | 1 | a0001c0002t0019g0144 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2059-242A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/21 | chrX | 153555807 | |||||||
| chrX:153555988 | T | C | 1 | a0001c0002t0001g0125 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2059-61T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/21 | chrX | 153555988 | |||||||
| chrX:153556005 | C | T | 2 | a0001c0002t0001g0016 a0001c0002t0003g0016 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2059-44C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 13/21 | chrX | 153556005 | |||||||
| chrX:153556255 | G | C | 1 | a0001c0002t0010g0093 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2238+27G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 14/21 | chrX | 153556255 | |||||||
| chrX:153556259 | C | A | 9 | a0001c0001t0001g0121 a0001c0001t0001g0202 a0001c0001t0002g0175 others(6): Show |
9 | HG00741.hp1 HG02486.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.2238+31C>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 14/21 | chrX | 153556259 | |||||||
| chrX:153556429 | C | T | 231 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(228): Show |
254 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.2326+11C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 15/21 | chrX | 153556429 | |||||||
| chrX:153556438 | C | T | 47 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(44): Show |
54 | HG00642.hp1 HG01109.hp1 HG01884.hp2 others(51): Show |
intron_variant | MODIFIER | c.2326+20C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 15/21 | chrX | 153556438 | |||||||
| chrX:153556604 | G | A | 1 | a0001c0001t0006g0066 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2326+186G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 15/21 | chrX | 153556604 | |||||||
| chrX:153556696 | A | G | 1 | a0001c0001t0044g0021 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2327-221A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 15/21 | chrX | 153556696 | |||||||
| chrX:153557272 | G | A | 1 | a0001c0002t0001g0126 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2433+249G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 16/21 | chrX | 153557272 | |||||||
| chrX:153557318 | C | T | 1 | a0001c0001t0039g0234 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2433+295C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 16/21 | chrX | 153557318 | |||||||
| chrX:153557859 | C | T | 42 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(39): Show |
49 | HG00642.hp1 HG01109.hp1 HG01884.hp2 others(46): Show |
intron_variant | MODIFIER | c.2434-253C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 16/21 | chrX | 153557859 | |||||||
| chrX:153557881 | A | AGC | 8 | a0001c0002t0001g0129 a0001c0002t0002g0185 a0001c0002t0002g0187 others(5): Show |
8 | HG00639.hp2 HG00741.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.2434-230_2434-229d others(4): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chrX | 153557881 | ||||||
| chrX:153557882 | G | GCGC | 74 | a0001c0001t0020g0199 a0001c0002t0001g0001 a0001c0002t0001g0011 others(71): Show |
86 | HG00558.hp1 HG00597.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.2434-229_2434-228i others(5): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chrX | 153557882 | ||||||
| chrX:153557882 | G | GCGCC | 25 | a0001c0002t0001g0004 a0001c0002t0001g0061 a0001c0002t0001g0082 others(22): Show |
26 | HG00408.hp1 HG00423.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.2434-229_2434-228i others(6): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chrX | 153557882 | ||||||
| chrX:153557883 | C | CG | 5 | a0001c0001t0044g0021 a0001c0003t0027g0227 a0001c0003t0040g0090 others(2): Show |
5 | HG02055.hp1 HG02109.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.2434-229_2434-228i others(3): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 16/21 | chrX | 153557883 | |||||||
| chrX:153557905 | T | C | 8 | a0001c0001t0044g0021 a0001c0003t0002g0080 a0001c0003t0002g0203 others(5): Show |
8 | HG01934.hp1 HG02055.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.2434-207T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 16/21 | chrX | 153557905 | |||||||
| chrX:153557941 | AT | A | 8 | a0001c0001t0044g0021 a0001c0003t0002g0080 a0001c0003t0002g0203 others(5): Show |
8 | HG01934.hp1 HG02055.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.2434-169delT | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chrX | 153557941 | ||||||
| chrX:153558445 | T | C | 1 | a0001c0002t0019g0144 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2625+142T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 17/21 | chrX | 153558445 | |||||||
| chrX:153558718 | T | C | 4 | a0001c0002t0002g0089 a0001c0002t0002g0166 a0001c0002t0015g0165 others(1): Show |
4 | NA18950.hp2 NA18957.hp1 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.2625+415T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 17/21 | chrX | 153558718 | |||||||
| chrX:153558744 | A | T | 15 | a0001c0001t0002g0175 a0001c0001t0005g0087 a0001c0001t0005g0127 others(12): Show |
15 | HG00741.hp1 HG01361.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.2625+441A>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 17/21 | chrX | 153558744 | |||||||
| chrX:153558816 | C | T | 123 | a0001c0001t0001g0121 a0001c0001t0002g0175 a0001c0001t0005g0087 others(120): Show |
136 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(133): Show |
intron_variant | MODIFIER | c.2625+513C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 17/21 | chrX | 153558816 | |||||||
| chrX:153558836 | G | C | 3 | a0001c0001t0005g0087 a0001c0001t0005g0127 a0001c0001t0014g0086 |
3 | HG03834.hp2 HG03927.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.2625+533G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 17/21 | chrX | 153558836 | |||||||
| chrX:153558884 | T | C | 1 | a0001c0001t0044g0021 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2625+581T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 17/21 | chrX | 153558884 | |||||||
| chrX:153558929 | A | C | 8 | a0001c0001t0002g0175 a0001c0001t0005g0087 a0001c0001t0005g0127 others(5): Show |
8 | HG00741.hp1 HG02451.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2625+626A>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 17/21 | chrX | 153558929 | |||||||
| chrX:153558972 | A | G | 60 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(57): Show |
68 | HG00642.hp1 HG01109.hp1 HG01884.hp2 others(65): Show |
intron_variant | MODIFIER | c.2625+669A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 17/21 | chrX | 153558972 | |||||||
| chrX:153559049 | TA | T | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(234): Show |
261 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(258): Show |
intron_variant | MODIFIER | c.2626-674delA | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chrX | 153559049 | ||||||
| chrX:153559334 | G | C | 187 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(184): Show |
208 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(205): Show |
intron_variant | MODIFIER | c.2626-395G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 17/21 | chrX | 153559334 | |||||||
| chrX:153559558 | G | C | 3 | a0001c0001t0002g0159 a0001c0001t0005g0157 a0001c0001t0005g0158 |
3 | HG03098.hp1 HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2626-171G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 17/21 | chrX | 153559558 | |||||||
| chrX:153559652 | C | T | 2 | a0001c0001t0002g0175 a0001c0001t0005g0201 |
2 | HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2626-77C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 17/21 | chrX | 153559652 | |||||||
| chrX:153559956 | G | T | 210 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(207): Show |
234 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.2839+14G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 18/21 | chrX | 153559956 | |||||||
| chrX:153559975 | A | G | 236 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(233): Show |
260 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(257): Show |
intron_variant | MODIFIER | c.2839+33A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 18/21 | chrX | 153559975 | |||||||
| chrX:153560047 | C | T | 2 | a0001c0001t0001g0118 a0001c0001t0019g0064 |
2 | HG01167.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.2839+105C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 18/21 | chrX | 153560047 | |||||||
| chrX:153560175 | G | C | 214 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(211): Show |
238 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.2839+233G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 18/21 | chrX | 153560175 | |||||||
| chrX:153560364 | TG | T | 7 | a0001c0001t0002g0175 a0001c0001t0005g0087 a0001c0001t0005g0127 others(4): Show |
7 | HG00741.hp1 HG02451.hp2 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.2840-306delG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chrX | 153560364 | ||||||
| chrX:153560415 | C | T | 8 | a0001c0001t0002g0175 a0001c0001t0005g0087 a0001c0001t0005g0127 others(5): Show |
8 | HG00741.hp1 HG02071.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.2840-261C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 18/21 | chrX | 153560415 | |||||||
| chrX:153560542 | T | A | 107 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(104): Show |
118 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.2840-134T>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 18/21 | chrX | 153560542 | |||||||
| chrX:153560547 | C | G | 1 | a0001c0001t0008g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2840-129C>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 18/21 | chrX | 153560547 | |||||||
| chrX:153560548 | G | A | 3 | a0001c0003t0027g0227 a0001c0003t0040g0090 a0001c0010t0005g0091 |
3 | HG02055.hp1 HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2840-128G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 18/21 | chrX | 153560548 | |||||||
| chrX:153560627 | C | T | 1 | a0001c0003t0024g0230 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2840-49C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 18/21 | chrX | 153560627 | |||||||
| chrX:153561081 | T | G | 2 | a0001c0002t0018g0128 a0001c0002t0018g0193 |
2 | HG00639.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.3051+194T>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 19/21 | chrX | 153561081 | |||||||
| chrX:153561105 | C | T | 1 | a0001c0002t0001g0182 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.3051+218C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 19/21 | chrX | 153561105 | |||||||
| chrX:153561134 | C | T | 9 | a0001c0001t0002g0175 a0001c0001t0005g0087 a0001c0001t0005g0127 others(6): Show |
9 | HG00741.hp1 HG02451.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.3051+247C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 19/21 | chrX | 153561134 | |||||||
| chrX:153561369 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.3051+482A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 19/21 | chrX | 153561369 | |||||||
| chrX:153561573 | A | G | 226 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(223): Show |
250 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(247): Show |
intron_variant | MODIFIER | c.3052-562A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 19/21 | chrX | 153561573 | |||||||
| chrX:153561584 | G | T | 226 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(223): Show |
250 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(247): Show |
intron_variant | MODIFIER | c.3052-551G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 19/21 | chrX | 153561584 | |||||||
| chrX:153561632 | G | T | 1 | a0003c0009t0005g0076 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3052-503G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 19/21 | chrX | 153561632 | |||||||
| chrX:153561847 | G | A | 2 | a0001c0001t0028g0232 a0001c0001t0044g0021 |
2 | HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.3052-288G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 19/21 | chrX | 153561847 | |||||||
| chrX:153561987 | A | G | 226 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(223): Show |
250 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(247): Show |
intron_variant | MODIFIER | c.3052-148A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 19/21 | chrX | 153561987 | |||||||
| chrX:153561995 | G | A | 3 | a0001c0003t0027g0227 a0001c0003t0040g0090 a0001c0010t0005g0091 |
3 | HG02055.hp1 HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.3052-140G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 19/21 | chrX | 153561995 | |||||||
| chrX:153562130 | C | T | 5 | a0001c0001t0001g0009 a0001c0001t0001g0058 a0001c0001t0001g0116 others(2): Show |
5 | HG01123.hp1 HG01928.hp1 HG01952.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.3052-5C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 19/21 | chrX | 153562130 | |||||||
| chrX:153562452 | A | G | 3 | a0001c0001t0017g0177 a0001c0002t0001g0072 a0001c0002t0017g0071 |
3 | HG01884.hp1 HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3159+210A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 20/21 | chrX | 153562452 | |||||||
| chrX:153562472 | G | A | 3 | a0001c0003t0002g0080 a0001c0003t0002g0203 a0003c0009t0005g0076 |
3 | HG01934.hp1 HG03041.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3159+230G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 20/21 | chrX | 153562472 | |||||||
| chrX:153562508 | C | T | 1 | a0001c0003t0040g0090 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3159+266C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 20/21 | chrX | 153562508 | |||||||
| chrX:153562660 | G | A | 1 | a0001c0002t0001g0132 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.3159+418G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 20/21 | chrX | 153562660 | |||||||
| chrX:153562703 | T | C | 105 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0121 others(102): Show |
117 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.3159+461T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 20/21 | chrX | 153562703 | |||||||
| chrX:153562728 | G | C | 3 | a0001c0001t0017g0177 a0001c0002t0001g0072 a0001c0002t0017g0071 |
3 | HG01884.hp1 HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3159+486G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 20/21 | chrX | 153562728 | |||||||
| chrX:153562819 | A | T | 1 | a0001c0002t0001g0072 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3159+577A>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 20/21 | chrX | 153562819 | |||||||
| chrX:153563127 | T | C | 218 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(215): Show |
240 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.3159+885T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 20/21 | chrX | 153563127 | |||||||
| chrX:153563136 | C | CTTT | 25 | a0001c0001t0001g0006 a0001c0001t0001g0054 a0001c0001t0001g0103 others(22): Show |
27 | HG00558.hp2 HG00639.hp1 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.3159+915_3159+917d others(5): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 153563136 | ||||||
| chrX:153563136 | C | CTTTT | 183 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(180): Show |
204 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.3159+914_3159+917d others(6): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 153563136 | ||||||
| chrX:153563136 | C | CTTTTT | 14 | a0001c0001t0001g0027 a0001c0001t0001g0110 a0001c0001t0001g0121 others(11): Show |
14 | HG00423.hp1 HG01123.hp2 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.3159+913_3159+917d others(7): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 153563136 | ||||||
| chrX:153563136 | CT | C | 15 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0002g0175 others(12): Show |
16 | HG00741.hp1 HG02451.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.3159+917delT | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chrX | 153563136 | ||||||
| chrX:153563243 | G | T | 1 | a0001c0002t0003g0131 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.3159+1001G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 20/21 | chrX | 153563243 | |||||||
| chrX:153563421 | G | T | 9 | a0001c0003t0001g0034 a0001c0003t0001g0035 a0001c0003t0002g0032 others(6): Show |
9 | HG01361.hp2 HG02257.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.3159+1179G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 20/21 | chrX | 153563421 | |||||||
| chrX:153563606 | G | A | 10 | a0001c0001t0002g0175 a0001c0001t0005g0087 a0001c0001t0005g0127 others(7): Show |
11 | HG00741.hp1 HG02451.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.3160-1315G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 20/21 | chrX | 153563606 | |||||||
| chrX:153563811 | T | G | 3 | a0001c0002t0001g0133 a0001c0002t0001g0154 a0001c0002t0001g0168 |
3 | HG01192.hp1 HG01978.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.3160-1110T>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 20/21 | chrX | 153563811 | |||||||
| chrX:153563940 | C | T | 98 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0121 others(95): Show |
110 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.3160-981C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 20/21 | chrX | 153563940 | |||||||
| chrX:153564118 | C | T | 10 | a0001c0001t0002g0175 a0001c0001t0005g0087 a0001c0001t0005g0127 others(7): Show |
11 | HG00741.hp1 HG02451.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.3160-803C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 20/21 | chrX | 153564118 | |||||||
| chrX:153564316 | C | T | 101 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0121 others(98): Show |
113 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.3160-605C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 20/21 | chrX | 153564316 | |||||||
| chrX:153564464 | C | G | 1 | a0001c0003t0024g0230 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3160-457C>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 20/21 | chrX | 153564464 | |||||||
| chrX:153564543 | G | A | 1 | a0001c0001t0028g0232 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3160-378G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 20/21 | chrX | 153564543 | |||||||
| chrX:153564722 | G | A | 3 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0022g0225 |
3 | HG02965.hp1 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3160-199G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 20/21 | chrX | 153564722 | |||||||
| chrX:153564864 | A | G | 226 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(223): Show |
249 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(246): Show |
intron_variant | MODIFIER | c.3160-57A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 20/21 | chrX | 153564864 | |||||||
| chrX:153565197 | G | A | 4 | a0001c0003t0027g0227 a0001c0003t0040g0090 a0001c0008t0026g0220 others(1): Show |
4 | HG02055.hp1 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.3342+94G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153565197 | |||||||
| chrX:153565226 | C | T | 221 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(218): Show |
244 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(241): Show |
intron_variant | MODIFIER | c.3342+123C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153565226 | |||||||
| chrX:153565304 | A | G | 240 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(237): Show |
264 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.3342+201A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153565304 | |||||||
| chrX:153565306 | C | T | 3 | a0001c0001t0021g0222 a0001c0004t0007g0218 a0001c0004t0016g0217 |
3 | HG01243.hp1 HG02280.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3342+203C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153565306 | |||||||
| chrX:153565307 | G | A | 2 | a0001c0001t0001g0055 a0001c0001t0037g0052 |
2 | HG03654.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.3342+204G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153565307 | |||||||
| chrX:153565434 | T | C | 1 | a0001c0001t0001g0123 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.3342+331T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153565434 | |||||||
| chrX:153565525 | T | A | 224 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(221): Show |
247 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.3342+422T>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153565525 | |||||||
| chrX:153565590 | T | C | 108 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(105): Show |
119 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.3342+487T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153565590 | |||||||
| chrX:153565609 | C | G | 13 | a0001c0003t0001g0034 a0001c0003t0001g0035 a0001c0003t0002g0032 others(10): Show |
13 | HG01361.hp2 HG01934.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.3342+506C>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153565609 | |||||||
| chrX:153565687 | T | C | 1 | a0001c0008t0026g0220 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3342+584T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153565687 | |||||||
| chrX:153565740 | C | T | 1 | a0001c0017t0025g0226 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3342+637C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153565740 | |||||||
| chrX:153566307 | A | G | 212 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(209): Show |
235 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.3342+1204A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153566307 | |||||||
| chrX:153566678 | A | G | 9 | a0001c0003t0001g0034 a0001c0003t0001g0035 a0001c0003t0002g0032 others(6): Show |
9 | HG01361.hp2 HG02257.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.3342+1575A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153566678 | |||||||
| chrX:153566865 | G | A | 1 | a0001c0001t0001g0049 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.3342+1762G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153566865 | |||||||
| chrX:153566884 | C | G | 3 | a0001c0001t0021g0222 a0001c0004t0007g0218 a0001c0004t0016g0217 |
3 | HG01243.hp1 HG02280.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3342+1781C>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153566884 | |||||||
| chrX:153566919 | G | A | 10 | a0001c0001t0002g0175 a0001c0001t0005g0087 a0001c0001t0005g0127 others(7): Show |
11 | HG00741.hp1 HG02451.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.3342+1816G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153566919 | |||||||
| chrX:153567154 | G | A | 12 | a0001c0001t0001g0102 a0001c0001t0001g0210 a0001c0001t0004g0018 others(9): Show |
13 | HG02027.hp1 NA18612.hp1 NA18939.hp1 others(10): Show |
intron_variant | MODIFIER | c.3342+2051G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153567154 | |||||||
| chrX:153567482 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3342+2379C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153567482 | |||||||
| chrX:153567516 | C | T | 1 | a0001c0001t0039g0234 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.3342+2413C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153567516 | |||||||
| chrX:153567694 | A | G | 226 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(223): Show |
249 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(246): Show |
intron_variant | MODIFIER | c.3342+2591A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153567694 | |||||||
| chrX:153567710 | G | A | 6 | a0001c0001t0001g0009 a0001c0001t0001g0058 a0001c0001t0001g0116 others(3): Show |
6 | HG01123.hp1 HG01928.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.3342+2607G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153567710 | |||||||
| chrX:153567735 | T | C | 239 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(236): Show |
263 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.3342+2632T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153567735 | |||||||
| chrX:153567739 | G | A | 225 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(222): Show |
248 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.3342+2636G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153567739 | |||||||
| chrX:153567798 | C | T | 3 | a0001c0002t0001g0109 a0001c0002t0001g0140 a0002c0006t0003g0139 |
3 | HG02080.hp2 NA18962.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.3342+2695C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153567798 | |||||||
| chrX:153567818 | C | A | 5 | a0001c0001t0001g0009 a0001c0001t0001g0058 a0001c0001t0001g0116 others(2): Show |
5 | HG01123.hp1 HG01928.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.3342+2715C>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153567818 | |||||||
| chrX:153567840 | A | T | 3 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0022g0225 |
3 | HG02965.hp1 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3342+2737A>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153567840 | |||||||
| chrX:153568045 | C | A | 1 | a0001c0002t0001g0170 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.3342+2942C>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153568045 | |||||||
| chrX:153568046 | A | C | 1 | a0001c0002t0001g0170 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.3342+2943A>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153568046 | |||||||
| chrX:153568223 | G | A | 4 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0022g0225 others(1): Show |
4 | HG02965.hp1 HG02976.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.3342+3120G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153568223 | |||||||
| chrX:153568263 | G | T | 3 | a0001c0001t0021g0222 a0001c0004t0007g0218 a0001c0004t0016g0217 |
3 | HG01243.hp1 HG02280.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3342+3160G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153568263 | |||||||
| chrX:153568300 | C | T | 2 | a0001c0002t0001g0149 a0001c0002t0001g0152 |
2 | NA19003.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.3342+3197C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153568300 | |||||||
| chrX:153568435 | A | G | 126 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(123): Show |
136 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.3342+3332A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153568435 | |||||||
| chrX:153568499 | C | T | 2 | a0001c0001t0001g0049 a0001c0001t0001g0235 |
2 | HG00609.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.3342+3396C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153568499 | |||||||
| chrX:153568545 | G | A | 3 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0022g0225 |
3 | HG02965.hp1 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3342+3442G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153568545 | |||||||
| chrX:153568634 | G | A | 4 | a0001c0002t0013g0083 a0001c0002t0013g0084 a0001c0002t0013g0085 others(1): Show |
4 | NA18948.hp1 NA18998.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.3342+3531G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153568634 | |||||||
| chrX:153568702 | G | A | 57 | a0001c0001t0001g0121 a0001c0002t0001g0001 a0001c0002t0001g0004 others(54): Show |
67 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.3342+3599G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153568702 | |||||||
| chrX:153568786 | C | T | 6 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0123 others(3): Show |
6 | HG00423.hp1 HG00558.hp2 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.3342+3683C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153568786 | |||||||
| chrX:153568984 | C | T | 3 | a0001c0001t0008g0017 a0001c0001t0008g0025 a0001c0001t0008g0160 |
4 | HG02280.hp2 HG02622.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.3342+3881C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153568984 | |||||||
| chrX:153569009 | C | T | 63 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0001g0121 others(60): Show |
73 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.3342+3906C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153569009 | |||||||
| chrX:153569158 | C | T | 1 | a0001c0001t0021g0222 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3342+4055C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153569158 | |||||||
| chrX:153569181 | G | A | 2 | a0001c0002t0001g0108 a0001c0002t0001g0208 |
2 | HG02015.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.3342+4078G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153569181 | |||||||
| chrX:153569278 | T | C | 67 | a0001c0001t0001g0044 a0001c0001t0001g0121 a0001c0001t0006g0010 others(64): Show |
78 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.3342+4175T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153569278 | |||||||
| chrX:153569312 | G | A | 1 | a0001c0001t0003g0204 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.3342+4209G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153569312 | |||||||
| chrX:153569433 | G | C | 68 | a0001c0001t0001g0044 a0001c0001t0001g0121 a0001c0001t0006g0010 others(65): Show |
79 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.3342+4330G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153569433 | |||||||
| chrX:153569501 | C | T | 2 | a0001c0001t0028g0232 a0001c0001t0044g0021 |
2 | HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.3342+4398C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153569501 | |||||||
| chrX:153569543 | C | G | 1 | a0001c0001t0001g0115 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.3342+4440C>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153569543 | |||||||
| chrX:153569764 | T | C | 3 | a0001c0001t0017g0177 a0001c0002t0001g0072 a0001c0002t0017g0071 |
3 | HG01884.hp1 HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3342+4661T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153569764 | |||||||
| chrX:153569843 | C | T | 1 | a0001c0002t0001g0099 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3342+4740C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153569843 | |||||||
| chrX:153570001 | G | A | 1 | a0001c0001t0021g0222 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3342+4898G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153570001 | |||||||
| chrX:153570071 | T | C | 3 | a0001c0001t0017g0177 a0001c0002t0001g0072 a0001c0002t0017g0071 |
3 | HG01884.hp1 HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3342+4968T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153570071 | |||||||
| chrX:153570121 | T | TG | 8 | a0001c0001t0002g0175 a0001c0001t0005g0087 a0001c0001t0005g0127 others(5): Show |
8 | HG00741.hp1 HG01243.hp1 HG03516.hp1 others(5): Show |
intron_variant | MODIFIER | c.3342+5019dupG | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153570121 | ||||||
| chrX:153570223 | A | C | 1 | a0001c0003t0045g0092 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3342+5120A>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153570223 | |||||||
| chrX:153570302 | C | T | 6 | a0001c0001t0008g0017 a0001c0001t0008g0025 a0001c0001t0008g0160 others(3): Show |
7 | HG01884.hp1 HG02280.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.3342+5199C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153570302 | |||||||
| chrX:153570387 | C | T | 1 | a0001c0001t0042g0078 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3342+5284C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153570387 | |||||||
| chrX:153570418 | C | T | 2 | a0001c0001t0002g0051 a0001c0001t0002g0068 |
2 | NA18979.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.3342+5315C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153570418 | |||||||
| chrX:153570441 | G | C | 6 | a0001c0001t0008g0017 a0001c0001t0008g0025 a0001c0001t0008g0160 others(3): Show |
7 | HG01884.hp1 HG02280.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.3342+5338G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153570441 | |||||||
| chrX:153570655 | T | C | 1 | a0001c0002t0002g0189 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.3342+5552T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153570655 | |||||||
| chrX:153570917 | A | G | 1 | a0001c0008t0026g0220 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3342+5814A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153570917 | |||||||
| chrX:153570962 | G | A | 1 | a0001c0017t0025g0226 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3342+5859G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153570962 | |||||||
| chrX:153571002 | G | A | 1 | a0001c0002t0001g0152 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.3342+5899G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153571002 | |||||||
| chrX:153571002 | G | GCA | 12 | a0001c0001t0002g0175 a0001c0001t0005g0087 a0001c0001t0005g0127 others(9): Show |
12 | HG01243.hp1 HG02257.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.3342+5899_3342+590 others(6): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153571002 | |||||||
| chrX:153571002 | GTACA | G | 3 | a0001c0003t0027g0227 a0001c0003t0040g0090 a0001c0010t0005g0091 |
3 | HG02055.hp1 HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.3342+5900_3342+590 others(8): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153571002 | |||||||
| chrX:153571002 | GTACACA | G | 4 | a0001c0001t0017g0177 a0001c0001t0042g0078 a0001c0002t0001g0072 others(1): Show |
4 | HG01884.hp1 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.3342+5900_3342+590 others(10): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153571002 | |||||||
| chrX:153571003 | T | C | 16 | a0001c0001t0002g0175 a0001c0001t0005g0087 a0001c0001t0005g0127 others(13): Show |
17 | HG00741.hp1 HG01243.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.3342+5900T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153571003 | |||||||
| chrX:153571003 | T | TAC | 78 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(75): Show |
88 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.3342+5935_3342+593 others(6): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153571003 | ||||||
| chrX:153571003 | T | TACAC | 59 | a0001c0001t0001g0026 a0001c0001t0001g0044 a0001c0001t0001g0073 others(56): Show |
68 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.3342+5933_3342+593 others(8): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153571003 | ||||||
| chrX:153571003 | T | TACACAC | 32 | a0001c0001t0001g0009 a0001c0001t0001g0028 a0001c0001t0001g0031 others(29): Show |
32 | HG00642.hp1 HG00735.hp2 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.3342+5931_3342+593 others(10): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153571003 | ||||||
| chrX:153571003 | T | TACACACA others(1): Show |
10 | a0001c0001t0004g0018 a0001c0001t0005g0158 a0001c0001t0032g0206 others(7): Show |
11 | HG00738.hp1 HG01081.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.3342+5929_3342+593 others(12): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153571003 | ||||||
| chrX:153571003 | T | TACACACA others(3): Show |
2 | a0001c0001t0001g0058 a0002c0006t0001g0147 |
2 | HG01123.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.3342+5927_3342+593 others(14): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153571003 | ||||||
| chrX:153571003 | TAC | T | 6 | a0001c0001t0001g0156 a0001c0001t0001g0198 a0001c0001t0001g0200 others(3): Show |
6 | HG00639.hp1 HG02109.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.3342+5935_3342+593 others(6): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153571003 | ||||||
| chrX:153571003 | TACAC | T | 3 | a0001c0001t0021g0222 a0001c0002t0002g0005 a0001c0002t0002g0189 |
5 | HG01123.hp2 HG01346.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.3342+5933_3342+593 others(8): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153571003 | ||||||
| chrX:153571010 | A | G | 1 | a0001c0001t0042g0078 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3342+5907A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153571010 | |||||||
| chrX:153571012 | A | G | 1 | a0001c0001t0042g0078 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3342+5909A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153571012 | |||||||
| chrX:153571157 | G | A | 1 | a0001c0001t0015g0056 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.3342+6054G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153571157 | |||||||
| chrX:153571220 | G | A | 4 | a0001c0002t0001g0100 a0001c0002t0001g0101 a0001c0002t0002g0041 others(1): Show |
4 | HG03688.hp1 HG03831.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.3342+6117G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153571220 | |||||||
| chrX:153571263 | G | A | 2 | a0001c0001t0028g0232 a0001c0001t0044g0021 |
2 | HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.3342+6160G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153571263 | |||||||
| chrX:153571498 | C | CAGGGGTG others(18): Show |
1 | a0001c0001t0009g0228 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3342+6397_3342+639 others(29): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153571498 | ||||||
| chrX:153571586 | G | A | 1 | a0001c0002t0003g0150 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.3342+6483G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153571586 | |||||||
| chrX:153571690 | G | A | 4 | a0001c0002t0001g0126 a0001c0002t0001g0154 a0001c0002t0018g0128 others(1): Show |
4 | HG00639.hp2 HG01192.hp1 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.3342+6587G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153571690 | |||||||
| chrX:153571792 | G | A | 7 | a0001c0001t0001g0009 a0001c0001t0001g0058 a0001c0001t0001g0116 others(4): Show |
7 | HG01123.hp1 HG01928.hp1 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.3342+6689G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153571792 | |||||||
| chrX:153571992 | T | C | 1 | a0001c0002t0001g0106 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.3342+6889T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153571992 | |||||||
| chrX:153572247 | C | T | 33 | a0001c0001t0002g0023 a0001c0001t0002g0159 a0001c0001t0009g0228 others(30): Show |
35 | HG00423.hp2 HG00544.hp1 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.3342+7144C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153572247 | |||||||
| chrX:153572273 | G | A | 39 | a0001c0001t0002g0023 a0001c0001t0002g0159 a0001c0001t0008g0017 others(36): Show |
42 | HG00423.hp2 HG00544.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.3342+7170G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153572273 | |||||||
| chrX:153572385 | G | A | 6 | a0001c0001t0011g0037 a0001c0001t0011g0038 a0001c0001t0011g0039 others(3): Show |
6 | HG02257.hp1 HG02486.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.3342+7282G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153572385 | |||||||
| chrX:153572628 | CAT | C | 239 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(236): Show |
263 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.3343-7347_3343-734 others(6): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153572628 | ||||||
| chrX:153572649 | T | C | 17 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0001g0198 others(14): Show |
17 | HG02109.hp2 HG02257.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.3343-7329T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153572649 | |||||||
| chrX:153572663 | C | T | 1 | a0001c0001t0021g0222 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3343-7315C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153572663 | |||||||
| chrX:153572896 | A | T | 2 | a0001c0001t0028g0232 a0001c0001t0044g0021 |
2 | HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.3343-7082A>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153572896 | |||||||
| chrX:153572966 | A | G | 1 | a0001c0001t0022g0225 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3343-7012A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153572966 | |||||||
| chrX:153573216 | T | G | 2 | a0001c0001t0028g0232 a0001c0001t0044g0021 |
2 | HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.3343-6762T>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153573216 | |||||||
| chrX:153573267 | G | A | 39 | a0001c0001t0002g0023 a0001c0001t0002g0159 a0001c0001t0008g0017 others(36): Show |
42 | HG00423.hp2 HG00544.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.3343-6711G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153573267 | |||||||
| chrX:153573311 | G | A | 44 | a0001c0001t0002g0023 a0001c0001t0002g0051 a0001c0001t0002g0068 others(41): Show |
47 | HG00423.hp2 HG00544.hp1 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.3343-6667G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153573311 | |||||||
| chrX:153573339 | G | A | 4 | a0001c0001t0011g0037 a0001c0001t0011g0038 a0001c0001t0011g0039 others(1): Show |
4 | HG02257.hp1 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.3343-6639G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153573339 | |||||||
| chrX:153573377 | T | C | 1 | a0001c0002t0001g0129 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.3343-6601T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153573377 | |||||||
| chrX:153573575 | A | T | 11 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0011g0037 others(8): Show |
11 | HG02109.hp2 HG02257.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.3343-6403A>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153573575 | |||||||
| chrX:153573654 | G | A | 66 | a0001c0001t0001g0044 a0001c0001t0001g0110 a0001c0001t0001g0111 others(63): Show |
76 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.3343-6324G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153573654 | |||||||
| chrX:153573680 | T | A | 137 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0001g0044 others(134): Show |
150 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.3343-6298T>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153573680 | |||||||
| chrX:153573783 | G | A | 1 | a0001c0001t0021g0222 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3343-6195G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153573783 | |||||||
| chrX:153573948 | C | G | 127 | a0001c0001t0001g0044 a0001c0001t0001g0110 a0001c0001t0001g0111 others(124): Show |
140 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.3343-6030C>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153573948 | |||||||
| chrX:153573969 | G | A | 1 | a0001c0001t0044g0021 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3343-6009G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153573969 | |||||||
| chrX:153574000 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3343-5978C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153574000 | |||||||
| chrX:153574011 | T | C | 126 | a0001c0001t0001g0044 a0001c0001t0001g0110 a0001c0001t0001g0111 others(123): Show |
139 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.3343-5967T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153574011 | |||||||
| chrX:153574025 | G | T | 130 | a0001c0001t0001g0044 a0001c0001t0001g0110 a0001c0001t0001g0111 others(127): Show |
143 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.3343-5953G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153574025 | |||||||
| chrX:153574239 | C | T | 13 | a0001c0001t0002g0175 a0001c0001t0005g0036 a0001c0001t0005g0087 others(10): Show |
13 | HG00741.hp1 HG01243.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.3343-5739C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153574239 | |||||||
| chrX:153574363 | G | C | 1 | a0001c0002t0001g0140 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.3343-5615G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153574363 | |||||||
| chrX:153574424 | G | A | 2 | a0001c0001t0028g0232 a0001c0001t0044g0021 |
2 | HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.3343-5554G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153574424 | |||||||
| chrX:153574493 | T | G | 11 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0011g0037 others(8): Show |
11 | HG02109.hp2 HG02257.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.3343-5485T>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153574493 | |||||||
| chrX:153574863 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.3343-5115G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153574863 | |||||||
| chrX:153574949 | A | G | 13 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0011g0037 others(10): Show |
13 | HG02109.hp2 HG02257.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.3343-5029A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153574949 | |||||||
| chrX:153575124 | G | A | 42 | a0001c0001t0002g0023 a0001c0001t0002g0051 a0001c0001t0002g0068 others(39): Show |
45 | HG00423.hp2 HG00544.hp1 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.3343-4854G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153575124 | |||||||
| chrX:153575150 | C | T | 1 | a0001c0001t0021g0222 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3343-4828C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153575150 | |||||||
| chrX:153575248 | G | A | 1 | a0001c0002t0010g0093 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.3343-4730G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153575248 | |||||||
| chrX:153575570 | C | T | 2 | a0001c0007t0001g0043 a0001c0007t0001g0062 |
2 | NA18944.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.3343-4408C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153575570 | |||||||
| chrX:153575638 | G | A | 3 | a0001c0001t0017g0177 a0001c0002t0001g0072 a0001c0002t0017g0071 |
3 | HG01884.hp1 HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3343-4340G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153575638 | |||||||
| chrX:153575765 | C | T | 1 | a0001c0002t0010g0093 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.3343-4213C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153575765 | |||||||
| chrX:153575863 | A | C | 11 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0011g0037 others(8): Show |
11 | HG02109.hp2 HG02257.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.3343-4115A>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153575863 | |||||||
| chrX:153575991 | G | A | 1 | a0001c0001t0006g0066 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.3343-3987G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153575991 | |||||||
| chrX:153576026 | A | T | 1 | a0001c0002t0002g0184 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.3343-3952A>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153576026 | |||||||
| chrX:153576034 | C | T | 1 | a0001c0001t0044g0021 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3343-3944C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153576034 | |||||||
| chrX:153576274 | T | A | 2 | a0001c0001t0028g0232 a0001c0001t0044g0021 |
2 | HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.3343-3704T>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153576274 | |||||||
| chrX:153576501 | C | T | 1 | a0001c0002t0001g0132 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.3343-3477C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153576501 | |||||||
| chrX:153576552 | G | A | 68 | a0001c0001t0001g0044 a0001c0001t0001g0110 a0001c0001t0001g0111 others(65): Show |
78 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.3343-3426G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153576552 | |||||||
| chrX:153576893 | T | C | 2 | a0001c0001t0009g0228 a0001c0003t0002g0080 |
2 | HG00642.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.3343-3085T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153576893 | |||||||
| chrX:153576919 | C | G | 4 | a0001c0001t0011g0037 a0001c0001t0011g0038 a0001c0001t0011g0039 others(1): Show |
4 | HG02257.hp1 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.3343-3059C>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153576919 | |||||||
| chrX:153577093 | C | T | 2 | a0001c0002t0018g0128 a0001c0002t0018g0193 |
2 | HG00639.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.3343-2885C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153577093 | |||||||
| chrX:153577094 | G | A | 1 | a0001c0002t0001g0125 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.3343-2884G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153577094 | |||||||
| chrX:153577174 | C | G | 1 | a0001c0001t0001g0202 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3343-2804C>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153577174 | |||||||
| chrX:153577209 | T | C | 8 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0022g0225 others(5): Show |
8 | HG02109.hp2 HG02257.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.3343-2769T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153577209 | |||||||
| chrX:153577283 | G | C | 67 | a0001c0001t0001g0044 a0001c0001t0001g0110 a0001c0001t0001g0111 others(64): Show |
77 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.3343-2695G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153577283 | |||||||
| chrX:153577284 | T | A | 8 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0022g0225 others(5): Show |
8 | HG02109.hp2 HG02257.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.3343-2694T>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153577284 | |||||||
| chrX:153577529 | C | T | 14 | a0001c0001t0002g0175 a0001c0001t0005g0036 a0001c0001t0005g0087 others(11): Show |
14 | HG00741.hp1 HG01243.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.3343-2449C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153577529 | |||||||
| chrX:153577669 | G | A | 43 | a0001c0001t0001g0121 a0001c0001t0001g0124 a0001c0001t0001g0210 others(40): Show |
52 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.3343-2309G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153577669 | |||||||
| chrX:153577705 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3343-2273G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153577705 | |||||||
| chrX:153577721 | C | T | 1 | a0001c0002t0002g0187 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.3343-2257C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153577721 | |||||||
| chrX:153577867 | G | A | 12 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0011g0037 others(9): Show |
12 | HG02109.hp2 HG02257.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.3343-2111G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153577867 | |||||||
| chrX:153577871 | C | T | 4 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0117 others(1): Show |
4 | HG00735.hp2 HG01069.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.3343-2107C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153577871 | |||||||
| chrX:153577899 | C | T | 83 | a0001c0001t0001g0044 a0001c0001t0001g0110 a0001c0001t0001g0111 others(80): Show |
93 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.3343-2079C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153577899 | |||||||
| chrX:153577932 | T | C | 4 | a0001c0001t0011g0037 a0001c0001t0011g0038 a0001c0001t0011g0039 others(1): Show |
4 | HG02257.hp1 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.3343-2046T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153577932 | |||||||
| chrX:153577957 | G | C | 1 | a0003c0009t0005g0076 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3343-2021G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153577957 | |||||||
| chrX:153578189 | GC | G | 4 | a0001c0001t0011g0037 a0001c0001t0011g0038 a0001c0001t0011g0039 others(1): Show |
4 | HG02257.hp1 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.3343-1785delC | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153578189 | ||||||
| chrX:153578518 | G | C | 7 | a0001c0002t0002g0015 a0001c0002t0002g0042 a0001c0002t0002g0178 others(4): Show |
7 | HG00423.hp2 HG01433.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.3343-1460G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153578518 | |||||||
| chrX:153578615 | A | C | 138 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(135): Show |
149 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.3343-1363A>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153578615 | |||||||
| chrX:153578638 | G | C | 1 | a0001c0001t0001g0075 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3343-1340G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153578638 | |||||||
| chrX:153578653 | T | G | 1 | a0001c0001t0011g0038 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3343-1325T>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153578653 | |||||||
| chrX:153578658 | C | T | 1 | a0001c0002t0003g0122 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.3343-1320C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153578658 | |||||||
| chrX:153578697 | G | A | 3 | a0001c0003t0007g0223 a0001c0003t0033g0030 a0001c0017t0025g0226 |
3 | HG02257.hp2 HG02886.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.3343-1281G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153578697 | |||||||
| chrX:153578701 | T | C | 1 | a0001c0001t0042g0078 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3343-1277T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153578701 | |||||||
| chrX:153578715 | G | T | 1 | a0001c0002t0030g0081 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.3343-1263G>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153578715 | |||||||
| chrX:153578772 | G | C | 3 | a0001c0001t0008g0017 a0001c0001t0008g0025 a0001c0001t0008g0160 |
4 | HG02280.hp2 HG02622.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.3343-1206G>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153578772 | |||||||
| chrX:153578777 | A | G | 81 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0001g0044 others(78): Show |
91 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.3343-1201A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153578777 | |||||||
| chrX:153578792 | T | C | 70 | a0001c0001t0001g0044 a0001c0001t0001g0102 a0001c0001t0001g0121 others(67): Show |
80 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.3343-1186T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153578792 | |||||||
| chrX:153578859 | A | G | 4 | a0001c0001t0021g0222 a0001c0001t0042g0078 a0001c0003t0002g0203 others(1): Show |
4 | HG01934.hp1 HG02451.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.3343-1119A>G | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153578859 | |||||||
| chrX:153578866 | G | A | 147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(144): Show |
161 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.3343-1112G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153578866 | |||||||
| chrX:153578901 | G | A | 2 | a0001c0003t0002g0203 a0001c0008t0026g0220 |
2 | HG01934.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.3343-1077G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153578901 | |||||||
| chrX:153578915 | A | ACAGGGGC others(7): Show |
1 | a0001c0008t0026g0220 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3343-1059_3343-104 others(18): Show |
ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chrX | 153578915 | ||||||
| chrX:153578950 | T | C | 1 | a0001c0015t0009g0221 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3343-1028T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153578950 | |||||||
| chrX:153578952 | C | T | 2 | a0001c0001t0009g0228 a0001c0003t0002g0080 |
2 | HG00642.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.3343-1026C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153578952 | |||||||
| chrX:153579091 | T | C | 76 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0001g0044 others(73): Show |
86 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.3343-887T>C | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153579091 | |||||||
| chrX:153579260 | G | A | 6 | a0001c0001t0021g0222 a0001c0001t0028g0232 a0001c0001t0042g0078 others(3): Show |
6 | HG01934.hp1 HG02451.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.3343-718G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153579260 | |||||||
| chrX:153579347 | G | A | 1 | a0001c0002t0001g0207 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.3343-631G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153579347 | |||||||
| chrX:153579619 | C | T | 1 | a0001c0001t0005g0158 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3343-359C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153579619 | |||||||
| chrX:153579716 | C | T | 4 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0001g0073 others(1): Show |
4 | HG02572.hp1 HG02647.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.3343-262C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153579716 | |||||||
| chrX:153579833 | C | T | 11 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0001g0073 others(8): Show |
11 | HG01934.hp1 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.3343-145C>T | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153579833 | |||||||
| chrX:153579834 | G | A | 1 | a0001c0002t0001g0126 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3343-144G>A | ATP2B3 | ENSG00000067842.19 | transcript | ENST00000263519.5 | protein_coding | 21/21 | chrX | 153579834 |