Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79832 |
| ensemblid | ENSG00000060749.17 |
| hgncid | 26154 |
| symbol | QSER1 |
| name | glutamine and serine rich 1 |
| refseq_nuc | NM_001076786.3 |
| refseq_prot | NP_001070254.2 |
| ensembl_nuc | ENST00000650167.2 |
| ensembl_prot | ENSP00000496900.1 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 32892811 |
| end | 32980270 |
| strand | + |
| ver | v1.2 |
| region | chr11:32892811-32980270 |
| region5000 | chr11:32887811-32985270 |
| regionname0 | QSER1_chr11_32892811_32980270 |
| regionname5000 | QSER1_chr11_32887811_32985270 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 1864 | 193 | 69 | 42 | 51 | 9 | 22 | 36 | QSER1_chr11_32887811_32985270 | QSER1 | MDRNY others(1859): Show |
chr11 | 32887811 | 32985270 |
| a0002 | 0/1 | 1864 | 13 | 3 | 2 | 2 | 0 | 5 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | MDRNY others(1859): Show |
chr11 | 32887811 | 32985270 |
| a0003 | 1/0 | 1864 | 10 | 9 | 0 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | MDRNY others(1859): Show |
chr11 | 32887811 | 32985270 |
| a0004 | 0/0 | 1864 | 6 | 0 | 3 | 0 | 1 | 2 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | MDRNY others(1859): Show |
chr11 | 32887811 | 32985270 |
| a0005 | 0/0 | 1870 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | MDRNY others(1865): Show |
chr11 | 32887811 | 32985270 |
| a0006 | 0/0 | 1865 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | MDRNY others(1860): Show |
chr11 | 32887811 | 32985270 |
| a0007 | 0/0 | 1864 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | QSER1_chr11_32887811_32985270 | QSER1 | MDRNY others(1859): Show |
chr11 | 32887811 | 32985270 |
| a0008 | 0/0 | 1864 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | MDRNY others(1859): Show |
chr11 | 32887811 | 32985270 |
| a0009 | 0/0 | 1864 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | MDRNY others(1859): Show |
chr11 | 32887811 | 32985270 |
| a0010 | 0/0 | 1864 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | MDRNY others(1859): Show |
chr11 | 32887811 | 32985270 |
| a0011 | 0/0 | 1864 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | MDRNY others(1859): Show |
chr11 | 32887811 | 32985270 |
| a0012 | 0/0 | 1864 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | MDRNY others(1859): Show |
chr11 | 32887811 | 32985270 |
| a0013 | 0/0 | 1864 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | MDRNY others(1859): Show |
chr11 | 32887811 | 32985270 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 5592 | 131 | 29 | 33 | 46 | 6 | 17 | QSER1_chr11_32887811_32985270 | QSER1 | ATGGA others(5587): Show |
chr11 | 32887811 | 32985270 | ||
| a0001c0002 | 0/0 | 5592 | 30 | 25 | 4 | 0 | 0 | 1 | QSER1_chr11_32887811_32985270 | QSER1 | ATGGA others(5587): Show |
chr11 | 32887811 | 32985270 | ||
| a0001c0003 | 0/0 | 5592 | 16 | 1 | 5 | 5 | 2 | 3 | QSER1_chr11_32887811_32985270 | QSER1 | ATGGA others(5587): Show |
chr11 | 32887811 | 32985270 | ||
| a0001c0006 | 0/0 | 5592 | 8 | 8 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | ATGGA others(5587): Show |
chr11 | 32887811 | 32985270 | ||
| a0001c0008 | 0/0 | 5592 | 4 | 4 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | ATGGA others(5587): Show |
chr11 | 32887811 | 32985270 | ||
| a0001c0011 | 0/0 | 5592 | 2 | 2 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | ATGGA others(5587): Show |
chr11 | 32887811 | 32985270 | ||
| a0001c0016 | 0/0 | 5592 | 1 | 0 | 0 | 0 | 1 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | ATGGA others(5587): Show |
chr11 | 32887811 | 32985270 | ||
| a0001c0020 | 0/0 | 5592 | 1 | 0 | 0 | 0 | 0 | 1 | QSER1_chr11_32887811_32985270 | QSER1 | ATGGA others(5587): Show |
chr11 | 32887811 | 32985270 | ||
| a0002c0004 | 0/0 | 5592 | 12 | 3 | 2 | 2 | 0 | 5 | QSER1_chr11_32887811_32985270 | QSER1 | ATGGA others(5587): Show |
chr11 | 32887811 | 32985270 | ||
| a0002c0013 | 0/1 | 5592 | 1 | 0 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | ATGGA others(5587): Show |
chr11 | 32887811 | 32985270 | ||
| a0003c0005 | 0/0 | 5592 | 9 | 9 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | ATGGA others(5587): Show |
chr11 | 32887811 | 32985270 | ||
| a0003c0018 | 1/0 | 5592 | 1 | 0 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | ATGGA others(5587): Show |
chr11 | 32887811 | 32985270 | ||
| a0004c0007 | 0/0 | 5592 | 6 | 0 | 3 | 0 | 1 | 2 | QSER1_chr11_32887811_32985270 | QSER1 | ATGGA others(5587): Show |
chr11 | 32887811 | 32985270 | ||
| a0005c0009 | 0/0 | 5610 | 4 | 4 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | ATGGA others(5605): Show |
chr11 | 32887811 | 32985270 | ||
| a0006c0022 | 0/0 | 5595 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | ATGGA others(5590): Show |
chr11 | 32887811 | 32985270 | ||
| a0006c0023 | 0/0 | 5595 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | ATGGA others(5590): Show |
chr11 | 32887811 | 32985270 | ||
| a0007c0010 | 0/0 | 5592 | 2 | 0 | 0 | 2 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | ATGGA others(5587): Show |
chr11 | 32887811 | 32985270 | ||
| a0008c0014 | 0/0 | 5592 | 1 | 0 | 0 | 1 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | ATGGA others(5587): Show |
chr11 | 32887811 | 32985270 | ||
| a0009c0017 | 0/0 | 5592 | 1 | 0 | 1 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | ATGGA others(5587): Show |
chr11 | 32887811 | 32985270 | ||
| a0010c0015 | 0/0 | 5592 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | ATGGA others(5587): Show |
chr11 | 32887811 | 32985270 | ||
| a0011c0012 | 0/0 | 5592 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | ATGGA others(5587): Show |
chr11 | 32887811 | 32985270 | ||
| a0012c0019 | 0/0 | 5592 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | ATGGA others(5587): Show |
chr11 | 32887811 | 32985270 | ||
| a0013c0021 | 0/0 | 5592 | 1 | 0 | 0 | 0 | 0 | 1 | QSER1_chr11_32887811_32985270 | QSER1 | ATGGA others(5587): Show |
chr11 | 32887811 | 32985270 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 9712 | 98 | 21 | 23 | 35 | 5 | 14 | QSER1_chr11_32887811_32985270 | QSER1 | ATCCT others(9707): Show |
chr11 | 32887811 | 32985270 |
| a0001c0001t0003 | 0/0 | 9712 | 8 | 0 | 0 | 7 | 0 | 1 | QSER1_chr11_32887811_32985270 | QSER1 | ATCCT others(9707): Show |
chr11 | 32887811 | 32985270 |
| a0001c0001t0005 | 0/0 | 9718 | 5 | 1 | 1 | 0 | 1 | 2 | QSER1_chr11_32887811_32985270 | QSER1 | ATCCT others(9713): Show |
chr11 | 32887811 | 32985270 |
| a0001c0001t0006 | 0/0 | 9709 | 5 | 5 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | ATCCT others(9704): Show |
chr11 | 32887811 | 32985270 |
| a0001c0001t0009 | 0/0 | 9718 | 3 | 0 | 3 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | ATCCT others(9713): Show |
chr11 | 32887811 | 32985270 |
| a0001c0001t0010 | 0/0 | 9712 | 3 | 0 | 3 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | ATCCT others(9707): Show |
chr11 | 32887811 | 32985270 |
| a0001c0001t0011 | 0/0 | 9712 | 2 | 0 | 2 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | ATCCT others(9707): Show |
chr11 | 32887811 | 32985270 |
| a0001c0001t0012 | 0/0 | 9712 | 3 | 0 | 1 | 2 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | ATCCT others(9707): Show |
chr11 | 32887811 | 32985270 |
| a0001c0001t0014 | 0/0 | 9712 | 2 | 0 | 0 | 2 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | ATCCT others(9707): Show |
chr11 | 32887811 | 32985270 |
| a0001c0001t0017 | 0/0 | 9721 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | ATCCT others(9716): Show |
chr11 | 32887811 | 32985270 |
| a0001c0001t0022 | 0/0 | 9712 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | ATCCT others(9707): Show |
chr11 | 32887811 | 32985270 |
| a0001c0002t0001 | 0/0 | 9712 | 10 | 9 | 1 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | ATCCT others(9707): Show |
chr11 | 32887811 | 32985270 |
| a0001c0002t0002 | 0/0 | 9706 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | ATCCT others(9701): Show |
chr11 | 32887811 | 32985270 |
| a0001c0002t0004 | 0/0 | 9712 | 8 | 6 | 2 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | ATCCT others(9707): Show |
chr11 | 32887811 | 32985270 |
| a0001c0002t0007 | 0/0 | 9715 | 4 | 3 | 1 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | ATCCT others(9710): Show |
chr11 | 32887811 | 32985270 |
| a0001c0002t0008 | 0/0 | 9715 | 2 | 2 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | ATCCT others(9710): Show |
chr11 | 32887811 | 32985270 |
| a0001c0002t0013 | 0/0 | 9718 | 2 | 2 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | ATCCT others(9713): Show |
chr11 | 32887811 | 32985270 |
| a0001c0002t0018 | 0/0 | 9715 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | ATCCT others(9710): Show |
chr11 | 32887811 | 32985270 |
| a0001c0002t0019 | 0/0 | 9712 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | ATCCT others(9707): Show |
chr11 | 32887811 | 32985270 |
| a0001c0002t0020 | 0/0 | 9712 | 1 | 0 | 0 | 0 | 0 | 1 | QSER1_chr11_32887811_32985270 | QSER1 | ATCCT others(9707): Show |
chr11 | 32887811 | 32985270 |
| a0001c0003t0002 | 0/0 | 9706 | 15 | 1 | 5 | 5 | 2 | 2 | QSER1_chr11_32887811_32985270 | QSER1 | ATCCT others(9701): Show |
chr11 | 32887811 | 32985270 |
| a0001c0003t0024 | 0/0 | 9706 | 1 | 0 | 0 | 0 | 0 | 1 | QSER1_chr11_32887811_32985270 | QSER1 | ATCCT others(9701): Show |
chr11 | 32887811 | 32985270 |
| a0001c0006t0001 | 0/0 | 9712 | 8 | 8 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | ATCCT others(9707): Show |
chr11 | 32887811 | 32985270 |
| a0001c0008t0001 | 0/0 | 9712 | 4 | 4 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | ATCCT others(9707): Show |
chr11 | 32887811 | 32985270 |
| a0001c0011t0001 | 0/0 | 9712 | 2 | 2 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | ATCCT others(9707): Show |
chr11 | 32887811 | 32985270 |
| a0001c0016t0002 | 0/0 | 9706 | 1 | 0 | 0 | 0 | 1 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | ATCCT others(9701): Show |
chr11 | 32887811 | 32985270 |
| a0001c0020t0001 | 0/0 | 9712 | 1 | 0 | 0 | 0 | 0 | 1 | QSER1_chr11_32887811_32985270 | QSER1 | ATCCT others(9707): Show |
chr11 | 32887811 | 32985270 |
| a0002c0004t0001 | 0/0 | 9712 | 8 | 1 | 0 | 2 | 0 | 5 | QSER1_chr11_32887811_32985270 | QSER1 | ATCCT others(9707): Show |
chr11 | 32887811 | 32985270 |
| a0002c0004t0008 | 0/0 | 9715 | 2 | 2 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | ATCCT others(9710): Show |
chr11 | 32887811 | 32985270 |
| a0002c0004t0015 | 0/0 | 9712 | 2 | 0 | 2 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | ATCCT others(9707): Show |
chr11 | 32887811 | 32985270 |
| a0002c0013t0001 | 0/1 | 9712 | 1 | 0 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | ATCCT others(9707): Show |
chr11 | 32887811 | 32985270 |
| a0003c0005t0001 | 0/0 | 9712 | 9 | 9 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | ATCCT others(9707): Show |
chr11 | 32887811 | 32985270 |
| a0003c0018t0002 | 1/0 | 9706 | 1 | 0 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | ATCCT others(9701): Show |
chr11 | 32887811 | 32985270 |
| a0004c0007t0001 | 0/0 | 9712 | 4 | 0 | 1 | 0 | 1 | 2 | QSER1_chr11_32887811_32985270 | QSER1 | ATCCT others(9707): Show |
chr11 | 32887811 | 32985270 |
| a0004c0007t0016 | 0/0 | 9712 | 2 | 0 | 2 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | ATCCT others(9707): Show |
chr11 | 32887811 | 32985270 |
| a0005c0009t0001 | 0/0 | 9730 | 4 | 4 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | ATCCT others(9725): Show |
chr11 | 32887811 | 32985270 |
| a0006c0022t0001 | 0/0 | 9715 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | ATCCT others(9710): Show |
chr11 | 32887811 | 32985270 |
| a0006c0023t0023 | 0/0 | 9715 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | ATCCT others(9710): Show |
chr11 | 32887811 | 32985270 |
| a0007c0010t0001 | 0/0 | 9712 | 2 | 0 | 0 | 2 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | ATCCT others(9707): Show |
chr11 | 32887811 | 32985270 |
| a0008c0014t0001 | 0/0 | 9712 | 1 | 0 | 0 | 1 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | ATCCT others(9707): Show |
chr11 | 32887811 | 32985270 |
| a0009c0017t0011 | 0/0 | 9712 | 1 | 0 | 1 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | ATCCT others(9707): Show |
chr11 | 32887811 | 32985270 |
| a0010c0015t0001 | 0/0 | 9712 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | ATCCT others(9707): Show |
chr11 | 32887811 | 32985270 |
| a0011c0012t0021 | 0/0 | 9712 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | ATCCT others(9707): Show |
chr11 | 32887811 | 32985270 |
| a0012c0019t0001 | 0/0 | 9712 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | ATCCT others(9707): Show |
chr11 | 32887811 | 32985270 |
| a0013c0021t0001 | 0/0 | 9712 | 1 | 0 | 0 | 0 | 0 | 1 | QSER1_chr11_32887811_32985270 | QSER1 | ATCCT others(9707): Show |
chr11 | 32887811 | 32985270 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0005g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0005g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0005g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0005g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0005g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0006g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0006g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0006g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0006g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0009g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0009g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0009g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0010g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0010g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0010g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0011g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0011g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0012g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0012g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0012g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0014g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0014g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0017g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0001t0022g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0002t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0002t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0002t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0002t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0002t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0002t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0002t0004g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0002t0004g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0002t0004g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0002t0004g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0002t0004g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0002t0004g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0002t0004g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0002t0004g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0002t0007g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0002t0007g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0002t0007g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0002t0007g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0002t0008g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0002t0008g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0002t0013g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0002t0013g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0002t0018g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0002t0019g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0002t0020g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0003t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0003t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0003t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0003t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0003t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0003t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0003t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0003t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0003t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0003t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0003t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0003t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0003t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0003t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0003t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0003t0024g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0006t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0006t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0006t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0006t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0006t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0006t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0006t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0006t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0008t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0008t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0008t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0008t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0011t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0011t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0016t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0001c0020t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0002c0004t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0002c0004t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0002c0004t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0002c0004t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0002c0004t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0002c0004t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0002c0004t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0002c0004t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0002c0004t0008g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0002c0004t0008g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0002c0004t0015g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0002c0004t0015g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0002c0013t0001g0152 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0003c0005t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0003c0005t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0003c0005t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0003c0005t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0003c0005t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0003c0005t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0003c0005t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0003c0005t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0003c0005t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0003c0018t0002g0217 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0004c0007t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0004c0007t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0004c0007t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0004c0007t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0004c0007t0016g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0004c0007t0016g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0005c0009t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0005c0009t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0005c0009t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0005c0009t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0006c0022t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0006c0023t0023g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0007c0010t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0007c0010t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0008c0014t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0009c0017t0011g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0010c0015t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0011c0012t0021g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0012c0019t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| a0013c0021t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0016 | t0002 | g0211 | EUR | GBR | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0085 | EUR | GBR | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0052 | EUR | GBR | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0159 | EUR | GBR | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG00280 | hp1 | a0004 | c0007 | t0001 | g0083 | EUR | FIN | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG00280 | hp2 | a0001 | c0001 | t0005 | g0035 | EUR | FIN | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | CHS | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG00621 | hp2 | a0001 | c0001 | t0012 | g0005 | EAS | CHS | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG00642 | hp1 | a0001 | c0001 | t0009 | g0006 | AMR | PUR | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG00673 | hp2 | a0008 | c0014 | t0001 | g0009 | EAS | CHS | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0011 | AMR | PUR | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG00735 | hp2 | a0004 | c0007 | t0001 | g0084 | AMR | PUR | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG01071 | hp1 | a0001 | c0001 | t0010 | g0143 | AMR | PUR | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG01071 | hp2 | a0001 | c0001 | t0009 | g0034 | AMR | PUR | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG01074 | hp1 | a0001 | c0003 | t0002 | g0215 | AMR | PUR | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG01099 | hp1 | a0001 | c0001 | t0005 | g0030 | AMR | PUR | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG01106 | hp1 | a0001 | c0001 | t0009 | g0036 | AMR | PUR | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG01167 | hp1 | a0001 | c0003 | t0002 | g0216 | AMR | PUR | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG01169 | hp2 | a0001 | c0003 | t0002 | g0220 | AMR | PUR | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG01175 | hp1 | a0009 | c0017 | t0011 | g0120 | AMR | PUR | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG01175 | hp2 | a0001 | c0001 | t0010 | g0104 | AMR | PUR | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG01243 | hp1 | a0001 | c0001 | t0011 | g0112 | AMR | PUR | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG01243 | hp2 | a0001 | c0002 | t0004 | g0227 | AMR | PUR | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG01256 | hp1 | a0001 | c0001 | t0012 | g0113 | AMR | CLM | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG01256 | hp2 | a0004 | c0007 | t0016 | g0115 | AMR | CLM | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG01257 | hp2 | a0001 | c0003 | t0002 | g0209 | AMR | CLM | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG01258 | hp2 | a0004 | c0007 | t0016 | g0114 | AMR | CLM | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG01261 | hp1 | a0001 | c0001 | t0011 | g0082 | AMR | CLM | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG01261 | hp2 | a0001 | c0003 | t0002 | g0219 | AMR | CLM | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG01346 | hp1 | a0001 | c0001 | t0010 | g0072 | AMR | CLM | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG01496 | hp1 | a0001 | c0002 | t0007 | g0191 | AMR | CLM | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG01496 | hp2 | a0001 | c0002 | t0004 | g0232 | AMR | CLM | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG01517 | hp1 | a0001 | c0003 | t0002 | g0210 | EUR | IBS | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0078 | EUR | IBS | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG01884 | hp1 | a0006 | c0023 | t0023 | g0186 | AFR | ACB | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG01884 | hp2 | a0001 | c0008 | t0001 | g0015 | AFR | ACB | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG01891 | hp1 | a0001 | c0001 | t0006 | g0166 | AFR | ACB | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG01891 | hp2 | a0001 | c0006 | t0001 | g0170 | AFR | ACB | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG01975 | hp1 | a0002 | c0004 | t0015 | g0032 | AMR | PEL | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG01981 | hp1 | a0002 | c0004 | t0015 | g0031 | AMR | PEL | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PEL | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02040 | hp2 | a0002 | c0004 | t0001 | g0023 | EAS | KHV | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0013 | AFR | ACB | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02145 | hp1 | a0003 | c0005 | t0001 | g0201 | AFR | ACB | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02145 | hp2 | a0001 | c0001 | t0017 | g0073 | AFR | ACB | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02257 | hp1 | a0001 | c0002 | t0013 | g0162 | AFR | ACB | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02257 | hp2 | a0001 | c0002 | t0004 | g0229 | AFR | ACB | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02280 | hp1 | a0001 | c0002 | t0002 | g0205 | AFR | ACB | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02280 | hp2 | a0001 | c0006 | t0001 | g0174 | AFR | ACB | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02451 | hp1 | a0001 | c0002 | t0007 | g0190 | AFR | ACB | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02572 | hp1 | a0001 | c0002 | t0004 | g0014 | AFR | GWD | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02572 | hp2 | a0001 | c0002 | t0008 | g0223 | AFR | GWD | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02622 | hp2 | a0003 | c0005 | t0001 | g0193 | AFR | GWD | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02683 | hp1 | a0001 | c0003 | t0002 | g0234 | SAS | PJL | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02698 | hp1 | a0001 | c0003 | t0024 | g0218 | SAS | PJL | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02698 | hp2 | a0001 | c0001 | t0005 | g0033 | SAS | PJL | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02717 | hp1 | a0003 | c0005 | t0001 | g0199 | AFR | GWD | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02723 | hp1 | a0001 | c0008 | t0001 | g0203 | AFR | GWD | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02723 | hp2 | a0002 | c0004 | t0001 | g0024 | AFR | GWD | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02809 | hp1 | a0006 | c0022 | t0001 | g0187 | AFR | GWD | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02809 | hp2 | a0003 | c0005 | t0001 | g0200 | AFR | GWD | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02818 | hp1 | a0001 | c0002 | t0018 | g0192 | AFR | GWD | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02818 | hp2 | a0005 | c0009 | t0001 | g0091 | AFR | GWD | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02886 | hp1 | a0001 | c0006 | t0001 | g0176 | AFR | GWD | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02886 | hp2 | a0001 | c0011 | t0001 | g0058 | AFR | GWD | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02895 | hp1 | a0005 | c0009 | t0001 | g0090 | AFR | GWD | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02895 | hp2 | a0005 | c0009 | t0001 | g0088 | AFR | GWD | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02896 | hp1 | a0001 | c0002 | t0004 | g0230 | AFR | GWD | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0178 | AFR | GWD | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02897 | hp1 | a0005 | c0009 | t0001 | g0089 | AFR | GWD | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0179 | AFR | GWD | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02922 | hp1 | a0010 | c0015 | t0001 | g0093 | AFR | ESN | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ESN | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02965 | hp1 | a0001 | c0002 | t0008 | g0206 | AFR | ESN | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02965 | hp2 | a0011 | c0012 | t0021 | g0188 | AFR | ESN | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0175 | AFR | ESN | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02970 | hp2 | a0001 | c0006 | t0001 | g0185 | AFR | ESN | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02976 | hp1 | a0001 | c0001 | t0006 | g0164 | AFR | ESN | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ESN | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG03041 | hp1 | a0001 | c0002 | t0004 | g0226 | AFR | GWD | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG03098 | hp1 | a0001 | c0002 | t0004 | g0233 | AFR | MSL | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG03098 | hp2 | a0002 | c0004 | t0008 | g0037 | AFR | MSL | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG03130 | hp1 | a0001 | c0001 | t0006 | g0002 | AFR | ESN | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG03130 | hp2 | a0001 | c0008 | t0001 | g0202 | AFR | ESN | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG03139 | hp2 | a0012 | c0019 | t0001 | g0173 | AFR | ESN | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG03195 | hp1 | a0001 | c0001 | t0006 | g0002 | AFR | ESN | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG03195 | hp2 | a0001 | c0006 | t0001 | g0171 | AFR | ESN | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0182 | AFR | MSL | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG03209 | hp2 | a0001 | c0011 | t0001 | g0057 | AFR | MSL | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG03225 | hp1 | a0001 | c0001 | t0006 | g0165 | AFR | MSL | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG03225 | hp2 | a0001 | c0006 | t0001 | g0172 | AFR | MSL | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | MSL | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG03453 | hp2 | a0001 | c0006 | t0001 | g0169 | AFR | MSL | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG03486 | hp1 | a0001 | c0002 | t0007 | g0189 | AFR | MSL | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG03486 | hp2 | a0001 | c0002 | t0013 | g0163 | AFR | MSL | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG03491 | hp2 | a0004 | c0007 | t0001 | g0147 | SAS | PJL | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG03492 | hp1 | a0004 | c0007 | t0001 | g0048 | SAS | PJL | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG03516 | hp1 | a0001 | c0002 | t0004 | g0228 | AFR | ESN | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0183 | AFR | MSL | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG03579 | hp2 | a0002 | c0004 | t0008 | g0038 | AFR | MSL | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG03669 | hp1 | a0002 | c0004 | t0001 | g0160 | SAS | PJL | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0097 | SAS | BEB | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG03831 | hp2 | a0001 | c0001 | t0005 | g0070 | SAS | BEB | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG03834 | hp1 | a0002 | c0004 | t0001 | g0044 | SAS | BEB | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | BEB | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG03927 | hp1 | a0001 | c0003 | t0002 | g0213 | SAS | BEB | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG03927 | hp2 | a0002 | c0004 | t0001 | g0022 | SAS | BEB | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG03942 | hp1 | a0002 | c0004 | t0001 | g0021 | SAS | BEB | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG03942 | hp2 | a0013 | c0021 | t0001 | g0154 | SAS | BEB | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | STU | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG04199 | hp2 | a0001 | c0002 | t0020 | g0231 | SAS | STU | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| NA18522 | hp1 | a0003 | c0005 | t0001 | g0195 | AFR | YRI | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0184 | AFR | YRI | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | CHB | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| NA18747 | hp2 | a0002 | c0004 | t0001 | g0027 | EAS | CHB | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | YRI | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| NA18906 | hp2 | a0003 | c0005 | t0001 | g0198 | AFR | YRI | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| NA18941 | hp1 | a0001 | c0003 | t0002 | g0221 | EAS | JPT | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| NA18967 | hp1 | a0001 | c0003 | t0002 | g0222 | EAS | JPT | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| NA18975 | hp2 | a0007 | c0010 | t0001 | g0068 | EAS | JPT | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| NA18979 | hp1 | a0001 | c0003 | t0002 | g0207 | EAS | JPT | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0158 | EAS | JPT | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| NA18984 | hp1 | a0001 | c0001 | t0014 | g0063 | EAS | JPT | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| NA19006 | hp1 | a0001 | c0001 | t0012 | g0116 | EAS | JPT | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| NA19006 | hp2 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| NA19030 | hp1 | a0001 | c0002 | t0007 | g0012 | AFR | LWK | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| NA19030 | hp2 | a0001 | c0008 | t0001 | g0204 | AFR | LWK | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| NA19043 | hp1 | a0001 | c0002 | t0019 | g0224 | AFR | LWK | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | LWK | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| NA19060 | hp1 | a0001 | c0003 | t0002 | g0214 | EAS | JPT | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| NA19076 | hp1 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| NA19076 | hp2 | a0007 | c0010 | t0001 | g0046 | EAS | JPT | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| NA19083 | hp1 | a0001 | c0001 | t0014 | g0045 | EAS | JPT | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| NA19083 | hp2 | a0001 | c0003 | t0002 | g0208 | EAS | JPT | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0103 | AFR | YRI | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0181 | AFR | YRI | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| NA20752 | hp1 | a0001 | c0003 | t0002 | g0212 | EUR | TSI | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0145 | EUR | TSI | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| NA20905 | hp1 | a0002 | c0004 | t0001 | g0026 | SAS | GIH | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| NA20905 | hp2 | a0001 | c0020 | t0001 | g0153 | SAS | GIH | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0180 | AFR | ACB | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02486 | hp1 | a0003 | c0005 | t0001 | g0196 | AFR | ACB | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG02559 | hp2 | a0003 | c0005 | t0001 | g0197 | AFR | ACB | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG03471 | hp1 | a0001 | c0006 | t0001 | g0177 | AFR | MSL | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| HG03471 | hp2 | a0001 | c0001 | t0022 | g0167 | AFR | MSL | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | USA | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | USA | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| NA21309 | hp1 | a0001 | c0003 | t0002 | g0225 | AFR | LWK | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| NA21309 | hp2 | a0003 | c0005 | t0001 | g0194 | AFR | LWK | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| homoSapiens | chm13v2 | a0002 | c0013 | t0001 | g0152 | REF | REF | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| homoSapiens | grch38p0 | a0003 | c0018 | t0002 | g0217 | REF | REF | QSER1_chr11_32887811_32985270 | QSER1 | chr11 | 32887811 | 32985270 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:32893160 | A | AGCC | 1 | a0006 | 2 | HG01884.hp1 HG02809.hp1 |
disruptive_inframe_insertion | MODERATE | c.54_56dupGCC | p.Pro19dup | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/13 | 372/9706 | 57/5595 | 19/1864 | INFO_REALIGN_3_PRIME | chr11 | 32893160 | ||
| chr11:32893243 | G | T | 1 | a0006 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.118G>T | p.Ala40Ser | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/13 | 433/9706 | 118/5595 | 40/1864 | chr11 | 32893243 | |||
| chr11:32893276 | A | AGCAGCAG others(11): Show |
1 | a0005 | 4 | HG02818.hp2 HG02895.hp1 HG02895.hp2 others(1): Show |
conservative_inframe_insertion | MODERATE | c.157_174dupAGCTGCAG others(10): Show |
p.Ser53_Ser58dup | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/13 | 490/9706 | 175/5595 | 59/1864 | INFO_REALIGN_3_PRIME | chr11 | 32893276 | ||
| chr11:32931970 | G | A | 1 | a0007 | 2 | NA18975.hp2 NA19076.hp2 |
missense_variant | MODERATE | c.712G>A | p.Val238Ile | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/13 | 1027/9706 | 712/5595 | 238/1864 | chr11 | 32931970 | |||
| chr11:32932286 | G | C | 1 | a0011 | 1 | HG02965.hp2 | missense_variant | MODERATE | c.1028G>C | p.Ser343Thr | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/13 | 1343/9706 | 1028/5595 | 343/1864 | chr11 | 32932286 | |||
| chr11:32932358 | T | C | 1 | a0008 | 1 | HG00673.hp2 | missense_variant | MODERATE | c.1100T>C | p.Ile367Thr | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/13 | 1415/9706 | 1100/5595 | 367/1864 | chr11 | 32932358 | |||
| chr11:32932798 | G | A | 11 | a0001 a0002 a0004 others(8): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
missense_variant | MODERATE | c.1540G>A | p.Val514Ile | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/13 | 1855/9706 | 1540/5595 | 514/1864 | chr11 | 32932798 | |||
| chr11:32932976 | A | G | 1 | a0013 | 1 | HG03942.hp2 | missense_variant | MODERATE | c.1718A>G | p.Tyr573Cys | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/13 | 2033/9706 | 1718/5595 | 573/1864 | chr11 | 32932976 | |||
| chr11:32933576 | A | G | 1 | a0002 | 12 | HG01975.hp1 HG01981.hp1 HG02040.hp2 others(9): Show |
missense_variant | MODERATE | c.2318A>G | p.Gln773Arg | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/13 | 2633/9706 | 2318/5595 | 773/1864 | chr11 | 32933576 | |||
| chr11:32933875 | G | A | 1 | a0010 | 1 | HG02922.hp1 | missense_variant | MODERATE | c.2617G>A | p.Gly873Ser | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/13 | 2932/9706 | 2617/5595 | 873/1864 | chr11 | 32933875 | |||
| chr11:32934336 | G | C | 1 | a0006 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.3078G>C | p.Arg1026Ser | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/13 | 3393/9706 | 3078/5595 | 1026/1864 | chr11 | 32934336 | |||
| chr11:32934698 | A | G | 12 | a0001 a0002 a0004 others(9): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
missense_variant | MODERATE | c.3440A>G | p.Asn1147Ser | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/13 | 3755/9706 | 3440/5595 | 1147/1864 | chr11 | 32934698 | |||
| chr11:32934946 | C | T | 1 | a0004 | 6 | HG00280.hp1 HG00735.hp2 HG01256.hp2 others(3): Show |
missense_variant | MODERATE | c.3688C>T | p.Arg1230Cys | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/13 | 4003/9706 | 3688/5595 | 1230/1864 | chr11 | 32934946 | |||
| chr11:32954076 | T | C | 1 | a0009 | 1 | HG01175.hp1 | missense_variant | MODERATE | c.4397T>C | p.Ile1466Thr | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 5/13 | 4712/9706 | 4397/5595 | 1466/1864 | chr11 | 32954076 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:32893149 | G | C | 3 | a0001c0008 a0003c0005 a0011c0012 |
14 | HG01884.hp2 HG02145.hp1 HG02486.hp1 others(11): Show |
synonymous_variant | LOW | c.24G>C | p.Ser8Ser | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/13 | 339/9706 | 24/5595 | 8/1864 | chr11 | 32893149 | |||
| chr11:32893296 | C | T | 1 | a0001c0011 | 2 | HG02886.hp2 HG03209.hp2 |
synonymous_variant | LOW | c.171C>T | p.Gly57Gly | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/13 | 486/9706 | 171/5595 | 57/1864 | chr11 | 32893296 | |||
| chr11:32932734 | C | T | 2 | a0001c0020 a0013c0021 |
2 | HG03942.hp2 NA20905.hp2 |
synonymous_variant | LOW | c.1476C>T | p.Ser492Ser | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/13 | 1791/9706 | 1476/5595 | 492/1864 | chr11 | 32932734 | |||
| chr11:32933883 | T | C | 1 | a0010c0015 | 1 | HG02922.hp1 | synonymous_variant | LOW | c.2625T>C | p.Gly875Gly | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/13 | 2940/9706 | 2625/5595 | 875/1864 | chr11 | 32933883 | |||
| chr11:32935074 | A | G | 11 | a0001c0001 a0001c0011 a0001c0020 others(8): Show |
162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
synonymous_variant | LOW | c.3816A>G | p.Pro1272Pro | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/13 | 4131/9706 | 3816/5595 | 1272/1864 | chr11 | 32935074 | |||
| chr11:32935269 | C | T | 1 | a0001c0016 | 1 | HG00099.hp1 | synonymous_variant | LOW | c.4011C>T | p.Gly1337Gly | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/13 | 4326/9706 | 4011/5595 | 1337/1864 | chr11 | 32935269 | |||
| chr11:32969134 | A | G | 2 | a0001c0006 a0012c0019 |
9 | HG01891.hp2 HG02280.hp2 HG02886.hp1 others(6): Show |
synonymous_variant | LOW | c.5196A>G | p.Gln1732Gln | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 10/13 | 5511/9706 | 5196/5595 | 1732/1864 | chr11 | 32969134 | |||
| chr11:32975259 | C | T | 2 | a0001c0003 a0001c0016 |
17 | HG00099.hp1 HG01074.hp1 HG01167.hp1 others(14): Show |
synonymous_variant | LOW | c.5370C>T | p.Val1790Val | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 12/13 | 5685/9706 | 5370/5595 | 1790/1864 | chr11 | 32975259 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:32892843 | G | GGCCGCC | 31 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(28): Show |
196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
5_prime_UTR_variant | MODIFIER | c.-269_-264dupCCGCCG | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/13 | 263 | INFO_REALIGN_3_PRIME | chr11 | 32892843 | |||||
| chr11:32892843 | G | GGCCGCCG others(2): Show |
4 | a0001c0002t0007 a0001c0002t0008 a0001c0002t0018 others(1): Show |
9 | HG01496.hp1 HG02451.hp1 HG02572.hp2 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-272_-264dupCCGCCG others(3): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/13 | 263 | INFO_REALIGN_3_PRIME | chr11 | 32892843 | |||||
| chr11:32892843 | G | GGCCGCCG others(5): Show |
3 | a0001c0001t0005 a0001c0001t0009 a0001c0002t0013 |
10 | HG00280.hp2 HG00642.hp1 HG01071.hp2 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-275_-264dupCCGCCG others(6): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/13 | 263 | INFO_REALIGN_3_PRIME | chr11 | 32892843 | |||||
| chr11:32892843 | G | GGCCGCCG others(8): Show |
1 | a0001c0001t0017 | 1 | HG02145.hp2 | 5_prime_UTR_variant | MODIFIER | c.-278_-264dupCCGCCG others(9): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/13 | 263 | INFO_REALIGN_3_PRIME | chr11 | 32892843 | |||||
| chr11:32892913 | G | T | 1 | a0006c0023t0023 | 1 | HG01884.hp1 | 5_prime_UTR_variant | MODIFIER | c.-213G>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/13 | 213 | chr11 | 32892913 | ||||||
| chr11:32893034 | T | C | 1 | a0001c0003t0024 | 1 | HG02698.hp1 | 5_prime_UTR_variant | MODIFIER | c.-92T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/13 | 92 | chr11 | 32893034 | ||||||
| chr11:32976768 | A | G | 1 | a0001c0001t0022 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*294A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 13/13 | 294 | chr11 | 32976768 | ||||||
| chr11:32976896 | C | T | 1 | a0001c0001t0012 | 3 | HG00621.hp2 HG01256.hp1 NA19006.hp1 |
3_prime_UTR_variant | MODIFIER | c.*422C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 13/13 | 422 | chr11 | 32976896 | ||||||
| chr11:32977450 | A | G | 1 | a0011c0012t0021 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*976A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 13/13 | 976 | chr11 | 32977450 | ||||||
| chr11:32977506 | A | G | 1 | a0004c0007t0016 | 2 | HG01256.hp2 HG01258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1032A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 13/13 | 1032 | chr11 | 32977506 | ||||||
| chr11:32977521 | C | T | 1 | a0002c0004t0015 | 2 | HG01975.hp1 HG01981.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1047C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 13/13 | 1047 | chr11 | 32977521 | ||||||
| chr11:32977916 | C | T | 2 | a0001c0002t0004 a0001c0002t0020 |
9 | HG01243.hp2 HG01496.hp2 HG02257.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1442C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 13/13 | 1442 | chr11 | 32977916 | ||||||
| chr11:32978072 | A | G | 2 | a0001c0002t0004 a0001c0002t0020 |
9 | HG01243.hp2 HG01496.hp2 HG02257.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1598A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 13/13 | 1598 | chr11 | 32978072 | ||||||
| chr11:32978656 | A | G | 1 | a0001c0002t0019 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2182A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 13/13 | 2182 | chr11 | 32978656 | ||||||
| chr11:32978674 | T | G | 1 | a0001c0002t0019 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2200T>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 13/13 | 2200 | chr11 | 32978674 | ||||||
| chr11:32978724 | T | C | 1 | a0001c0001t0010 | 3 | HG01071.hp1 HG01175.hp2 HG01346.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2250T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 13/13 | 2250 | chr11 | 32978724 | ||||||
| chr11:32978753 | A | C | 1 | a0001c0002t0020 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2279A>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 13/13 | 2279 | chr11 | 32978753 | ||||||
| chr11:32978763 | T | A | 2 | a0001c0001t0011 a0009c0017t0011 |
3 | HG01175.hp1 HG01243.hp1 HG01261.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2289T>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 13/13 | 2289 | chr11 | 32978763 | ||||||
| chr11:32978844 | C | T | 1 | a0001c0002t0013 | 2 | HG02257.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2370C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 13/13 | 2370 | chr11 | 32978844 | ||||||
| chr11:32978845 | G | A | 1 | a0001c0001t0009 | 3 | HG00642.hp1 HG01071.hp2 HG01106.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2371G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 13/13 | 2371 | chr11 | 32978845 | ||||||
| chr11:32978888 | G | A | 1 | a0001c0001t0003 | 8 | HG03831.hp1 NA18951.hp1 NA18964.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2414G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 13/13 | 2414 | chr11 | 32978888 | ||||||
| chr11:32978940 | T | C | 2 | a0001c0002t0004 a0001c0002t0020 |
9 | HG01243.hp2 HG01496.hp2 HG02257.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2466T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 13/13 | 2466 | chr11 | 32978940 | ||||||
| chr11:32979142 | C | T | 1 | a0002c0004t0015 | 2 | HG01975.hp1 HG01981.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2668C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 13/13 | 2668 | chr11 | 32979142 | ||||||
| chr11:32979143 | G | A | 2 | a0001c0002t0007 a0001c0002t0018 |
5 | HG01496.hp1 HG02451.hp1 HG02818.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2669G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 13/13 | 2669 | chr11 | 32979143 | ||||||
| chr11:32979634 | ACTT | A | 1 | a0001c0001t0006 | 5 | HG01891.hp1 HG02976.hp1 HG03130.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3164_*3166delCTT | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 13/13 | 3164 | INFO_REALIGN_3_PRIME | chr11 | 32979634 | |||||
| chr11:32979967 | C | G | 1 | a0001c0001t0014 | 2 | NA18984.hp1 NA19083.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3493C>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 13/13 | 3493 | chr11 | 32979967 | ||||||
| chr11:32979981 | G | T | 1 | a0001c0002t0018 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3507G>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 13/13 | 3507 | chr11 | 32979981 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:32893352 | C | CG | 12 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(9): Show |
12 | HG00621.hp2 HG00642.hp1 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.209+22dupG | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 32893352 | ||||||
| chr11:32893570 | G | C | 1 | a0001c0001t0001g0003 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.209+236G>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32893570 | |||||||
| chr11:32893646 | A | G | 1 | a0001c0003t0002g0234 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.209+312A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32893646 | |||||||
| chr11:32893838 | G | A | 1 | a0001c0008t0001g0015 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.209+504G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32893838 | |||||||
| chr11:32893938 | G | A | 1 | a0001c0001t0001g0016 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.209+604G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32893938 | |||||||
| chr11:32894459 | G | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(151): Show |
155 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.209+1125G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32894459 | |||||||
| chr11:32894500 | A | G | 9 | a0001c0002t0004g0014 a0001c0002t0004g0226 a0001c0002t0004g0227 others(6): Show |
9 | HG01243.hp2 HG01496.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.209+1166A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32894500 | |||||||
| chr11:32894603 | G | C | 2 | a0001c0002t0013g0162 a0001c0002t0013g0163 |
2 | HG02257.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.209+1269G>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32894603 | |||||||
| chr11:32894674 | T | C | 26 | a0001c0001t0001g0168 a0001c0001t0006g0002 a0001c0001t0006g0164 others(23): Show |
27 | HG00735.hp1 HG01884.hp1 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.209+1340T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32894674 | |||||||
| chr11:32894957 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.209+1623A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32894957 | |||||||
| chr11:32895096 | C | G | 26 | a0001c0001t0001g0168 a0001c0001t0006g0002 a0001c0001t0006g0164 others(23): Show |
27 | HG00735.hp1 HG01884.hp1 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.209+1762C>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32895096 | |||||||
| chr11:32895285 | G | C | 21 | a0001c0002t0002g0205 a0001c0002t0007g0012 a0001c0002t0007g0189 others(18): Show |
21 | HG01496.hp1 HG01884.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.209+1951G>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32895285 | |||||||
| chr11:32895334 | C | T | 1 | a0001c0003t0002g0225 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.209+2000C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32895334 | |||||||
| chr11:32895532 | T | A | 4 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(1): Show |
4 | HG00673.hp1 HG02083.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.209+2198T>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32895532 | |||||||
| chr11:32895646 | A | G | 2 | a0001c0002t0001g0013 a0001c0002t0019g0224 |
2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.209+2312A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32895646 | |||||||
| chr11:32895693 | C | T | 1 | a0006c0022t0001g0187 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.209+2359C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32895693 | |||||||
| chr11:32895959 | A | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(151): Show |
155 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.209+2625A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32895959 | |||||||
| chr11:32896024 | G | A | 1 | a0001c0001t0001g0020 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.209+2690G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32896024 | |||||||
| chr11:32896118 | A | C | 1 | a0001c0002t0001g0013 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.209+2784A>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32896118 | |||||||
| chr11:32896231 | T | C | 2 | a0001c0002t0013g0162 a0001c0002t0013g0163 |
2 | HG02257.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.209+2897T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32896231 | |||||||
| chr11:32896524 | A | G | 2 | a0001c0002t0002g0205 a0001c0002t0008g0206 |
2 | HG02280.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.209+3190A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32896524 | |||||||
| chr11:32896725 | A | G | 1 | a0002c0004t0001g0160 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.209+3391A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32896725 | |||||||
| chr11:32896769 | G | A | 1 | a0011c0012t0021g0188 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.209+3435G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32896769 | |||||||
| chr11:32896940 | C | A | 2 | a0001c0002t0013g0162 a0001c0002t0013g0163 |
2 | HG02257.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.209+3606C>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32896940 | |||||||
| chr11:32897087 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.209+3753C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32897087 | |||||||
| chr11:32897461 | A | G | 2 | a0001c0002t0001g0013 a0001c0002t0019g0224 |
2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.209+4127A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32897461 | |||||||
| chr11:32897537 | C | T | 2 | a0001c0001t0003g0157 a0001c0001t0003g0158 |
2 | NA18964.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.209+4203C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32897537 | |||||||
| chr11:32897647 | T | C | 1 | a0001c0001t0012g0005 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.209+4313T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32897647 | |||||||
| chr11:32897778 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.209+4444C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32897778 | |||||||
| chr11:32897799 | A | G | 1 | a0001c0001t0001g0155 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.209+4465A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32897799 | |||||||
| chr11:32898008 | G | C | 1 | a0001c0008t0001g0015 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.209+4674G>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32898008 | |||||||
| chr11:32898114 | A | G | 4 | a0001c0008t0001g0202 a0001c0008t0001g0203 a0001c0008t0001g0204 others(1): Show |
4 | HG02723.hp1 HG02965.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.209+4780A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32898114 | |||||||
| chr11:32898206 | C | G | 4 | a0001c0008t0001g0202 a0001c0008t0001g0203 a0001c0008t0001g0204 others(1): Show |
4 | HG02723.hp1 HG02965.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.209+4872C>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32898206 | |||||||
| chr11:32898464 | C | T | 2 | a0001c0020t0001g0153 a0013c0021t0001g0154 |
2 | HG03942.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.209+5130C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32898464 | |||||||
| chr11:32898482 | T | TCA | 7 | a0001c0003t0002g0209 a0001c0003t0002g0210 a0001c0003t0002g0212 others(4): Show |
7 | HG00099.hp1 HG01074.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.209+5195_209+5196d others(4): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 32898482 | ||||||
| chr11:32898482 | T | TCACA | 7 | a0001c0001t0001g0025 a0001c0001t0001g0028 a0001c0001t0001g0029 others(4): Show |
7 | HG02040.hp2 HG02559.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.209+5193_209+5196d others(6): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 32898482 | ||||||
| chr11:32898482 | T | TCACACA | 7 | a0001c0003t0002g0207 a0001c0003t0002g0208 a0001c0008t0001g0202 others(4): Show |
7 | HG02723.hp1 HG03130.hp2 HG03927.hp2 others(4): Show |
intron_variant | MODIFIER | c.209+5191_209+5196d others(8): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 32898482 | ||||||
| chr11:32898482 | TCA | T | 22 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0040 others(19): Show |
22 | HG00280.hp2 HG00642.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.209+5195_209+5196d others(4): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 32898482 | ||||||
| chr11:32898482 | TCACA | T | 59 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(56): Show |
60 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.209+5193_209+5196d others(6): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 32898482 | ||||||
| chr11:32898482 | TCACACA | T | 38 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0098 others(35): Show |
38 | HG01106.hp2 HG01169.hp1 HG01175.hp1 others(35): Show |
intron_variant | MODIFIER | c.209+5191_209+5196d others(8): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 32898482 | ||||||
| chr11:32898482 | TCACACAC others(1): Show |
T | 24 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0123 others(21): Show |
24 | HG00673.hp1 HG00738.hp1 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.209+5189_209+5196d others(10): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 32898482 | ||||||
| chr11:32898482 | TCACACAC others(3): Show |
T | 28 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(25): Show |
28 | HG00140.hp2 HG00621.hp1 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.209+5187_209+5196d others(12): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 32898482 | ||||||
| chr11:32898482 | TCACACAC others(5): Show |
T | 20 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0168 others(17): Show |
21 | HG01891.hp2 HG02040.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.209+5185_209+5196d others(14): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 32898482 | ||||||
| chr11:32898482 | TCACACAC others(9): Show |
T | 9 | a0001c0002t0001g0011 a0001c0002t0001g0180 a0001c0002t0001g0181 others(6): Show |
9 | HG00735.hp1 HG01884.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.209+5181_209+5196d others(18): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 32898482 | ||||||
| chr11:32898798 | T | C | 1 | a0001c0001t0005g0030 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.209+5464T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32898798 | |||||||
| chr11:32898855 | G | A | 1 | a0001c0008t0001g0015 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.209+5521G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32898855 | |||||||
| chr11:32899019 | C | A | 9 | a0003c0005t0001g0193 a0003c0005t0001g0194 a0003c0005t0001g0195 others(6): Show |
9 | HG02145.hp1 HG02486.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.209+5685C>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32899019 | |||||||
| chr11:32899027 | G | C | 1 | a0007c0010t0001g0046 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.209+5693G>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32899027 | |||||||
| chr11:32899073 | C | A | 2 | a0003c0005t0001g0197 a0003c0005t0001g0198 |
2 | HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.209+5739C>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32899073 | |||||||
| chr11:32899090 | A | G | 1 | a0006c0023t0023g0186 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.209+5756A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32899090 | |||||||
| chr11:32899230 | A | C | 1 | a0001c0002t0008g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.209+5896A>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32899230 | |||||||
| chr11:32899310 | C | T | 9 | a0001c0002t0004g0014 a0001c0002t0004g0226 a0001c0002t0004g0227 others(6): Show |
9 | HG01243.hp2 HG01496.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.209+5976C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32899310 | |||||||
| chr11:32899430 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.209+6096G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32899430 | |||||||
| chr11:32899661 | G | GA | 25 | a0001c0001t0001g0168 a0001c0001t0006g0002 a0001c0001t0006g0164 others(22): Show |
26 | HG00735.hp1 HG01891.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.209+6337dupA | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 32899661 | ||||||
| chr11:32899819 | G | A | 2 | a0001c0001t0001g0047 a0004c0007t0001g0048 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.209+6485G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32899819 | |||||||
| chr11:32900074 | A | C | 9 | a0003c0005t0001g0193 a0003c0005t0001g0194 a0003c0005t0001g0195 others(6): Show |
9 | HG02145.hp1 HG02486.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.209+6740A>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32900074 | |||||||
| chr11:32900076 | A | C | 9 | a0003c0005t0001g0193 a0003c0005t0001g0194 a0003c0005t0001g0195 others(6): Show |
9 | HG02145.hp1 HG02486.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.209+6742A>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32900076 | |||||||
| chr11:32900151 | C | T | 3 | a0001c0008t0001g0202 a0001c0008t0001g0203 a0001c0008t0001g0204 |
3 | HG02723.hp1 HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.209+6817C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32900151 | |||||||
| chr11:32900227 | G | A | 2 | a0002c0004t0015g0031 a0002c0004t0015g0032 |
2 | HG01975.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.209+6893G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32900227 | |||||||
| chr11:32900390 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.209+7056C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32900390 | |||||||
| chr11:32900507 | T | C | 215 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(212): Show |
217 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.209+7173T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32900507 | |||||||
| chr11:32900589 | GCCTACAA others(3): Show |
G | 1 | a0001c0001t0001g0122 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.209+7259_209+7268d others(12): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 32900589 | ||||||
| chr11:32900677 | G | A | 9 | a0001c0001t0001g0159 a0001c0001t0003g0049 a0001c0001t0003g0094 others(6): Show |
9 | HG00140.hp2 HG03831.hp1 NA18951.hp1 others(6): Show |
intron_variant | MODIFIER | c.209+7343G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32900677 | |||||||
| chr11:32900682 | A | G | 1 | a0010c0015t0001g0093 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.209+7348A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32900682 | |||||||
| chr11:32900968 | G | A | 1 | a0001c0003t0002g0234 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.209+7634G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32900968 | |||||||
| chr11:32901295 | ATGTC | A | 2 | a0001c0002t0004g0228 a0001c0002t0004g0229 |
2 | HG02257.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.209+7964_209+7967d others(6): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 32901295 | ||||||
| chr11:32901354 | A | T | 20 | a0001c0002t0001g0011 a0001c0002t0001g0175 a0001c0002t0001g0178 others(17): Show |
20 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.209+8020A>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32901354 | |||||||
| chr11:32901748 | G | A | 2 | a0001c0002t0013g0162 a0001c0002t0013g0163 |
2 | HG02257.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.209+8414G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32901748 | |||||||
| chr11:32901809 | C | T | 9 | a0003c0005t0001g0193 a0003c0005t0001g0194 a0003c0005t0001g0195 others(6): Show |
9 | HG02145.hp1 HG02486.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.209+8475C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32901809 | |||||||
| chr11:32901818 | T | C | 6 | a0001c0001t0005g0030 a0001c0001t0005g0033 a0001c0001t0005g0035 others(3): Show |
6 | HG00280.hp2 HG00642.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.209+8484T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32901818 | |||||||
| chr11:32902476 | A | C | 1 | a0001c0002t0018g0192 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.209+9142A>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32902476 | |||||||
| chr11:32902522 | G | A | 2 | a0002c0004t0008g0037 a0002c0004t0008g0038 |
2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.209+9188G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32902522 | |||||||
| chr11:32902647 | C | A | 9 | a0001c0002t0001g0175 a0001c0006t0001g0169 a0001c0006t0001g0170 others(6): Show |
9 | HG01891.hp2 HG02280.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.209+9313C>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32902647 | |||||||
| chr11:32902929 | A | T | 1 | a0001c0002t0001g0013 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.209+9595A>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32902929 | |||||||
| chr11:32903282 | A | T | 1 | a0003c0005t0001g0198 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.209+9948A>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32903282 | |||||||
| chr11:32903578 | G | C | 1 | a0006c0023t0023g0186 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.209+10244G>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32903578 | |||||||
| chr11:32903597 | A | ATTTG | 4 | a0001c0002t0007g0189 a0001c0002t0008g0223 a0001c0002t0013g0162 others(1): Show |
4 | HG02257.hp1 HG02572.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.209+10289_209+1029 others(8): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 32903597 | ||||||
| chr11:32903597 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.209+10263A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32903597 | |||||||
| chr11:32903597 | ATTTGTTT others(1): Show |
A | 6 | a0001c0001t0001g0168 a0001c0001t0006g0002 a0001c0001t0006g0164 others(3): Show |
7 | HG01891.hp1 HG02976.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.209+10285_209+1029 others(12): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 32903597 | ||||||
| chr11:32903657 | A | G | 1 | a0001c0008t0001g0015 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.209+10323A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32903657 | |||||||
| chr11:32904146 | C | G | 5 | a0001c0001t0001g0121 a0001c0001t0001g0136 a0001c0001t0001g0148 others(2): Show |
5 | HG02602.hp1 HG02683.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.209+10812C>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32904146 | |||||||
| chr11:32904189 | C | CT | 5 | a0001c0002t0004g0227 a0001c0002t0004g0233 a0005c0009t0001g0089 others(2): Show |
5 | HG01243.hp2 HG02818.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.209+10871dupT | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 32904189 | ||||||
| chr11:32904189 | CT | C | 10 | a0001c0003t0002g0216 a0003c0005t0001g0193 a0003c0005t0001g0194 others(7): Show |
10 | HG01167.hp1 HG02145.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.209+10871delT | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 32904189 | ||||||
| chr11:32904256 | A | G | 183 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(180): Show |
185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.209+10922A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32904256 | |||||||
| chr11:32904420 | G | C | 1 | a0001c0001t0001g0125 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.209+11086G>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32904420 | |||||||
| chr11:32904601 | C | CT | 23 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0029 others(20): Show |
23 | HG00621.hp1 HG00621.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.209+11287dupT | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 32904601 | ||||||
| chr11:32904601 | C | CTT | 6 | a0001c0002t0001g0013 a0001c0002t0004g0232 a0001c0002t0007g0012 others(3): Show |
6 | HG01496.hp1 HG01496.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.209+11286_209+1128 others(6): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 32904601 | ||||||
| chr11:32904601 | CT | C | 22 | a0001c0001t0001g0050 a0001c0002t0001g0011 a0001c0002t0001g0175 others(19): Show |
22 | HG00735.hp1 HG01257.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.209+11287delT | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 32904601 | ||||||
| chr11:32904679 | A | G | 1 | a0001c0008t0001g0015 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.209+11345A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32904679 | |||||||
| chr11:32904757 | C | T | 1 | a0001c0001t0001g0086 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.209+11423C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32904757 | |||||||
| chr11:32905034 | A | G | 1 | a0009c0017t0011g0120 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.209+11700A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32905034 | |||||||
| chr11:32905155 | A | C | 3 | a0001c0001t0001g0085 a0001c0001t0001g0119 a0001c0001t0001g0145 |
3 | HG00099.hp2 HG03239.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.209+11821A>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32905155 | |||||||
| chr11:32905353 | G | T | 17 | a0001c0003t0002g0207 a0001c0003t0002g0208 a0001c0003t0002g0209 others(14): Show |
17 | HG00099.hp1 HG01074.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.209+12019G>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32905353 | |||||||
| chr11:32905530 | AG | A | 20 | a0001c0002t0001g0011 a0001c0002t0001g0175 a0001c0002t0001g0178 others(17): Show |
20 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.209+12197delG | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32905530 | |||||||
| chr11:32905553 | T | C | 20 | a0001c0002t0001g0011 a0001c0002t0001g0175 a0001c0002t0001g0178 others(17): Show |
20 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.209+12219T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32905553 | |||||||
| chr11:32906104 | G | GT | 28 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0136 others(25): Show |
28 | HG00735.hp1 HG00735.hp2 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.209+12790dupT | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 32906104 | ||||||
| chr11:32906104 | GT | G | 22 | a0001c0003t0002g0207 a0001c0003t0002g0208 a0001c0003t0002g0209 others(19): Show |
22 | HG00099.hp1 HG01074.hp1 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.209+12790delT | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 32906104 | ||||||
| chr11:32906112 | T | G | 1 | a0011c0012t0021g0188 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.209+12778T>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32906112 | |||||||
| chr11:32906232 | G | T | 6 | a0001c0001t0001g0047 a0004c0007t0001g0048 a0004c0007t0001g0083 others(3): Show |
6 | HG00280.hp1 HG00735.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.209+12898G>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32906232 | |||||||
| chr11:32906235 | T | A | 1 | a0001c0001t0003g0097 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.209+12901T>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32906235 | |||||||
| chr11:32906357 | G | A | 4 | a0001c0008t0001g0202 a0001c0008t0001g0203 a0001c0008t0001g0204 others(1): Show |
4 | HG02723.hp1 HG02965.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.209+13023G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32906357 | |||||||
| chr11:32907168 | T | C | 1 | a0003c0005t0001g0196 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.209+13834T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32907168 | |||||||
| chr11:32907873 | A | G | 1 | a0001c0003t0002g0215 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.209+14539A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32907873 | |||||||
| chr11:32907886 | G | A | 1 | a0002c0004t0001g0024 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.209+14552G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32907886 | |||||||
| chr11:32907929 | C | T | 2 | a0003c0005t0001g0194 a0003c0005t0001g0195 |
2 | NA18522.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.209+14595C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32907929 | |||||||
| chr11:32908303 | A | G | 1 | a0005c0009t0001g0088 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.209+14969A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32908303 | |||||||
| chr11:32908350 | C | T | 1 | a0001c0001t0003g0158 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.209+15016C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32908350 | |||||||
| chr11:32908454 | T | C | 4 | a0001c0008t0001g0202 a0001c0008t0001g0203 a0001c0008t0001g0204 others(1): Show |
4 | HG02723.hp1 HG02965.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.209+15120T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32908454 | |||||||
| chr11:32908631 | T | C | 1 | a0001c0001t0001g0016 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.209+15297T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32908631 | |||||||
| chr11:32908816 | A | G | 1 | a0001c0001t0001g0123 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.209+15482A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32908816 | |||||||
| chr11:32908893 | T | C | 72 | a0001c0002t0001g0011 a0001c0002t0001g0013 a0001c0002t0001g0175 others(69): Show |
72 | HG00099.hp1 HG00735.hp1 HG01074.hp1 others(69): Show |
intron_variant | MODIFIER | c.209+15559T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32908893 | |||||||
| chr11:32908954 | G | C | 1 | a0001c0001t0001g0137 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.209+15620G>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32908954 | |||||||
| chr11:32909121 | C | T | 1 | a0001c0001t0001g0016 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.209+15787C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32909121 | |||||||
| chr11:32909352 | G | A | 1 | a0001c0002t0001g0180 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.209+16018G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32909352 | |||||||
| chr11:32909433 | C | T | 1 | a0002c0004t0001g0044 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.209+16099C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32909433 | |||||||
| chr11:32909484 | G | C | 6 | a0001c0001t0001g0007 a0001c0001t0001g0051 a0001c0001t0001g0052 others(3): Show |
6 | HG00140.hp1 HG01346.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.209+16150G>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32909484 | |||||||
| chr11:32909840 | T | G | 1 | a0001c0001t0001g0017 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.209+16506T>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32909840 | |||||||
| chr11:32909845 | A | G | 20 | a0001c0002t0001g0011 a0001c0002t0001g0175 a0001c0002t0001g0178 others(17): Show |
20 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.209+16511A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32909845 | |||||||
| chr11:32909869 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.209+16535C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32909869 | |||||||
| chr11:32910401 | T | G | 1 | a0002c0004t0001g0023 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.210-16756T>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32910401 | |||||||
| chr11:32910483 | A | G | 2 | a0001c0003t0002g0221 a0001c0003t0002g0222 |
2 | NA18941.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.210-16674A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32910483 | |||||||
| chr11:32910561 | G | C | 2 | a0001c0001t0001g0047 a0004c0007t0001g0048 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.210-16596G>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32910561 | |||||||
| chr11:32910772 | A | G | 1 | a0001c0002t0013g0163 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.210-16385A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32910772 | |||||||
| chr11:32910846 | T | C | 1 | a0001c0001t0012g0116 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.210-16311T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32910846 | |||||||
| chr11:32910892 | G | T | 2 | a0001c0002t0001g0013 a0001c0002t0019g0224 |
2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.210-16265G>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32910892 | |||||||
| chr11:32911030 | T | C | 1 | a0001c0008t0001g0015 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.210-16127T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32911030 | |||||||
| chr11:32911092 | C | G | 3 | a0001c0003t0002g0207 a0001c0003t0002g0208 a0001c0003t0002g0214 |
3 | NA18979.hp1 NA19060.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.210-16065C>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32911092 | |||||||
| chr11:32911431 | A | C | 1 | a0003c0005t0001g0195 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.210-15726A>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32911431 | |||||||
| chr11:32911442 | T | TA | 3 | a0001c0002t0007g0190 a0001c0002t0007g0191 a0001c0002t0018g0192 |
3 | HG01496.hp1 HG02451.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.210-15714dupA | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 32911442 | ||||||
| chr11:32911565 | T | C | 72 | a0001c0002t0001g0011 a0001c0002t0001g0013 a0001c0002t0001g0175 others(69): Show |
72 | HG00099.hp1 HG00735.hp1 HG01074.hp1 others(69): Show |
intron_variant | MODIFIER | c.210-15592T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32911565 | |||||||
| chr11:32911703 | A | G | 1 | a0001c0001t0011g0082 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.210-15454A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32911703 | |||||||
| chr11:32912594 | G | A | 10 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0001g0055 others(7): Show |
10 | HG00642.hp2 HG02109.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.210-14563G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32912594 | |||||||
| chr11:32912594 | G | C | 1 | a0001c0001t0001g0100 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.210-14563G>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32912594 | |||||||
| chr11:32912597 | G | C | 1 | a0001c0001t0001g0100 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.210-14560G>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32912597 | |||||||
| chr11:32912901 | A | G | 2 | a0001c0002t0002g0205 a0001c0002t0008g0206 |
2 | HG02280.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.210-14256A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32912901 | |||||||
| chr11:32912932 | T | G | 16 | a0001c0002t0002g0205 a0001c0002t0008g0206 a0001c0008t0001g0015 others(13): Show |
16 | HG01884.hp2 HG02145.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.210-14225T>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32912932 | |||||||
| chr11:32913038 | C | A | 4 | a0001c0001t0001g0001 a0001c0001t0001g0060 a0001c0001t0001g0061 others(1): Show |
5 | HG02523.hp1 NA18951.hp2 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.210-14119C>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32913038 | |||||||
| chr11:32913049 | A | G | 6 | a0001c0001t0001g0018 a0001c0002t0007g0012 a0001c0002t0007g0189 others(3): Show |
6 | HG01496.hp1 HG02451.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.210-14108A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32913049 | |||||||
| chr11:32913172 | C | T | 1 | a0001c0001t0012g0113 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.210-13985C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32913172 | |||||||
| chr11:32913179 | C | CT | 90 | a0001c0001t0001g0019 a0001c0001t0001g0028 a0001c0001t0001g0029 others(87): Show |
90 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.210-13949dupT | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 32913179 | ||||||
| chr11:32913179 | C | CTT | 10 | a0001c0001t0001g0118 a0001c0001t0001g0125 a0001c0001t0001g0148 others(7): Show |
10 | HG02683.hp2 HG02809.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.210-13950_210-1394 others(6): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 32913179 | ||||||
| chr11:32913179 | CT | C | 22 | a0001c0001t0003g0049 a0001c0001t0006g0164 a0001c0001t0014g0063 others(19): Show |
22 | HG01243.hp2 HG01496.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.210-13949delT | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 32913179 | ||||||
| chr11:32913179 | CTTTTTTT others(7): Show |
C | 3 | a0001c0002t0001g0011 a0001c0002t0001g0181 a0001c0002t0001g0182 |
3 | HG00735.hp1 HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.210-13962_210-1394 others(18): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 32913179 | ||||||
| chr11:32913179 | CTTTTTTT others(11): Show |
C | 2 | a0001c0002t0004g0228 a0001c0002t0004g0229 |
2 | HG02257.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.210-13966_210-1394 others(22): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 32913179 | ||||||
| chr11:32913338 | G | A | 21 | a0001c0002t0002g0205 a0001c0002t0007g0012 a0001c0002t0007g0189 others(18): Show |
21 | HG01496.hp1 HG01884.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.210-13819G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32913338 | |||||||
| chr11:32913385 | A | G | 72 | a0001c0002t0001g0011 a0001c0002t0001g0013 a0001c0002t0001g0175 others(69): Show |
72 | HG00099.hp1 HG00735.hp1 HG01074.hp1 others(69): Show |
intron_variant | MODIFIER | c.210-13772A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32913385 | |||||||
| chr11:32913479 | TACCGCA | T | 5 | a0001c0002t0007g0012 a0001c0002t0007g0189 a0001c0002t0007g0190 others(2): Show |
5 | HG01496.hp1 HG02451.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.210-13677_210-1367 others(10): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32913479 | |||||||
| chr11:32913486 | C | G | 5 | a0001c0002t0007g0012 a0001c0002t0007g0189 a0001c0002t0007g0190 others(2): Show |
5 | HG01496.hp1 HG02451.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.210-13671C>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32913486 | |||||||
| chr11:32914112 | A | G | 72 | a0001c0002t0001g0011 a0001c0002t0001g0013 a0001c0002t0001g0175 others(69): Show |
72 | HG00099.hp1 HG00735.hp1 HG01074.hp1 others(69): Show |
intron_variant | MODIFIER | c.210-13045A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32914112 | |||||||
| chr11:32914334 | C | G | 4 | a0001c0001t0001g0155 a0001c0001t0011g0082 a0001c0001t0011g0112 others(1): Show |
4 | HG01175.hp1 HG01243.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.210-12823C>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32914334 | |||||||
| chr11:32914928 | G | A | 2 | a0001c0001t0010g0072 a0001c0001t0010g0104 |
2 | HG01175.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.210-12229G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32914928 | |||||||
| chr11:32914993 | C | T | 1 | a0001c0003t0024g0218 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.210-12164C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32914993 | |||||||
| chr11:32915243 | T | A | 2 | a0001c0002t0002g0205 a0001c0002t0008g0206 |
2 | HG02280.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.210-11914T>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32915243 | |||||||
| chr11:32915244 | A | T | 7 | a0001c0001t0001g0007 a0001c0001t0001g0051 a0001c0001t0001g0052 others(4): Show |
7 | HG00140.hp1 HG01346.hp2 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.210-11913A>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32915244 | |||||||
| chr11:32915259 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.210-11898C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32915259 | |||||||
| chr11:32915326 | C | T | 1 | a0001c0002t0004g0228 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.210-11831C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32915326 | |||||||
| chr11:32915687 | C | T | 5 | a0001c0002t0007g0012 a0001c0002t0007g0189 a0001c0002t0007g0190 others(2): Show |
5 | HG01496.hp1 HG02451.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.210-11470C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32915687 | |||||||
| chr11:32915775 | T | G | 1 | a0001c0001t0001g0064 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.210-11382T>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32915775 | |||||||
| chr11:32915860 | T | C | 45 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(42): Show |
46 | HG00408.hp2 HG00621.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.210-11297T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32915860 | |||||||
| chr11:32916026 | C | T | 160 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(157): Show |
162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.210-11131C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32916026 | |||||||
| chr11:32916619 | A | G | 72 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(69): Show |
73 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.210-10538A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32916619 | |||||||
| chr11:32916782 | A | AT | 27 | a0001c0002t0001g0011 a0001c0002t0001g0175 a0001c0002t0001g0178 others(24): Show |
27 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.210-10361dupT | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 32916782 | ||||||
| chr11:32916782 | AT | A | 160 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(157): Show |
162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.210-10361delT | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 32916782 | ||||||
| chr11:32916976 | G | A | 9 | a0001c0002t0004g0014 a0001c0002t0004g0226 a0001c0002t0004g0227 others(6): Show |
9 | HG01243.hp2 HG01496.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.210-10181G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32916976 | |||||||
| chr11:32917081 | C | T | 1 | a0001c0001t0010g0143 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.210-10076C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32917081 | |||||||
| chr11:32917215 | A | G | 1 | a0001c0001t0003g0097 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.210-9942A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32917215 | |||||||
| chr11:32917532 | A | T | 160 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(157): Show |
162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.210-9625A>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32917532 | |||||||
| chr11:32917542 | A | C | 1 | a0011c0012t0021g0188 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.210-9615A>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32917542 | |||||||
| chr11:32917711 | A | G | 1 | a0003c0005t0001g0194 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.210-9446A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32917711 | |||||||
| chr11:32917821 | C | CA | 87 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(84): Show |
87 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.210-9313dupA | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 32917821 | ||||||
| chr11:32917821 | C | CAA | 84 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(81): Show |
86 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.210-9314_210-9313d others(4): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 32917821 | ||||||
| chr11:32917821 | C | CAAA | 8 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0064 others(5): Show |
8 | HG00408.hp2 HG00642.hp2 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.210-9315_210-9313d others(5): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 32917821 | ||||||
| chr11:32917835 | A | C | 2 | a0001c0003t0002g0212 a0001c0003t0002g0234 |
2 | HG02683.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.210-9322A>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32917835 | |||||||
| chr11:32917840 | A | C | 9 | a0001c0002t0004g0014 a0001c0002t0004g0226 a0001c0002t0004g0227 others(6): Show |
9 | HG01243.hp2 HG01496.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.210-9317A>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32917840 | |||||||
| chr11:32918307 | A | G | 17 | a0001c0003t0002g0207 a0001c0003t0002g0208 a0001c0003t0002g0209 others(14): Show |
17 | HG00099.hp1 HG01074.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.210-8850A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32918307 | |||||||
| chr11:32918328 | G | A | 1 | a0001c0001t0022g0167 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.210-8829G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32918328 | |||||||
| chr11:32918426 | A | G | 3 | a0001c0006t0001g0174 a0001c0006t0001g0176 a0001c0006t0001g0177 |
3 | HG02280.hp2 HG02886.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.210-8731A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32918426 | |||||||
| chr11:32918839 | G | A | 20 | a0001c0002t0001g0011 a0001c0002t0001g0175 a0001c0002t0001g0178 others(17): Show |
20 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.210-8318G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32918839 | |||||||
| chr11:32919092 | T | C | 1 | a0001c0008t0001g0015 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.210-8065T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32919092 | |||||||
| chr11:32919693 | C | T | 3 | a0001c0001t0001g0053 a0001c0001t0001g0137 a0001c0001t0001g0138 |
3 | HG01346.hp2 HG01934.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.210-7464C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32919693 | |||||||
| chr11:32919711 | G | A | 1 | a0001c0002t0002g0205 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.210-7446G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32919711 | |||||||
| chr11:32919735 | T | A | 1 | a0001c0001t0001g0086 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.210-7422T>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32919735 | |||||||
| chr11:32920037 | G | T | 1 | a0001c0001t0001g0042 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.210-7120G>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32920037 | |||||||
| chr11:32920045 | A | G | 1 | a0001c0002t0004g0226 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.210-7112A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32920045 | |||||||
| chr11:32920088 | T | C | 17 | a0001c0003t0002g0207 a0001c0003t0002g0208 a0001c0003t0002g0209 others(14): Show |
17 | HG00099.hp1 HG01074.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.210-7069T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32920088 | |||||||
| chr11:32920168 | C | T | 6 | a0001c0001t0001g0168 a0001c0001t0006g0002 a0001c0001t0006g0164 others(3): Show |
7 | HG01891.hp1 HG02976.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.210-6989C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32920168 | |||||||
| chr11:32920443 | A | C | 2 | a0001c0002t0004g0014 a0001c0002t0004g0226 |
2 | HG02572.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.210-6714A>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32920443 | |||||||
| chr11:32920541 | T | A | 1 | a0001c0002t0008g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.210-6616T>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32920541 | |||||||
| chr11:32920702 | T | TGTGA | 2 | a0001c0001t0001g0111 a0001c0001t0003g0124 |
2 | NA18966.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.210-6452_210-6449d others(6): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 32920702 | ||||||
| chr11:32920724 | G | C | 1 | a0002c0004t0001g0027 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.210-6433G>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32920724 | |||||||
| chr11:32920765 | C | G | 3 | a0003c0005t0001g0197 a0003c0005t0001g0198 a0003c0005t0001g0200 |
3 | HG02559.hp2 HG02809.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.210-6392C>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32920765 | |||||||
| chr11:32921032 | A | G | 1 | a0006c0023t0023g0186 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.210-6125A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32921032 | |||||||
| chr11:32921728 | A | T | 16 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0122 others(13): Show |
16 | HG01975.hp1 HG01981.hp1 HG02040.hp2 others(13): Show |
intron_variant | MODIFIER | c.210-5429A>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32921728 | |||||||
| chr11:32921756 | A | G | 1 | a0001c0002t0019g0224 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.210-5401A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32921756 | |||||||
| chr11:32921789 | C | T | 1 | a0001c0001t0001g0155 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.210-5368C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32921789 | |||||||
| chr11:32921829 | T | G | 1 | a0001c0002t0008g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.210-5328T>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32921829 | |||||||
| chr11:32921934 | G | A | 10 | a0001c0002t0001g0011 a0001c0002t0001g0175 a0001c0002t0001g0178 others(7): Show |
10 | HG00735.hp1 HG02109.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.210-5223G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32921934 | |||||||
| chr11:32921951 | A | G | 2 | a0001c0002t0013g0162 a0001c0002t0013g0163 |
2 | HG02257.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.210-5206A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32921951 | |||||||
| chr11:32922037 | G | A | 2 | a0001c0001t0001g0075 a0001c0001t0001g0106 |
2 | HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.210-5120G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32922037 | |||||||
| chr11:32922318 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.210-4839A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32922318 | |||||||
| chr11:32922479 | A | AT | 14 | a0001c0002t0004g0014 a0001c0002t0004g0226 a0001c0002t0004g0232 others(11): Show |
14 | HG01496.hp1 HG01496.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.210-4655dupT | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 32922479 | ||||||
| chr11:32922479 | A | ATT | 5 | a0001c0002t0004g0227 a0001c0002t0004g0228 a0001c0002t0004g0229 others(2): Show |
5 | HG01243.hp2 HG02257.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.210-4656_210-4655d others(4): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 32922479 | ||||||
| chr11:32922479 | AT | A | 54 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0051 others(51): Show |
55 | HG00140.hp1 HG00621.hp1 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.210-4655delT | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 32922479 | ||||||
| chr11:32922479 | ATT | A | 131 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(128): Show |
132 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.210-4656_210-4655d others(4): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 32922479 | ||||||
| chr11:32922479 | ATTT | A | 7 | a0001c0001t0001g0018 a0001c0001t0001g0065 a0001c0001t0001g0087 others(4): Show |
7 | HG00738.hp2 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.210-4657_210-4655d others(5): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 32922479 | ||||||
| chr11:32922903 | C | T | 2 | a0001c0002t0013g0162 a0001c0002t0013g0163 |
2 | HG02257.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.210-4254C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32922903 | |||||||
| chr11:32922992 | A | G | 1 | a0001c0001t0003g0049 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.210-4165A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32922992 | |||||||
| chr11:32922997 | T | A | 2 | a0003c0005t0001g0194 a0003c0005t0001g0195 |
2 | NA18522.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.210-4160T>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32922997 | |||||||
| chr11:32923244 | A | G | 9 | a0001c0006t0001g0169 a0001c0006t0001g0170 a0001c0006t0001g0171 others(6): Show |
9 | HG01891.hp2 HG02280.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.210-3913A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32923244 | |||||||
| chr11:32923284 | A | G | 20 | a0001c0002t0001g0011 a0001c0002t0001g0175 a0001c0002t0001g0178 others(17): Show |
20 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.210-3873A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32923284 | |||||||
| chr11:32923538 | C | T | 17 | a0001c0003t0002g0207 a0001c0003t0002g0208 a0001c0003t0002g0209 others(14): Show |
17 | HG00099.hp1 HG01074.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.210-3619C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32923538 | |||||||
| chr11:32923678 | CA | C | 211 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(208): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.210-3470delA | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 32923678 | ||||||
| chr11:32923691 | C | T | 1 | a0001c0001t0001g0042 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.210-3466C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32923691 | |||||||
| chr11:32923692 | G | A | 2 | a0001c0002t0001g0013 a0001c0002t0019g0224 |
2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.210-3465G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32923692 | |||||||
| chr11:32923787 | G | T | 1 | a0001c0001t0001g0042 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.210-3370G>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32923787 | |||||||
| chr11:32924030 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.210-3127C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32924030 | |||||||
| chr11:32924242 | CT | C | 160 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(157): Show |
162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.210-2914delT | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32924242 | |||||||
| chr11:32924560 | C | CA | 28 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(25): Show |
28 | HG00099.hp1 HG00099.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.210-2578dupA | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 32924560 | ||||||
| chr11:32924579 | AG | A | 8 | a0001c0002t0004g0014 a0001c0002t0004g0226 a0001c0002t0004g0227 others(5): Show |
8 | HG01243.hp2 HG02257.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.210-2576delG | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 32924579 | ||||||
| chr11:32924584 | T | G | 1 | a0001c0001t0001g0087 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.210-2573T>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32924584 | |||||||
| chr11:32924585 | A | G | 1 | a0001c0001t0001g0087 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.210-2572A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32924585 | |||||||
| chr11:32924651 | C | T | 2 | a0001c0002t0013g0162 a0001c0002t0013g0163 |
2 | HG02257.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.210-2506C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32924651 | |||||||
| chr11:32925160 | T | G | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG01433.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.210-1997T>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32925160 | |||||||
| chr11:32925491 | C | CTTTT | 12 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0001g0109 others(9): Show |
12 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.210-1663_210-1660d others(6): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 32925491 | ||||||
| chr11:32925494 | T | TTTTA | 42 | a0001c0001t0001g0017 a0001c0001t0001g0047 a0001c0001t0001g0077 others(39): Show |
42 | HG00099.hp2 HG00621.hp1 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.210-1619_210-1616d others(6): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 32925494 | ||||||
| chr11:32925494 | T | TTTTATTT others(1): Show |
11 | a0001c0001t0001g0100 a0001c0001t0001g0107 a0001c0001t0001g0118 others(8): Show |
11 | HG00738.hp2 HG01981.hp1 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.210-1623_210-1616d others(10): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 32925494 | ||||||
| chr11:32925494 | T | TTTTATTT others(5): Show |
1 | a0001c0001t0001g0122 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.210-1627_210-1616d others(14): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 32925494 | ||||||
| chr11:32925494 | TTTTA | T | 16 | a0001c0001t0001g0010 a0001c0001t0001g0087 a0001c0002t0001g0183 others(13): Show |
16 | HG01099.hp2 HG01167.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.210-1619_210-1616d others(6): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 32925494 | ||||||
| chr11:32925494 | TTTTATTT others(1): Show |
T | 16 | a0001c0001t0001g0040 a0001c0002t0001g0011 a0001c0002t0001g0013 others(13): Show |
16 | HG00735.hp1 HG02055.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.210-1623_210-1616d others(10): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 32925494 | ||||||
| chr11:32925494 | TTTTATTT others(5): Show |
T | 25 | a0001c0001t0001g0008 a0001c0001t0001g0041 a0001c0001t0001g0043 others(22): Show |
25 | HG00099.hp1 HG01074.hp1 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.210-1627_210-1616d others(14): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 32925494 | ||||||
| chr11:32925498 | A | T | 24 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0051 others(21): Show |
25 | HG00140.hp1 HG01346.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.210-1659A>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32925498 | |||||||
| chr11:32925638 | G | A | 9 | a0001c0002t0004g0014 a0001c0002t0004g0226 a0001c0002t0004g0227 others(6): Show |
9 | HG01243.hp2 HG01496.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.210-1519G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32925638 | |||||||
| chr11:32925668 | G | A | 2 | a0001c0002t0001g0178 a0001c0002t0001g0179 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.210-1489G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32925668 | |||||||
| chr11:32925728 | A | G | 1 | a0008c0014t0001g0009 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.210-1429A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32925728 | |||||||
| chr11:32926164 | G | A | 1 | a0001c0001t0003g0097 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.210-993G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32926164 | |||||||
| chr11:32926184 | CACTGAT | C | 12 | a0002c0004t0001g0021 a0002c0004t0001g0022 a0002c0004t0001g0023 others(9): Show |
12 | HG01975.hp1 HG01981.hp1 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.210-969_210-964del others(6): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 32926184 | ||||||
| chr11:32926237 | A | C | 17 | a0001c0003t0002g0207 a0001c0003t0002g0208 a0001c0003t0002g0209 others(14): Show |
17 | HG00099.hp1 HG01074.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.210-920A>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32926237 | |||||||
| chr11:32926250 | A | G | 1 | a0001c0001t0001g0019 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.210-907A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32926250 | |||||||
| chr11:32926406 | A | G | 1 | a0001c0001t0001g0008 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.210-751A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32926406 | |||||||
| chr11:32926646 | G | A | 5 | a0001c0002t0007g0012 a0001c0002t0007g0189 a0001c0002t0007g0190 others(2): Show |
5 | HG01496.hp1 HG02451.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.210-511G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32926646 | |||||||
| chr11:32926666 | G | T | 9 | a0001c0006t0001g0169 a0001c0006t0001g0170 a0001c0006t0001g0171 others(6): Show |
9 | HG01891.hp2 HG02280.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.210-491G>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32926666 | |||||||
| chr11:32926706 | G | A | 160 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(157): Show |
162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.210-451G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32926706 | |||||||
| chr11:32926763 | T | A | 9 | a0001c0002t0004g0014 a0001c0002t0004g0226 a0001c0002t0004g0227 others(6): Show |
9 | HG01243.hp2 HG01496.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.210-394T>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32926763 | |||||||
| chr11:32926968 | C | CTTACTAA others(38): Show |
1 | a0005c0009t0001g0088 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.210-187_210-143dup others(45): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 32926968 | ||||||
| chr11:32927013 | G | A | 5 | a0001c0002t0007g0012 a0001c0002t0007g0189 a0001c0002t0007g0190 others(2): Show |
5 | HG01496.hp1 HG02451.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.210-144G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 1/12 | chr11 | 32927013 | |||||||
| chr11:32927468 | C | T | 73 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(70): Show |
74 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.322+199C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 2/12 | chr11 | 32927468 | |||||||
| chr11:32927491 | T | C | 160 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(157): Show |
162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.322+222T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 2/12 | chr11 | 32927491 | |||||||
| chr11:32927501 | G | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
2 | HG02559.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.322+232G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 2/12 | chr11 | 32927501 | |||||||
| chr11:32927687 | A | G | 160 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(157): Show |
162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.323-275A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 2/12 | chr11 | 32927687 | |||||||
| chr11:32927727 | C | T | 4 | a0001c0008t0001g0202 a0001c0008t0001g0203 a0001c0008t0001g0204 others(1): Show |
4 | HG02723.hp1 HG02965.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.323-235C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 2/12 | chr11 | 32927727 | |||||||
| chr11:32927917 | A | AT | 187 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(184): Show |
189 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.323-32dupT | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr11 | 32927917 | ||||||
| chr11:32927917 | A | ATT | 19 | a0001c0002t0001g0175 a0001c0002t0001g0184 a0001c0003t0002g0207 others(16): Show |
19 | HG00099.hp1 HG01074.hp1 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.323-33_323-32dupTT | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr11 | 32927917 | ||||||
| chr11:32928941 | T | A | 4 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(1): Show |
4 | HG00738.hp1 HG01257.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.484+818T>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 3/12 | chr11 | 32928941 | |||||||
| chr11:32929103 | T | C | 4 | a0003c0005t0001g0193 a0003c0005t0001g0194 a0003c0005t0001g0195 others(1): Show |
4 | HG02486.hp1 HG02622.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.484+980T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 3/12 | chr11 | 32929103 | |||||||
| chr11:32929168 | A | G | 1 | a0001c0002t0008g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.484+1045A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 3/12 | chr11 | 32929168 | |||||||
| chr11:32929486 | T | C | 1 | a0006c0023t0023g0186 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.484+1363T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 3/12 | chr11 | 32929486 | |||||||
| chr11:32929594 | G | A | 2 | a0004c0007t0016g0114 a0004c0007t0016g0115 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.484+1471G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 3/12 | chr11 | 32929594 | |||||||
| chr11:32929643 | C | T | 2 | a0001c0001t0001g0111 a0001c0001t0003g0124 |
2 | NA18966.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.484+1520C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 3/12 | chr11 | 32929643 | |||||||
| chr11:32929731 | A | G | 1 | a0001c0002t0001g0183 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.484+1608A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 3/12 | chr11 | 32929731 | |||||||
| chr11:32929914 | T | A | 1 | a0001c0003t0002g0221 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.484+1791T>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 3/12 | chr11 | 32929914 | |||||||
| chr11:32929984 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.485-1759C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 3/12 | chr11 | 32929984 | |||||||
| chr11:32930043 | C | T | 2 | a0002c0004t0001g0021 a0002c0004t0001g0022 |
2 | HG03927.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.485-1700C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 3/12 | chr11 | 32930043 | |||||||
| chr11:32930642 | A | C | 20 | a0001c0002t0001g0011 a0001c0002t0001g0175 a0001c0002t0001g0178 others(17): Show |
20 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.485-1101A>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 3/12 | chr11 | 32930642 | |||||||
| chr11:32930684 | T | C | 1 | a0001c0003t0024g0218 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.485-1059T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 3/12 | chr11 | 32930684 | |||||||
| chr11:32930710 | T | G | 3 | a0001c0008t0001g0202 a0001c0008t0001g0203 a0001c0008t0001g0204 |
3 | HG02723.hp1 HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.485-1033T>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 3/12 | chr11 | 32930710 | |||||||
| chr11:32930803 | A | G | 2 | a0001c0002t0013g0162 a0001c0002t0013g0163 |
2 | HG02257.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.485-940A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 3/12 | chr11 | 32930803 | |||||||
| chr11:32931490 | G | A | 2 | a0001c0002t0001g0013 a0001c0002t0019g0224 |
2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.485-253G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 3/12 | chr11 | 32931490 | |||||||
| chr11:32931501 | G | A | 1 | a0001c0001t0001g0010 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.485-242G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 3/12 | chr11 | 32931501 | |||||||
| chr11:32931545 | C | T | 1 | a0001c0002t0008g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.485-198C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 3/12 | chr11 | 32931545 | |||||||
| chr11:32931547 | T | TA | 21 | a0001c0002t0001g0011 a0001c0002t0001g0175 a0001c0002t0001g0178 others(18): Show |
21 | HG00735.hp1 HG01261.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.485-186dupA | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr11 | 32931547 | ||||||
| chr11:32935585 | T | A | 1 | a0001c0001t0005g0030 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.4177+150T>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32935585 | |||||||
| chr11:32935962 | T | G | 1 | a0001c0001t0001g0039 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.4177+527T>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32935962 | |||||||
| chr11:32936077 | T | G | 1 | a0001c0001t0005g0033 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.4177+642T>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32936077 | |||||||
| chr11:32936187 | C | G | 1 | a0002c0004t0001g0027 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.4177+752C>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32936187 | |||||||
| chr11:32937063 | G | A | 180 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(177): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.4177+1628G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32937063 | |||||||
| chr11:32937303 | G | C | 3 | a0001c0002t0008g0223 a0001c0002t0013g0162 a0001c0002t0013g0163 |
3 | HG02257.hp1 HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4177+1868G>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32937303 | |||||||
| chr11:32937372 | A | T | 1 | a0001c0002t0019g0224 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4177+1937A>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32937372 | |||||||
| chr11:32937502 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4177+2067G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32937502 | |||||||
| chr11:32937572 | G | A | 160 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(157): Show |
162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.4177+2137G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32937572 | |||||||
| chr11:32937781 | A | T | 3 | a0001c0002t0008g0223 a0001c0002t0013g0162 a0001c0002t0013g0163 |
3 | HG02257.hp1 HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4177+2346A>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32937781 | |||||||
| chr11:32938203 | A | G | 1 | a0001c0001t0005g0030 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.4177+2768A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32938203 | |||||||
| chr11:32938253 | C | T | 1 | a0009c0017t0011g0120 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.4177+2818C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32938253 | |||||||
| chr11:32938254 | G | A | 1 | a0008c0014t0001g0009 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.4177+2819G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32938254 | |||||||
| chr11:32938510 | A | G | 1 | a0005c0009t0001g0088 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.4177+3075A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32938510 | |||||||
| chr11:32939013 | A | G | 5 | a0001c0001t0001g0069 a0001c0001t0017g0073 a0005c0009t0001g0089 others(2): Show |
5 | HG01433.hp2 HG02145.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.4177+3578A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32939013 | |||||||
| chr11:32939391 | A | G | 1 | a0001c0001t0005g0103 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.4177+3956A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32939391 | |||||||
| chr11:32939420 | A | AT | 20 | a0001c0002t0001g0011 a0001c0002t0001g0175 a0001c0002t0001g0178 others(17): Show |
20 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.4177+3994dupT | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 32939420 | ||||||
| chr11:32939499 | T | A | 160 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(157): Show |
162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.4177+4064T>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32939499 | |||||||
| chr11:32939698 | T | A | 1 | a0006c0023t0023g0186 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4177+4263T>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32939698 | |||||||
| chr11:32939788 | G | A | 223 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(220): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.4177+4353G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32939788 | |||||||
| chr11:32939805 | C | T | 1 | a0001c0002t0004g0230 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.4177+4370C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32939805 | |||||||
| chr11:32939948 | A | AT | 10 | a0001c0002t0004g0228 a0001c0002t0004g0229 a0001c0002t0004g0232 others(7): Show |
10 | HG01496.hp1 HG01496.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.4177+4534dupT | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 32939948 | ||||||
| chr11:32939948 | AT | A | 72 | a0001c0001t0001g0010 a0001c0001t0001g0042 a0001c0001t0001g0051 others(69): Show |
72 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.4177+4534delT | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 32939948 | ||||||
| chr11:32939948 | ATT | A | 5 | a0001c0001t0001g0047 a0001c0001t0001g0106 a0001c0001t0001g0139 others(2): Show |
5 | HG01175.hp1 HG03041.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.4177+4533_4177+453 others(6): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 32939948 | ||||||
| chr11:32940002 | T | C | 1 | a0001c0001t0001g0065 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.4177+4567T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32940002 | |||||||
| chr11:32940126 | C | G | 1 | a0001c0001t0001g0086 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.4177+4691C>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32940126 | |||||||
| chr11:32940464 | T | C | 2 | a0001c0002t0001g0013 a0001c0002t0019g0224 |
2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.4177+5029T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32940464 | |||||||
| chr11:32940476 | A | C | 2 | a0001c0002t0001g0013 a0001c0002t0019g0224 |
2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.4177+5041A>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32940476 | |||||||
| chr11:32940696 | A | G | 10 | a0001c0002t0001g0011 a0001c0002t0001g0175 a0001c0002t0001g0178 others(7): Show |
10 | HG00735.hp1 HG02109.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.4177+5261A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32940696 | |||||||
| chr11:32941132 | TCA | T | 3 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0161 |
3 | HG00738.hp1 HG01257.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.4177+5698_4177+569 others(6): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32941132 | |||||||
| chr11:32941171 | A | C | 2 | a0001c0002t0001g0013 a0001c0002t0019g0224 |
2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.4177+5736A>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32941171 | |||||||
| chr11:32941182 | T | G | 1 | a0001c0001t0001g0148 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.4177+5747T>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32941182 | |||||||
| chr11:32941212 | T | TTTA | 6 | a0001c0002t0007g0012 a0001c0002t0007g0189 a0001c0002t0007g0190 others(3): Show |
6 | HG00099.hp1 HG01496.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.4177+5801_4177+580 others(7): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 32941212 | ||||||
| chr11:32941212 | TTTA | T | 162 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(159): Show |
164 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.4177+5801_4177+580 others(7): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 32941212 | ||||||
| chr11:32941239 | T | A | 2 | a0001c0002t0002g0205 a0001c0002t0008g0206 |
2 | HG02280.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.4177+5804T>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32941239 | |||||||
| chr11:32941339 | C | T | 1 | a0001c0008t0001g0015 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.4177+5904C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32941339 | |||||||
| chr11:32941384 | T | C | 1 | a0004c0007t0001g0147 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.4177+5949T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32941384 | |||||||
| chr11:32941384 | T | TC | 101 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(98): Show |
102 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.4177+5951dupC | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 32941384 | ||||||
| chr11:32941393 | C | A | 9 | a0001c0002t0004g0014 a0001c0002t0004g0226 a0001c0002t0004g0227 others(6): Show |
9 | HG01243.hp2 HG01496.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.4177+5958C>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32941393 | |||||||
| chr11:32941544 | C | T | 4 | a0003c0005t0001g0193 a0003c0005t0001g0194 a0003c0005t0001g0195 others(1): Show |
4 | HG02486.hp1 HG02622.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.4177+6109C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32941544 | |||||||
| chr11:32941557 | G | A | 20 | a0001c0002t0001g0011 a0001c0002t0001g0175 a0001c0002t0001g0178 others(17): Show |
20 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.4177+6122G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32941557 | |||||||
| chr11:32941859 | G | C | 1 | a0001c0001t0003g0049 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.4177+6424G>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32941859 | |||||||
| chr11:32941983 | T | A | 3 | a0005c0009t0001g0089 a0005c0009t0001g0090 a0005c0009t0001g0091 |
3 | HG02818.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4177+6548T>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32941983 | |||||||
| chr11:32942050 | A | G | 20 | a0001c0002t0001g0011 a0001c0002t0001g0175 a0001c0002t0001g0178 others(17): Show |
20 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.4177+6615A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32942050 | |||||||
| chr11:32942076 | GTTGT | G | 9 | a0001c0002t0004g0014 a0001c0002t0004g0226 a0001c0002t0004g0227 others(6): Show |
9 | HG01243.hp2 HG01496.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.4177+6648_4177+665 others(8): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 32942076 | ||||||
| chr11:32942106 | G | C | 1 | a0001c0001t0001g0077 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.4177+6671G>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32942106 | |||||||
| chr11:32942194 | G | C | 223 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(220): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.4177+6759G>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32942194 | |||||||
| chr11:32942251 | T | A | 10 | a0001c0002t0001g0011 a0001c0002t0001g0175 a0001c0002t0001g0178 others(7): Show |
10 | HG00735.hp1 HG02109.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.4177+6816T>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32942251 | |||||||
| chr11:32942391 | TC | T | 9 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0001g0055 others(6): Show |
9 | HG00642.hp2 HG02109.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.4177+6957delC | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32942391 | |||||||
| chr11:32942855 | C | T | 1 | a0001c0002t0008g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4177+7420C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32942855 | |||||||
| chr11:32942881 | C | T | 1 | a0001c0001t0005g0035 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.4177+7446C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32942881 | |||||||
| chr11:32942907 | A | C | 1 | a0001c0001t0001g0018 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.4177+7472A>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32942907 | |||||||
| chr11:32943000 | A | G | 9 | a0001c0002t0004g0014 a0001c0002t0004g0226 a0001c0002t0004g0227 others(6): Show |
9 | HG01243.hp2 HG01496.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.4177+7565A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32943000 | |||||||
| chr11:32943018 | G | C | 1 | a0001c0001t0001g0123 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.4177+7583G>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32943018 | |||||||
| chr11:32943200 | C | T | 1 | a0001c0003t0002g0215 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.4177+7765C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32943200 | |||||||
| chr11:32943548 | G | A | 14 | a0001c0001t0001g0122 a0002c0004t0001g0021 a0002c0004t0001g0022 others(11): Show |
14 | HG01975.hp1 HG01981.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.4177+8113G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32943548 | |||||||
| chr11:32943779 | C | G | 1 | a0001c0002t0008g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4177+8344C>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32943779 | |||||||
| chr11:32943791 | A | G | 1 | a0001c0003t0002g0234 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.4177+8356A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32943791 | |||||||
| chr11:32943832 | C | G | 2 | a0001c0001t0005g0070 a0001c0001t0005g0103 |
2 | HG03831.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.4177+8397C>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32943832 | |||||||
| chr11:32944021 | G | A | 3 | a0001c0001t0001g0132 a0001c0002t0004g0232 a0001c0002t0020g0231 |
3 | HG00738.hp2 HG01496.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.4177+8586G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32944021 | |||||||
| chr11:32944214 | G | GT | 3 | a0001c0002t0007g0190 a0001c0002t0007g0191 a0001c0002t0018g0192 |
3 | HG01496.hp1 HG02451.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.4177+8785dupT | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 32944214 | ||||||
| chr11:32944403 | T | G | 20 | a0001c0002t0001g0011 a0001c0002t0001g0175 a0001c0002t0001g0178 others(17): Show |
20 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.4177+8968T>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32944403 | |||||||
| chr11:32944589 | T | C | 2 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
2 | HG02559.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.4177+9154T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32944589 | |||||||
| chr11:32944601 | T | C | 1 | a0001c0001t0001g0077 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.4177+9166T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32944601 | |||||||
| chr11:32945113 | T | C | 1 | a0002c0004t0001g0024 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.4178-8744T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32945113 | |||||||
| chr11:32945191 | A | G | 4 | a0001c0008t0001g0202 a0001c0008t0001g0203 a0001c0008t0001g0204 others(1): Show |
4 | HG02723.hp1 HG02965.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.4178-8666A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32945191 | |||||||
| chr11:32945220 | C | A | 3 | a0001c0001t0012g0005 a0001c0001t0012g0113 a0001c0001t0012g0116 |
3 | HG00621.hp2 HG01256.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.4178-8637C>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32945220 | |||||||
| chr11:32945262 | A | C | 1 | a0001c0008t0001g0203 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.4178-8595A>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32945262 | |||||||
| chr11:32945457 | G | C | 3 | a0001c0008t0001g0202 a0001c0008t0001g0203 a0001c0008t0001g0204 |
3 | HG02723.hp1 HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.4178-8400G>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32945457 | |||||||
| chr11:32945724 | C | T | 21 | a0001c0001t0001g0047 a0001c0001t0001g0105 a0001c0001t0001g0110 others(18): Show |
21 | HG00621.hp1 HG01071.hp1 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.4178-8133C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32945724 | |||||||
| chr11:32945855 | C | A | 5 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0060 others(2): Show |
6 | HG02523.hp1 NA18951.hp2 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.4178-8002C>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32945855 | |||||||
| chr11:32945962 | T | C | 1 | a0001c0002t0008g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4178-7895T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32945962 | |||||||
| chr11:32946025 | G | A | 1 | a0001c0002t0001g0013 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4178-7832G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32946025 | |||||||
| chr11:32946056 | C | T | 1 | a0001c0001t0001g0040 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.4178-7801C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32946056 | |||||||
| chr11:32946212 | C | T | 183 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(180): Show |
185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.4178-7645C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32946212 | |||||||
| chr11:32946346 | CT | C | 3 | a0001c0002t0008g0223 a0001c0002t0013g0162 a0001c0002t0013g0163 |
3 | HG02257.hp1 HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4178-7506delT | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 32946346 | ||||||
| chr11:32946352 | C | G | 3 | a0001c0002t0008g0223 a0001c0002t0013g0162 a0001c0002t0013g0163 |
3 | HG02257.hp1 HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4178-7505C>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32946352 | |||||||
| chr11:32946402 | T | C | 223 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(220): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.4178-7455T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32946402 | |||||||
| chr11:32946493 | G | A | 3 | a0001c0002t0008g0223 a0001c0002t0013g0162 a0001c0002t0013g0163 |
3 | HG02257.hp1 HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4178-7364G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32946493 | |||||||
| chr11:32946674 | T | C | 2 | a0001c0001t0001g0107 a0001c0001t0001g0118 |
2 | HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.4178-7183T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32946674 | |||||||
| chr11:32946765 | A | G | 220 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(217): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.4178-7092A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32946765 | |||||||
| chr11:32946773 | C | T | 1 | a0001c0001t0001g0025 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.4178-7084C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32946773 | |||||||
| chr11:32946838 | A | G | 220 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(217): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.4178-7019A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32946838 | |||||||
| chr11:32946914 | C | T | 1 | a0001c0001t0022g0167 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4178-6943C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32946914 | |||||||
| chr11:32946928 | G | A | 2 | a0001c0001t0001g0066 a0001c0001t0001g0067 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.4178-6929G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32946928 | |||||||
| chr11:32946934 | C | T | 10 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0001g0055 others(7): Show |
10 | HG00642.hp2 HG02109.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.4178-6923C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32946934 | |||||||
| chr11:32947090 | G | A | 3 | a0001c0001t0001g0041 a0001c0002t0013g0162 a0001c0002t0013g0163 |
3 | HG01981.hp2 HG02257.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.4178-6767G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32947090 | |||||||
| chr11:32947091 | C | T | 2 | a0001c0003t0002g0221 a0001c0003t0002g0222 |
2 | NA18941.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.4178-6766C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32947091 | |||||||
| chr11:32947182 | C | T | 2 | a0001c0002t0001g0175 a0001c0002t0001g0184 |
2 | HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.4178-6675C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32947182 | |||||||
| chr11:32947235 | C | T | 3 | a0001c0001t0001g0085 a0001c0001t0001g0119 a0001c0001t0001g0145 |
3 | HG00099.hp2 HG03239.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.4178-6622C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32947235 | |||||||
| chr11:32947326 | A | C | 1 | a0001c0003t0002g0219 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.4178-6531A>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32947326 | |||||||
| chr11:32947552 | G | A | 4 | a0001c0008t0001g0202 a0001c0008t0001g0203 a0001c0008t0001g0204 others(1): Show |
4 | HG02723.hp1 HG02965.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.4178-6305G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32947552 | |||||||
| chr11:32947676 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.4178-6181C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32947676 | |||||||
| chr11:32947685 | C | T | 1 | a0001c0001t0001g0029 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.4178-6172C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32947685 | |||||||
| chr11:32947686 | CTTAT | C | 5 | a0001c0002t0007g0012 a0001c0002t0007g0189 a0001c0002t0007g0190 others(2): Show |
5 | HG01496.hp1 HG02451.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.4178-6168_4178-616 others(8): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 32947686 | ||||||
| chr11:32947921 | T | C | 1 | a0001c0001t0001g0039 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.4178-5936T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32947921 | |||||||
| chr11:32947968 | G | A | 1 | a0001c0006t0001g0170 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.4178-5889G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32947968 | |||||||
| chr11:32948338 | G | A | 20 | a0001c0002t0001g0011 a0001c0002t0001g0175 a0001c0002t0001g0178 others(17): Show |
20 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.4178-5519G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32948338 | |||||||
| chr11:32948434 | G | A | 1 | a0001c0002t0019g0224 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4178-5423G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32948434 | |||||||
| chr11:32948460 | T | C | 1 | a0011c0012t0021g0188 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.4178-5397T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32948460 | |||||||
| chr11:32948653 | C | G | 211 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(208): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.4178-5204C>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32948653 | |||||||
| chr11:32948764 | T | C | 1 | a0001c0001t0001g0122 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4178-5093T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32948764 | |||||||
| chr11:32949024 | C | T | 1 | a0001c0001t0001g0020 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.4178-4833C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32949024 | |||||||
| chr11:32949522 | T | A | 1 | a0001c0001t0001g0122 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4178-4335T>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32949522 | |||||||
| chr11:32949536 | A | C | 2 | a0001c0002t0004g0228 a0001c0002t0004g0229 |
2 | HG02257.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.4178-4321A>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32949536 | |||||||
| chr11:32949627 | C | T | 160 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(157): Show |
162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.4178-4230C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32949627 | |||||||
| chr11:32949689 | T | A | 2 | a0001c0002t0002g0205 a0001c0002t0008g0206 |
2 | HG02280.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.4178-4168T>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32949689 | |||||||
| chr11:32949730 | A | G | 1 | a0001c0001t0001g0064 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.4178-4127A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32949730 | |||||||
| chr11:32949778 | G | A | 1 | a0001c0008t0001g0203 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.4178-4079G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32949778 | |||||||
| chr11:32949798 | T | C | 2 | a0001c0002t0001g0013 a0001c0002t0019g0224 |
2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.4178-4059T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32949798 | |||||||
| chr11:32949826 | A | G | 2 | a0001c0002t0013g0162 a0001c0002t0013g0163 |
2 | HG02257.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.4178-4031A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32949826 | |||||||
| chr11:32950007 | T | G | 1 | a0001c0001t0001g0071 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.4178-3850T>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32950007 | |||||||
| chr11:32950102 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.4178-3755T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32950102 | |||||||
| chr11:32950419 | T | C | 9 | a0001c0002t0004g0014 a0001c0002t0004g0226 a0001c0002t0004g0227 others(6): Show |
9 | HG01243.hp2 HG01496.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.4178-3438T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32950419 | |||||||
| chr11:32950516 | T | C | 3 | a0001c0002t0008g0223 a0001c0002t0013g0162 a0001c0002t0013g0163 |
3 | HG02257.hp1 HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4178-3341T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32950516 | |||||||
| chr11:32950974 | G | C | 1 | a0001c0001t0001g0074 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.4178-2883G>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32950974 | |||||||
| chr11:32951021 | G | A | 220 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(217): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.4178-2836G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32951021 | |||||||
| chr11:32951026 | A | G | 1 | a0001c0002t0007g0189 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.4178-2831A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32951026 | |||||||
| chr11:32951434 | T | G | 1 | a0001c0001t0001g0137 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.4178-2423T>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32951434 | |||||||
| chr11:32951543 | C | A | 1 | a0001c0001t0001g0064 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.4178-2314C>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32951543 | |||||||
| chr11:32951614 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.4178-2243T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32951614 | |||||||
| chr11:32951672 | T | G | 1 | a0001c0001t0001g0137 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.4178-2185T>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32951672 | |||||||
| chr11:32951838 | A | AT | 154 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(151): Show |
156 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.4178-2003dupT | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 32951838 | ||||||
| chr11:32952093 | G | C | 1 | a0001c0001t0006g0165 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4178-1764G>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32952093 | |||||||
| chr11:32952241 | G | A | 1 | a0005c0009t0001g0088 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.4178-1616G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32952241 | |||||||
| chr11:32952384 | A | G | 1 | a0003c0005t0001g0196 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4178-1473A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32952384 | |||||||
| chr11:32952399 | AAC | A | 160 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(157): Show |
162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.4178-1454_4178-145 others(6): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 32952399 | ||||||
| chr11:32952466 | GGTCATAT others(1): Show |
G | 6 | a0001c0001t0005g0030 a0001c0001t0005g0033 a0001c0001t0005g0035 others(3): Show |
6 | HG00280.hp2 HG00642.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.4178-1388_4178-138 others(12): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 32952466 | ||||||
| chr11:32952473 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.4178-1384T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32952473 | |||||||
| chr11:32952493 | G | T | 1 | a0001c0008t0001g0204 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4178-1364G>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32952493 | |||||||
| chr11:32952747 | CT | C | 6 | a0001c0001t0001g0105 a0001c0001t0010g0072 a0001c0001t0010g0104 others(3): Show |
6 | HG01071.hp1 HG01175.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.4178-1097delT | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 32952747 | ||||||
| chr11:32952803 | C | CT | 5 | a0001c0001t0001g0074 a0001c0001t0017g0073 a0005c0009t0001g0089 others(2): Show |
5 | HG02145.hp2 HG02818.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.4178-1037dupT | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr11 | 32952803 | ||||||
| chr11:32952961 | C | T | 6 | a0001c0002t0004g0014 a0001c0002t0004g0226 a0001c0002t0004g0227 others(3): Show |
6 | HG01243.hp2 HG01496.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.4178-896C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32952961 | |||||||
| chr11:32953051 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.4178-806T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32953051 | |||||||
| chr11:32953270 | T | A | 1 | a0001c0001t0001g0137 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.4178-587T>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32953270 | |||||||
| chr11:32953364 | A | T | 1 | a0001c0001t0001g0109 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.4178-493A>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32953364 | |||||||
| chr11:32953503 | A | G | 3 | a0001c0002t0008g0223 a0001c0002t0013g0162 a0001c0002t0013g0163 |
3 | HG02257.hp1 HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4178-354A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32953503 | |||||||
| chr11:32953787 | T | G | 160 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(157): Show |
162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.4178-70T>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 4/12 | chr11 | 32953787 | |||||||
| chr11:32954261 | G | A | 5 | a0001c0002t0007g0012 a0001c0002t0007g0189 a0001c0002t0007g0190 others(2): Show |
5 | HG01496.hp1 HG02451.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.4500+82G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 5/12 | chr11 | 32954261 | |||||||
| chr11:32954357 | T | C | 1 | a0001c0002t0019g0224 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4500+178T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 5/12 | chr11 | 32954357 | |||||||
| chr11:32954872 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4501-424C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 5/12 | chr11 | 32954872 | |||||||
| chr11:32955009 | A | G | 2 | a0001c0003t0002g0216 a0001c0003t0002g0220 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.4501-287A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 5/12 | chr11 | 32955009 | |||||||
| chr11:32955881 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.4618-107A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 6/12 | chr11 | 32955881 | |||||||
| chr11:32956466 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.4751+345A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 7/12 | chr11 | 32956466 | |||||||
| chr11:32956470 | A | T | 2 | a0001c0002t0002g0205 a0001c0002t0008g0206 |
2 | HG02280.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.4751+349A>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 7/12 | chr11 | 32956470 | |||||||
| chr11:32956508 | T | TA | 22 | a0001c0001t0001g0065 a0001c0001t0001g0092 a0001c0002t0001g0011 others(19): Show |
22 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.4751+394dupA | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr11 | 32956508 | ||||||
| chr11:32956624 | C | T | 45 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(42): Show |
46 | HG00408.hp2 HG00621.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.4751+503C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 7/12 | chr11 | 32956624 | |||||||
| chr11:32957065 | G | T | 2 | a0001c0011t0001g0057 a0001c0011t0001g0058 |
2 | HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.4752-804G>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 7/12 | chr11 | 32957065 | |||||||
| chr11:32957134 | C | CT | 16 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0050 others(13): Show |
16 | HG00642.hp2 HG00738.hp1 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.4752-719dupT | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr11 | 32957134 | ||||||
| chr11:32957222 | A | T | 1 | a0001c0001t0005g0035 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.4752-647A>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 7/12 | chr11 | 32957222 | |||||||
| chr11:32957517 | C | T | 2 | a0001c0002t0001g0013 a0001c0002t0019g0224 |
2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.4752-352C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 7/12 | chr11 | 32957517 | |||||||
| chr11:32957553 | T | TC | 5 | a0001c0002t0001g0011 a0001c0002t0001g0180 a0001c0002t0001g0181 others(2): Show |
5 | HG00735.hp1 HG02109.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.4752-315dupC | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr11 | 32957553 | ||||||
| chr11:32957554 | C | A | 9 | a0001c0002t0004g0014 a0001c0002t0004g0226 a0001c0002t0004g0227 others(6): Show |
9 | HG01243.hp2 HG01496.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.4752-315C>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 7/12 | chr11 | 32957554 | |||||||
| chr11:32957829 | G | A | 1 | a0001c0002t0018g0192 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4752-40G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 7/12 | chr11 | 32957829 | |||||||
| chr11:32958353 | G | C | 1 | a0001c0001t0001g0055 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4969+267G>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32958353 | |||||||
| chr11:32958392 | CT | C | 9 | a0001c0002t0004g0014 a0001c0002t0004g0226 a0001c0002t0004g0227 others(6): Show |
9 | HG01243.hp2 HG01496.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.4969+319delT | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 32958392 | ||||||
| chr11:32958427 | G | A | 3 | a0001c0001t0001g0141 a0001c0002t0001g0178 a0001c0002t0001g0179 |
3 | HG01934.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.4969+341G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32958427 | |||||||
| chr11:32958529 | G | A | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG01433.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.4969+443G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32958529 | |||||||
| chr11:32958658 | G | A | 1 | a0001c0002t0019g0224 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4969+572G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32958658 | |||||||
| chr11:32958673 | C | A | 1 | a0001c0002t0008g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4969+587C>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32958673 | |||||||
| chr11:32958693 | T | A | 2 | a0001c0002t0001g0013 a0001c0002t0019g0224 |
2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.4969+607T>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32958693 | |||||||
| chr11:32958840 | T | C | 20 | a0001c0002t0001g0011 a0001c0002t0001g0175 a0001c0002t0001g0178 others(17): Show |
20 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.4969+754T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32958840 | |||||||
| chr11:32958882 | G | T | 183 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(180): Show |
185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.4969+796G>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32958882 | |||||||
| chr11:32959212 | T | A | 1 | a0001c0001t0001g0130 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.4969+1126T>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32959212 | |||||||
| chr11:32959305 | C | T | 3 | a0005c0009t0001g0089 a0005c0009t0001g0090 a0005c0009t0001g0091 |
3 | HG02818.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4969+1219C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32959305 | |||||||
| chr11:32959719 | T | TA | 8 | a0001c0002t0001g0011 a0001c0002t0001g0175 a0001c0002t0001g0180 others(5): Show |
8 | HG00735.hp1 HG02109.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.4969+1641dupA | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 32959719 | ||||||
| chr11:32959886 | T | C | 1 | a0001c0002t0008g0206 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4969+1800T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32959886 | |||||||
| chr11:32960015 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.4969+1929C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32960015 | |||||||
| chr11:32960412 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.4969+2326A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32960412 | |||||||
| chr11:32960463 | G | A | 19 | a0001c0002t0001g0011 a0001c0002t0001g0175 a0001c0002t0001g0178 others(16): Show |
19 | HG00735.hp1 HG01891.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.4969+2377G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32960463 | |||||||
| chr11:32960595 | G | A | 1 | a0001c0002t0019g0224 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4969+2509G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32960595 | |||||||
| chr11:32960930 | A | G | 8 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0002t0004g0014 others(5): Show |
8 | HG01243.hp2 HG01496.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.4969+2844A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32960930 | |||||||
| chr11:32961063 | G | C | 5 | a0001c0001t0001g0075 a0001c0001t0001g0100 a0001c0001t0001g0106 others(2): Show |
5 | HG02630.hp1 HG02922.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.4969+2977G>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32961063 | |||||||
| chr11:32961184 | C | T | 2 | a0001c0002t0001g0013 a0001c0002t0019g0224 |
2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.4969+3098C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32961184 | |||||||
| chr11:32961459 | C | T | 2 | a0001c0002t0001g0013 a0001c0002t0019g0224 |
2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.4969+3373C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32961459 | |||||||
| chr11:32961691 | C | T | 1 | a0006c0023t0023g0186 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4969+3605C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32961691 | |||||||
| chr11:32961714 | G | A | 2 | a0001c0001t0001g0075 a0001c0001t0001g0106 |
2 | HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.4969+3628G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32961714 | |||||||
| chr11:32961981 | T | G | 1 | a0001c0001t0001g0107 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.4969+3895T>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32961981 | |||||||
| chr11:32962035 | G | A | 4 | a0001c0008t0001g0202 a0001c0008t0001g0203 a0001c0008t0001g0204 others(1): Show |
4 | HG02723.hp1 HG02965.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.4969+3949G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32962035 | |||||||
| chr11:32962052 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.4969+3966A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32962052 | |||||||
| chr11:32962112 | G | A | 2 | a0001c0001t0001g0066 a0001c0001t0001g0067 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.4969+4026G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32962112 | |||||||
| chr11:32962242 | A | G | 9 | a0001c0006t0001g0169 a0001c0006t0001g0170 a0001c0006t0001g0171 others(6): Show |
9 | HG01891.hp2 HG02280.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.4970-4058A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32962242 | |||||||
| chr11:32962492 | C | T | 5 | a0001c0002t0007g0012 a0001c0002t0007g0189 a0001c0002t0007g0190 others(2): Show |
5 | HG01496.hp1 HG02451.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.4970-3808C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32962492 | |||||||
| chr11:32962551 | T | G | 2 | a0001c0001t0014g0045 a0001c0001t0014g0063 |
2 | NA18984.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.4970-3749T>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32962551 | |||||||
| chr11:32962725 | A | C | 1 | a0001c0003t0002g0225 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.4970-3575A>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32962725 | |||||||
| chr11:32962754 | A | C | 1 | a0001c0002t0007g0012 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4970-3546A>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32962754 | |||||||
| chr11:32962932 | T | C | 14 | a0001c0001t0001g0122 a0002c0004t0001g0021 a0002c0004t0001g0022 others(11): Show |
14 | HG01975.hp1 HG01981.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.4970-3368T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32962932 | |||||||
| chr11:32963305 | AT | A | 20 | a0001c0002t0001g0011 a0001c0002t0001g0175 a0001c0002t0001g0178 others(17): Show |
20 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.4970-2988delT | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 32963305 | ||||||
| chr11:32963444 | C | G | 1 | a0001c0001t0003g0124 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.4970-2856C>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32963444 | |||||||
| chr11:32963518 | CT | C | 5 | a0001c0001t0001g0075 a0001c0001t0001g0100 a0001c0001t0001g0106 others(2): Show |
5 | HG02630.hp1 HG02922.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.4970-2776delT | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 32963518 | ||||||
| chr11:32964232 | C | T | 5 | a0001c0002t0007g0012 a0001c0002t0007g0189 a0001c0002t0007g0190 others(2): Show |
5 | HG01496.hp1 HG02451.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.4970-2068C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32964232 | |||||||
| chr11:32964701 | G | GA | 183 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(180): Show |
185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.4970-1587dupA | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 32964701 | ||||||
| chr11:32964712 | A | T | 17 | a0001c0003t0002g0207 a0001c0003t0002g0208 a0001c0003t0002g0209 others(14): Show |
17 | HG00099.hp1 HG01074.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.4970-1588A>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32964712 | |||||||
| chr11:32964717 | C | CAT | 65 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(62): Show |
67 | HG00140.hp1 HG00621.hp2 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.4970-1561_4970-156 others(6): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 32964717 | ||||||
| chr11:32964717 | C | CATAT | 54 | a0001c0001t0001g0010 a0001c0001t0001g0042 a0001c0001t0001g0047 others(51): Show |
54 | HG00280.hp2 HG00408.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.4970-1563_4970-156 others(8): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 32964717 | ||||||
| chr11:32964717 | C | CATATAT | 19 | a0001c0001t0001g0016 a0001c0001t0001g0056 a0001c0001t0001g0064 others(16): Show |
19 | HG00099.hp2 HG00408.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.4970-1565_4970-156 others(10): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 32964717 | ||||||
| chr11:32964717 | C | CATATATA others(1): Show |
10 | a0001c0001t0001g0029 a0001c0001t0001g0100 a0001c0001t0001g0151 others(7): Show |
10 | HG00280.hp1 HG00735.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.4970-1567_4970-156 others(12): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 32964717 | ||||||
| chr11:32964717 | C | CATATATA others(3): Show |
1 | a0001c0001t0005g0103 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.4970-1569_4970-156 others(14): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 32964717 | ||||||
| chr11:32964717 | C | CATATATA others(5): Show |
2 | a0001c0001t0001g0028 a0001c0001t0001g0039 |
2 | HG02083.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.4970-1571_4970-156 others(16): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 32964717 | ||||||
| chr11:32964717 | C | CATATATA others(7): Show |
3 | a0001c0002t0004g0227 a0004c0007t0001g0048 a0004c0007t0001g0147 |
3 | HG01243.hp2 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.4970-1573_4970-156 others(18): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 32964717 | ||||||
| chr11:32964717 | C | CATATATA others(9): Show |
3 | a0001c0002t0004g0233 a0001c0002t0008g0223 a0006c0023t0023g0186 |
3 | HG01884.hp1 HG02572.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.4970-1575_4970-156 others(20): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 32964717 | ||||||
| chr11:32964717 | C | CATATATA others(11): Show |
4 | a0001c0001t0001g0105 a0001c0001t0001g0110 a0001c0002t0004g0014 others(1): Show |
4 | HG02572.hp1 HG02896.hp1 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.4970-1577_4970-156 others(22): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 32964717 | ||||||
| chr11:32964717 | C | CATATATA others(13): Show |
1 | a0001c0002t0004g0228 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4970-1579_4970-156 others(24): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 32964717 | ||||||
| chr11:32964717 | C | CATATATA others(15): Show |
2 | a0001c0002t0004g0226 a0001c0002t0020g0231 |
2 | HG03041.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.4970-1581_4970-156 others(26): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 32964717 | ||||||
| chr11:32964717 | C | CATATATA others(17): Show |
1 | a0001c0002t0004g0229 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.4970-1560_4970-155 others(28): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 32964717 | ||||||
| chr11:32964717 | CAT | C | 7 | a0001c0002t0002g0205 a0001c0003t0002g0225 a0003c0005t0001g0194 others(4): Show |
7 | HG02280.hp1 HG02486.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.4970-1561_4970-156 others(6): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 32964717 | ||||||
| chr11:32964717 | CATAT | C | 2 | a0001c0002t0008g0206 a0001c0003t0002g0213 |
2 | HG02965.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.4970-1563_4970-156 others(8): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 32964717 | ||||||
| chr11:32964717 | CATATATA others(3): Show |
C | 2 | a0001c0003t0002g0212 a0001c0003t0002g0234 |
2 | HG02683.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.4970-1569_4970-156 others(14): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 32964717 | ||||||
| chr11:32964731 | T | TACAC | 2 | a0001c0003t0002g0209 a0001c0003t0002g0219 |
2 | HG01257.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.4970-1568_4970-156 others(8): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 32964731 | ||||||
| chr11:32964731 | T | TACACACA others(1): Show |
3 | a0001c0003t0002g0210 a0001c0003t0002g0214 a0001c0016t0002g0211 |
3 | HG00099.hp1 HG01517.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.4970-1568_4970-156 others(12): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 32964731 | ||||||
| chr11:32964733 | T | C | 6 | a0001c0003t0002g0209 a0001c0003t0002g0210 a0001c0003t0002g0214 others(3): Show |
6 | HG00099.hp1 HG01257.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.4970-1567T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32964733 | |||||||
| chr11:32964733 | T | TACACAC | 2 | a0001c0003t0002g0207 a0001c0003t0002g0208 |
2 | NA18979.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.4970-1566_4970-156 others(10): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 32964733 | ||||||
| chr11:32964733 | T | TACACACA others(1): Show |
3 | a0001c0003t0002g0216 a0001c0003t0002g0220 a0001c0003t0002g0221 |
3 | HG01167.hp1 HG01169.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.4970-1566_4970-156 others(12): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 32964733 | ||||||
| chr11:32964733 | T | TACACACA others(3): Show |
1 | a0001c0003t0002g0215 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.4970-1566_4970-156 others(14): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 32964733 | ||||||
| chr11:32964733 | T | TACACACA others(5): Show |
1 | a0001c0003t0002g0222 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.4970-1566_4970-156 others(16): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 32964733 | ||||||
| chr11:32964733 | TATATATA others(7): Show |
T | 1 | a0001c0008t0001g0015 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.4970-1565_4970-155 others(18): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 32964733 | ||||||
| chr11:32964735 | T | C | 14 | a0001c0003t0002g0207 a0001c0003t0002g0208 a0001c0003t0002g0209 others(11): Show |
14 | HG00099.hp1 HG01074.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.4970-1565T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32964735 | |||||||
| chr11:32964737 | T | C | 15 | a0001c0003t0002g0207 a0001c0003t0002g0208 a0001c0003t0002g0209 others(12): Show |
15 | HG00099.hp1 HG01074.hp1 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.4970-1563T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32964737 | |||||||
| chr11:32964737 | TATAC | T | 2 | a0001c0002t0018g0192 a0003c0005t0001g0200 |
2 | HG02809.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.4970-1561_4970-155 others(8): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 32964737 | ||||||
| chr11:32964739 | T | C | 16 | a0001c0003t0002g0207 a0001c0003t0002g0208 a0001c0003t0002g0209 others(13): Show |
16 | HG00099.hp1 HG01074.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.4970-1561T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32964739 | |||||||
| chr11:32964739 | T | TATAC | 3 | a0001c0001t0001g0117 a0001c0001t0003g0094 a0011c0012t0021g0188 |
3 | HG01169.hp1 HG02965.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.4970-1560_4970-155 others(8): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 32964739 | ||||||
| chr11:32964739 | T | TATATATA others(9): Show |
1 | a0001c0002t0004g0232 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.4970-1560_4970-155 others(20): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 32964739 | ||||||
| chr11:32964739 | TAC | T | 5 | a0001c0001t0003g0097 a0001c0002t0007g0012 a0001c0002t0007g0190 others(2): Show |
5 | HG01496.hp1 HG01981.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.4970-1519_4970-151 others(6): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 32964739 | ||||||
| chr11:32964739 | TACACACA others(7): Show |
T | 1 | a0001c0001t0001g0159 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.4970-1531_4970-151 others(18): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 32964739 | ||||||
| chr11:32964741 | C | T | 178 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(175): Show |
180 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.4970-1559C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32964741 | |||||||
| chr11:32964743 | C | T | 146 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(143): Show |
148 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.4970-1557C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32964743 | |||||||
| chr11:32964745 | C | T | 33 | a0001c0001t0001g0122 a0001c0001t0001g0130 a0001c0001t0001g0135 others(30): Show |
33 | HG00621.hp1 HG00735.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.4970-1555C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32964745 | |||||||
| chr11:32964747 | C | T | 21 | a0001c0001t0001g0135 a0001c0001t0001g0142 a0001c0001t0001g0146 others(18): Show |
21 | HG00621.hp1 HG00735.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.4970-1553C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32964747 | |||||||
| chr11:32964755 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.4970-1545C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32964755 | |||||||
| chr11:32964767 | C | T | 2 | a0001c0002t0001g0175 a0001c0002t0001g0184 |
2 | HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.4970-1533C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32964767 | |||||||
| chr11:32964769 | C | T | 188 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(185): Show |
190 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.4970-1531C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32964769 | |||||||
| chr11:32964773 | C | T | 2 | a0001c0002t0004g0227 a0001c0002t0004g0233 |
2 | HG01243.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.4970-1527C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32964773 | |||||||
| chr11:32964781 | CAT | C | 2 | a0001c0002t0001g0175 a0001c0002t0001g0184 |
2 | HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.4970-1517_4970-151 others(6): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 32964781 | ||||||
| chr11:32964783 | T | C | 12 | a0001c0002t0001g0011 a0001c0002t0001g0178 a0001c0002t0001g0179 others(9): Show |
12 | HG00735.hp1 HG01243.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.4970-1517T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32964783 | |||||||
| chr11:32964787 | C | T | 2 | a0001c0002t0004g0227 a0001c0002t0004g0233 |
2 | HG01243.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.4970-1513C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32964787 | |||||||
| chr11:32964793 | T | C | 2 | a0001c0002t0004g0227 a0001c0002t0004g0233 |
2 | HG01243.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.4970-1507T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32964793 | |||||||
| chr11:32965109 | C | A | 9 | a0001c0001t0001g0085 a0001c0001t0001g0119 a0001c0001t0001g0145 others(6): Show |
9 | HG00099.hp2 HG00280.hp1 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.4970-1191C>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32965109 | |||||||
| chr11:32965139 | C | A | 6 | a0001c0001t0001g0007 a0001c0001t0001g0051 a0001c0001t0001g0052 others(3): Show |
6 | HG00140.hp1 HG01346.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.4970-1161C>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32965139 | |||||||
| chr11:32965286 | A | T | 186 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(183): Show |
188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.4970-1014A>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32965286 | |||||||
| chr11:32965303 | C | T | 2 | a0001c0002t0002g0205 a0001c0002t0008g0206 |
2 | HG02280.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.4970-997C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32965303 | |||||||
| chr11:32965304 | G | A | 10 | a0001c0002t0001g0011 a0001c0002t0001g0175 a0001c0002t0001g0178 others(7): Show |
10 | HG00735.hp1 HG02109.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.4970-996G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32965304 | |||||||
| chr11:32965499 | C | T | 1 | a0006c0023t0023g0186 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4970-801C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32965499 | |||||||
| chr11:32965601 | A | T | 1 | a0001c0001t0001g0020 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.4970-699A>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32965601 | |||||||
| chr11:32965604 | A | C | 1 | a0001c0001t0001g0020 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.4970-696A>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32965604 | |||||||
| chr11:32965707 | T | G | 1 | a0001c0002t0007g0012 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4970-593T>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32965707 | |||||||
| chr11:32965718 | A | G | 20 | a0001c0002t0001g0011 a0001c0002t0001g0175 a0001c0002t0001g0178 others(17): Show |
20 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.4970-582A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32965718 | |||||||
| chr11:32965782 | A | G | 5 | a0001c0001t0001g0010 a0001c0001t0001g0127 a0001c0001t0001g0128 others(2): Show |
5 | HG00738.hp1 HG01099.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.4970-518A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32965782 | |||||||
| chr11:32965944 | A | AAC | 13 | a0001c0002t0004g0228 a0001c0002t0004g0232 a0001c0002t0008g0223 others(10): Show |
13 | HG01496.hp2 HG01884.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.4970-315_4970-314d others(4): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 32965944 | ||||||
| chr11:32965944 | A | AACAC | 10 | a0001c0001t0003g0049 a0001c0002t0001g0011 a0001c0002t0004g0014 others(7): Show |
10 | HG00735.hp1 HG01243.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.4970-317_4970-314d others(6): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 32965944 | ||||||
| chr11:32965944 | A | AACACAC | 16 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0029 others(13): Show |
16 | HG00099.hp2 HG00738.hp2 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.4970-319_4970-314d others(8): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 32965944 | ||||||
| chr11:32965944 | A | AACACACA others(1): Show |
32 | a0001c0001t0001g0018 a0001c0001t0001g0028 a0001c0001t0001g0065 others(29): Show |
32 | HG00280.hp1 HG00738.hp1 HG01169.hp1 others(29): Show |
intron_variant | MODIFIER | c.4970-321_4970-314d others(10): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 32965944 | ||||||
| chr11:32965944 | A | AACACACA others(3): Show |
33 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(30): Show |
33 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.4970-323_4970-314d others(12): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 32965944 | ||||||
| chr11:32965944 | A | AACACACA others(5): Show |
33 | a0001c0001t0001g0001 a0001c0001t0001g0025 a0001c0001t0001g0051 others(30): Show |
33 | HG00408.hp1 HG00408.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.4970-325_4970-314d others(14): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 32965944 | ||||||
| chr11:32965944 | A | AACACACA others(7): Show |
23 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0040 others(20): Show |
23 | HG00140.hp2 HG00621.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.4970-327_4970-314d others(16): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 32965944 | ||||||
| chr11:32965944 | A | AACACACA others(9): Show |
15 | a0001c0001t0001g0020 a0001c0001t0001g0039 a0001c0001t0001g0043 others(12): Show |
15 | HG01074.hp2 HG01175.hp1 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.4970-329_4970-314d others(18): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 32965944 | ||||||
| chr11:32965944 | A | AACACACA others(11): Show |
4 | a0001c0001t0001g0069 a0001c0001t0001g0150 a0001c0001t0012g0005 others(1): Show |
4 | HG00621.hp2 HG01256.hp1 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.4970-331_4970-314d others(20): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 32965944 | ||||||
| chr11:32965944 | A | AACACACA others(13): Show |
2 | a0001c0001t0001g0133 a0001c0001t0001g0151 |
2 | HG01993.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.4970-333_4970-314d others(22): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 32965944 | ||||||
| chr11:32965944 | A | AACACACA others(15): Show |
1 | a0001c0001t0014g0063 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.4970-335_4970-314d others(24): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 32965944 | ||||||
| chr11:32965944 | A | ACACACAC others(6): Show |
2 | a0001c0001t0001g0047 a0001c0002t0007g0189 |
2 | HG03486.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.4970-356_4970-355i others(15): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32965944 | |||||||
| chr11:32965944 | A | ACACACAC others(8): Show |
1 | a0001c0001t0001g0079 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.4970-356_4970-355i others(17): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32965944 | |||||||
| chr11:32965944 | AAC | A | 7 | a0001c0002t0001g0013 a0001c0002t0001g0175 a0001c0002t0001g0178 others(4): Show |
7 | HG01884.hp1 HG02055.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.4970-315_4970-314d others(4): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 32965944 | ||||||
| chr11:32965944 | AACACAC | A | 15 | a0001c0001t0003g0096 a0001c0003t0002g0207 a0001c0003t0002g0208 others(12): Show |
15 | HG00099.hp1 HG01074.hp1 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.4970-319_4970-314d others(8): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 32965944 | ||||||
| chr11:32965944 | AACACACA others(9): Show |
A | 1 | a0001c0003t0002g0234 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.4970-329_4970-314d others(18): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 32965944 | ||||||
| chr11:32966229 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4970-71C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 8/12 | chr11 | 32966229 | |||||||
| chr11:32966474 | T | C | 1 | a0001c0002t0001g0180 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.5107+37T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 9/12 | chr11 | 32966474 | |||||||
| chr11:32966501 | CTGTTAGT others(8): Show |
C | 1 | a0001c0001t0001g0140 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.5107+66_5107+80del others(15): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 32966501 | ||||||
| chr11:32966891 | T | C | 1 | a0001c0008t0001g0015 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.5107+454T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 9/12 | chr11 | 32966891 | |||||||
| chr11:32966961 | C | G | 1 | a0006c0022t0001g0187 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.5107+524C>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 9/12 | chr11 | 32966961 | |||||||
| chr11:32967358 | A | C | 1 | a0001c0001t0001g0085 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.5107+921A>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 9/12 | chr11 | 32967358 | |||||||
| chr11:32967487 | GT | G | 17 | a0001c0003t0002g0207 a0001c0003t0002g0208 a0001c0003t0002g0209 others(14): Show |
17 | HG00099.hp1 HG01074.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.5107+1058delT | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 32967487 | ||||||
| chr11:32968706 | A | G | 10 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0001g0055 others(7): Show |
10 | HG00642.hp2 HG02109.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.5108-340A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 9/12 | chr11 | 32968706 | |||||||
| chr11:32968802 | A | G | 9 | a0001c0002t0004g0014 a0001c0002t0004g0226 a0001c0002t0004g0227 others(6): Show |
9 | HG01243.hp2 HG01496.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.5108-244A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 9/12 | chr11 | 32968802 | |||||||
| chr11:32969004 | T | C | 1 | a0011c0012t0021g0188 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.5108-42T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 9/12 | chr11 | 32969004 | |||||||
| chr11:32969296 | G | T | 211 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(208): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.5205+153G>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 10/12 | chr11 | 32969296 | |||||||
| chr11:32969400 | G | A | 17 | a0001c0003t0002g0207 a0001c0003t0002g0208 a0001c0003t0002g0209 others(14): Show |
17 | HG00099.hp1 HG01074.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.5205+257G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 10/12 | chr11 | 32969400 | |||||||
| chr11:32969472 | G | A | 2 | a0002c0004t0008g0037 a0002c0004t0008g0038 |
2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.5205+329G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 10/12 | chr11 | 32969472 | |||||||
| chr11:32969531 | G | A | 1 | a0001c0001t0014g0063 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.5205+388G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 10/12 | chr11 | 32969531 | |||||||
| chr11:32969686 | C | CT | 17 | a0001c0003t0002g0207 a0001c0003t0002g0208 a0001c0003t0002g0209 others(14): Show |
17 | HG00099.hp1 HG01074.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.5205+559dupT | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr11 | 32969686 | ||||||
| chr11:32969690 | T | TC | 10 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0001g0055 others(7): Show |
10 | HG00642.hp2 HG02109.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.5205+547_5205+548i others(3): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 10/12 | chr11 | 32969690 | |||||||
| chr11:32969691 | T | C | 1 | a0001c0002t0001g0013 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.5205+548T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 10/12 | chr11 | 32969691 | |||||||
| chr11:32969733 | A | G | 20 | a0001c0002t0001g0011 a0001c0002t0001g0175 a0001c0002t0001g0178 others(17): Show |
20 | HG00735.hp1 HG01884.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.5205+590A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 10/12 | chr11 | 32969733 | |||||||
| chr11:32969981 | G | A | 1 | a0001c0002t0004g0232 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.5205+838G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 10/12 | chr11 | 32969981 | |||||||
| chr11:32970064 | C | T | 1 | a0001c0001t0005g0035 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.5205+921C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 10/12 | chr11 | 32970064 | |||||||
| chr11:32970351 | G | A | 2 | a0001c0002t0004g0227 a0001c0002t0004g0233 |
2 | HG01243.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.5205+1208G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 10/12 | chr11 | 32970351 | |||||||
| chr11:32970443 | C | T | 4 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(1): Show |
4 | HG00738.hp1 HG01257.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.5205+1300C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 10/12 | chr11 | 32970443 | |||||||
| chr11:32970657 | C | T | 17 | a0001c0003t0002g0207 a0001c0003t0002g0208 a0001c0003t0002g0209 others(14): Show |
17 | HG00099.hp1 HG01074.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.5205+1514C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 10/12 | chr11 | 32970657 | |||||||
| chr11:32970946 | C | CT | 121 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(118): Show |
123 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.5205+1827dupT | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr11 | 32970946 | ||||||
| chr11:32970946 | C | CTT | 34 | a0001c0001t0001g0008 a0001c0001t0001g0047 a0001c0001t0001g0060 others(31): Show |
34 | HG00642.hp1 HG01071.hp1 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.5205+1826_5205+182 others(6): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr11 | 32970946 | ||||||
| chr11:32970946 | CT | C | 14 | a0001c0002t0001g0178 a0001c0002t0001g0179 a0001c0002t0001g0183 others(11): Show |
14 | HG01167.hp1 HG01884.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.5205+1827delT | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr11 | 32970946 | ||||||
| chr11:32970946 | CTT | C | 6 | a0001c0002t0001g0011 a0001c0002t0001g0175 a0001c0002t0001g0180 others(3): Show |
6 | HG00735.hp1 HG02109.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.5205+1826_5205+182 others(6): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr11 | 32970946 | ||||||
| chr11:32971536 | A | G | 1 | a0001c0008t0001g0015 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.5206-1861A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 10/12 | chr11 | 32971536 | |||||||
| chr11:32971575 | A | C | 1 | a0001c0001t0001g0148 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.5206-1822A>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 10/12 | chr11 | 32971575 | |||||||
| chr11:32971860 | G | A | 17 | a0001c0003t0002g0207 a0001c0003t0002g0208 a0001c0003t0002g0209 others(14): Show |
17 | HG00099.hp1 HG01074.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.5206-1537G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 10/12 | chr11 | 32971860 | |||||||
| chr11:32972032 | T | C | 45 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(42): Show |
46 | HG00408.hp2 HG00621.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.5206-1365T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 10/12 | chr11 | 32972032 | |||||||
| chr11:32972062 | C | CA | 9 | a0001c0002t0007g0012 a0001c0002t0007g0189 a0001c0002t0007g0190 others(6): Show |
9 | HG01496.hp1 HG01981.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.5206-1320dupA | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr11 | 32972062 | ||||||
| chr11:32972062 | CA | C | 22 | a0001c0002t0001g0013 a0001c0002t0008g0223 a0001c0002t0013g0162 others(19): Show |
22 | HG00099.hp1 HG01074.hp1 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.5206-1320delA | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr11 | 32972062 | ||||||
| chr11:32972062 | CAA | C | 29 | a0001c0002t0001g0011 a0001c0002t0001g0175 a0001c0002t0001g0178 others(26): Show |
29 | HG00735.hp1 HG01243.hp2 HG01496.hp2 others(26): Show |
intron_variant | MODIFIER | c.5206-1321_5206-132 others(6): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr11 | 32972062 | ||||||
| chr11:32972089 | T | C | 223 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(220): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.5206-1308T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 10/12 | chr11 | 32972089 | |||||||
| chr11:32972182 | C | T | 1 | a0001c0002t0007g0189 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.5206-1215C>T | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 10/12 | chr11 | 32972182 | |||||||
| chr11:32972341 | G | A | 160 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(157): Show |
162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.5206-1056G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 10/12 | chr11 | 32972341 | |||||||
| chr11:32972406 | C | CTTAT | 21 | a0001c0001t0001g0020 a0001c0001t0001g0052 a0001c0001t0001g0053 others(18): Show |
21 | HG00140.hp1 HG01074.hp2 HG01934.hp1 others(18): Show |
intron_variant | MODIFIER | c.5206-947_5206-944d others(6): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr11 | 32972406 | ||||||
| chr11:32972406 | C | CTTATTTA others(1): Show |
9 | a0001c0001t0001g0054 a0001c0001t0001g0105 a0001c0001t0001g0110 others(6): Show |
9 | HG00140.hp2 HG01981.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.5206-951_5206-944d others(10): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr11 | 32972406 | ||||||
| chr11:32972406 | C | CTTATTTA others(5): Show |
1 | a0001c0001t0003g0094 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.5206-955_5206-944d others(14): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr11 | 32972406 | ||||||
| chr11:32972406 | CTTAT | C | 75 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0029 others(72): Show |
76 | HG00099.hp2 HG00621.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.5206-947_5206-944d others(6): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr11 | 32972406 | ||||||
| chr11:32972406 | CTTATTTA others(1): Show |
C | 32 | a0001c0001t0001g0016 a0001c0001t0001g0051 a0001c0001t0012g0116 others(29): Show |
32 | HG00099.hp1 HG01074.hp1 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.5206-951_5206-944d others(10): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr11 | 32972406 | ||||||
| chr11:32972406 | CTTATTTA others(9): Show |
C | 5 | a0001c0001t0001g0122 a0001c0001t0001g0168 a0001c0002t0013g0162 others(2): Show |
5 | HG01884.hp1 HG02257.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.5206-959_5206-944d others(18): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr11 | 32972406 | ||||||
| chr11:32972670 | A | C | 28 | a0001c0002t0001g0011 a0001c0002t0001g0175 a0001c0002t0001g0178 others(25): Show |
28 | HG00735.hp1 HG01243.hp2 HG01496.hp2 others(25): Show |
intron_variant | MODIFIER | c.5206-727A>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 10/12 | chr11 | 32972670 | |||||||
| chr11:32973241 | A | ACACACAC others(27): Show |
1 | a0001c0001t0001g0086 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.5206-112_5206-79du others(35): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr11 | 32973241 | ||||||
| chr11:32973241 | ACACACAC others(27): Show |
A | 1 | a0001c0008t0001g0015 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.5206-112_5206-79de others(35): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr11 | 32973241 | ||||||
| chr11:32973294 | A | C | 1 | a0001c0001t0001g0077 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.5206-103A>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 10/12 | chr11 | 32973294 | |||||||
| chr11:32973677 | A | G | 1 | a0001c0001t0003g0049 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.5358+128A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 11/12 | chr11 | 32973677 | |||||||
| chr11:32973683 | G | A | 1 | a0001c0002t0004g0230 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.5358+134G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 11/12 | chr11 | 32973683 | |||||||
| chr11:32973715 | G | C | 1 | a0001c0002t0008g0206 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.5358+166G>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 11/12 | chr11 | 32973715 | |||||||
| chr11:32974143 | A | G | 1 | a0001c0008t0001g0015 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.5358+594A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 11/12 | chr11 | 32974143 | |||||||
| chr11:32974334 | G | C | 1 | a0001c0002t0008g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.5358+785G>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 11/12 | chr11 | 32974334 | |||||||
| chr11:32974365 | G | A | 1 | a0002c0004t0001g0023 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.5358+816G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 11/12 | chr11 | 32974365 | |||||||
| chr11:32974425 | CA | C | 28 | a0001c0001t0001g0056 a0001c0001t0001g0117 a0001c0001t0011g0082 others(25): Show |
28 | HG00735.hp1 HG01169.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.5359-807delA | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr11 | 32974425 | ||||||
| chr11:32974430 | A | G | 4 | a0001c0001t0001g0069 a0005c0009t0001g0089 a0005c0009t0001g0090 others(1): Show |
4 | HG01433.hp2 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.5359-818A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 11/12 | chr11 | 32974430 | |||||||
| chr11:32974564 | G | A | 3 | a0001c0008t0001g0202 a0001c0008t0001g0203 a0001c0008t0001g0204 |
3 | HG02723.hp1 HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.5359-684G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 11/12 | chr11 | 32974564 | |||||||
| chr11:32974721 | T | C | 1 | a0002c0004t0001g0044 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.5359-527T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 11/12 | chr11 | 32974721 | |||||||
| chr11:32975031 | A | G | 2 | a0002c0004t0015g0031 a0002c0004t0015g0032 |
2 | HG01975.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.5359-217A>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 11/12 | chr11 | 32975031 | |||||||
| chr11:32975036 | G | A | 1 | a0001c0002t0007g0189 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.5359-212G>A | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 11/12 | chr11 | 32975036 | |||||||
| chr11:32975134 | CAT | C | 2 | a0003c0005t0001g0194 a0003c0005t0001g0195 |
2 | NA18522.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.5359-109_5359-108d others(4): Show |
QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr11 | 32975134 | ||||||
| chr11:32975554 | T | C | 1 | a0001c0001t0003g0097 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.5454+211T>C | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 12/12 | chr11 | 32975554 | |||||||
| chr11:32975996 | T | G | 4 | a0001c0008t0001g0202 a0001c0008t0001g0203 a0001c0008t0001g0204 others(1): Show |
4 | HG02723.hp1 HG02965.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.5455-338T>G | QSER1 | ENSG00000060749.17 | transcript | ENST00000650167.2 | protein_coding | 12/12 | chr11 | 32975996 |