Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79269 |
| ensemblid | ENSG00000122741.16 |
| hgncid | 23686 |
| symbol | DCAF10 |
| name | DDB1 and CUL4 associated factor 10 |
| refseq_nuc | NM_024345.5 |
| refseq_prot | NP_077321.3 |
| ensembl_nuc | ENST00000377724.8 |
| ensembl_prot | ENSP00000366953.3 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 37800797 |
| end | 37867664 |
| strand | + |
| ver | v1.2 |
| region | chr9:37800797-37867664 |
| region5000 | chr9:37795797-37872664 |
| regionname0 | DCAF10_chr9_37800797_37867664 |
| regionname5000 | DCAF10_chr9_37795797_37872664 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 559 | 354 | 77 | 72 | 147 | 12 | 44 | 111 | DCAF10_chr9_37795797_37872664 | DCAF10 | MFPFG others(554): Show |
chr9 | 37795797 | 37872664 |
| a0002 | 0/0 | 559 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | MFSFG others(554): Show |
chr9 | 37795797 | 37872664 |
| a0003 | 0/0 | 559 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | MFPFG others(554): Show |
chr9 | 37795797 | 37872664 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1677 | 348 | 73 | 71 | 146 | 12 | 44 | DCAF10_chr9_37795797_37872664 | DCAF10 | ATGTT others(1672): Show |
chr9 | 37795797 | 37872664 | ||
| a0001c0002 | 0/0 | 1677 | 3 | 3 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | ATGTT others(1672): Show |
chr9 | 37795797 | 37872664 | ||
| a0001c0003 | 0/0 | 1677 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | ATGTT others(1672): Show |
chr9 | 37795797 | 37872664 | ||
| a0001c0004 | 0/0 | 1677 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | ATGTT others(1672): Show |
chr9 | 37795797 | 37872664 | ||
| a0001c0006 | 0/0 | 1677 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | ATGTT others(1672): Show |
chr9 | 37795797 | 37872664 | ||
| a0002c0007 | 0/0 | 1677 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | ATGTT others(1672): Show |
chr9 | 37795797 | 37872664 | ||
| a0003c0005 | 0/0 | 1677 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | ATGTT others(1672): Show |
chr9 | 37795797 | 37872664 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 7906 | 107 | 19 | 24 | 49 | 3 | 10 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7901): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0002 | 0/0 | 7905 | 51 | 5 | 9 | 25 | 2 | 10 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7900): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0003 | 0/0 | 7906 | 39 | 2 | 12 | 16 | 1 | 8 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7901): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0004 | 0/0 | 7906 | 24 | 7 | 4 | 7 | 2 | 4 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7901): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0005 | 0/0 | 7921 | 11 | 1 | 2 | 6 | 1 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7916): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0006 | 0/0 | 7906 | 9 | 1 | 3 | 4 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7901): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0007 | 0/0 | 7905 | 8 | 1 | 0 | 7 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7900): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0008 | 0/0 | 7904 | 6 | 6 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7899): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0009 | 0/0 | 7922 | 6 | 0 | 0 | 5 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7917): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0010 | 0/0 | 7907 | 5 | 1 | 0 | 3 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7902): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0011 | 0/0 | 7906 | 5 | 0 | 0 | 5 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7901): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0012 | 0/0 | 7907 | 4 | 4 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7902): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0013 | 0/0 | 7906 | 4 | 0 | 4 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7901): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0014 | 0/0 | 7901 | 4 | 4 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7896): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0015 | 0/0 | 7909 | 4 | 3 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7904): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0016 | 0/0 | 7906 | 3 | 0 | 2 | 0 | 1 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7901): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0017 | 0/0 | 7905 | 3 | 0 | 0 | 2 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7900): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0018 | 0/0 | 7904 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7899): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0019 | 0/0 | 7911 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7906): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0020 | 0/0 | 7911 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7906): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0021 | 0/0 | 7911 | 2 | 1 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7906): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0022 | 0/0 | 7906 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7901): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0023 | 0/0 | 7907 | 2 | 0 | 1 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7902): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0024 | 0/0 | 7906 | 2 | 0 | 0 | 0 | 1 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7901): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0025 | 0/0 | 7906 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7901): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0026 | 0/0 | 7906 | 2 | 0 | 2 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7901): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0027 | 0/0 | 7923 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7918): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0028 | 0/0 | 7921 | 2 | 0 | 2 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7916): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0029 | 0/0 | 7906 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7901): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0031 | 0/0 | 7910 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7905): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0032 | 0/0 | 7911 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7906): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0033 | 0/0 | 7907 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7902): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0034 | 0/0 | 7905 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7900): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0035 | 0/0 | 7907 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7902): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0036 | 0/0 | 7907 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7902): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0037 | 0/0 | 7907 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7902): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0038 | 0/0 | 7907 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7902): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0039 | 0/0 | 7906 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7901): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0040 | 0/0 | 7906 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7901): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0041 | 0/0 | 7906 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7901): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0042 | 0/0 | 7907 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7902): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0043 | 0/0 | 7906 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7901): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0044 | 0/0 | 7906 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7901): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0045 | 0/0 | 7906 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7901): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0046 | 0/0 | 7906 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7901): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0048 | 0/0 | 7907 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7902): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0049 | 0/0 | 7906 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7901): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0050 | 0/0 | 7905 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7900): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0051 | 0/0 | 7905 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7900): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0052 | 0/0 | 7905 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7900): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0053 | 0/0 | 7905 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7900): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0054 | 0/0 | 7905 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7900): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0055 | 0/0 | 7905 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7900): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0056 | 0/0 | 7905 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7900): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0057 | 0/0 | 7906 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7901): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0058 | 0/0 | 7906 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7901): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0059 | 0/0 | 7924 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7919): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0060 | 0/0 | 7922 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7917): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0061 | 0/0 | 7922 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7917): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0062 | 0/0 | 7913 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7908): Show |
chr9 | 37795797 | 37872664 |
| a0001c0001t0063 | 0/0 | 7909 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7904): Show |
chr9 | 37795797 | 37872664 |
| a0001c0002t0004 | 0/0 | 7906 | 3 | 3 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7901): Show |
chr9 | 37795797 | 37872664 |
| a0001c0003t0030 | 0/0 | 7924 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7919): Show |
chr9 | 37795797 | 37872664 |
| a0001c0004t0047 | 0/0 | 7905 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7900): Show |
chr9 | 37795797 | 37872664 |
| a0001c0006t0003 | 0/0 | 7906 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7901): Show |
chr9 | 37795797 | 37872664 |
| a0002c0007t0008 | 0/0 | 7904 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7899): Show |
chr9 | 37795797 | 37872664 |
| a0003c0005t0001 | 0/0 | 7906 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | AGCTG others(7901): Show |
chr9 | 37795797 | 37872664 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0092 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0104 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0002g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0002g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0002g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0003g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0004g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0004g0010 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0004g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0004g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0004g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0004g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0004g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0004g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0004g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0004g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0004g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0004g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0004g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0004g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0004g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0004g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0004g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0005g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0005g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0005g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0005g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0005g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0005g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0005g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0005g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0005g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0005g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0005g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0006g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0006g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0006g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0006g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0006g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0006g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0006g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0006g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0006g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0007g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0007g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0007g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0007g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0007g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0007g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0007g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0007g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0008g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0008g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0008g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0008g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0008g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0008g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0009g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0009g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0009g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0009g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0009g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0010g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0010g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0010g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0010g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0010g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0011g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0011g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0011g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0011g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0011g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0012g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0012g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0012g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0013g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0013g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0013g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0013g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0014g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0014g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0014g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0015g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0015g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0015g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0015g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0016g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0016g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0016g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0017g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0017g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0017g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0018g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0019g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0019g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0020g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0020g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0021g0004 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0022g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0022g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0023g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0023g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0024g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0024g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0025g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0025g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0026g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0027g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0027g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0028g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0028g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0029g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0031g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0032g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0033g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0034g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0035g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0036g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0037g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0038g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0039g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0040g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0041g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0042g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0043g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0044g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0045g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0046g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0048g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0049g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0050g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0051g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0052g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0053g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0054g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0055g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0056g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0057g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0058g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0059g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0060g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0061g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0062g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0001t0063g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0002t0004g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0002t0004g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0002t0004g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0003t0030g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0004t0047g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0001c0006t0003g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0002c0007t0008g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| a0003c0005t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0274 | EUR | GBR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0089 | EUR | GBR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG00140 | hp1 | a0001 | c0001 | t0024 | g0140 | EUR | GBR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0010 | EUR | GBR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0152 | EUR | FIN | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG00323 | hp2 | a0001 | c0001 | t0004 | g0211 | EUR | FIN | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG00438 | hp1 | a0001 | c0001 | t0035 | g0189 | EAS | CHS | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG00438 | hp2 | a0001 | c0001 | t0010 | g0155 | EAS | CHS | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG00597 | hp1 | a0001 | c0001 | t0058 | g0096 | EAS | CHS | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG00597 | hp2 | a0001 | c0001 | t0004 | g0232 | EAS | CHS | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0203 | EAS | CHS | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG00639 | hp1 | a0001 | c0006 | t0003 | g0222 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG00639 | hp2 | a0001 | c0001 | t0026 | g0007 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0233 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0268 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG00733 | hp2 | a0001 | c0001 | t0013 | g0061 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG00735 | hp1 | a0001 | c0001 | t0041 | g0154 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0168 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0088 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG00738 | hp2 | a0001 | c0001 | t0026 | g0007 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG00741 | hp1 | a0001 | c0001 | t0016 | g0195 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0167 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0219 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG01081 | hp1 | a0001 | c0001 | t0028 | g0034 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0307 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG01106 | hp2 | a0001 | c0001 | t0016 | g0194 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0260 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG01109 | hp2 | a0001 | c0001 | t0023 | g0213 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG01168 | hp1 | a0001 | c0001 | t0005 | g0037 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0193 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG01192 | hp2 | a0001 | c0001 | t0028 | g0033 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG01243 | hp1 | a0001 | c0001 | t0021 | g0004 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0273 | AMR | CLM | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG01256 | hp1 | a0001 | c0001 | t0013 | g0064 | AMR | CLM | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG01256 | hp2 | a0001 | c0001 | t0004 | g0171 | AMR | CLM | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG01258 | hp2 | a0001 | c0001 | t0013 | g0062 | AMR | CLM | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0287 | AMR | CLM | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG01346 | hp1 | a0001 | c0001 | t0013 | g0186 | AMR | CLM | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG01346 | hp2 | a0001 | c0001 | t0004 | g0063 | AMR | CLM | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG01361 | hp1 | a0001 | c0001 | t0037 | g0223 | AMR | CLM | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG01361 | hp2 | a0001 | c0001 | t0006 | g0255 | AMR | CLM | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0218 | AMR | CLM | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG01496 | hp2 | a0001 | c0001 | t0063 | g0044 | AMR | CLM | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG01515 | hp1 | a0001 | c0001 | t0005 | g0031 | EUR | IBS | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG01515 | hp2 | a0001 | c0001 | t0016 | g0212 | EUR | IBS | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0311 | EUR | IBS | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0227 | EUR | IBS | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0172 | AFR | ACB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0308 | AFR | ACB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0221 | AMR | PEL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG01975 | hp1 | a0001 | c0001 | t0043 | g0192 | AMR | PEL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG01975 | hp2 | a0001 | c0001 | t0006 | g0256 | AMR | PEL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG01978 | hp2 | a0001 | c0001 | t0006 | g0321 | AMR | PEL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0184 | AMR | PEL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0304 | AMR | PEL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0226 | AMR | PEL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0011 | AMR | PEL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02004 | hp2 | a0001 | c0001 | t0004 | g0306 | AMR | PEL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0179 | EAS | KHV | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0316 | AFR | ACB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02055 | hp2 | a0001 | c0001 | t0010 | g0090 | AFR | ACB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0196 | EAS | KHV | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02074 | hp1 | a0001 | c0004 | t0047 | g0288 | EAS | KHV | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | KHV | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0320 | EAS | KHV | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02080 | hp2 | a0001 | c0001 | t0057 | g0077 | EAS | KHV | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02083 | hp1 | a0001 | c0001 | t0007 | g0289 | EAS | KHV | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02083 | hp2 | a0001 | c0001 | t0004 | g0253 | EAS | KHV | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0201 | EAS | KHV | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0312 | EAS | KHV | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0093 | EAS | KHV | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0202 | AFR | ACB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0303 | AMR | PEL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02155 | hp1 | a0001 | c0001 | t0045 | g0264 | EAS | CDX | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | CDX | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02165 | hp1 | a0001 | c0001 | t0034 | g0331 | EAS | CDX | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | CDX | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02257 | hp2 | a0001 | c0001 | t0031 | g0337 | AFR | ACB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0207 | AMR | PEL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0310 | AMR | PEL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02280 | hp1 | a0001 | c0002 | t0004 | g0215 | AFR | ACB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0145 | AFR | ACB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0011 | AMR | PEL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02300 | hp1 | a0001 | c0001 | t0005 | g0022 | AMR | PEL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0302 | AMR | PEL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | ACB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02451 | hp2 | a0001 | c0001 | t0008 | g0047 | AFR | ACB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0283 | EAS | KHV | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0325 | AFR | GWD | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02572 | hp2 | a0001 | c0001 | t0038 | g0332 | AFR | GWD | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0300 | SAS | PJL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0170 | SAS | PJL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0240 | AFR | GWD | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02622 | hp2 | a0001 | c0001 | t0062 | g0019 | AFR | GWD | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02630 | hp1 | a0001 | c0001 | t0015 | g0017 | AFR | GWD | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02647 | hp2 | a0001 | c0001 | t0012 | g0005 | AFR | GWD | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0200 | SAS | PJL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02717 | hp1 | a0001 | c0003 | t0030 | g0045 | AFR | GWD | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02717 | hp2 | a0001 | c0001 | t0025 | g0206 | AFR | GWD | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02735 | hp1 | a0001 | c0001 | t0004 | g0010 | SAS | PJL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02738 | hp1 | a0001 | c0001 | t0024 | g0141 | SAS | PJL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0334 | SAS | PJL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02818 | hp1 | a0001 | c0001 | t0032 | g0056 | AFR | GWD | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02818 | hp2 | a0001 | c0001 | t0008 | g0046 | AFR | GWD | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02895 | hp2 | a0001 | c0001 | t0012 | g0005 | AFR | GWD | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02897 | hp2 | a0001 | c0001 | t0012 | g0059 | AFR | GWD | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02922 | hp1 | a0001 | c0001 | t0008 | g0050 | AFR | ESN | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02922 | hp2 | a0001 | c0001 | t0021 | g0004 | AFR | ESN | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02965 | hp1 | a0001 | c0001 | t0051 | g0177 | AFR | ESN | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02965 | hp2 | a0001 | c0001 | t0053 | g0241 | AFR | ESN | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02970 | hp1 | a0001 | c0001 | t0022 | g0335 | AFR | ESN | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | ESN | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0150 | AFR | ESN | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02976 | hp2 | a0001 | c0001 | t0018 | g0016 | AFR | ESN | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG03017 | hp1 | a0001 | c0001 | t0044 | g0157 | SAS | PJL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG03041 | hp1 | a0001 | c0001 | t0022 | g0336 | AFR | GWD | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG03139 | hp1 | a0001 | c0001 | t0020 | g0054 | AFR | ESN | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0178 | AFR | ESN | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0143 | AFR | ESN | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG03195 | hp2 | a0001 | c0001 | t0007 | g0294 | AFR | ESN | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG03209 | hp1 | a0001 | c0001 | t0015 | g0038 | AFR | MSL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG03209 | hp2 | a0001 | c0001 | t0014 | g0012 | AFR | MSL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0323 | SAS | PJL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0217 | SAS | PJL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | MSL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG03453 | hp2 | a0001 | c0001 | t0008 | g0051 | AFR | MSL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG03486 | hp1 | a0001 | c0001 | t0012 | g0060 | AFR | MSL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG03486 | hp2 | a0001 | c0001 | t0025 | g0209 | AFR | MSL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0271 | SAS | PJL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0231 | SAS | PJL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG03491 | hp2 | a0001 | c0001 | t0050 | g0142 | SAS | PJL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0230 | SAS | PJL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG03516 | hp1 | a0001 | c0001 | t0020 | g0053 | AFR | ESN | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | ESN | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG03540 | hp2 | a0001 | c0001 | t0014 | g0012 | AFR | GWD | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG03654 | hp2 | a0001 | c0001 | t0005 | g0032 | SAS | PJL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG03688 | hp1 | a0001 | c0001 | t0036 | g0151 | SAS | STU | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG03688 | hp2 | a0001 | c0001 | t0006 | g0259 | SAS | STU | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0324 | SAS | PJL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0299 | SAS | PJL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG03710 | hp2 | a0001 | c0001 | t0010 | g0108 | SAS | PJL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG03831 | hp1 | a0001 | c0001 | t0061 | g0036 | SAS | BEB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG03831 | hp2 | a0001 | c0001 | t0004 | g0136 | SAS | BEB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0322 | SAS | BEB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | BEB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0197 | SAS | BEB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0330 | SAS | BEB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0329 | SAS | STU | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG04115 | hp2 | a0001 | c0001 | t0017 | g0080 | SAS | STU | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG04184 | hp1 | a0001 | c0001 | t0023 | g0153 | SAS | BEB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG04184 | hp2 | a0001 | c0001 | t0059 | g0039 | SAS | BEB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG04199 | hp1 | a0001 | c0001 | t0009 | g0028 | SAS | STU | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG04199 | hp2 | a0001 | c0001 | t0004 | g0275 | SAS | STU | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | STU | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0199 | SAS | STU | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0328 | SAS | STU | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0234 | SAS | STU | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18522 | hp1 | a0001 | c0001 | t0008 | g0049 | AFR | YRI | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0276 | AFR | YRI | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | CHB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | CHB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18747 | hp1 | a0001 | c0001 | t0004 | g0166 | EAS | CHB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | CHB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | YRI | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18906 | hp2 | a0002 | c0007 | t0008 | g0052 | AFR | YRI | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18943 | hp2 | a0001 | c0001 | t0006 | g0254 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18944 | hp1 | a0001 | c0001 | t0009 | g0023 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18946 | hp1 | a0001 | c0001 | t0054 | g0008 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18948 | hp2 | a0001 | c0001 | t0015 | g0040 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18951 | hp1 | a0001 | c0001 | t0005 | g0035 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18951 | hp2 | a0001 | c0001 | t0004 | g0208 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18952 | hp2 | a0001 | c0001 | t0007 | g0267 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18957 | hp1 | a0001 | c0001 | t0027 | g0020 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18957 | hp2 | a0003 | c0005 | t0001 | g0074 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18959 | hp2 | a0001 | c0001 | t0052 | g0169 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18960 | hp2 | a0001 | c0001 | t0009 | g0003 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18965 | hp1 | a0001 | c0001 | t0009 | g0041 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18965 | hp2 | a0001 | c0001 | t0049 | g0120 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0291 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18967 | hp2 | a0001 | c0001 | t0039 | g0280 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18968 | hp2 | a0001 | c0001 | t0005 | g0026 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18969 | hp2 | a0001 | c0001 | t0004 | g0121 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18970 | hp2 | a0001 | c0001 | t0042 | g0278 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18972 | hp1 | a0001 | c0001 | t0005 | g0030 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18974 | hp2 | a0001 | c0001 | t0048 | g0163 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18977 | hp2 | a0001 | c0001 | t0056 | g0309 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18978 | hp1 | a0001 | c0001 | t0055 | g0266 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18978 | hp2 | a0001 | c0001 | t0005 | g0027 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18979 | hp1 | a0001 | c0001 | t0011 | g0164 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18979 | hp2 | a0001 | c0001 | t0007 | g0269 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18980 | hp1 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18980 | hp2 | a0001 | c0001 | t0046 | g0099 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18982 | hp2 | a0001 | c0001 | t0004 | g0176 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18988 | hp1 | a0001 | c0001 | t0027 | g0021 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18989 | hp1 | a0001 | c0001 | t0011 | g0159 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18995 | hp1 | a0001 | c0001 | t0010 | g0112 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18995 | hp2 | a0001 | c0001 | t0006 | g0261 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA19000 | hp1 | a0001 | c0001 | t0011 | g0156 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA19000 | hp2 | a0001 | c0001 | t0007 | g0318 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA19004 | hp1 | a0001 | c0001 | t0005 | g0024 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0182 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA19011 | hp1 | a0001 | c0001 | t0011 | g0158 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA19030 | hp1 | a0001 | c0001 | t0008 | g0048 | AFR | LWK | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA19030 | hp2 | a0001 | c0001 | t0014 | g0165 | AFR | LWK | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0091 | AFR | LWK | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | LWK | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA19056 | hp1 | a0001 | c0001 | t0006 | g0279 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA19057 | hp1 | a0001 | c0001 | t0009 | g0003 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA19060 | hp1 | a0001 | c0001 | t0007 | g0270 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA19063 | hp2 | a0001 | c0001 | t0007 | g0272 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA19076 | hp1 | a0001 | c0001 | t0009 | g0042 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA19076 | hp2 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA19079 | hp1 | a0001 | c0001 | t0007 | g0293 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA19079 | hp2 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA19083 | hp1 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA19084 | hp1 | a0001 | c0001 | t0010 | g0013 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA19084 | hp2 | a0001 | c0001 | t0006 | g0262 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA19091 | hp1 | a0001 | c0001 | t0005 | g0029 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA19091 | hp2 | a0001 | c0001 | t0017 | g0327 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA19240 | hp1 | a0001 | c0001 | t0014 | g0237 | AFR | YRI | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA19240 | hp2 | a0001 | c0001 | t0033 | g0058 | AFR | YRI | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA20129 | hp1 | a0001 | c0001 | t0015 | g0025 | AFR | ASW | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA20129 | hp2 | a0001 | c0002 | t0004 | g0214 | AFR | ASW | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA20752 | hp1 | a0001 | c0001 | t0029 | g0137 | EUR | TSI | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0205 | EUR | TSI | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0317 | SAS | GIH | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA20905 | hp2 | a0001 | c0001 | t0004 | g0333 | SAS | GIH | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | CLM | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG01123 | hp2 | a0001 | c0001 | t0060 | g0018 | AMR | CLM | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0228 | AFR | ACB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02486 | hp1 | a0001 | c0002 | t0004 | g0220 | AFR | ACB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02486 | hp2 | a0001 | c0001 | t0019 | g0055 | AFR | ACB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02559 | hp1 | a0001 | c0001 | t0019 | g0057 | AFR | ACB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | ACB | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | MSL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0295 | AFR | MSL | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG06807 | hp1 | a0001 | c0001 | t0040 | g0235 | AFR | USA | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | USA | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18955 | hp1 | a0001 | c0001 | t0011 | g0160 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA18955 | hp2 | a0001 | c0001 | t0017 | g0326 | EAS | JPT | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA20300 | hp1 | a0001 | c0001 | t0018 | g0016 | AFR | USA | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA20300 | hp2 | a0001 | c0001 | t0006 | g0257 | AFR | USA | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | LWK | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| NA21309 | hp2 | a0001 | c0001 | t0005 | g0043 | AFR | LWK | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0092 | REF | REF | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0104 | REF | REF | DCAF10_chr9_37795797_37872664 | DCAF10 | chr9 | 37795797 | 37872664 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:37800873 | C | T | 1 | a0002 | 1 | NA18906.hp2 | missense_variant | MODERATE | c.7C>T | p.Pro3Ser | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/7 | 77/7906 | 7/1680 | 3/559 | chr9 | 37800873 | |||
| chr9:37860086 | G | A | 1 | a0003 | 1 | NA18957.hp2 | missense_variant | MODERATE | c.1204G>A | p.Glu402Lys | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 6/7 | 1274/7906 | 1204/1680 | 402/559 | chr9 | 37860086 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:37800908 | G | A | 1 | a0001c0003 | 1 | HG02717.hp1 | synonymous_variant | LOW | c.42G>A | p.Ser14Ser | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/7 | 112/7906 | 42/1680 | 14/559 | chr9 | 37800908 | |||
| chr9:37800965 | G | A | 1 | a0001c0004 | 1 | HG02074.hp1 | synonymous_variant | LOW | c.99G>A | p.Gly33Gly | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/7 | 169/7906 | 99/1680 | 33/559 | chr9 | 37800965 | |||
| chr9:37801370 | C | T | 1 | a0001c0006 | 1 | HG00639.hp1 | synonymous_variant | LOW | c.504C>T | p.His168His | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/7 | 574/7906 | 504/1680 | 168/559 | chr9 | 37801370 | |||
| chr9:37861481 | G | A | 1 | a0001c0002 | 3 | HG02280.hp1 HG02486.hp1 NA20129.hp2 |
synonymous_variant | LOW | c.1653G>A | p.Arg551Arg | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 1723/7906 | 1653/1680 | 551/559 | chr9 | 37861481 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:37800841 | C | A | 1 | a0001c0001t0029 | 1 | NA20752.hp1 | 5_prime_UTR_variant | MODIFIER | c.-26C>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/7 | 26 | chr9 | 37800841 | ||||||
| chr9:37861684 | A | ATC | 10 | a0001c0001t0005 a0001c0001t0009 a0001c0001t0015 others(7): Show |
30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*179_*180dupTC | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 181 | INFO_REALIGN_3_PRIME | chr9 | 37861684 | |||||
| chr9:37861797 | C | A | 22 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0009 others(19): Show |
55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*289C>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 289 | chr9 | 37861797 | ||||||
| chr9:37862004 | T | G | 1 | a0001c0001t0034 | 1 | HG02165.hp1 | 3_prime_UTR_variant | MODIFIER | c.*496T>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 496 | chr9 | 37862004 | ||||||
| chr9:37862069 | A | G | 1 | a0001c0001t0058 | 1 | HG00597.hp1 | 3_prime_UTR_variant | MODIFIER | c.*561A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 561 | chr9 | 37862069 | ||||||
| chr9:37862127 | A | T | 10 | a0001c0001t0005 a0001c0001t0009 a0001c0001t0015 others(7): Show |
30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*619A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 619 | chr9 | 37862127 | ||||||
| chr9:37862181 | A | T | 10 | a0001c0001t0005 a0001c0001t0009 a0001c0001t0015 others(7): Show |
30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*673A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 673 | chr9 | 37862181 | ||||||
| chr9:37862632 | G | A | 1 | a0001c0001t0018 | 2 | HG02976.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1124G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 1124 | chr9 | 37862632 | ||||||
| chr9:37862781 | G | A | 22 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0009 others(19): Show |
55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*1273G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 1273 | chr9 | 37862781 | ||||||
| chr9:37862871 | A | G | 1 | a0001c0001t0057 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1363A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 1363 | chr9 | 37862871 | ||||||
| chr9:37863065 | T | C | 22 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0009 others(19): Show |
55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*1557T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 1557 | chr9 | 37863065 | ||||||
| chr9:37863152 | G | C | 22 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0009 others(19): Show |
55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*1644G>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 1644 | chr9 | 37863152 | ||||||
| chr9:37863171 | C | T | 1 | a0001c0001t0056 | 1 | NA18977.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1663C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 1663 | chr9 | 37863171 | ||||||
| chr9:37863199 | A | G | 22 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0009 others(19): Show |
55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*1691A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 1691 | chr9 | 37863199 | ||||||
| chr9:37863228 | A | G | 1 | a0001c0001t0055 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1720A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 1720 | chr9 | 37863228 | ||||||
| chr9:37863262 | G | C | 2 | a0001c0001t0013 a0001c0001t0018 |
6 | HG00733.hp2 HG01256.hp1 HG01258.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1754G>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 1754 | chr9 | 37863262 | ||||||
| chr9:37863275 | G | A | 4 | a0001c0001t0008 a0001c0001t0018 a0001c0003t0030 others(1): Show |
10 | HG02451.hp2 HG02717.hp1 HG02818.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1767G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 1767 | chr9 | 37863275 | ||||||
| chr9:37863325 | C | CA | 8 | a0001c0001t0006 a0001c0001t0010 a0001c0001t0023 others(5): Show |
21 | HG00438.hp1 HG00438.hp2 HG01109.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1841dupA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 1842 | INFO_REALIGN_3_PRIME | chr9 | 37863325 | |||||
| chr9:37863325 | C | CAAAA | 6 | a0001c0001t0019 a0001c0001t0020 a0001c0001t0021 others(3): Show |
9 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1838_*1841dupAAAA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 1842 | INFO_REALIGN_3_PRIME | chr9 | 37863325 | |||||
| chr9:37863325 | C | CAAAAAAA others(5): Show |
2 | a0001c0001t0005 a0001c0001t0028 |
13 | HG01081.hp1 HG01168.hp1 HG01192.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1830_*1841dupAAAA others(8): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 1842 | INFO_REALIGN_3_PRIME | chr9 | 37863325 | |||||
| chr9:37863325 | C | CAAAAAAA others(6): Show |
3 | a0001c0001t0009 a0001c0001t0060 a0001c0001t0061 |
8 | HG01123.hp2 HG03831.hp1 HG04199.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1829_*1841dupAAAA others(9): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 1842 | INFO_REALIGN_3_PRIME | chr9 | 37863325 | |||||
| chr9:37863325 | C | CAAAAAAA others(7): Show |
1 | a0001c0001t0027 | 2 | NA18957.hp1 NA18988.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1828_*1841dupAAAA others(10): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 1842 | INFO_REALIGN_3_PRIME | chr9 | 37863325 | |||||
| chr9:37863325 | C | CAAAAAAA others(8): Show |
1 | a0001c0001t0059 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1827_*1841dupAAAA others(11): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 1842 | INFO_REALIGN_3_PRIME | chr9 | 37863325 | |||||
| chr9:37863325 | C | CAAAAAAA others(10): Show |
1 | a0001c0003t0030 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1825_*1841dupAAAA others(13): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 1842 | INFO_REALIGN_3_PRIME | chr9 | 37863325 | |||||
| chr9:37863325 | CA | C | 6 | a0001c0001t0017 a0001c0001t0050 a0001c0001t0051 others(3): Show |
8 | HG02965.hp1 HG02965.hp2 HG03491.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1841delA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 1841 | INFO_REALIGN_3_PRIME | chr9 | 37863325 | |||||
| chr9:37863325 | CAAA | C | 3 | a0001c0001t0008 a0001c0001t0018 a0002c0007t0008 |
9 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1839_*1841delAAA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 1839 | INFO_REALIGN_3_PRIME | chr9 | 37863325 | |||||
| chr9:37863357 | C | T | 1 | a0001c0001t0049 | 1 | NA18965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1849C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 1849 | chr9 | 37863357 | ||||||
| chr9:37863482 | A | G | 1 | a0001c0003t0030 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1974A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 1974 | chr9 | 37863482 | ||||||
| chr9:37863648 | T | C | 6 | a0001c0001t0019 a0001c0001t0020 a0001c0001t0021 others(3): Show |
10 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2140T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 2140 | chr9 | 37863648 | ||||||
| chr9:37863893 | G | T | 3 | a0001c0001t0011 a0001c0001t0048 a0001c0001t0054 |
7 | NA18946.hp1 NA18955.hp1 NA18974.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2385G>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 2385 | chr9 | 37863893 | ||||||
| chr9:37863958 | T | C | 1 | a0001c0001t0035 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2450T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 2450 | chr9 | 37863958 | ||||||
| chr9:37864022 | AC | A | 8 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0007 others(5): Show |
73 | HG00099.hp1 HG00558.hp1 HG00642.hp2 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*2515delC | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 2515 | chr9 | 37864022 | ||||||
| chr9:37864060 | A | C | 1 | a0001c0001t0021 | 2 | HG01243.hp1 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2552A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 2552 | chr9 | 37864060 | ||||||
| chr9:37864097 | G | A | 2 | a0001c0001t0024 a0001c0001t0050 |
3 | HG00140.hp1 HG02738.hp1 HG03491.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2589G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 2589 | chr9 | 37864097 | ||||||
| chr9:37864163 | G | A | 1 | a0001c0001t0040 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2655G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 2655 | chr9 | 37864163 | ||||||
| chr9:37864234 | C | G | 1 | a0001c0001t0038 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2726C>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 2726 | chr9 | 37864234 | ||||||
| chr9:37864239 | T | A | 2 | a0001c0001t0022 a0001c0001t0031 |
3 | HG02257.hp2 HG02970.hp1 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2731T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 2731 | chr9 | 37864239 | ||||||
| chr9:37864265 | A | G | 22 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0009 others(19): Show |
55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*2757A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 2757 | chr9 | 37864265 | ||||||
| chr9:37864477 | A | C | 1 | a0001c0001t0063 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2969A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 2969 | chr9 | 37864477 | ||||||
| chr9:37864478 | G | T | 1 | a0001c0001t0063 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2970G>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 2970 | chr9 | 37864478 | ||||||
| chr9:37864533 | G | A | 1 | a0001c0001t0028 | 2 | HG01081.hp1 HG01192.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3025G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 3025 | chr9 | 37864533 | ||||||
| chr9:37864539 | G | A | 2 | a0001c0001t0025 a0001c0001t0051 |
3 | HG02717.hp2 HG02965.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3031G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 3031 | chr9 | 37864539 | ||||||
| chr9:37864542 | C | T | 1 | a0001c0001t0061 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3034C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 3034 | chr9 | 37864542 | ||||||
| chr9:37864583 | C | CA | 5 | a0001c0001t0019 a0001c0001t0020 a0001c0001t0032 others(2): Show |
7 | HG02486.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3092dupA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 3093 | INFO_REALIGN_3_PRIME | chr9 | 37864583 | |||||
| chr9:37864596 | A | AT | 17 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0009 others(14): Show |
47 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*3088_*3089insT | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 3089 | chr9 | 37864596 | ||||||
| chr9:37864596 | A | T | 13 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(10): Show |
97 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*3088A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 3088 | chr9 | 37864596 | ||||||
| chr9:37864597 | A | T | 7 | a0001c0001t0003 a0001c0001t0035 a0001c0001t0037 others(4): Show |
45 | HG00099.hp2 HG00438.hp1 HG00621.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*3089A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 3089 | chr9 | 37864597 | ||||||
| chr9:37865058 | T | C | 10 | a0001c0001t0005 a0001c0001t0009 a0001c0001t0015 others(7): Show |
30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*3550T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 3550 | chr9 | 37865058 | ||||||
| chr9:37865307 | C | G | 4 | a0001c0001t0008 a0001c0001t0018 a0001c0003t0030 others(1): Show |
10 | HG02451.hp2 HG02717.hp1 HG02818.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3799C>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 3799 | chr9 | 37865307 | ||||||
| chr9:37865409 | T | C | 1 | a0001c0001t0033 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3901T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 3901 | chr9 | 37865409 | ||||||
| chr9:37865590 | T | G | 1 | a0001c0001t0060 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4082T>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 4082 | chr9 | 37865590 | ||||||
| chr9:37865754 | G | A | 5 | a0001c0001t0019 a0001c0001t0020 a0001c0001t0021 others(2): Show |
9 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4246G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 4246 | chr9 | 37865754 | ||||||
| chr9:37865795 | A | G | 1 | a0001c0001t0046 | 1 | NA18980.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4287A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 4287 | chr9 | 37865795 | ||||||
| chr9:37865822 | TAAGAA | T | 1 | a0001c0001t0014 | 4 | HG03209.hp2 HG03540.hp2 NA19030.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4318_*4322delAAAA others(1): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 4318 | INFO_REALIGN_3_PRIME | chr9 | 37865822 | |||||
| chr9:37865907 | T | C | 1 | a0001c0003t0030 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4399T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 4399 | chr9 | 37865907 | ||||||
| chr9:37865946 | A | G | 22 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0009 others(19): Show |
55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*4438A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 4438 | chr9 | 37865946 | ||||||
| chr9:37866010 | G | A | 1 | a0001c0001t0058 | 1 | HG00597.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4502G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 4502 | chr9 | 37866010 | ||||||
| chr9:37866024 | G | A | 1 | a0001c0001t0036 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4516G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 4516 | chr9 | 37866024 | ||||||
| chr9:37866065 | A | G | 1 | a0001c0001t0041 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4557A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 4557 | chr9 | 37866065 | ||||||
| chr9:37866222 | T | C | 1 | a0001c0001t0043 | 1 | HG01975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4714T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 4714 | chr9 | 37866222 | ||||||
| chr9:37866528 | G | A | 1 | a0001c0001t0026 | 2 | HG00639.hp2 HG00738.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5020G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 5020 | chr9 | 37866528 | ||||||
| chr9:37866554 | C | T | 10 | a0001c0001t0005 a0001c0001t0009 a0001c0001t0015 others(7): Show |
30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*5046C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 5046 | chr9 | 37866554 | ||||||
| chr9:37866556 | A | G | 1 | a0001c0001t0044 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5048A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 5048 | chr9 | 37866556 | ||||||
| chr9:37866590 | C | T | 1 | a0001c0003t0030 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5082C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 5082 | chr9 | 37866590 | ||||||
| chr9:37866635 | G | A | 10 | a0001c0001t0005 a0001c0001t0009 a0001c0001t0015 others(7): Show |
30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*5127G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 5127 | chr9 | 37866635 | ||||||
| chr9:37867036 | A | C | 1 | a0001c0001t0016 | 3 | HG00741.hp1 HG01106.hp2 HG01515.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5528A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 5528 | chr9 | 37867036 | ||||||
| chr9:37867110 | T | C | 3 | a0001c0001t0039 a0001c0001t0045 a0001c0004t0047 |
3 | HG02074.hp1 HG02155.hp1 NA18967.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5602T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 5602 | chr9 | 37867110 | ||||||
| chr9:37867194 | T | C | 19 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0009 others(16): Show |
50 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*5686T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 5686 | chr9 | 37867194 | ||||||
| chr9:37867321 | T | C | 2 | a0001c0001t0022 a0001c0001t0031 |
3 | HG02257.hp2 HG02970.hp1 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5813T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 7/7 | 5813 | chr9 | 37867321 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:37801447 | G | A | 29 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(26): Show |
30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.539+42G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37801447 | |||||||
| chr9:37801462 | G | A | 1 | a0001c0003t0030g0045 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.539+57G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37801462 | |||||||
| chr9:37801465 | C | T | 3 | a0001c0001t0022g0335 a0001c0001t0022g0336 a0001c0001t0031g0337 |
3 | HG02257.hp2 HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.539+60C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37801465 | |||||||
| chr9:37801488 | G | C | 49 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(46): Show |
52 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(49): Show |
intron_variant | MODIFIER | c.539+83G>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37801488 | |||||||
| chr9:37801717 | G | C | 4 | a0001c0001t0004g0063 a0001c0001t0013g0061 a0001c0001t0013g0062 others(1): Show |
4 | HG00733.hp2 HG01256.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.539+312G>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37801717 | |||||||
| chr9:37801815 | C | T | 1 | a0001c0001t0001g0334 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.539+410C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37801815 | |||||||
| chr9:37801859 | C | T | 1 | a0001c0001t0004g0333 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.539+454C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37801859 | |||||||
| chr9:37802177 | A | T | 1 | a0001c0001t0001g0334 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.539+772A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37802177 | |||||||
| chr9:37802237 | A | G | 51 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(48): Show |
55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.539+832A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37802237 | |||||||
| chr9:37802455 | T | C | 1 | a0001c0001t0002g0065 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.539+1050T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37802455 | |||||||
| chr9:37802665 | A | G | 1 | a0001c0001t0038g0332 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.539+1260A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37802665 | |||||||
| chr9:37802761 | A | G | 4 | a0001c0001t0012g0005 a0001c0001t0012g0059 a0001c0001t0012g0060 others(1): Show |
5 | HG02647.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.539+1356A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37802761 | |||||||
| chr9:37802868 | C | G | 1 | a0001c0001t0034g0331 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.539+1463C>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37802868 | |||||||
| chr9:37803213 | T | C | 50 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(47): Show |
54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.539+1808T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37803213 | |||||||
| chr9:37803300 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.539+1895T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37803300 | |||||||
| chr9:37803412 | TTTTATA | T | 8 | a0001c0001t0008g0046 a0001c0001t0008g0047 a0001c0001t0008g0048 others(5): Show |
9 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.539+2015_539+2020d others(8): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37803412 | ||||||
| chr9:37803527 | C | T | 8 | a0001c0001t0008g0046 a0001c0001t0008g0047 a0001c0001t0008g0048 others(5): Show |
9 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.539+2122C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37803527 | |||||||
| chr9:37803894 | T | C | 3 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 |
3 | HG02647.hp1 HG02897.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.539+2489T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37803894 | |||||||
| chr9:37803951 | G | A | 3 | a0001c0001t0022g0335 a0001c0001t0022g0336 a0001c0001t0031g0337 |
3 | HG02257.hp2 HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.539+2546G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37803951 | |||||||
| chr9:37803989 | A | G | 1 | a0001c0001t0019g0057 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.539+2584A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37803989 | |||||||
| chr9:37804028 | T | C | 1 | a0001c0003t0030g0045 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.539+2623T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37804028 | |||||||
| chr9:37804036 | A | T | 1 | a0001c0003t0030g0045 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.539+2631A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37804036 | |||||||
| chr9:37804040 | A | G | 1 | a0001c0001t0019g0057 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.539+2635A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37804040 | |||||||
| chr9:37804194 | AAC | A | 13 | a0001c0001t0012g0005 a0001c0001t0012g0059 a0001c0001t0012g0060 others(10): Show |
15 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.539+2793_539+2794d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37804194 | ||||||
| chr9:37804356 | A | G | 1 | a0001c0001t0001g0015 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.539+2951A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37804356 | |||||||
| chr9:37804439 | T | G | 28 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(25): Show |
29 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.539+3034T>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37804439 | |||||||
| chr9:37804519 | G | A | 1 | a0001c0001t0015g0017 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.539+3114G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37804519 | |||||||
| chr9:37804546 | G | A | 2 | a0001c0001t0001g0070 a0001c0001t0001g0071 |
2 | HG00733.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.539+3141G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37804546 | |||||||
| chr9:37804598 | G | A | 4 | a0001c0001t0008g0046 a0001c0001t0008g0047 a0001c0001t0008g0048 others(1): Show |
4 | HG02451.hp2 HG02818.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.539+3193G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37804598 | |||||||
| chr9:37804716 | C | T | 1 | a0001c0003t0030g0045 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.539+3311C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37804716 | |||||||
| chr9:37804846 | C | A | 7 | a0001c0001t0008g0046 a0001c0001t0008g0047 a0001c0001t0008g0048 others(4): Show |
7 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.539+3441C>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37804846 | |||||||
| chr9:37804871 | G | C | 2 | a0001c0001t0020g0053 a0001c0001t0020g0054 |
2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.539+3466G>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37804871 | |||||||
| chr9:37804881 | C | T | 1 | a0001c0003t0030g0045 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.539+3476C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37804881 | |||||||
| chr9:37804957 | G | T | 1 | a0002c0007t0008g0052 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.539+3552G>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37804957 | |||||||
| chr9:37804958 | A | T | 1 | a0002c0007t0008g0052 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.539+3553A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37804958 | |||||||
| chr9:37805007 | A | G | 1 | a0001c0001t0018g0016 | 2 | HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.539+3602A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37805007 | |||||||
| chr9:37805196 | G | A | 1 | a0001c0001t0060g0018 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.539+3791G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37805196 | |||||||
| chr9:37805327 | C | CA | 4 | a0001c0001t0012g0005 a0001c0001t0012g0059 a0001c0001t0012g0060 others(1): Show |
5 | HG02647.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.539+3929dupA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37805327 | ||||||
| chr9:37805343 | G | A | 1 | a0001c0003t0030g0045 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.539+3938G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37805343 | |||||||
| chr9:37805432 | G | A | 1 | a0001c0003t0030g0045 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.539+4027G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37805432 | |||||||
| chr9:37805653 | A | G | 6 | a0001c0001t0019g0055 a0001c0001t0019g0057 a0001c0001t0020g0053 others(3): Show |
7 | HG01243.hp1 HG02486.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.539+4248A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37805653 | |||||||
| chr9:37805822 | C | T | 7 | a0001c0001t0008g0046 a0001c0001t0008g0047 a0001c0001t0008g0048 others(4): Show |
7 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.539+4417C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37805822 | |||||||
| chr9:37805954 | G | A | 29 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(26): Show |
30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.539+4549G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37805954 | |||||||
| chr9:37806009 | G | A | 29 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(26): Show |
30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.539+4604G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37806009 | |||||||
| chr9:37806028 | G | A | 17 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0075 others(14): Show |
17 | HG00621.hp2 HG02071.hp2 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.539+4623G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37806028 | |||||||
| chr9:37806094 | A | T | 4 | a0001c0001t0002g0328 a0001c0001t0002g0329 a0001c0001t0002g0330 others(1): Show |
4 | HG03942.hp2 HG04115.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.539+4689A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37806094 | |||||||
| chr9:37806248 | T | C | 49 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(46): Show |
52 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(49): Show |
intron_variant | MODIFIER | c.539+4843T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37806248 | |||||||
| chr9:37806428 | A | C | 50 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(47): Show |
53 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(50): Show |
intron_variant | MODIFIER | c.539+5023A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37806428 | |||||||
| chr9:37806465 | C | T | 49 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(46): Show |
52 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(49): Show |
intron_variant | MODIFIER | c.539+5060C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37806465 | |||||||
| chr9:37806497 | C | G | 1 | a0002c0007t0008g0052 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.539+5092C>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37806497 | |||||||
| chr9:37806580 | T | C | 29 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(26): Show |
30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.539+5175T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37806580 | |||||||
| chr9:37806633 | T | C | 2 | a0001c0001t0003g0088 a0001c0001t0003g0089 |
2 | HG00099.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.539+5228T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37806633 | |||||||
| chr9:37806894 | A | C | 4 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(1): Show |
4 | NA18968.hp1 NA18988.hp2 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.539+5489A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37806894 | |||||||
| chr9:37807061 | C | A | 50 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(47): Show |
53 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(50): Show |
intron_variant | MODIFIER | c.539+5656C>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37807061 | |||||||
| chr9:37807064 | T | C | 29 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(26): Show |
30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.539+5659T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37807064 | |||||||
| chr9:37807225 | T | G | 1 | a0001c0001t0010g0090 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.539+5820T>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37807225 | |||||||
| chr9:37807275 | T | G | 1 | a0001c0001t0004g0091 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.539+5870T>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37807275 | |||||||
| chr9:37807287 | T | C | 1 | a0001c0001t0008g0050 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.539+5882T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37807287 | |||||||
| chr9:37807570 | T | A | 1 | a0001c0001t0018g0016 | 2 | HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.539+6165T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37807570 | |||||||
| chr9:37807621 | T | C | 1 | a0001c0001t0062g0019 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.539+6216T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37807621 | |||||||
| chr9:37807653 | CTTTTCTT others(3): Show |
C | 4 | a0001c0001t0008g0046 a0001c0001t0008g0047 a0001c0001t0008g0048 others(1): Show |
4 | HG02451.hp2 HG02818.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.539+6253_539+6262d others(12): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37807653 | ||||||
| chr9:37807658 | CT | C | 279 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(276): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.539+6274delT | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37807658 | ||||||
| chr9:37807658 | CTT | C | 8 | a0001c0001t0001g0015 a0001c0001t0001g0081 a0001c0001t0001g0122 others(5): Show |
8 | HG01169.hp2 HG03209.hp2 HG04184.hp1 others(5): Show |
intron_variant | MODIFIER | c.539+6273_539+6274d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37807658 | ||||||
| chr9:37807773 | C | T | 2 | a0001c0001t0017g0326 a0001c0001t0017g0327 |
2 | NA18955.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.539+6368C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37807773 | |||||||
| chr9:37807823 | C | T | 77 | a0001c0001t0001g0263 a0001c0001t0001g0282 a0001c0001t0001g0319 others(74): Show |
80 | HG00099.hp1 HG00558.hp1 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.539+6418C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37807823 | |||||||
| chr9:37807824 | G | A | 1 | a0001c0003t0030g0045 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.539+6419G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37807824 | |||||||
| chr9:37807906 | C | G | 1 | a0001c0001t0004g0253 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.539+6501C>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37807906 | |||||||
| chr9:37808049 | A | G | 1 | a0001c0001t0001g0252 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.539+6644A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37808049 | |||||||
| chr9:37808118 | C | T | 2 | a0001c0001t0001g0014 a0001c0001t0001g0251 |
3 | HG01081.hp2 HG01243.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.539+6713C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37808118 | |||||||
| chr9:37808153 | A | G | 2 | a0001c0001t0001g0249 a0001c0001t0001g0250 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.539+6748A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37808153 | |||||||
| chr9:37808214 | A | C | 1 | a0001c0001t0002g0325 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.539+6809A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37808214 | |||||||
| chr9:37808463 | T | A | 2 | a0001c0001t0027g0020 a0001c0001t0027g0021 |
2 | NA18957.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.539+7058T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37808463 | |||||||
| chr9:37808464 | A | T | 3 | a0001c0001t0001g0013 a0001c0001t0001g0248 a0001c0001t0010g0013 |
3 | NA18943.hp1 NA18947.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.539+7059A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37808464 | |||||||
| chr9:37808473 | T | TATATATT others(25): Show |
1 | a0001c0001t0003g0093 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.539+7088_539+7119d others(34): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808473 | ||||||
| chr9:37808505 | C | T | 29 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(26): Show |
30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.539+7100C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37808505 | |||||||
| chr9:37808505 | CAT | C | 9 | a0001c0001t0019g0055 a0001c0001t0019g0057 a0001c0001t0020g0053 others(6): Show |
10 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.539+7105_539+7106d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808505 | ||||||
| chr9:37808513 | TATATA | T | 5 | a0001c0001t0002g0330 a0001c0001t0012g0005 a0001c0001t0012g0059 others(2): Show |
6 | HG02647.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.539+7114_539+7118d others(7): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808513 | ||||||
| chr9:37808524 | T | TAAATATA others(20): Show |
1 | a0001c0001t0063g0044 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.539+7119_539+7120i others(29): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37808524 | |||||||
| chr9:37808524 | T | TAAATATA others(52): Show |
28 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(25): Show |
29 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.539+7119_539+7120i others(61): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37808524 | |||||||
| chr9:37808572 | T | C | 1 | a0001c0001t0006g0254 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.539+7167T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37808572 | |||||||
| chr9:37808610 | A | AATATAAT others(31): Show |
7 | a0001c0001t0008g0046 a0001c0001t0008g0047 a0001c0001t0008g0048 others(4): Show |
7 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.539+7222_539+7223i others(40): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808610 | ||||||
| chr9:37808628 | A | T | 36 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(33): Show |
37 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.539+7223A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37808628 | |||||||
| chr9:37808637 | TA | T | 6 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0244 others(3): Show |
6 | HG02155.hp2 NA18959.hp1 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.539+7237delA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808637 | ||||||
| chr9:37808642 | A | ATATAT | 268 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0014 others(265): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.539+7238_539+7242d others(7): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808642 | ||||||
| chr9:37808642 | A | ATATATTA others(23): Show |
4 | a0001c0001t0002g0323 a0001c0001t0002g0324 a0001c0001t0004g0240 others(1): Show |
4 | HG02622.hp1 HG02965.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.539+7242_539+7243i others(32): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808642 | ||||||
| chr9:37808733 | AAT | A | 49 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(46): Show |
52 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(49): Show |
intron_variant | MODIFIER | c.539+7334_539+7335d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808733 | ||||||
| chr9:37808748 | A | ATATATAA others(138): Show |
1 | a0001c0001t0003g0093 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.539+7345_539+7346i others(147): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808748 | ||||||
| chr9:37808748 | A | ATATATAA others(157): Show |
1 | a0001c0003t0030g0045 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.539+7345_539+7346i others(166): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808748 | ||||||
| chr9:37808748 | A | ATATATAA others(148): Show |
1 | a0001c0001t0014g0165 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.539+7345_539+7346i others(157): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808748 | ||||||
| chr9:37808748 | A | ATATATAA others(153): Show |
89 | a0001c0001t0001g0014 a0001c0001t0001g0122 a0001c0001t0001g0123 others(86): Show |
93 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.539+7345_539+7346i others(162): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808748 | ||||||
| chr9:37808748 | A | ATATATAA others(155): Show |
1 | a0001c0001t0001g0238 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.539+7345_539+7346i others(164): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808748 | ||||||
| chr9:37808748 | A | ATATATAA others(155): Show |
2 | a0001c0001t0001g0013 a0001c0001t0010g0013 |
2 | NA18943.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.539+7345_539+7346i others(164): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808748 | ||||||
| chr9:37808748 | A | ATATATAA others(154): Show |
1 | a0001c0001t0001g0239 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.539+7345_539+7346i others(163): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808748 | ||||||
| chr9:37808748 | A | ATATATAA others(150): Show |
1 | a0001c0001t0002g0001 | 4 | HG00558.hp1 NA18971.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.539+7345_539+7346i others(159): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808748 | ||||||
| chr9:37808748 | A | ATATATAA others(154): Show |
1 | a0001c0001t0001g0247 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.539+7345_539+7346i others(163): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808748 | ||||||
| chr9:37808748 | A | ATATATAA others(153): Show |
2 | a0001c0001t0001g0319 a0001c0001t0002g0320 |
2 | HG02080.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.539+7345_539+7346i others(162): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808748 | ||||||
| chr9:37808748 | A | ATATATAA others(156): Show |
2 | a0001c0001t0002g0322 a0001c0001t0006g0321 |
2 | HG01978.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.539+7345_539+7346i others(165): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808748 | ||||||
| chr9:37808748 | A | ATATATAA others(154): Show |
8 | a0001c0001t0001g0006 a0001c0001t0001g0125 a0001c0001t0001g0126 others(5): Show |
9 | HG01069.hp2 HG01928.hp2 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.539+7345_539+7346i others(163): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808748 | ||||||
| chr9:37808748 | A | ATATATAA others(237): Show |
1 | a0001c0001t0008g0051 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.539+7345_539+7346i others(246): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808748 | ||||||
| chr9:37808748 | A | ATATATAA others(176): Show |
1 | a0001c0001t0005g0022 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.539+7345_539+7346i others(185): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808748 | ||||||
| chr9:37808748 | A | ATATATAA others(191): Show |
2 | a0001c0001t0005g0024 a0001c0001t0009g0023 |
2 | NA18944.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.539+7345_539+7346i others(200): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808748 | ||||||
| chr9:37808748 | A | ATATATAA others(208): Show |
4 | a0001c0001t0015g0017 a0001c0001t0015g0025 a0001c0001t0060g0018 others(1): Show |
4 | HG01123.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.539+7345_539+7346i others(217): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808748 | ||||||
| chr9:37808748 | A | ATATATAA others(207): Show |
13 | a0001c0001t0005g0026 a0001c0001t0005g0027 a0001c0001t0005g0029 others(10): Show |
13 | HG01081.hp1 HG01168.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.539+7345_539+7346i others(216): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808748 | ||||||
| chr9:37808748 | A | ATATATAA others(195): Show |
1 | a0001c0001t0063g0044 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.539+7345_539+7346i others(204): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808748 | ||||||
| chr9:37808748 | A | ATATATAA others(234): Show |
1 | a0001c0001t0008g0046 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.539+7345_539+7346i others(243): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808748 | ||||||
| chr9:37808748 | A | ATATATAA others(238): Show |
3 | a0001c0001t0008g0047 a0001c0001t0008g0048 a0001c0001t0008g0049 |
3 | HG02451.hp2 NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.539+7345_539+7346i others(247): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808748 | ||||||
| chr9:37808748 | A | ATATATAA others(77): Show |
4 | a0001c0001t0012g0005 a0001c0001t0012g0059 a0001c0001t0012g0060 others(1): Show |
5 | HG02647.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.539+7345_539+7346i others(86): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808748 | ||||||
| chr9:37808748 | A | ATATATAA others(107): Show |
9 | a0001c0001t0019g0055 a0001c0001t0019g0057 a0001c0001t0020g0053 others(6): Show |
10 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.539+7345_539+7346i others(116): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808748 | ||||||
| chr9:37808748 | A | ATATATAA others(207): Show |
1 | a0001c0001t0015g0038 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.539+7345_539+7346i others(216): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808748 | ||||||
| chr9:37808748 | A | ATATATAA others(206): Show |
7 | a0001c0001t0009g0003 a0001c0001t0009g0041 a0001c0001t0009g0042 others(4): Show |
8 | HG04184.hp2 NA18948.hp2 NA18957.hp1 others(5): Show |
intron_variant | MODIFIER | c.539+7345_539+7346i others(215): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808748 | ||||||
| chr9:37808748 | A | ATATATAA others(223): Show |
1 | a0001c0001t0008g0050 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.539+7345_539+7346i others(232): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808748 | ||||||
| chr9:37808748 | A | ATATATAA others(202): Show |
1 | a0002c0007t0008g0052 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.539+7345_539+7346i others(211): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37808748 | ||||||
| chr9:37809093 | G | GAA | 45 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(42): Show |
48 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(45): Show |
intron_variant | MODIFIER | c.539+7702_539+7703d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37809093 | ||||||
| chr9:37809124 | C | T | 2 | a0001c0001t0001g0013 a0001c0001t0010g0013 |
2 | NA18943.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.539+7719C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37809124 | |||||||
| chr9:37809394 | TA | T | 33 | a0001c0001t0001g0009 a0001c0001t0001g0066 a0001c0001t0001g0083 others(30): Show |
38 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.539+8003delA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37809394 | ||||||
| chr9:37809394 | TAA | T | 6 | a0001c0001t0008g0046 a0001c0001t0008g0047 a0001c0001t0008g0048 others(3): Show |
6 | HG02451.hp2 HG02818.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.539+8002_539+8003d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37809394 | ||||||
| chr9:37809394 | TAAAA | T | 29 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(26): Show |
30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.539+8000_539+8003d others(6): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37809394 | ||||||
| chr9:37809903 | C | T | 49 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(46): Show |
52 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(49): Show |
intron_variant | MODIFIER | c.539+8498C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37809903 | |||||||
| chr9:37809996 | C | T | 1 | a0001c0003t0030g0045 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.539+8591C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37809996 | |||||||
| chr9:37810152 | T | TA | 8 | a0001c0001t0002g0258 a0001c0001t0002g0260 a0001c0001t0006g0255 others(5): Show |
8 | HG01109.hp1 HG01361.hp2 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.539+8761dupA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37810152 | ||||||
| chr9:37810152 | TA | T | 5 | a0001c0001t0001g0082 a0001c0001t0001g0236 a0001c0001t0004g0121 others(2): Show |
6 | HG01168.hp1 HG01169.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.539+8761delA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37810152 | ||||||
| chr9:37810396 | G | T | 49 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(46): Show |
52 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(49): Show |
intron_variant | MODIFIER | c.540-8892G>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37810396 | |||||||
| chr9:37810459 | C | CTT | 28 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(25): Show |
29 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.540-8827_540-8826d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37810459 | ||||||
| chr9:37810463 | C | T | 49 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(46): Show |
52 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(49): Show |
intron_variant | MODIFIER | c.540-8825C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37810463 | |||||||
| chr9:37810467 | T | C | 88 | a0001c0001t0001g0014 a0001c0001t0001g0122 a0001c0001t0001g0123 others(85): Show |
91 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.540-8821T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37810467 | |||||||
| chr9:37810525 | A | G | 51 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(48): Show |
55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.540-8763A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37810525 | |||||||
| chr9:37810859 | C | T | 49 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(46): Show |
52 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(49): Show |
intron_variant | MODIFIER | c.540-8429C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37810859 | |||||||
| chr9:37810929 | C | G | 1 | a0001c0001t0018g0016 | 2 | HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.540-8359C>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37810929 | |||||||
| chr9:37811137 | C | G | 1 | a0001c0001t0003g0234 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.540-8151C>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37811137 | |||||||
| chr9:37811224 | C | T | 1 | a0001c0001t0008g0049 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.540-8064C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37811224 | |||||||
| chr9:37811291 | CACT | C | 29 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(26): Show |
30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.540-7994_540-7992d others(5): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37811291 | ||||||
| chr9:37811303 | G | A | 3 | a0001c0001t0014g0012 a0001c0001t0014g0165 a0001c0001t0014g0237 |
4 | HG03209.hp2 HG03540.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.540-7985G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37811303 | |||||||
| chr9:37811407 | G | A | 3 | a0001c0001t0008g0047 a0001c0001t0008g0048 a0001c0001t0008g0049 |
3 | HG02451.hp2 NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.540-7881G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37811407 | |||||||
| chr9:37811462 | T | C | 29 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(26): Show |
30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.540-7826T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37811462 | |||||||
| chr9:37811772 | GA | G | 17 | a0001c0001t0001g0009 a0001c0001t0001g0161 a0001c0001t0001g0162 others(14): Show |
19 | HG00438.hp2 HG00639.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.540-7513delA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37811772 | ||||||
| chr9:37811815 | A | G | 1 | a0001c0001t0053g0241 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.540-7473A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37811815 | |||||||
| chr9:37811956 | G | A | 1 | a0001c0001t0018g0016 | 2 | HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.540-7332G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37811956 | |||||||
| chr9:37811991 | A | G | 1 | a0001c0001t0003g0233 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.540-7297A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37811991 | |||||||
| chr9:37812169 | CCTT | C | 91 | a0001c0001t0001g0014 a0001c0001t0001g0122 a0001c0001t0001g0123 others(88): Show |
95 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.540-7116_540-7114d others(5): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37812169 | ||||||
| chr9:37812317 | A | G | 1 | a0001c0001t0007g0318 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.540-6971A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37812317 | |||||||
| chr9:37812342 | T | A | 1 | a0001c0001t0001g0263 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.540-6946T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37812342 | |||||||
| chr9:37812343 | A | T | 1 | a0001c0001t0001g0263 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.540-6945A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37812343 | |||||||
| chr9:37812561 | G | A | 76 | a0001c0001t0001g0282 a0001c0001t0001g0319 a0001c0001t0002g0001 others(73): Show |
79 | HG00099.hp1 HG00558.hp1 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.540-6727G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37812561 | |||||||
| chr9:37812612 | G | A | 13 | a0001c0001t0012g0005 a0001c0001t0012g0059 a0001c0001t0012g0060 others(10): Show |
15 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.540-6676G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37812612 | |||||||
| chr9:37812706 | T | A | 1 | a0001c0001t0001g0094 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.540-6582T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37812706 | |||||||
| chr9:37812752 | G | C | 1 | a0002c0007t0008g0052 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.540-6536G>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37812752 | |||||||
| chr9:37812792 | G | A | 1 | a0001c0001t0004g0166 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.540-6496G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37812792 | |||||||
| chr9:37812792 | G | T | 2 | a0001c0001t0001g0152 a0001c0001t0023g0153 |
2 | HG00323.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.540-6496G>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37812792 | |||||||
| chr9:37812794 | T | A | 14 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0070 others(11): Show |
17 | HG00323.hp1 HG00733.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.540-6494T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37812794 | |||||||
| chr9:37812865 | A | G | 9 | a0001c0001t0019g0055 a0001c0001t0019g0057 a0001c0001t0020g0053 others(6): Show |
10 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.540-6423A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37812865 | |||||||
| chr9:37813732 | A | G | 1 | a0002c0007t0008g0052 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.540-5556A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37813732 | |||||||
| chr9:37813735 | A | C | 1 | a0001c0001t0031g0337 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.540-5553A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37813735 | |||||||
| chr9:37814018 | A | G | 23 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0070 others(20): Show |
26 | HG00323.hp1 HG00733.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.540-5270A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37814018 | |||||||
| chr9:37814054 | T | C | 76 | a0001c0001t0001g0282 a0001c0001t0001g0319 a0001c0001t0002g0001 others(73): Show |
79 | HG00099.hp1 HG00558.hp1 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.540-5234T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37814054 | |||||||
| chr9:37814080 | C | CTA | 33 | a0001c0001t0001g0013 a0001c0001t0001g0068 a0001c0001t0001g0069 others(30): Show |
33 | HG00323.hp1 HG00741.hp1 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.540-5162_540-5161d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37814080 | ||||||
| chr9:37814080 | C | CTATA | 32 | a0001c0001t0001g0006 a0001c0001t0001g0067 a0001c0001t0001g0073 others(29): Show |
34 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.540-5164_540-5161d others(6): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37814080 | ||||||
| chr9:37814080 | C | CTATATA | 19 | a0001c0001t0001g0126 a0001c0001t0001g0147 a0001c0001t0001g0248 others(16): Show |
20 | HG00140.hp1 HG00140.hp2 HG00597.hp1 others(17): Show |
intron_variant | MODIFIER | c.540-5166_540-5161d others(8): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37814080 | ||||||
| chr9:37814080 | C | CTATATAT others(1): Show |
19 | a0001c0001t0001g0072 a0001c0001t0001g0125 a0001c0001t0001g0133 others(16): Show |
19 | HG01074.hp1 HG01099.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.540-5168_540-5161d others(10): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37814080 | ||||||
| chr9:37814080 | C | CTATATAT others(3): Show |
7 | a0001c0001t0001g0132 a0001c0001t0002g0274 a0001c0001t0003g0170 others(4): Show |
7 | HG00099.hp1 HG00438.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.540-5170_540-5161d others(12): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37814080 | ||||||
| chr9:37814080 | C | CTATATAT others(5): Show |
10 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0002g0268 others(7): Show |
10 | HG00558.hp2 HG00642.hp2 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.540-5172_540-5161d others(14): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37814080 | ||||||
| chr9:37814080 | C | CTATATAT others(7): Show |
3 | a0001c0001t0003g0167 a0001c0001t0007g0267 a0001c0001t0055g0266 |
3 | HG01071.hp2 NA18952.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.540-5174_540-5161d others(16): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37814080 | ||||||
| chr9:37814080 | C | CTATATAT others(9): Show |
1 | a0001c0001t0002g0265 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.540-5176_540-5161d others(18): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37814080 | ||||||
| chr9:37814080 | C | CTATATAT others(11): Show |
1 | a0001c0001t0045g0264 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.540-5178_540-5161d others(20): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37814080 | ||||||
| chr9:37814080 | CTA | C | 31 | a0001c0001t0001g0066 a0001c0001t0001g0076 a0001c0001t0001g0109 others(28): Show |
32 | HG00099.hp2 HG00741.hp2 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.540-5162_540-5161d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37814080 | ||||||
| chr9:37814080 | CTATA | C | 25 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0071 others(22): Show |
30 | HG00323.hp2 HG00558.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.540-5164_540-5161d others(6): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37814080 | ||||||
| chr9:37814080 | CTATATA | C | 17 | a0001c0001t0001g0002 a0001c0001t0001g0117 a0001c0001t0001g0118 others(14): Show |
20 | HG00639.hp1 HG01074.hp2 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.540-5166_540-5161d others(8): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37814080 | ||||||
| chr9:37814080 | CTATATAT others(1): Show |
C | 5 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0083 others(2): Show |
6 | HG00621.hp2 HG01243.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.540-5168_540-5161d others(10): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37814080 | ||||||
| chr9:37814080 | CTATATAT others(3): Show |
C | 10 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0227 others(7): Show |
10 | HG01516.hp2 HG01993.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.540-5170_540-5161d others(12): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37814080 | ||||||
| chr9:37814080 | CTATATAT others(5): Show |
C | 7 | a0001c0001t0001g0229 a0001c0001t0004g0228 a0001c0001t0009g0042 others(4): Show |
7 | HG02109.hp1 HG02257.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.540-5172_540-5161d others(14): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37814080 | ||||||
| chr9:37814080 | CTATATAT others(7): Show |
C | 9 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0246 others(6): Show |
9 | HG00597.hp2 HG02155.hp2 HG03491.hp1 others(6): Show |
intron_variant | MODIFIER | c.540-5174_540-5161d others(16): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37814080 | ||||||
| chr9:37814080 | CTATATAT others(9): Show |
C | 1 | a0001c0001t0032g0056 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.540-5176_540-5161d others(18): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37814080 | ||||||
| chr9:37814080 | CTATATAT others(11): Show |
C | 6 | a0001c0001t0001g0081 a0001c0001t0004g0063 a0001c0001t0013g0062 others(3): Show |
6 | HG01256.hp1 HG01258.hp2 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.540-5178_540-5161d others(20): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37814080 | ||||||
| chr9:37814080 | CTATATAT others(13): Show |
C | 8 | a0001c0001t0002g0316 a0001c0001t0004g0240 a0001c0001t0012g0005 others(5): Show |
9 | HG02055.hp1 HG02622.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.540-5180_540-5161d others(22): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37814080 | ||||||
| chr9:37814080 | CTATATAT others(19): Show |
C | 2 | a0001c0001t0006g0261 a0001c0001t0006g0262 |
2 | NA18995.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.540-5186_540-5161d others(28): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37814080 | ||||||
| chr9:37814080 | CTATATAT others(21): Show |
C | 1 | a0001c0001t0002g0317 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.540-5188_540-5161d others(30): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37814080 | ||||||
| chr9:37814080 | CTATATAT others(23): Show |
C | 1 | a0002c0007t0008g0052 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.540-5190_540-5161d others(32): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37814080 | ||||||
| chr9:37814107 | TATATATA others(10): Show |
T | 2 | a0001c0001t0005g0043 a0001c0001t0015g0025 |
2 | NA20129.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.540-5180_540-5164d others(19): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37814107 | |||||||
| chr9:37814109 | TATATATA others(8): Show |
T | 24 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(21): Show |
25 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.540-5178_540-5164d others(17): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37814109 | |||||||
| chr9:37814111 | TATATATA others(6): Show |
T | 2 | a0001c0001t0027g0020 a0001c0001t0063g0044 |
2 | HG01496.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.540-5176_540-5164d others(15): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37814111 | |||||||
| chr9:37814119 | TATATATA others(4): Show |
T | 1 | a0001c0001t0008g0046 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.540-5168_540-5158d others(13): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37814119 | |||||||
| chr9:37814119 | TATATATA others(7): Show |
T | 1 | a0001c0001t0002g0065 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.540-5168_540-5155d others(16): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37814119 | |||||||
| chr9:37814122 | A | T | 8 | a0001c0001t0009g0042 a0001c0001t0019g0055 a0001c0001t0019g0057 others(5): Show |
9 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.540-5166A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37814122 | |||||||
| chr9:37814124 | A | G | 8 | a0001c0001t0009g0042 a0001c0001t0019g0055 a0001c0001t0019g0057 others(5): Show |
9 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.540-5164A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37814124 | |||||||
| chr9:37814124 | A | T | 1 | a0001c0001t0008g0051 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.540-5164A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37814124 | |||||||
| chr9:37814125 | TATTTG | T | 3 | a0001c0001t0008g0047 a0001c0001t0008g0048 a0001c0001t0008g0049 |
3 | HG02451.hp2 NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.540-5162_540-5158d others(7): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37814125 | |||||||
| chr9:37814126 | A | G | 1 | a0001c0001t0008g0051 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.540-5162A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37814126 | |||||||
| chr9:37814126 | A | T | 37 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(34): Show |
39 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.540-5162A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37814126 | |||||||
| chr9:37814127 | T | G | 37 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(34): Show |
39 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.540-5161T>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37814127 | |||||||
| chr9:37814127 | T | TATATATA others(4): Show |
1 | a0001c0001t0002g0307 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.540-5161_540-5160i others(13): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37814127 | |||||||
| chr9:37814127 | T | TATATATA others(6): Show |
1 | a0001c0001t0018g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.540-5161_540-5160i others(15): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37814127 | |||||||
| chr9:37814127 | T | TATATATA others(4): Show |
2 | a0001c0001t0003g0199 a0001c0001t0018g0016 |
2 | HG04204.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.540-5161_540-5160i others(13): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37814127 | |||||||
| chr9:37814129 | T | A | 1 | a0001c0001t0001g0161 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.540-5159T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37814129 | |||||||
| chr9:37814130 | G | T | 1 | a0001c0001t0001g0161 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.540-5158G>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37814130 | |||||||
| chr9:37814192 | G | T | 1 | a0001c0001t0014g0165 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.540-5096G>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37814192 | |||||||
| chr9:37814201 | C | T | 1 | a0001c0001t0001g0009 | 2 | NA18986.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.540-5087C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37814201 | |||||||
| chr9:37814241 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.540-5047C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37814241 | |||||||
| chr9:37814301 | C | CT | 28 | a0001c0001t0001g0082 a0001c0001t0001g0115 a0001c0001t0001g0128 others(25): Show |
28 | HG00597.hp1 HG00621.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.540-4966dupT | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37814301 | ||||||
| chr9:37814301 | CT | C | 38 | a0001c0001t0001g0242 a0001c0001t0005g0022 a0001c0001t0005g0024 others(35): Show |
40 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.540-4966delT | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37814301 | ||||||
| chr9:37814301 | CTT | C | 6 | a0001c0001t0008g0047 a0001c0001t0008g0049 a0001c0001t0008g0050 others(3): Show |
7 | HG01496.hp2 HG02451.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.540-4967_540-4966d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37814301 | ||||||
| chr9:37814452 | A | G | 8 | a0001c0001t0008g0046 a0001c0001t0008g0047 a0001c0001t0008g0048 others(5): Show |
9 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.540-4836A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37814452 | |||||||
| chr9:37814495 | A | G | 50 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(47): Show |
54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.540-4793A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37814495 | |||||||
| chr9:37814704 | G | T | 1 | a0001c0001t0037g0223 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.540-4584G>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37814704 | |||||||
| chr9:37814722 | T | C | 50 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(47): Show |
54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.540-4566T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37814722 | |||||||
| chr9:37814876 | C | T | 92 | a0001c0001t0001g0014 a0001c0001t0001g0122 a0001c0001t0001g0123 others(89): Show |
96 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.540-4412C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37814876 | |||||||
| chr9:37814950 | T | C | 1 | a0001c0001t0040g0235 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.540-4338T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37814950 | |||||||
| chr9:37815017 | T | C | 1 | a0001c0001t0003g0172 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.540-4271T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37815017 | |||||||
| chr9:37815204 | C | G | 51 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(48): Show |
55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.540-4084C>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37815204 | |||||||
| chr9:37815306 | T | A | 3 | a0001c0001t0004g0063 a0001c0001t0013g0062 a0001c0001t0013g0064 |
3 | HG01256.hp1 HG01258.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.540-3982T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37815306 | |||||||
| chr9:37815380 | C | A | 50 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(47): Show |
54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.540-3908C>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37815380 | |||||||
| chr9:37815443 | G | A | 1 | a0001c0001t0012g0060 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.540-3845G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37815443 | |||||||
| chr9:37815517 | C | T | 1 | a0001c0001t0014g0165 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.540-3771C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37815517 | |||||||
| chr9:37815541 | A | T | 9 | a0001c0001t0019g0055 a0001c0001t0019g0057 a0001c0001t0020g0053 others(6): Show |
10 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.540-3747A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37815541 | |||||||
| chr9:37815547 | C | T | 50 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(47): Show |
54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.540-3741C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37815547 | |||||||
| chr9:37815606 | T | C | 29 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(26): Show |
30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.540-3682T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37815606 | |||||||
| chr9:37815633 | A | AAAACTCT others(3): Show |
1 | a0001c0003t0030g0045 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.540-3648_540-3647i others(12): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37815633 | ||||||
| chr9:37815649 | T | TA | 39 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(36): Show |
42 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(39): Show |
intron_variant | MODIFIER | c.540-3627dupA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37815649 | ||||||
| chr9:37815667 | A | G | 1 | a0001c0001t0018g0016 | 2 | HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.540-3621A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37815667 | |||||||
| chr9:37815711 | A | C | 15 | a0001c0001t0001g0009 a0001c0001t0001g0161 a0001c0001t0001g0162 others(12): Show |
17 | HG00438.hp2 HG00639.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.540-3577A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37815711 | |||||||
| chr9:37815719 | TAATAG | T | 9 | a0001c0001t0019g0055 a0001c0001t0019g0057 a0001c0001t0020g0053 others(6): Show |
10 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.540-3563_540-3559d others(7): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37815719 | ||||||
| chr9:37815736 | C | T | 51 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(48): Show |
55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.540-3552C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37815736 | |||||||
| chr9:37815810 | T | G | 1 | a0001c0001t0008g0049 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.540-3478T>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37815810 | |||||||
| chr9:37815883 | TC | T | 8 | a0001c0001t0008g0046 a0001c0001t0008g0047 a0001c0001t0008g0048 others(5): Show |
9 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.540-3402delC | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37815883 | ||||||
| chr9:37815926 | T | C | 1 | a0001c0001t0025g0209 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.540-3362T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37815926 | |||||||
| chr9:37815975 | G | A | 1 | a0001c0001t0003g0179 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.540-3313G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37815975 | |||||||
| chr9:37816064 | A | G | 51 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(48): Show |
55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.540-3224A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37816064 | |||||||
| chr9:37816129 | T | TA | 42 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(39): Show |
45 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(42): Show |
intron_variant | MODIFIER | c.540-3150dupA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37816129 | ||||||
| chr9:37816129 | T | TAA | 8 | a0001c0001t0008g0046 a0001c0001t0008g0047 a0001c0001t0008g0048 others(5): Show |
9 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.540-3151_540-3150d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37816129 | ||||||
| chr9:37816343 | C | A | 1 | a0001c0001t0019g0057 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.540-2945C>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37816343 | |||||||
| chr9:37816498 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.540-2790G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37816498 | |||||||
| chr9:37816590 | CA | C | 51 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(48): Show |
55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.540-2689delA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37816590 | ||||||
| chr9:37816659 | G | GGGGGGGG others(13): Show |
3 | a0001c0001t0009g0003 a0001c0001t0027g0020 a0001c0001t0027g0021 |
4 | NA18957.hp1 NA18960.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.540-2628_540-2627i others(22): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37816659 | ||||||
| chr9:37816659 | G | GGGGGGGG others(18): Show |
1 | a0001c0001t0059g0039 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.540-2628_540-2627i others(27): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37816659 | ||||||
| chr9:37816659 | G | GGGGGGGG others(7): Show |
1 | a0001c0001t0061g0036 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.540-2628_540-2627i others(16): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37816659 | ||||||
| chr9:37816659 | G | GGGGGGGG others(11): Show |
1 | a0001c0001t0015g0040 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.540-2628_540-2627i others(20): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37816659 | ||||||
| chr9:37816659 | G | GGGGGGGG others(13): Show |
2 | a0001c0001t0009g0041 a0001c0001t0009g0042 |
2 | NA18965.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.540-2628_540-2627i others(22): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37816659 | ||||||
| chr9:37816659 | G | GGGGGGTG others(7): Show |
2 | a0001c0001t0005g0026 a0001c0001t0005g0027 |
2 | NA18968.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.540-2628_540-2627i others(16): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37816659 | ||||||
| chr9:37816659 | G | GGGGGGTG others(9): Show |
2 | a0001c0001t0005g0029 a0001c0001t0009g0028 |
2 | HG04199.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.540-2628_540-2627i others(18): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37816659 | ||||||
| chr9:37816659 | G | GGGGGGTG others(11): Show |
2 | a0001c0001t0005g0030 a0001c0001t0015g0038 |
2 | HG03209.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.540-2628_540-2627i others(20): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37816659 | ||||||
| chr9:37816659 | G | GGGGGGTG others(13): Show |
4 | a0001c0001t0005g0022 a0001c0001t0005g0031 a0001c0001t0005g0032 others(1): Show |
4 | HG01515.hp1 HG02300.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.540-2628_540-2627i others(22): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37816659 | ||||||
| chr9:37816659 | G | GGGGGGTG others(15): Show |
3 | a0001c0001t0005g0037 a0001c0001t0028g0033 a0001c0001t0028g0034 |
3 | HG01081.hp1 HG01168.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.540-2628_540-2627i others(24): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37816659 | ||||||
| chr9:37816659 | G | GGGGGTGT others(10): Show |
1 | a0001c0001t0015g0017 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.540-2628_540-2627i others(19): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37816659 | ||||||
| chr9:37816659 | G | GGGGTGTG others(7): Show |
1 | a0001c0001t0009g0023 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.540-2628_540-2627i others(16): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37816659 | ||||||
| chr9:37816659 | G | GGGGTGTG others(9): Show |
1 | a0001c0001t0005g0035 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.540-2628_540-2627i others(18): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37816659 | ||||||
| chr9:37816659 | G | GGGGTGTG others(11): Show |
3 | a0001c0001t0005g0024 a0001c0001t0005g0043 a0001c0001t0063g0044 |
3 | HG01496.hp2 NA19004.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.540-2628_540-2627i others(20): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37816659 | ||||||
| chr9:37816659 | G | GGGGTGTG others(13): Show |
1 | a0001c0001t0060g0018 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.540-2628_540-2627i others(22): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37816659 | ||||||
| chr9:37816659 | G | GGGGTGTG others(21): Show |
1 | a0001c0001t0015g0025 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.540-2628_540-2627i others(30): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37816659 | ||||||
| chr9:37816659 | G | GGT | 29 | a0001c0001t0001g0014 a0001c0001t0001g0114 a0001c0001t0001g0118 others(26): Show |
32 | HG00639.hp2 HG00738.hp2 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.540-2598_540-2597d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37816659 | ||||||
| chr9:37816659 | G | GGTGT | 21 | a0001c0001t0001g0009 a0001c0001t0001g0107 a0001c0001t0001g0161 others(18): Show |
23 | HG00438.hp1 HG00438.hp2 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.540-2600_540-2597d others(6): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37816659 | ||||||
| chr9:37816659 | G | GGTGTGT | 8 | a0001c0001t0008g0046 a0001c0001t0008g0051 a0001c0001t0019g0055 others(5): Show |
8 | HG02257.hp2 HG02486.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.540-2602_540-2597d others(8): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37816659 | ||||||
| chr9:37816659 | G | GGTGTGTG others(1): Show |
5 | a0001c0001t0008g0047 a0001c0001t0008g0048 a0001c0001t0012g0005 others(2): Show |
6 | HG02451.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.540-2604_540-2597d others(10): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37816659 | ||||||
| chr9:37816659 | G | GGTGTGTG others(3): Show |
2 | a0001c0001t0008g0049 a0001c0001t0012g0059 |
2 | HG02897.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.540-2606_540-2597d others(12): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37816659 | ||||||
| chr9:37816661 | T | G | 5 | a0001c0001t0001g0139 a0001c0001t0001g0334 a0001c0001t0024g0140 others(2): Show |
5 | HG00140.hp1 HG01074.hp1 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.540-2627T>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37816661 | |||||||
| chr9:37816884 | A | G | 1 | a0001c0001t0061g0036 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.540-2404A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37816884 | |||||||
| chr9:37816930 | A | C | 7 | a0001c0001t0008g0046 a0001c0001t0008g0047 a0001c0001t0008g0048 others(4): Show |
7 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.540-2358A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37816930 | |||||||
| chr9:37816963 | C | T | 51 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(48): Show |
55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.540-2325C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37816963 | |||||||
| chr9:37817033 | T | A | 1 | a0001c0003t0030g0045 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.540-2255T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37817033 | |||||||
| chr9:37817082 | G | C | 4 | a0001c0001t0012g0005 a0001c0001t0012g0059 a0001c0001t0012g0060 others(1): Show |
5 | HG02647.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.540-2206G>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37817082 | |||||||
| chr9:37817178 | C | A | 1 | a0001c0001t0009g0041 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.540-2110C>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37817178 | |||||||
| chr9:37817198 | T | C | 1 | a0001c0001t0001g0242 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.540-2090T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37817198 | |||||||
| chr9:37817226 | C | T | 1 | a0001c0001t0002g0271 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.540-2062C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37817226 | |||||||
| chr9:37817279 | A | G | 1 | a0001c0001t0009g0041 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.540-2009A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37817279 | |||||||
| chr9:37817353 | C | A | 5 | a0001c0001t0008g0046 a0001c0001t0008g0047 a0001c0001t0008g0048 others(2): Show |
5 | HG02451.hp2 HG02818.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.540-1935C>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37817353 | |||||||
| chr9:37817467 | G | A | 1 | a0001c0001t0002g0297 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.540-1821G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37817467 | |||||||
| chr9:37817592 | CGTCTCAG others(19): Show |
C | 29 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(26): Show |
30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.540-1691_540-1666d others(28): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37817592 | ||||||
| chr9:37817593 | G | A | 4 | a0001c0001t0012g0005 a0001c0001t0012g0059 a0001c0001t0012g0060 others(1): Show |
5 | HG02647.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.540-1695G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37817593 | |||||||
| chr9:37817687 | G | A | 1 | a0001c0001t0063g0044 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.540-1601G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37817687 | |||||||
| chr9:37817717 | A | G | 29 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(26): Show |
30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.540-1571A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37817717 | |||||||
| chr9:37817738 | C | CA | 13 | a0001c0001t0012g0005 a0001c0001t0012g0059 a0001c0001t0012g0060 others(10): Show |
15 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.540-1540dupA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37817738 | ||||||
| chr9:37817904 | A | C | 50 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(47): Show |
54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.540-1384A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37817904 | |||||||
| chr9:37817935 | G | A | 51 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(48): Show |
55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.540-1353G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37817935 | |||||||
| chr9:37818037 | T | G | 50 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(47): Show |
54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.540-1251T>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37818037 | |||||||
| chr9:37818282 | C | T | 5 | a0001c0001t0002g0260 a0001c0001t0006g0255 a0001c0001t0006g0256 others(2): Show |
5 | HG01109.hp1 HG01361.hp2 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.540-1006C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37818282 | |||||||
| chr9:37818290 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.540-998G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37818290 | |||||||
| chr9:37818481 | TAATC | T | 4 | a0001c0001t0012g0005 a0001c0001t0012g0059 a0001c0001t0012g0060 others(1): Show |
5 | HG02647.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.540-804_540-801del others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37818481 | ||||||
| chr9:37818596 | C | T | 13 | a0001c0001t0012g0005 a0001c0001t0012g0059 a0001c0001t0012g0060 others(10): Show |
15 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.540-692C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37818596 | |||||||
| chr9:37818723 | T | C | 13 | a0001c0001t0012g0005 a0001c0001t0012g0059 a0001c0001t0012g0060 others(10): Show |
15 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.540-565T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37818723 | |||||||
| chr9:37818733 | G | A | 1 | a0001c0003t0030g0045 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.540-555G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37818733 | |||||||
| chr9:37819008 | T | C | 1 | a0001c0001t0001g0094 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.540-280T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37819008 | |||||||
| chr9:37819062 | G | C | 51 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(48): Show |
55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.540-226G>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37819062 | |||||||
| chr9:37819149 | A | C | 1 | a0001c0001t0008g0050 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.540-139A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | chr9 | 37819149 | |||||||
| chr9:37819178 | CA | C | 50 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(47): Show |
54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.540-99delA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 37819178 | ||||||
| chr9:37819525 | T | C | 4 | a0001c0001t0012g0005 a0001c0001t0012g0059 a0001c0001t0012g0060 others(1): Show |
5 | HG02647.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.653+124T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37819525 | |||||||
| chr9:37819684 | T | C | 2 | a0001c0001t0019g0055 a0001c0001t0019g0057 |
2 | HG02486.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.653+283T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37819684 | |||||||
| chr9:37819732 | T | A | 1 | a0001c0001t0016g0195 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.653+331T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37819732 | |||||||
| chr9:37819790 | T | C | 28 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(25): Show |
29 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.653+389T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37819790 | |||||||
| chr9:37819909 | T | G | 1 | a0001c0001t0002g0271 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.653+508T>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37819909 | |||||||
| chr9:37819996 | T | TAGG | 50 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(47): Show |
54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.653+597_653+598ins others(3): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37819996 | ||||||
| chr9:37820127 | T | C | 1 | a0002c0007t0008g0052 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.653+726T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37820127 | |||||||
| chr9:37820143 | A | G | 9 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(6): Show |
9 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.653+742A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37820143 | |||||||
| chr9:37820226 | T | A | 1 | a0001c0001t0003g0200 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.653+825T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37820226 | |||||||
| chr9:37820397 | A | G | 8 | a0001c0001t0001g0006 a0001c0001t0001g0125 a0001c0001t0001g0126 others(5): Show |
9 | HG01069.hp2 HG01928.hp2 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.653+996A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37820397 | |||||||
| chr9:37820416 | C | T | 2 | a0001c0001t0002g0283 a0001c0001t0007g0289 |
2 | HG02083.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.653+1015C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37820416 | |||||||
| chr9:37820419 | G | A | 91 | a0001c0001t0001g0014 a0001c0001t0001g0122 a0001c0001t0001g0123 others(88): Show |
95 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.653+1018G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37820419 | |||||||
| chr9:37820464 | T | A | 6 | a0001c0001t0019g0055 a0001c0001t0019g0057 a0001c0001t0020g0053 others(3): Show |
7 | HG01243.hp1 HG02486.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.653+1063T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37820464 | |||||||
| chr9:37820515 | A | C | 1 | a0001c0001t0008g0051 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.653+1114A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37820515 | |||||||
| chr9:37820528 | A | G | 1 | a0001c0001t0018g0016 | 2 | HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.653+1127A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37820528 | |||||||
| chr9:37820691 | G | A | 29 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(26): Show |
30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.653+1290G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37820691 | |||||||
| chr9:37820795 | A | G | 71 | a0001c0001t0001g0282 a0001c0001t0001g0319 a0001c0001t0002g0001 others(68): Show |
74 | HG00099.hp1 HG00558.hp1 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.653+1394A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37820795 | |||||||
| chr9:37820820 | A | G | 1 | a0001c0001t0017g0080 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.653+1419A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37820820 | |||||||
| chr9:37820829 | C | T | 87 | a0001c0001t0001g0014 a0001c0001t0001g0122 a0001c0001t0001g0123 others(84): Show |
90 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.653+1428C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37820829 | |||||||
| chr9:37821090 | C | CAT | 12 | a0001c0001t0001g0282 a0001c0001t0004g0240 a0001c0001t0007g0267 others(9): Show |
13 | HG02622.hp1 HG02965.hp2 HG02976.hp2 others(10): Show |
intron_variant | MODIFIER | c.653+1703_653+1704d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37821090 | ||||||
| chr9:37821090 | C | CATATAT | 10 | a0001c0001t0019g0055 a0001c0001t0019g0057 a0001c0001t0020g0053 others(7): Show |
11 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.653+1699_653+1704d others(8): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37821090 | ||||||
| chr9:37821090 | C | CATATATA others(1): Show |
4 | a0001c0001t0008g0046 a0001c0001t0008g0047 a0001c0001t0008g0048 others(1): Show |
4 | HG02451.hp2 HG02818.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.653+1697_653+1704d others(10): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37821090 | ||||||
| chr9:37821090 | C | CATATATA others(3): Show |
2 | a0001c0001t0008g0051 a0001c0001t0063g0044 |
2 | HG01496.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.653+1695_653+1704d others(12): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37821090 | ||||||
| chr9:37821090 | C | CATATATA others(11): Show |
1 | a0001c0001t0008g0050 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.653+1704_653+1705i others(20): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37821090 | ||||||
| chr9:37821090 | CAT | C | 90 | a0001c0001t0001g0014 a0001c0001t0001g0122 a0001c0001t0001g0123 others(87): Show |
94 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.653+1703_653+1704d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37821090 | ||||||
| chr9:37821097 | A | G | 1 | a0001c0001t0002g0258 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.653+1696A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37821097 | |||||||
| chr9:37821104 | T | TATATAC | 28 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(25): Show |
29 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.653+1704_653+1705i others(8): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37821104 | ||||||
| chr9:37821106 | C | T | 10 | a0001c0001t0008g0046 a0001c0001t0008g0047 a0001c0001t0008g0048 others(7): Show |
12 | HG02451.hp2 HG02647.hp2 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.653+1705C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37821106 | |||||||
| chr9:37821125 | A | G | 1 | a0001c0001t0001g0069 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.653+1724A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37821125 | |||||||
| chr9:37821164 | T | C | 9 | a0001c0001t0019g0055 a0001c0001t0019g0057 a0001c0001t0020g0053 others(6): Show |
10 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.653+1763T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37821164 | |||||||
| chr9:37821179 | C | T | 50 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(47): Show |
54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.653+1778C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37821179 | |||||||
| chr9:37821674 | T | A | 1 | a0001c0001t0002g0298 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.653+2273T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37821674 | |||||||
| chr9:37821675 | A | T | 2 | a0001c0001t0004g0240 a0001c0001t0053g0241 |
2 | HG02622.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.653+2274A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37821675 | |||||||
| chr9:37822072 | G | A | 50 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(47): Show |
54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.653+2671G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37822072 | |||||||
| chr9:37822073 | C | T | 13 | a0001c0001t0012g0005 a0001c0001t0012g0059 a0001c0001t0012g0060 others(10): Show |
15 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.653+2672C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37822073 | |||||||
| chr9:37822074 | C | T | 1 | a0001c0003t0030g0045 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.653+2673C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37822074 | |||||||
| chr9:37822268 | A | G | 29 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(26): Show |
30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.653+2867A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37822268 | |||||||
| chr9:37822317 | G | C | 9 | a0001c0001t0019g0055 a0001c0001t0019g0057 a0001c0001t0020g0053 others(6): Show |
10 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.653+2916G>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37822317 | |||||||
| chr9:37822353 | C | T | 1 | a0001c0001t0002g0297 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.653+2952C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37822353 | |||||||
| chr9:37822404 | G | GAT | 16 | a0001c0001t0001g0014 a0001c0001t0001g0067 a0001c0001t0001g0078 others(13): Show |
17 | HG00621.hp2 HG01081.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.653+3040_653+3041d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37822404 | ||||||
| chr9:37822404 | G | GATAT | 9 | a0001c0001t0001g0068 a0001c0001t0001g0081 a0001c0001t0001g0087 others(6): Show |
9 | HG02132.hp2 HG02280.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.653+3038_653+3041d others(6): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37822404 | ||||||
| chr9:37822404 | G | GATATAT | 5 | a0001c0001t0001g0069 a0001c0001t0001g0084 a0001c0001t0001g0086 others(2): Show |
5 | HG02055.hp2 HG02897.hp1 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.653+3036_653+3041d others(8): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37822404 | ||||||
| chr9:37822404 | G | GATATATA others(1): Show |
5 | a0001c0001t0003g0190 a0001c0001t0003g0198 a0001c0001t0003g0201 others(2): Show |
5 | HG00642.hp1 HG02129.hp1 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.653+3034_653+3041d others(10): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37822404 | ||||||
| chr9:37822404 | G | GATATATA others(3): Show |
4 | a0001c0001t0001g0085 a0001c0001t0003g0175 a0001c0001t0003g0197 others(1): Show |
4 | HG03710.hp2 HG03942.hp1 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.653+3032_653+3041d others(12): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37822404 | ||||||
| chr9:37822404 | G | GATATATA others(5): Show |
2 | a0001c0001t0003g0193 a0001c0002t0004g0215 |
2 | HG01192.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.653+3030_653+3041d others(14): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37822404 | ||||||
| chr9:37822404 | G | GATATATA others(7): Show |
4 | a0001c0001t0003g0170 a0001c0001t0003g0174 a0001c0001t0003g0182 others(1): Show |
4 | HG01981.hp1 HG02602.hp2 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.653+3028_653+3041d others(16): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37822404 | ||||||
| chr9:37822404 | G | GATATATA others(9): Show |
7 | a0001c0001t0003g0173 a0001c0001t0003g0181 a0001c0001t0003g0183 others(4): Show |
7 | HG00621.hp1 HG01975.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.653+3026_653+3041d others(18): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37822404 | ||||||
| chr9:37822404 | G | GATATATA others(11): Show |
5 | a0001c0001t0003g0089 a0001c0001t0003g0179 a0001c0001t0003g0196 others(2): Show |
5 | HG00099.hp2 HG00438.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.653+3024_653+3041d others(20): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37822404 | ||||||
| chr9:37822404 | G | GATATATA others(13): Show |
5 | a0001c0001t0003g0088 a0001c0001t0003g0167 a0001c0001t0003g0200 others(2): Show |
5 | HG00738.hp1 HG01071.hp2 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.653+3022_653+3041d others(22): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37822404 | ||||||
| chr9:37822404 | G | GATATATA others(15): Show |
4 | a0001c0001t0003g0093 a0001c0001t0003g0180 a0001c0001t0037g0223 others(1): Show |
4 | HG01361.hp1 HG02135.hp1 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.653+3020_653+3041d others(24): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37822404 | ||||||
| chr9:37822404 | G | GATATATA others(17): Show |
3 | a0001c0001t0003g0230 a0001c0001t0003g0231 a0001c0001t0003g0234 |
3 | HG03491.hp1 HG03492.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.653+3018_653+3041d others(26): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37822404 | ||||||
| chr9:37822404 | GAT | G | 12 | a0001c0001t0001g0101 a0001c0001t0001g0105 a0001c0001t0001g0114 others(9): Show |
12 | HG01123.hp1 HG01257.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.653+3040_653+3041d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37822404 | ||||||
| chr9:37822404 | GATAT | G | 39 | a0001c0001t0001g0006 a0001c0001t0001g0070 a0001c0001t0001g0073 others(36): Show |
40 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.653+3038_653+3041d others(6): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37822404 | ||||||
| chr9:37822404 | GATATAT | G | 37 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0066 others(34): Show |
40 | HG00323.hp1 HG00741.hp2 HG01168.hp2 others(37): Show |
intron_variant | MODIFIER | c.653+3036_653+3041d others(8): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37822404 | ||||||
| chr9:37822404 | GATATATA others(1): Show |
G | 5 | a0001c0001t0002g0065 a0001c0001t0002g0283 a0001c0001t0002g0290 others(2): Show |
5 | HG02165.hp1 HG02523.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.653+3034_653+3041d others(10): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37822404 | ||||||
| chr9:37822404 | GATATATA others(3): Show |
G | 17 | a0001c0001t0002g0273 a0001c0001t0002g0276 a0001c0001t0002g0295 others(14): Show |
17 | HG01255.hp1 HG01516.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.653+3032_653+3041d others(12): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37822404 | ||||||
| chr9:37822404 | GATATATA others(5): Show |
G | 56 | a0001c0001t0001g0282 a0001c0001t0001g0319 a0001c0001t0002g0001 others(53): Show |
59 | HG00099.hp1 HG00558.hp1 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.653+3030_653+3041d others(14): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37822404 | ||||||
| chr9:37822404 | GATATATA others(7): Show |
G | 21 | a0001c0001t0001g0009 a0001c0001t0001g0161 a0001c0001t0001g0162 others(18): Show |
24 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.653+3028_653+3041d others(16): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37822404 | ||||||
| chr9:37822404 | GATATATA others(13): Show |
G | 9 | a0001c0001t0003g0011 a0001c0001t0003g0202 a0001c0001t0003g0207 others(6): Show |
10 | HG00639.hp1 HG01074.hp2 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.653+3022_653+3041d others(22): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37822404 | ||||||
| chr9:37822404 | GATATATA others(19): Show |
G | 50 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(47): Show |
54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.653+3016_653+3041d others(28): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37822404 | ||||||
| chr9:37822576 | T | C | 1 | a0001c0001t0061g0036 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.653+3175T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37822576 | |||||||
| chr9:37822605 | G | T | 5 | a0001c0001t0004g0178 a0001c0001t0023g0213 a0001c0002t0004g0214 others(2): Show |
5 | HG01109.hp2 HG02280.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.653+3204G>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37822605 | |||||||
| chr9:37822638 | A | C | 37 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(34): Show |
39 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.653+3237A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37822638 | |||||||
| chr9:37822734 | T | C | 51 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(48): Show |
55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.653+3333T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37822734 | |||||||
| chr9:37822762 | G | A | 51 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(48): Show |
55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.653+3361G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37822762 | |||||||
| chr9:37822911 | T | G | 2 | a0001c0001t0003g0088 a0001c0001t0003g0089 |
2 | HG00099.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.653+3510T>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37822911 | |||||||
| chr9:37822941 | T | G | 1 | a0001c0001t0009g0028 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.653+3540T>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37822941 | |||||||
| chr9:37822964 | C | T | 1 | a0001c0001t0061g0036 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.653+3563C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37822964 | |||||||
| chr9:37823248 | A | G | 2 | a0001c0001t0002g0274 a0001c0001t0002g0307 |
2 | HG00099.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.653+3847A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37823248 | |||||||
| chr9:37823540 | T | C | 4 | a0001c0001t0012g0005 a0001c0001t0012g0059 a0001c0001t0012g0060 others(1): Show |
5 | HG02647.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.653+4139T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37823540 | |||||||
| chr9:37823586 | G | A | 29 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(26): Show |
30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.653+4185G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37823586 | |||||||
| chr9:37823589 | G | GT | 37 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(34): Show |
40 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.653+4195dupT | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37823589 | ||||||
| chr9:37823596 | T | TTG | 13 | a0001c0001t0008g0046 a0001c0001t0008g0047 a0001c0001t0008g0048 others(10): Show |
14 | HG01243.hp1 HG02257.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.653+4195_653+4196i others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37823596 | |||||||
| chr9:37823599 | C | G | 51 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(48): Show |
55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.653+4198C>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37823599 | |||||||
| chr9:37823600 | G | A | 1 | a0001c0001t0003g0093 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.653+4199G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37823600 | |||||||
| chr9:37823699 | T | C | 1 | a0001c0001t0003g0199 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.653+4298T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37823699 | |||||||
| chr9:37823876 | C | CT | 19 | a0001c0001t0001g0070 a0001c0001t0001g0073 a0001c0001t0002g0281 others(16): Show |
19 | HG00733.hp1 HG01978.hp2 HG02071.hp2 others(16): Show |
intron_variant | MODIFIER | c.653+4497dupT | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37823876 | ||||||
| chr9:37823876 | CT | C | 20 | a0001c0001t0001g0009 a0001c0001t0001g0069 a0001c0001t0001g0134 others(17): Show |
22 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(19): Show |
intron_variant | MODIFIER | c.653+4497delT | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37823876 | ||||||
| chr9:37823919 | TGCCCAGG others(15): Show |
T | 1 | a0001c0001t0005g0027 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.653+4520_653+4541d others(24): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37823919 | ||||||
| chr9:37824062 | G | A | 50 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(47): Show |
54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.653+4661G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37824062 | |||||||
| chr9:37824083 | G | A | 12 | a0001c0001t0016g0194 a0001c0001t0016g0195 a0001c0001t0016g0212 others(9): Show |
13 | HG00741.hp1 HG01106.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.653+4682G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37824083 | |||||||
| chr9:37824170 | C | T | 1 | a0001c0001t0020g0054 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.653+4769C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37824170 | |||||||
| chr9:37824182 | T | C | 13 | a0001c0001t0012g0005 a0001c0001t0012g0059 a0001c0001t0012g0060 others(10): Show |
15 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.653+4781T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37824182 | |||||||
| chr9:37824306 | G | A | 13 | a0001c0001t0012g0005 a0001c0001t0012g0059 a0001c0001t0012g0060 others(10): Show |
15 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.653+4905G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37824306 | |||||||
| chr9:37824320 | A | C | 1 | a0001c0003t0030g0045 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.653+4919A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37824320 | |||||||
| chr9:37824420 | T | C | 8 | a0001c0001t0008g0046 a0001c0001t0008g0047 a0001c0001t0008g0048 others(5): Show |
9 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.653+5019T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37824420 | |||||||
| chr9:37824508 | A | G | 1 | a0001c0001t0002g0271 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.653+5107A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37824508 | |||||||
| chr9:37824554 | TA | T | 29 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(26): Show |
30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.653+5165delA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37824554 | ||||||
| chr9:37824728 | T | G | 51 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(48): Show |
55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.653+5327T>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37824728 | |||||||
| chr9:37824939 | A | G | 1 | a0001c0001t0018g0016 | 2 | HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.653+5538A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37824939 | |||||||
| chr9:37825014 | C | A | 1 | a0001c0001t0002g0325 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.653+5613C>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825014 | |||||||
| chr9:37825036 | T | C | 1 | a0001c0001t0002g0325 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.653+5635T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825036 | |||||||
| chr9:37825179 | G | C | 1 | a0001c0001t0002g0290 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.653+5778G>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825179 | |||||||
| chr9:37825181 | G | A | 1 | a0001c0001t0002g0290 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.653+5780G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825181 | |||||||
| chr9:37825190 | T | A | 1 | a0001c0001t0002g0290 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.653+5789T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825190 | |||||||
| chr9:37825194 | A | T | 1 | a0001c0001t0002g0290 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.653+5793A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825194 | |||||||
| chr9:37825197 | C | G | 1 | a0001c0001t0002g0290 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.653+5796C>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825197 | |||||||
| chr9:37825200 | A | G | 1 | a0001c0001t0002g0290 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.653+5799A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825200 | |||||||
| chr9:37825203 | A | C | 1 | a0001c0001t0002g0290 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.653+5802A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825203 | |||||||
| chr9:37825204 | A | T | 1 | a0001c0001t0002g0290 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.653+5803A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825204 | |||||||
| chr9:37825205 | C | A | 1 | a0001c0001t0002g0290 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.653+5804C>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825205 | |||||||
| chr9:37825207 | A | T | 1 | a0001c0001t0002g0290 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.653+5806A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825207 | |||||||
| chr9:37825208 | C | T | 1 | a0001c0001t0002g0290 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.653+5807C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825208 | |||||||
| chr9:37825213 | A | T | 1 | a0001c0001t0002g0290 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.653+5812A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825213 | |||||||
| chr9:37825214 | T | C | 1 | a0001c0001t0002g0290 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.653+5813T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825214 | |||||||
| chr9:37825221 | C | A | 1 | a0001c0001t0002g0290 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.653+5820C>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825221 | |||||||
| chr9:37825228 | C | T | 2 | a0001c0001t0005g0024 a0001c0001t0009g0023 |
2 | NA18944.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.653+5827C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825228 | |||||||
| chr9:37825232 | T | G | 1 | a0001c0001t0002g0290 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.653+5831T>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825232 | |||||||
| chr9:37825235 | C | T | 1 | a0001c0001t0002g0290 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.653+5834C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825235 | |||||||
| chr9:37825238 | G | T | 1 | a0001c0001t0002g0290 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.653+5837G>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825238 | |||||||
| chr9:37825241 | A | C | 1 | a0001c0001t0002g0290 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.653+5840A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825241 | |||||||
| chr9:37825243 | A | T | 1 | a0001c0001t0002g0290 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.653+5842A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825243 | |||||||
| chr9:37825245 | A | T | 1 | a0001c0001t0002g0290 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.653+5844A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825245 | |||||||
| chr9:37825246 | C | T | 1 | a0001c0001t0002g0290 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.653+5845C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825246 | |||||||
| chr9:37825249 | A | T | 1 | a0001c0001t0002g0290 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.653+5848A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825249 | |||||||
| chr9:37825250 | A | C | 1 | a0001c0001t0002g0290 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.653+5849A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825250 | |||||||
| chr9:37825251 | A | C | 1 | a0001c0001t0002g0290 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.653+5850A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825251 | |||||||
| chr9:37825257 | A | C | 1 | a0001c0001t0002g0290 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.653+5856A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825257 | |||||||
| chr9:37825280 | C | T | 1 | a0001c0001t0002g0290 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.653+5879C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825280 | |||||||
| chr9:37825281 | A | T | 1 | a0001c0001t0002g0290 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.653+5880A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825281 | |||||||
| chr9:37825344 | T | C | 1 | a0001c0001t0003g0217 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.653+5943T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825344 | |||||||
| chr9:37825565 | C | T | 3 | a0001c0001t0022g0335 a0001c0001t0022g0336 a0001c0001t0031g0337 |
3 | HG02257.hp2 HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.653+6164C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825565 | |||||||
| chr9:37825705 | A | G | 1 | a0001c0001t0014g0012 | 2 | HG03209.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.653+6304A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825705 | |||||||
| chr9:37825860 | A | G | 1 | a0001c0001t0004g0121 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.653+6459A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825860 | |||||||
| chr9:37825903 | C | T | 1 | a0001c0001t0015g0017 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.653+6502C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825903 | |||||||
| chr9:37825904 | G | A | 1 | a0001c0001t0026g0007 | 2 | HG00639.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.653+6503G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825904 | |||||||
| chr9:37825912 | G | A | 29 | a0001c0001t0001g0014 a0001c0001t0001g0122 a0001c0001t0001g0123 others(26): Show |
31 | HG00140.hp2 HG00323.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.653+6511G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825912 | |||||||
| chr9:37825913 | T | G | 15 | a0001c0001t0001g0009 a0001c0001t0001g0161 a0001c0001t0001g0162 others(12): Show |
17 | HG00438.hp2 HG00639.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.653+6512T>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825913 | |||||||
| chr9:37825928 | A | G | 51 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(48): Show |
55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.653+6527A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825928 | |||||||
| chr9:37825992 | G | A | 50 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(47): Show |
54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.653+6591G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37825992 | |||||||
| chr9:37826003 | C | A | 1 | a0001c0001t0001g0247 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.653+6602C>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37826003 | |||||||
| chr9:37826014 | G | A | 51 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(48): Show |
55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.653+6613G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37826014 | |||||||
| chr9:37826039 | GA | G | 45 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(42): Show |
48 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(45): Show |
intron_variant | MODIFIER | c.653+6650delA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37826039 | ||||||
| chr9:37826051 | A | G | 1 | a0001c0001t0005g0027 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.653+6650A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37826051 | |||||||
| chr9:37826052 | G | T | 1 | a0001c0001t0005g0027 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.653+6651G>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37826052 | |||||||
| chr9:37826055 | T | A | 1 | a0001c0001t0005g0027 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.653+6654T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37826055 | |||||||
| chr9:37826076 | T | TA | 15 | a0001c0001t0001g0009 a0001c0001t0001g0161 a0001c0001t0001g0162 others(12): Show |
17 | HG00438.hp2 HG00639.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.653+6687dupA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37826076 | ||||||
| chr9:37826076 | TA | T | 51 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(48): Show |
55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.653+6687delA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37826076 | ||||||
| chr9:37826221 | T | C | 4 | a0001c0001t0003g0011 a0001c0001t0003g0207 a0001c0001t0003g0221 others(1): Show |
5 | HG01928.hp1 HG01993.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.653+6820T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37826221 | |||||||
| chr9:37826288 | G | A | 50 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(47): Show |
54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.653+6887G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37826288 | |||||||
| chr9:37826294 | A | G | 1 | a0001c0001t0036g0151 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.653+6893A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37826294 | |||||||
| chr9:37826422 | A | G | 29 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(26): Show |
30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.653+7021A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37826422 | |||||||
| chr9:37826580 | C | T | 8 | a0001c0001t0008g0046 a0001c0001t0008g0047 a0001c0001t0008g0048 others(5): Show |
9 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.653+7179C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37826580 | |||||||
| chr9:37826614 | C | T | 6 | a0001c0001t0008g0046 a0001c0001t0008g0047 a0001c0001t0008g0048 others(3): Show |
6 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.653+7213C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37826614 | |||||||
| chr9:37826820 | C | CT | 11 | a0001c0001t0001g0081 a0001c0001t0001g0083 a0001c0001t0001g0097 others(8): Show |
11 | HG02135.hp1 HG02135.hp2 NA18747.hp2 others(8): Show |
intron_variant | MODIFIER | c.653+7441dupT | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37826820 | ||||||
| chr9:37826820 | CTT | C | 36 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(33): Show |
38 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(35): Show |
intron_variant | MODIFIER | c.653+7440_653+7441d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37826820 | ||||||
| chr9:37826820 | CTTT | C | 5 | a0001c0001t0012g0005 a0001c0001t0012g0059 a0001c0001t0012g0060 others(2): Show |
6 | HG02647.hp2 HG02717.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.653+7439_653+7441d others(5): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37826820 | ||||||
| chr9:37826820 | CTTTT | C | 9 | a0001c0001t0019g0055 a0001c0001t0019g0057 a0001c0001t0020g0053 others(6): Show |
10 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.653+7438_653+7441d others(6): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37826820 | ||||||
| chr9:37826878 | A | T | 51 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(48): Show |
55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.653+7477A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37826878 | |||||||
| chr9:37826895 | G | A | 1 | a0001c0001t0001g0162 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.653+7494G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37826895 | |||||||
| chr9:37827240 | T | C | 2 | a0001c0001t0001g0152 a0001c0001t0023g0153 |
2 | HG00323.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.653+7839T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37827240 | |||||||
| chr9:37827320 | A | G | 2 | a0001c0001t0003g0221 a0001c0001t0003g0226 |
2 | HG01928.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.653+7919A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37827320 | |||||||
| chr9:37827771 | G | A | 1 | a0001c0001t0003g0172 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.653+8370G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37827771 | |||||||
| chr9:37827886 | C | CTTATT | 3 | a0001c0001t0004g0091 a0001c0001t0014g0237 a0001c0001t0018g0016 |
4 | HG02976.hp2 NA19043.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.653+8499_653+8503d others(7): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37827886 | ||||||
| chr9:37827886 | C | CTTATTTT others(3): Show |
1 | a0001c0001t0014g0165 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.653+8494_653+8503d others(12): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37827886 | ||||||
| chr9:37828223 | G | A | 49 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(46): Show |
53 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(50): Show |
intron_variant | MODIFIER | c.653+8822G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37828223 | |||||||
| chr9:37828327 | ACAAATAT others(35): Show |
A | 2 | a0001c0001t0001g0070 a0001c0001t0001g0071 |
2 | HG00733.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.653+8928_653+8969d others(44): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37828327 | ||||||
| chr9:37828452 | G | GA | 13 | a0001c0001t0012g0005 a0001c0001t0012g0059 a0001c0001t0012g0060 others(10): Show |
15 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.653+9057dupA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37828452 | ||||||
| chr9:37828458 | AG | A | 6 | a0001c0001t0008g0046 a0001c0001t0008g0047 a0001c0001t0008g0048 others(3): Show |
6 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.653+9058delG | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37828458 | |||||||
| chr9:37828459 | G | A | 45 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(42): Show |
49 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(46): Show |
intron_variant | MODIFIER | c.653+9058G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37828459 | |||||||
| chr9:37828758 | C | G | 51 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(48): Show |
55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.653+9357C>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37828758 | |||||||
| chr9:37829221 | C | G | 1 | a0001c0001t0005g0030 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.653+9820C>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37829221 | |||||||
| chr9:37829231 | G | C | 1 | a0001c0001t0004g0091 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.653+9830G>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37829231 | |||||||
| chr9:37829266 | C | T | 1 | a0001c0001t0008g0050 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.653+9865C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37829266 | |||||||
| chr9:37829269 | G | A | 13 | a0001c0001t0012g0005 a0001c0001t0012g0059 a0001c0001t0012g0060 others(10): Show |
15 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.653+9868G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37829269 | |||||||
| chr9:37829296 | C | T | 1 | a0001c0001t0007g0267 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.653+9895C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37829296 | |||||||
| chr9:37829306 | C | G | 51 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(48): Show |
55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.653+9905C>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37829306 | |||||||
| chr9:37829365 | G | A | 4 | a0001c0001t0012g0005 a0001c0001t0012g0059 a0001c0001t0012g0060 others(1): Show |
5 | HG02647.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.653+9964G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37829365 | |||||||
| chr9:37829368 | A | G | 1 | a0001c0001t0008g0050 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.653+9967A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37829368 | |||||||
| chr9:37829380 | C | T | 1 | a0001c0001t0003g0234 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.653+9979C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37829380 | |||||||
| chr9:37829603 | C | T | 6 | a0001c0001t0019g0055 a0001c0001t0019g0057 a0001c0001t0020g0053 others(3): Show |
7 | HG01243.hp1 HG02486.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.653+10202C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37829603 | |||||||
| chr9:37829734 | T | C | 1 | a0001c0001t0003g0201 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.653+10333T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37829734 | |||||||
| chr9:37829740 | C | T | 1 | a0001c0003t0030g0045 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.653+10339C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37829740 | |||||||
| chr9:37829796 | C | G | 3 | a0001c0001t0004g0176 a0001c0001t0004g0208 a0001c0001t0004g0232 |
3 | HG00597.hp2 NA18951.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.653+10395C>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37829796 | |||||||
| chr9:37829807 | G | C | 8 | a0001c0001t0008g0046 a0001c0001t0008g0047 a0001c0001t0008g0048 others(5): Show |
9 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.653+10406G>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37829807 | |||||||
| chr9:37829889 | C | T | 1 | a0001c0003t0030g0045 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.653+10488C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37829889 | |||||||
| chr9:37829949 | G | C | 1 | a0001c0001t0001g0002 | 3 | HG02735.hp2 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.653+10548G>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37829949 | |||||||
| chr9:37830091 | TAGAG | T | 52 | a0001c0001t0002g0273 a0001c0001t0002g0276 a0001c0001t0002g0295 others(49): Show |
55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.653+10694_653+1069 others(8): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37830091 | ||||||
| chr9:37830143 | T | G | 5 | a0001c0001t0004g0178 a0001c0001t0023g0213 a0001c0002t0004g0214 others(2): Show |
5 | HG01109.hp2 HG02280.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.653+10742T>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37830143 | |||||||
| chr9:37830213 | T | A | 5 | a0001c0001t0008g0046 a0001c0001t0008g0047 a0001c0001t0008g0048 others(2): Show |
5 | HG02451.hp2 HG02818.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.653+10812T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37830213 | |||||||
| chr9:37830554 | C | T | 51 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(48): Show |
55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.653+11153C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37830554 | |||||||
| chr9:37830636 | G | T | 1 | a0001c0003t0030g0045 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.653+11235G>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37830636 | |||||||
| chr9:37831095 | C | T | 5 | a0001c0001t0002g0273 a0001c0001t0002g0276 a0001c0001t0002g0295 others(2): Show |
5 | HG01255.hp1 HG01891.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.654-10994C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37831095 | |||||||
| chr9:37831101 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.654-10988C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37831101 | |||||||
| chr9:37831131 | C | T | 52 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(49): Show |
56 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(53): Show |
intron_variant | MODIFIER | c.654-10958C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37831131 | |||||||
| chr9:37831215 | TC | T | 4 | a0001c0001t0012g0005 a0001c0001t0012g0059 a0001c0001t0012g0060 others(1): Show |
5 | HG02647.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.654-10873delC | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37831215 | |||||||
| chr9:37831216 | C | CA | 29 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(26): Show |
30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.654-10864dupA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37831216 | ||||||
| chr9:37831241 | A | G | 51 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(48): Show |
55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.654-10848A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37831241 | |||||||
| chr9:37831365 | T | A | 1 | a0001c0003t0030g0045 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.654-10724T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37831365 | |||||||
| chr9:37831366 | C | T | 1 | a0001c0003t0030g0045 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.654-10723C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37831366 | |||||||
| chr9:37831559 | G | A | 29 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(26): Show |
30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.654-10530G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37831559 | |||||||
| chr9:37831727 | T | C | 3 | a0001c0001t0022g0335 a0001c0001t0022g0336 a0001c0001t0031g0337 |
3 | HG02257.hp2 HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.654-10362T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37831727 | |||||||
| chr9:37831823 | T | C | 51 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(48): Show |
55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.654-10266T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37831823 | |||||||
| chr9:37832108 | C | G | 1 | a0002c0007t0008g0052 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.654-9981C>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37832108 | |||||||
| chr9:37832150 | A | T | 1 | a0001c0001t0001g0263 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.654-9939A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37832150 | |||||||
| chr9:37832150 | AAAT | A | 86 | a0001c0001t0001g0014 a0001c0001t0001g0122 a0001c0001t0001g0123 others(83): Show |
90 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.654-9929_654-9927d others(5): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37832150 | ||||||
| chr9:37832153 | T | A | 1 | a0001c0003t0030g0045 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.654-9936T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37832153 | |||||||
| chr9:37832195 | T | C | 18 | a0001c0001t0003g0093 a0001c0001t0003g0170 a0001c0001t0003g0173 others(15): Show |
18 | HG00621.hp1 HG01192.hp1 HG01975.hp1 others(15): Show |
intron_variant | MODIFIER | c.654-9894T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37832195 | |||||||
| chr9:37832223 | C | T | 4 | a0001c0001t0020g0053 a0001c0001t0020g0054 a0001c0001t0021g0004 others(1): Show |
5 | HG01243.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.654-9866C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37832223 | |||||||
| chr9:37832233 | G | A | 1 | a0001c0003t0030g0045 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.654-9856G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37832233 | |||||||
| chr9:37832261 | C | T | 1 | a0001c0001t0009g0028 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.654-9828C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37832261 | |||||||
| chr9:37832303 | C | G | 1 | a0001c0001t0018g0016 | 2 | HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.654-9786C>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37832303 | |||||||
| chr9:37832327 | G | A | 3 | a0001c0001t0022g0335 a0001c0001t0022g0336 a0001c0001t0031g0337 |
3 | HG02257.hp2 HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.654-9762G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37832327 | |||||||
| chr9:37832415 | G | A | 18 | a0001c0001t0002g0277 a0001c0001t0002g0281 a0001c0001t0002g0283 others(15): Show |
18 | HG01516.hp1 HG01978.hp2 HG02083.hp1 others(15): Show |
intron_variant | MODIFIER | c.654-9674G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37832415 | |||||||
| chr9:37832458 | C | CA | 10 | a0001c0001t0018g0016 a0001c0001t0019g0055 a0001c0001t0019g0057 others(7): Show |
12 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.654-9616dupA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37832458 | ||||||
| chr9:37832789 | C | T | 50 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(47): Show |
54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.654-9300C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37832789 | |||||||
| chr9:37832872 | T | C | 8 | a0001c0001t0008g0046 a0001c0001t0008g0047 a0001c0001t0008g0048 others(5): Show |
9 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.654-9217T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37832872 | |||||||
| chr9:37832879 | TTTTTTG | T | 13 | a0001c0001t0012g0005 a0001c0001t0012g0059 a0001c0001t0012g0060 others(10): Show |
15 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.654-9192_654-9187d others(8): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37832879 | ||||||
| chr9:37832957 | T | C | 1 | a0001c0001t0018g0016 | 2 | HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.654-9132T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37832957 | |||||||
| chr9:37833069 | T | A | 1 | a0001c0001t0004g0091 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.654-9020T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37833069 | |||||||
| chr9:37833298 | C | T | 1 | a0001c0001t0063g0044 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.654-8791C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37833298 | |||||||
| chr9:37833784 | A | T | 1 | a0001c0003t0030g0045 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.654-8305A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37833784 | |||||||
| chr9:37833815 | C | T | 1 | a0001c0001t0040g0235 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.654-8274C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37833815 | |||||||
| chr9:37833844 | G | C | 2 | a0001c0001t0019g0055 a0001c0001t0019g0057 |
2 | HG02486.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.654-8245G>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37833844 | |||||||
| chr9:37834053 | C | T | 2 | a0001c0001t0001g0067 a0001c0001t0033g0058 |
2 | NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.654-8036C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37834053 | |||||||
| chr9:37834058 | G | C | 1 | a0002c0007t0008g0052 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.654-8031G>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37834058 | |||||||
| chr9:37834098 | C | T | 1 | a0001c0001t0014g0165 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.654-7991C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37834098 | |||||||
| chr9:37834165 | T | C | 51 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(48): Show |
55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.654-7924T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37834165 | |||||||
| chr9:37834214 | G | A | 51 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(48): Show |
55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.654-7875G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37834214 | |||||||
| chr9:37834373 | C | T | 50 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(47): Show |
54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.654-7716C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37834373 | |||||||
| chr9:37834444 | A | G | 1 | a0001c0001t0004g0211 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.654-7645A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37834444 | |||||||
| chr9:37834790 | C | T | 1 | a0001c0001t0003g0219 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.654-7299C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37834790 | |||||||
| chr9:37834794 | C | CTTTTTTT others(1): Show |
38 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(35): Show |
40 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.654-7291_654-7284d others(10): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37834794 | ||||||
| chr9:37834794 | C | CTTTTTTT others(2): Show |
6 | a0001c0001t0012g0005 a0001c0001t0012g0059 a0001c0001t0012g0060 others(3): Show |
7 | HG02647.hp2 HG02717.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.654-7292_654-7284d others(11): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37834794 | ||||||
| chr9:37834794 | C | CTTTTTTT others(3): Show |
7 | a0001c0001t0008g0046 a0001c0001t0008g0047 a0001c0001t0008g0048 others(4): Show |
8 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.654-7293_654-7284d others(12): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37834794 | ||||||
| chr9:37834891 | A | C | 51 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(48): Show |
55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.654-7198A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37834891 | |||||||
| chr9:37835156 | C | T | 1 | a0001c0001t0003g0200 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.654-6933C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37835156 | |||||||
| chr9:37835303 | G | A | 4 | a0001c0001t0001g0139 a0001c0001t0024g0140 a0001c0001t0024g0141 others(1): Show |
4 | HG00140.hp1 HG01074.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.654-6786G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37835303 | |||||||
| chr9:37835352 | G | A | 1 | a0001c0001t0006g0255 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.654-6737G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37835352 | |||||||
| chr9:37835382 | C | T | 61 | a0001c0001t0001g0282 a0001c0001t0002g0001 a0001c0001t0002g0065 others(58): Show |
64 | HG00099.hp1 HG00558.hp1 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.654-6707C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37835382 | |||||||
| chr9:37835533 | G | A | 1 | a0001c0001t0063g0044 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.654-6556G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37835533 | |||||||
| chr9:37835567 | G | C | 2 | a0001c0001t0001g0109 a0001c0001t0001g0110 |
2 | NA18994.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.654-6522G>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37835567 | |||||||
| chr9:37835691 | G | A | 50 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(47): Show |
54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.654-6398G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37835691 | |||||||
| chr9:37836101 | G | A | 13 | a0001c0001t0012g0005 a0001c0001t0012g0059 a0001c0001t0012g0060 others(10): Show |
15 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.654-5988G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37836101 | |||||||
| chr9:37836262 | G | T | 51 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(48): Show |
55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.654-5827G>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37836262 | |||||||
| chr9:37836511 | T | C | 50 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(47): Show |
54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.654-5578T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37836511 | |||||||
| chr9:37836629 | GA | G | 50 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(47): Show |
54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.654-5459delA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37836629 | |||||||
| chr9:37836716 | T | A | 1 | a0001c0001t0001g0146 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.654-5373T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37836716 | |||||||
| chr9:37836944 | T | C | 51 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(48): Show |
55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.654-5145T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37836944 | |||||||
| chr9:37837044 | G | C | 50 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(47): Show |
54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.654-5045G>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37837044 | |||||||
| chr9:37837102 | A | G | 1 | a0001c0001t0001g0244 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.654-4987A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37837102 | |||||||
| chr9:37837143 | C | A | 50 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(47): Show |
54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.654-4946C>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37837143 | |||||||
| chr9:37837328 | A | G | 50 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(47): Show |
54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.654-4761A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37837328 | |||||||
| chr9:37837415 | C | T | 1 | a0001c0003t0030g0045 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.654-4674C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37837415 | |||||||
| chr9:37837433 | T | G | 1 | a0001c0001t0034g0331 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.654-4656T>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37837433 | |||||||
| chr9:37837450 | T | C | 1 | a0001c0001t0004g0333 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.654-4639T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37837450 | |||||||
| chr9:37837453 | A | G | 50 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(47): Show |
54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.654-4636A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37837453 | |||||||
| chr9:37837457 | C | CA | 9 | a0001c0001t0001g0071 a0001c0001t0001g0078 a0001c0001t0001g0109 others(6): Show |
9 | HG00621.hp2 HG01981.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.654-4614dupA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37837457 | ||||||
| chr9:37837457 | CAAAA | C | 49 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(46): Show |
53 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(50): Show |
intron_variant | MODIFIER | c.654-4617_654-4614d others(6): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37837457 | ||||||
| chr9:37837472 | A | G | 1 | a0001c0001t0001g0248 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.654-4617A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37837472 | |||||||
| chr9:37837520 | A | C | 50 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(47): Show |
54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.654-4569A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37837520 | |||||||
| chr9:37837650 | G | T | 48 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(45): Show |
52 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(49): Show |
intron_variant | MODIFIER | c.654-4439G>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37837650 | |||||||
| chr9:37837845 | C | CA | 34 | a0001c0001t0001g0095 a0001c0001t0001g0187 a0001c0001t0001g0188 others(31): Show |
35 | HG00558.hp2 HG01081.hp1 HG01123.hp2 others(32): Show |
intron_variant | MODIFIER | c.654-4230dupA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37837845 | ||||||
| chr9:37837845 | C | CAA | 13 | a0001c0001t0012g0005 a0001c0001t0012g0059 a0001c0001t0012g0060 others(10): Show |
15 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.654-4231_654-4230d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37837845 | ||||||
| chr9:37837845 | C | CAAA | 9 | a0001c0001t0008g0046 a0001c0001t0008g0047 a0001c0001t0008g0048 others(6): Show |
10 | HG01496.hp2 HG02451.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.654-4232_654-4230d others(5): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37837845 | ||||||
| chr9:37838063 | A | G | 1 | a0001c0001t0008g0050 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.654-4026A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37838063 | |||||||
| chr9:37838071 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.654-4018T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37838071 | |||||||
| chr9:37838438 | T | TA | 51 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(48): Show |
55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.654-3644dupA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37838438 | ||||||
| chr9:37839018 | C | CAGAAATT others(5): Show |
1 | a0002c0007t0008g0052 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.654-3070_654-3069i others(14): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37839018 | ||||||
| chr9:37839020 | T | A | 1 | a0002c0007t0008g0052 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.654-3069T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37839020 | |||||||
| chr9:37839021 | C | A | 1 | a0002c0007t0008g0052 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.654-3068C>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37839021 | |||||||
| chr9:37839048 | A | AT | 13 | a0001c0001t0012g0005 a0001c0001t0012g0059 a0001c0001t0012g0060 others(10): Show |
15 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.654-3031dupT | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37839048 | ||||||
| chr9:37839065 | C | CT | 21 | a0001c0001t0008g0046 a0001c0001t0008g0047 a0001c0001t0008g0048 others(18): Show |
24 | HG01243.hp1 HG02257.hp2 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.654-3016dupT | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37839065 | ||||||
| chr9:37839065 | C | CTT | 29 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(26): Show |
30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.654-3017_654-3016d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37839065 | ||||||
| chr9:37839148 | G | A | 1 | a0001c0001t0055g0266 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.654-2941G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37839148 | |||||||
| chr9:37839247 | A | G | 1 | a0001c0001t0002g0316 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.654-2842A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37839247 | |||||||
| chr9:37839347 | A | G | 1 | a0001c0001t0001g0083 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.654-2742A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37839347 | |||||||
| chr9:37839359 | C | T | 3 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0246 |
3 | NA18959.hp1 NA19062.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.654-2730C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37839359 | |||||||
| chr9:37839529 | C | A | 22 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0070 others(19): Show |
25 | HG00323.hp1 HG00733.hp1 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.654-2560C>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37839529 | |||||||
| chr9:37839531 | C | T | 1 | a0001c0001t0001g0079 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.654-2558C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37839531 | |||||||
| chr9:37839795 | C | T | 50 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(47): Show |
54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.654-2294C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37839795 | |||||||
| chr9:37839822 | C | G | 51 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(48): Show |
55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.654-2267C>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37839822 | |||||||
| chr9:37839875 | G | A | 1 | a0001c0001t0018g0016 | 2 | HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.654-2214G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37839875 | |||||||
| chr9:37839949 | C | T | 1 | a0001c0001t0015g0038 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.654-2140C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37839949 | |||||||
| chr9:37840024 | C | G | 50 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(47): Show |
54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.654-2065C>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37840024 | |||||||
| chr9:37840161 | A | C | 1 | a0001c0001t0002g0314 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.654-1928A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37840161 | |||||||
| chr9:37840294 | G | C | 1 | a0001c0001t0001g0111 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.654-1795G>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37840294 | |||||||
| chr9:37840364 | C | G | 4 | a0001c0001t0012g0005 a0001c0001t0012g0059 a0001c0001t0012g0060 others(1): Show |
5 | HG02647.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.654-1725C>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37840364 | |||||||
| chr9:37840446 | T | A | 1 | a0001c0001t0016g0195 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.654-1643T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37840446 | |||||||
| chr9:37840539 | T | C | 50 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(47): Show |
54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.654-1550T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37840539 | |||||||
| chr9:37840555 | C | T | 1 | a0001c0001t0005g0032 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.654-1534C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37840555 | |||||||
| chr9:37840616 | C | T | 6 | a0001c0001t0008g0046 a0001c0001t0008g0047 a0001c0001t0008g0048 others(3): Show |
6 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.654-1473C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37840616 | |||||||
| chr9:37840670 | T | A | 1 | a0001c0001t0018g0016 | 2 | HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.654-1419T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37840670 | |||||||
| chr9:37840690 | A | G | 1 | a0001c0001t0018g0016 | 2 | HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.654-1399A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37840690 | |||||||
| chr9:37840892 | A | G | 2 | a0001c0001t0001g0073 a0001c0001t0017g0080 |
2 | HG02071.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.654-1197A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37840892 | |||||||
| chr9:37840898 | ATACT | A | 3 | a0001c0001t0001g0124 a0001c0001t0013g0061 a0001c0001t0013g0062 |
3 | HG00733.hp2 HG01255.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.654-1187_654-1184d others(6): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 37840898 | ||||||
| chr9:37840905 | C | T | 4 | a0001c0001t0002g0281 a0001c0001t0002g0284 a0001c0001t0002g0285 others(1): Show |
4 | NA18994.hp2 NA19062.hp1 NA19081.hp2 others(1): Show |
intron_variant | MODIFIER | c.654-1184C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37840905 | |||||||
| chr9:37840912 | G | T | 1 | a0001c0001t0001g0014 | 2 | HG01081.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.654-1177G>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37840912 | |||||||
| chr9:37840953 | C | A | 4 | a0001c0001t0012g0005 a0001c0001t0012g0059 a0001c0001t0012g0060 others(1): Show |
5 | HG02647.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.654-1136C>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37840953 | |||||||
| chr9:37840991 | T | C | 1 | a0002c0007t0008g0052 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.654-1098T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37840991 | |||||||
| chr9:37841166 | G | A | 8 | a0001c0001t0002g0258 a0001c0001t0002g0260 a0001c0001t0006g0255 others(5): Show |
8 | HG01109.hp1 HG01361.hp2 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.654-923G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37841166 | |||||||
| chr9:37841176 | C | G | 107 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0122 others(104): Show |
113 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.654-913C>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37841176 | |||||||
| chr9:37841201 | G | A | 7 | a0001c0001t0008g0046 a0001c0001t0008g0047 a0001c0001t0008g0048 others(4): Show |
7 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.654-888G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37841201 | |||||||
| chr9:37841251 | T | C | 42 | a0001c0001t0003g0011 a0001c0001t0003g0088 a0001c0001t0003g0089 others(39): Show |
43 | HG00099.hp2 HG00438.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.654-838T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37841251 | |||||||
| chr9:37841383 | A | G | 50 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(47): Show |
54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.654-706A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37841383 | |||||||
| chr9:37841585 | A | C | 1 | a0001c0001t0008g0050 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.654-504A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 2/6 | chr9 | 37841585 | |||||||
| chr9:37842340 | G | C | 6 | a0001c0001t0019g0055 a0001c0001t0019g0057 a0001c0001t0020g0053 others(3): Show |
7 | HG01243.hp1 HG02486.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.851+54G>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37842340 | |||||||
| chr9:37842611 | T | C | 4 | a0001c0001t0012g0005 a0001c0001t0012g0059 a0001c0001t0012g0060 others(1): Show |
5 | HG02647.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.851+325T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37842611 | |||||||
| chr9:37842719 | G | A | 3 | a0001c0001t0009g0003 a0001c0001t0027g0020 a0001c0001t0027g0021 |
4 | NA18957.hp1 NA18960.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.851+433G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37842719 | |||||||
| chr9:37842975 | T | C | 1 | a0001c0001t0002g0315 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.851+689T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37842975 | |||||||
| chr9:37842994 | C | A | 8 | a0001c0001t0008g0046 a0001c0001t0008g0047 a0001c0001t0008g0048 others(5): Show |
9 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.851+708C>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37842994 | |||||||
| chr9:37843049 | G | A | 15 | a0001c0001t0001g0009 a0001c0001t0001g0161 a0001c0001t0001g0162 others(12): Show |
17 | HG00438.hp2 HG00639.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.851+763G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37843049 | |||||||
| chr9:37843099 | A | T | 1 | a0001c0001t0062g0019 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.851+813A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37843099 | |||||||
| chr9:37843268 | T | C | 51 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(48): Show |
55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.851+982T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37843268 | |||||||
| chr9:37843324 | C | T | 3 | a0001c0001t0022g0335 a0001c0001t0022g0336 a0001c0001t0031g0337 |
3 | HG02257.hp2 HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.851+1038C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37843324 | |||||||
| chr9:37843362 | G | A | 2 | a0001c0001t0004g0240 a0001c0001t0053g0241 |
2 | HG02622.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.851+1076G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37843362 | |||||||
| chr9:37843432 | G | C | 6 | a0001c0001t0008g0046 a0001c0001t0008g0047 a0001c0001t0008g0048 others(3): Show |
6 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.851+1146G>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37843432 | |||||||
| chr9:37843688 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.851+1402T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37843688 | |||||||
| chr9:37844032 | C | T | 1 | a0001c0001t0006g0261 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.851+1746C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37844032 | |||||||
| chr9:37844242 | C | T | 8 | a0001c0001t0002g0258 a0001c0001t0002g0260 a0001c0001t0006g0255 others(5): Show |
8 | HG01109.hp1 HG01361.hp2 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.851+1956C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37844242 | |||||||
| chr9:37844243 | G | A | 37 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(34): Show |
39 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.851+1957G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37844243 | |||||||
| chr9:37844293 | G | A | 1 | a0001c0001t0001g0247 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.851+2007G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37844293 | |||||||
| chr9:37844374 | C | T | 29 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(26): Show |
30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.851+2088C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37844374 | |||||||
| chr9:37844398 | C | T | 1 | a0001c0003t0030g0045 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.851+2112C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37844398 | |||||||
| chr9:37844471 | A | G | 236 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0122 others(233): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.851+2185A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37844471 | |||||||
| chr9:37844533 | C | A | 1 | a0001c0001t0002g0317 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.851+2247C>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37844533 | |||||||
| chr9:37844592 | C | T | 1 | a0001c0003t0030g0045 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.851+2306C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37844592 | |||||||
| chr9:37844605 | T | C | 1 | a0001c0001t0021g0004 | 2 | HG01243.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.851+2319T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37844605 | |||||||
| chr9:37844699 | G | T | 1 | a0001c0001t0021g0004 | 2 | HG01243.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.851+2413G>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37844699 | |||||||
| chr9:37844750 | C | T | 42 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(39): Show |
45 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(42): Show |
intron_variant | MODIFIER | c.851+2464C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37844750 | |||||||
| chr9:37844827 | TAAC | T | 50 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(47): Show |
54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.851+2553_851+2555d others(5): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37844827 | ||||||
| chr9:37844856 | G | A | 13 | a0001c0001t0012g0005 a0001c0001t0012g0059 a0001c0001t0012g0060 others(10): Show |
15 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.851+2570G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37844856 | |||||||
| chr9:37844904 | AT | A | 29 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(26): Show |
30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.851+2621delT | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37844904 | ||||||
| chr9:37845332 | G | A | 1 | a0001c0001t0041g0154 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.851+3046G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37845332 | |||||||
| chr9:37845560 | A | T | 1 | a0001c0001t0001g0117 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.851+3274A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37845560 | |||||||
| chr9:37845706 | A | G | 51 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(48): Show |
55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.851+3420A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37845706 | |||||||
| chr9:37845743 | C | T | 1 | a0001c0001t0004g0121 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.851+3457C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37845743 | |||||||
| chr9:37845803 | T | G | 29 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(26): Show |
30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.851+3517T>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37845803 | |||||||
| chr9:37845965 | A | G | 50 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(47): Show |
54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.851+3679A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37845965 | |||||||
| chr9:37846353 | A | G | 1 | a0001c0001t0015g0038 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.851+4067A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37846353 | |||||||
| chr9:37846398 | C | T | 3 | a0001c0001t0002g0295 a0001c0001t0002g0308 a0001c0001t0007g0294 |
3 | HG01891.hp2 HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.851+4112C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37846398 | |||||||
| chr9:37846412 | G | A | 1 | a0002c0007t0008g0052 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.851+4126G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37846412 | |||||||
| chr9:37846489 | G | A | 29 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(26): Show |
30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.851+4203G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37846489 | |||||||
| chr9:37846691 | A | G | 77 | a0001c0001t0001g0282 a0001c0001t0002g0001 a0001c0001t0002g0065 others(74): Show |
80 | HG00099.hp1 HG00558.hp1 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.851+4405A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37846691 | |||||||
| chr9:37846703 | A | G | 50 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(47): Show |
54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.851+4417A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37846703 | |||||||
| chr9:37846724 | G | A | 6 | a0001c0001t0008g0046 a0001c0001t0008g0047 a0001c0001t0008g0048 others(3): Show |
6 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.851+4438G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37846724 | |||||||
| chr9:37846920 | C | T | 3 | a0001c0001t0022g0335 a0001c0001t0022g0336 a0001c0001t0031g0337 |
3 | HG02257.hp2 HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.851+4634C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37846920 | |||||||
| chr9:37846924 | T | C | 3 | a0001c0001t0022g0335 a0001c0001t0022g0336 a0001c0001t0031g0337 |
3 | HG02257.hp2 HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.851+4638T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37846924 | |||||||
| chr9:37847024 | C | T | 8 | a0001c0001t0002g0065 a0001c0001t0002g0320 a0001c0001t0008g0046 others(5): Show |
8 | HG02080.hp1 HG02451.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.851+4738C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37847024 | |||||||
| chr9:37847146 | A | G | 50 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(47): Show |
54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.851+4860A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37847146 | |||||||
| chr9:37847213 | A | G | 1 | a0001c0001t0002g0313 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.851+4927A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37847213 | |||||||
| chr9:37847226 | C | A | 1 | a0001c0001t0001g0227 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.851+4940C>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37847226 | |||||||
| chr9:37847253 | C | CA | 12 | a0001c0001t0001g0071 a0001c0001t0001g0097 a0001c0001t0001g0105 others(9): Show |
12 | HG00323.hp2 HG00735.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.851+4991dupA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37847253 | ||||||
| chr9:37847253 | CA | C | 16 | a0001c0001t0001g0111 a0001c0001t0001g0129 a0001c0001t0001g0139 others(13): Show |
16 | HG00140.hp1 HG01069.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.851+4991delA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37847253 | ||||||
| chr9:37847253 | CAA | C | 31 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(28): Show |
33 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(30): Show |
intron_variant | MODIFIER | c.851+4990_851+4991d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37847253 | ||||||
| chr9:37847253 | CAAAA | C | 13 | a0001c0001t0012g0005 a0001c0001t0012g0059 a0001c0001t0012g0060 others(10): Show |
15 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.851+4988_851+4991d others(6): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37847253 | ||||||
| chr9:37847253 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0009g0041 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.851+4982_851+4991d others(12): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37847253 | ||||||
| chr9:37847253 | CAAAAAAA others(5): Show |
C | 4 | a0001c0001t0004g0178 a0001c0002t0004g0214 a0001c0002t0004g0215 others(1): Show |
4 | HG02280.hp1 HG02486.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.851+4980_851+4991d others(14): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37847253 | ||||||
| chr9:37847296 | T | C | 50 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(47): Show |
54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.851+5010T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37847296 | |||||||
| chr9:37847300 | TA | T | 9 | a0001c0001t0019g0055 a0001c0001t0019g0057 a0001c0001t0020g0053 others(6): Show |
10 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.851+5025delA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37847300 | ||||||
| chr9:37847322 | A | G | 8 | a0001c0001t0001g0282 a0001c0001t0007g0267 a0001c0001t0007g0269 others(5): Show |
8 | NA18947.hp1 NA18952.hp2 NA18978.hp1 others(5): Show |
intron_variant | MODIFIER | c.851+5036A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37847322 | |||||||
| chr9:37847330 | C | A | 8 | a0001c0001t0001g0282 a0001c0001t0007g0267 a0001c0001t0007g0269 others(5): Show |
8 | NA18947.hp1 NA18952.hp2 NA18978.hp1 others(5): Show |
intron_variant | MODIFIER | c.851+5044C>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37847330 | |||||||
| chr9:37848037 | G | T | 1 | a0001c0001t0003g0093 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.851+5751G>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37848037 | |||||||
| chr9:37848256 | CA | C | 4 | a0001c0001t0011g0158 a0001c0001t0011g0159 a0001c0001t0011g0160 others(1): Show |
4 | NA18955.hp1 NA18979.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.851+5973delA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37848256 | ||||||
| chr9:37848282 | G | T | 9 | a0001c0001t0019g0055 a0001c0001t0019g0057 a0001c0001t0020g0053 others(6): Show |
10 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.851+5996G>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37848282 | |||||||
| chr9:37848352 | G | A | 1 | a0001c0001t0009g0028 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.851+6066G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37848352 | |||||||
| chr9:37848378 | A | C | 50 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(47): Show |
54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.851+6092A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37848378 | |||||||
| chr9:37848413 | G | A | 3 | a0001c0001t0022g0335 a0001c0001t0022g0336 a0001c0001t0031g0337 |
3 | HG02257.hp2 HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.851+6127G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37848413 | |||||||
| chr9:37848486 | C | T | 7 | a0001c0001t0008g0046 a0001c0001t0008g0047 a0001c0001t0008g0048 others(4): Show |
7 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.851+6200C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37848486 | |||||||
| chr9:37848526 | T | C | 9 | a0001c0001t0019g0055 a0001c0001t0019g0057 a0001c0001t0020g0053 others(6): Show |
10 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.851+6240T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37848526 | |||||||
| chr9:37848572 | A | G | 1 | a0001c0001t0008g0051 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.852-6208A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37848572 | |||||||
| chr9:37848602 | A | C | 4 | a0001c0001t0012g0005 a0001c0001t0012g0059 a0001c0001t0012g0060 others(1): Show |
5 | HG02647.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.852-6178A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37848602 | |||||||
| chr9:37848626 | C | A | 2 | a0001c0001t0001g0115 a0001c0001t0001g0128 |
2 | HG02027.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.852-6154C>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37848626 | |||||||
| chr9:37848635 | G | A | 4 | a0001c0001t0012g0005 a0001c0001t0012g0059 a0001c0001t0012g0060 others(1): Show |
5 | HG02647.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.852-6145G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37848635 | |||||||
| chr9:37848737 | C | T | 1 | a0001c0001t0003g0226 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.852-6043C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37848737 | |||||||
| chr9:37848741 | G | T | 8 | a0001c0001t0008g0046 a0001c0001t0008g0047 a0001c0001t0008g0048 others(5): Show |
9 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.852-6039G>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37848741 | |||||||
| chr9:37848742 | GA | G | 51 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(48): Show |
55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.852-6037delA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37848742 | |||||||
| chr9:37848798 | T | C | 51 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(48): Show |
55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.852-5982T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37848798 | |||||||
| chr9:37848967 | T | C | 50 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(47): Show |
54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.852-5813T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37848967 | |||||||
| chr9:37848972 | C | CA | 11 | a0001c0001t0001g0135 a0001c0001t0002g0268 a0001c0001t0003g0233 others(8): Show |
12 | HG00438.hp2 HG00642.hp1 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.852-5789dupA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37848972 | ||||||
| chr9:37848972 | CAA | C | 13 | a0001c0001t0012g0005 a0001c0001t0012g0059 a0001c0001t0012g0060 others(10): Show |
15 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.852-5790_852-5789d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37848972 | ||||||
| chr9:37848972 | CAAA | C | 37 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(34): Show |
39 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.852-5791_852-5789d others(5): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37848972 | ||||||
| chr9:37848989 | A | C | 1 | a0001c0001t0001g0252 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.852-5791A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37848989 | |||||||
| chr9:37849247 | A | G | 1 | a0001c0001t0018g0016 | 2 | HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.852-5533A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37849247 | |||||||
| chr9:37849441 | A | G | 1 | a0001c0001t0001g0334 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.852-5339A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37849441 | |||||||
| chr9:37849476 | C | A | 51 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(48): Show |
55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.852-5304C>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37849476 | |||||||
| chr9:37849512 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.852-5268C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37849512 | |||||||
| chr9:37849603 | C | T | 1 | a0001c0001t0018g0016 | 2 | HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.852-5177C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37849603 | |||||||
| chr9:37849610 | C | G | 1 | a0001c0001t0004g0150 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.852-5170C>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37849610 | |||||||
| chr9:37849835 | G | A | 37 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(34): Show |
39 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.852-4945G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37849835 | |||||||
| chr9:37849847 | T | A | 1 | a0001c0001t0032g0056 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.852-4933T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37849847 | |||||||
| chr9:37849894 | C | A | 2 | a0001c0001t0004g0240 a0001c0001t0053g0241 |
2 | HG02622.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.852-4886C>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37849894 | |||||||
| chr9:37849897 | A | C | 1 | a0001c0003t0030g0045 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.852-4883A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37849897 | |||||||
| chr9:37849925 | C | T | 5 | a0001c0001t0001g0124 a0001c0001t0013g0061 a0001c0001t0013g0062 others(2): Show |
5 | HG00733.hp2 HG01255.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.852-4855C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37849925 | |||||||
| chr9:37849949 | C | T | 1 | a0001c0001t0016g0212 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.852-4831C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37849949 | |||||||
| chr9:37849960 | G | A | 4 | a0001c0001t0008g0046 a0001c0001t0008g0047 a0001c0001t0008g0048 others(1): Show |
4 | HG02451.hp2 HG02818.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.852-4820G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37849960 | |||||||
| chr9:37849984 | A | T | 1 | a0001c0003t0030g0045 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.852-4796A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37849984 | |||||||
| chr9:37850082 | GGGCCAAA others(11): Show |
G | 1 | a0002c0007t0008g0052 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.852-4690_852-4673d others(20): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850082 | ||||||
| chr9:37850128 | T | C | 1 | a0001c0001t0010g0090 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.852-4652T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37850128 | |||||||
| chr9:37850253 | T | A | 1 | a0001c0003t0030g0045 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.852-4527T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37850253 | |||||||
| chr9:37850312 | A | G | 50 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(47): Show |
54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.852-4468A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37850312 | |||||||
| chr9:37850475 | G | A | 50 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(47): Show |
54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.852-4305G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37850475 | |||||||
| chr9:37850736 | A | G | 3 | a0001c0001t0004g0176 a0001c0001t0004g0208 a0001c0001t0004g0232 |
3 | HG00597.hp2 NA18951.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.852-4044A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37850736 | |||||||
| chr9:37850818 | GATATATT others(6): Show |
G | 1 | a0001c0001t0003g0198 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.852-3955_852-3943d others(15): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850818 | ||||||
| chr9:37850820 | T | C | 2 | a0001c0001t0017g0326 a0001c0001t0017g0327 |
2 | NA18955.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.852-3960T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37850820 | |||||||
| chr9:37850823 | A | T | 1 | a0001c0001t0003g0231 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.852-3957A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37850823 | |||||||
| chr9:37850825 | T | A | 1 | a0002c0007t0008g0052 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.852-3955T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37850825 | |||||||
| chr9:37850825 | TTTATATA others(4): Show |
T | 1 | a0001c0001t0003g0231 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.852-3953_852-3943d others(13): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850825 | ||||||
| chr9:37850826 | T | A | 2 | a0001c0001t0001g0095 a0001c0001t0007g0294 |
2 | HG00558.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.852-3954T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37850826 | |||||||
| chr9:37850826 | T | TTA | 24 | a0001c0001t0001g0070 a0001c0001t0001g0109 a0001c0001t0001g0118 others(21): Show |
24 | HG00733.hp1 HG01261.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.852-3899_852-3898d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850826 | ||||||
| chr9:37850826 | T | TTATA | 21 | a0001c0001t0001g0002 a0001c0001t0001g0073 a0001c0001t0001g0075 others(18): Show |
22 | HG01978.hp2 HG02071.hp2 HG02074.hp1 others(19): Show |
intron_variant | MODIFIER | c.852-3901_852-3898d others(6): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850826 | ||||||
| chr9:37850826 | T | TTATATA | 10 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0002g0300 others(7): Show |
11 | HG01168.hp2 HG01169.hp2 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.852-3903_852-3898d others(8): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850826 | ||||||
| chr9:37850826 | T | TTATATAT others(1): Show |
8 | a0001c0001t0001g0013 a0001c0001t0001g0129 a0001c0001t0001g0248 others(5): Show |
8 | HG01069.hp2 HG02080.hp2 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.852-3905_852-3898d others(10): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850826 | ||||||
| chr9:37850826 | T | TTATATAT others(3): Show |
10 | a0001c0001t0001g0069 a0001c0001t0001g0082 a0001c0001t0001g0084 others(7): Show |
10 | HG02080.hp1 HG02897.hp1 HG03710.hp1 others(7): Show |
intron_variant | MODIFIER | c.852-3907_852-3898d others(12): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850826 | ||||||
| chr9:37850826 | T | TTATATAT others(5): Show |
2 | a0001c0001t0001g0125 a0001c0001t0002g0313 |
2 | HG01928.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.852-3909_852-3898d others(14): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850826 | ||||||
| chr9:37850826 | T | TTATATAT others(9): Show |
1 | a0001c0001t0006g0279 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.852-3913_852-3898d others(18): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850826 | ||||||
| chr9:37850826 | T | TTATATAT others(11): Show |
2 | a0001c0001t0001g0101 a0001c0001t0002g0260 |
2 | HG01109.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.852-3915_852-3898d others(20): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850826 | ||||||
| chr9:37850826 | T | TTATATAT others(15): Show |
1 | a0001c0001t0002g0329 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.852-3919_852-3898d others(24): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850826 | ||||||
| chr9:37850826 | TTA | T | 27 | a0001c0001t0001g0009 a0001c0001t0001g0097 a0001c0001t0001g0107 others(24): Show |
28 | HG00438.hp2 HG00642.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.852-3899_852-3898d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850826 | ||||||
| chr9:37850826 | TTATA | T | 18 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0068 others(15): Show |
18 | HG00558.hp1 HG01099.hp1 HG01993.hp1 others(15): Show |
intron_variant | MODIFIER | c.852-3901_852-3898d others(6): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850826 | ||||||
| chr9:37850826 | TTATATA | T | 14 | a0001c0001t0001g0006 a0001c0001t0001g0071 a0001c0001t0001g0078 others(11): Show |
14 | HG00621.hp2 HG01978.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.852-3903_852-3898d others(8): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850826 | ||||||
| chr9:37850826 | TTATATAT others(1): Show |
T | 10 | a0001c0001t0001g0094 a0001c0001t0001g0103 a0001c0001t0001g0113 others(7): Show |
10 | HG01074.hp1 HG01123.hp2 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.852-3905_852-3898d others(10): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850826 | ||||||
| chr9:37850826 | TTATATAT others(3): Show |
T | 7 | a0001c0001t0002g0258 a0001c0001t0005g0024 a0001c0001t0008g0046 others(4): Show |
8 | HG00140.hp1 HG02074.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.852-3907_852-3898d others(12): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850826 | ||||||
| chr9:37850826 | TTATATAT others(5): Show |
T | 13 | a0001c0001t0001g0111 a0001c0001t0001g0135 a0001c0001t0001g0245 others(10): Show |
14 | HG00741.hp2 HG01975.hp2 HG02155.hp2 others(11): Show |
intron_variant | MODIFIER | c.852-3909_852-3898d others(14): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850826 | ||||||
| chr9:37850826 | TTATATAT others(7): Show |
T | 11 | a0001c0001t0001g0067 a0001c0001t0003g0193 a0001c0001t0005g0029 others(8): Show |
11 | HG01192.hp1 HG01975.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.852-3911_852-3898d others(16): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850826 | ||||||
| chr9:37850826 | TTATATAT others(9): Show |
T | 10 | a0001c0001t0003g0233 a0001c0001t0004g0091 a0001c0001t0005g0026 others(7): Show |
10 | HG00642.hp1 HG00741.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.852-3913_852-3898d others(18): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850826 | ||||||
| chr9:37850826 | TTATATAT others(11): Show |
T | 19 | a0001c0001t0001g0250 a0001c0001t0003g0167 a0001c0001t0003g0172 others(16): Show |
19 | HG00621.hp1 HG01071.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.852-3915_852-3898d others(20): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850826 | ||||||
| chr9:37850826 | TTATATAT others(13): Show |
T | 20 | a0001c0001t0001g0124 a0001c0001t0001g0187 a0001c0001t0001g0188 others(17): Show |
21 | HG00099.hp2 HG00738.hp1 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.852-3917_852-3898d others(22): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850826 | ||||||
| chr9:37850826 | TTATATAT others(15): Show |
T | 40 | a0001c0001t0001g0123 a0001c0001t0001g0144 a0001c0001t0001g0204 others(37): Show |
42 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.852-3919_852-3898d others(24): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850826 | ||||||
| chr9:37850826 | TTATATAT others(17): Show |
T | 9 | a0001c0001t0001g0014 a0001c0001t0001g0122 a0001c0001t0001g0185 others(6): Show |
10 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.852-3921_852-3898d others(26): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850826 | ||||||
| chr9:37850826 | TTATATAT others(19): Show |
T | 3 | a0001c0001t0001g0117 a0001c0001t0016g0212 a0001c0001t0040g0235 |
3 | HG01515.hp2 HG06807.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.852-3923_852-3898d others(28): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850826 | ||||||
| chr9:37850826 | TTATATAT others(21): Show |
T | 1 | a0001c0001t0001g0116 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.852-3925_852-3898d others(30): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850826 | ||||||
| chr9:37850826 | TTATATAT others(23): Show |
T | 1 | a0001c0001t0001g0134 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.852-3927_852-3898d others(32): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850826 | ||||||
| chr9:37850826 | TTATATAT others(27): Show |
T | 6 | a0001c0001t0019g0055 a0001c0001t0019g0057 a0001c0001t0020g0053 others(3): Show |
7 | HG01243.hp1 HG02486.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.852-3931_852-3898d others(36): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850826 | ||||||
| chr9:37850826 | TTATATAT others(33): Show |
T | 4 | a0001c0001t0012g0005 a0001c0001t0012g0059 a0001c0001t0012g0060 others(1): Show |
5 | HG02647.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.852-3937_852-3898d others(42): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850826 | ||||||
| chr9:37850827 | TATATATA others(14): Show |
T | 2 | a0001c0001t0003g0181 a0001c0001t0003g0182 |
2 | NA18970.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.852-3952_852-3932d others(23): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37850827 | |||||||
| chr9:37850832 | A | ATATATAT others(3): Show |
1 | a0001c0001t0026g0007 | 2 | HG00639.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.852-3939_852-3938i others(12): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850832 | ||||||
| chr9:37850834 | A | T | 3 | a0001c0001t0003g0173 a0001c0001t0003g0174 a0001c0001t0003g0175 |
3 | NA18960.hp1 NA18980.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.852-3946A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37850834 | |||||||
| chr9:37850836 | A | T | 2 | a0001c0001t0001g0139 a0001c0001t0050g0142 |
2 | HG01074.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.852-3944A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37850836 | |||||||
| chr9:37850838 | A | T | 2 | a0001c0001t0024g0140 a0001c0001t0024g0141 |
2 | HG00140.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.852-3942A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37850838 | |||||||
| chr9:37850840 | A | T | 1 | a0001c0001t0003g0199 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.852-3940A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37850840 | |||||||
| chr9:37850842 | A | G | 2 | a0001c0001t0011g0159 a0001c0001t0044g0157 |
2 | HG03017.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.852-3938A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37850842 | |||||||
| chr9:37850842 | A | T | 3 | a0001c0001t0003g0193 a0001c0001t0014g0165 a0001c0001t0043g0192 |
3 | HG01192.hp1 HG01975.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.852-3938A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37850842 | |||||||
| chr9:37850844 | A | G | 11 | a0001c0001t0001g0009 a0001c0001t0001g0162 a0001c0001t0004g0008 others(8): Show |
12 | HG00438.hp2 HG00735.hp1 NA18946.hp1 others(9): Show |
intron_variant | MODIFIER | c.852-3936A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37850844 | |||||||
| chr9:37850844 | A | T | 1 | a0001c0001t0003g0233 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.852-3936A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37850844 | |||||||
| chr9:37850846 | A | G | 2 | a0001c0001t0001g0161 a0001c0001t0048g0163 |
2 | HG01099.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.852-3934A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37850846 | |||||||
| chr9:37850846 | A | T | 8 | a0001c0001t0001g0250 a0001c0001t0003g0167 a0001c0001t0003g0172 others(5): Show |
8 | HG00621.hp1 HG01071.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.852-3934A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37850846 | |||||||
| chr9:37850848 | A | T | 17 | a0001c0001t0001g0124 a0001c0001t0001g0187 a0001c0001t0001g0188 others(14): Show |
18 | HG00099.hp2 HG00738.hp1 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.852-3932A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37850848 | |||||||
| chr9:37850850 | A | T | 35 | a0001c0001t0001g0123 a0001c0001t0001g0144 a0001c0001t0001g0204 others(32): Show |
37 | HG00140.hp2 HG00438.hp1 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.852-3930A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37850850 | |||||||
| chr9:37850852 | A | T | 5 | a0001c0001t0001g0014 a0001c0001t0001g0185 a0001c0001t0003g0196 others(2): Show |
6 | HG00323.hp2 HG01081.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.852-3928A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37850852 | |||||||
| chr9:37850854 | A | T | 1 | a0001c0001t0040g0235 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.852-3926A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37850854 | |||||||
| chr9:37850878 | A | G | 8 | a0001c0001t0008g0046 a0001c0001t0008g0047 a0001c0001t0008g0048 others(5): Show |
9 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.852-3902A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37850878 | |||||||
| chr9:37850881 | T | A | 13 | a0001c0001t0001g0009 a0001c0001t0001g0162 a0001c0001t0004g0008 others(10): Show |
15 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.852-3899T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37850881 | |||||||
| chr9:37850881 | T | TATATATA others(7): Show |
1 | a0001c0001t0002g0323 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.852-3898_852-3897i others(16): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37850881 | ||||||
| chr9:37850882 | A | ATATATAT others(6): Show |
1 | a0001c0001t0006g0254 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.852-3898_852-3897i others(15): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37850882 | |||||||
| chr9:37851060 | A | G | 1 | a0001c0001t0044g0157 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.852-3720A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37851060 | |||||||
| chr9:37851099 | C | G | 5 | a0001c0001t0002g0273 a0001c0001t0002g0276 a0001c0001t0002g0295 others(2): Show |
5 | HG01255.hp1 HG01891.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.852-3681C>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37851099 | |||||||
| chr9:37851390 | G | A | 51 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(48): Show |
55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.852-3390G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37851390 | |||||||
| chr9:37851421 | C | T | 22 | a0001c0001t0008g0046 a0001c0001t0008g0047 a0001c0001t0008g0048 others(19): Show |
25 | HG01243.hp1 HG02257.hp2 HG02451.hp2 others(22): Show |
intron_variant | MODIFIER | c.852-3359C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37851421 | |||||||
| chr9:37851433 | G | T | 3 | a0001c0001t0001g0015 a0001c0001t0001g0132 a0001c0001t0001g0133 |
4 | HG01099.hp2 HG01168.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.852-3347G>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37851433 | |||||||
| chr9:37851553 | G | C | 6 | a0001c0001t0019g0055 a0001c0001t0019g0057 a0001c0001t0020g0053 others(3): Show |
7 | HG01243.hp1 HG02486.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.852-3227G>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37851553 | |||||||
| chr9:37851560 | C | T | 1 | a0001c0001t0004g0136 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.852-3220C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37851560 | |||||||
| chr9:37851668 | G | A | 51 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(48): Show |
55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.852-3112G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37851668 | |||||||
| chr9:37851680 | G | A | 13 | a0001c0001t0012g0005 a0001c0001t0012g0059 a0001c0001t0012g0060 others(10): Show |
15 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.852-3100G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37851680 | |||||||
| chr9:37851688 | G | A | 2 | a0001c0001t0002g0260 a0001c0001t0006g0259 |
2 | HG01109.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.852-3092G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37851688 | |||||||
| chr9:37851693 | G | GCTGAGGC others(12): Show |
1 | a0001c0001t0001g0152 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.852-3086_852-3068d others(21): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37851693 | ||||||
| chr9:37851788 | A | AAAAT | 3 | a0001c0001t0006g0255 a0001c0001t0006g0256 a0001c0001t0006g0257 |
3 | HG01361.hp2 HG01975.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.852-2970_852-2967d others(6): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37851788 | ||||||
| chr9:37851788 | AAAAT | A | 6 | a0001c0001t0001g0185 a0001c0001t0001g0210 a0001c0001t0001g0224 others(3): Show |
6 | HG02451.hp1 HG02559.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.852-2970_852-2967d others(6): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37851788 | ||||||
| chr9:37851791 | AT | A | 50 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(47): Show |
54 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.852-2988delT | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37851791 | |||||||
| chr9:37851796 | T | A | 1 | a0001c0001t0008g0051 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.852-2984T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37851796 | |||||||
| chr9:37851810 | A | T | 15 | a0001c0001t0001g0009 a0001c0001t0001g0161 a0001c0001t0001g0162 others(12): Show |
17 | HG00438.hp2 HG00639.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.852-2970A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37851810 | |||||||
| chr9:37851866 | C | CCGAAA | 6 | a0001c0001t0019g0055 a0001c0001t0019g0057 a0001c0001t0020g0053 others(3): Show |
7 | HG01243.hp1 HG02486.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.852-2914_852-2913i others(7): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37851866 | |||||||
| chr9:37851866 | C | CTGAAA | 45 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(42): Show |
48 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(45): Show |
intron_variant | MODIFIER | c.852-2908_852-2904d others(7): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37851866 | ||||||
| chr9:37852080 | A | C | 1 | a0001c0001t0032g0056 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.852-2700A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37852080 | |||||||
| chr9:37852140 | C | A | 51 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(48): Show |
55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.852-2640C>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37852140 | |||||||
| chr9:37852602 | A | AAG | 51 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(48): Show |
55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.852-2175_852-2174d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37852602 | ||||||
| chr9:37852648 | C | A | 12 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0078 others(9): Show |
12 | HG00621.hp2 HG02080.hp2 NA18747.hp2 others(9): Show |
intron_variant | MODIFIER | c.852-2132C>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37852648 | |||||||
| chr9:37852681 | C | T | 2 | a0001c0001t0002g0274 a0001c0001t0015g0040 |
2 | HG00099.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.852-2099C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37852681 | |||||||
| chr9:37852682 | G | A | 13 | a0001c0001t0012g0005 a0001c0001t0012g0059 a0001c0001t0012g0060 others(10): Show |
15 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.852-2098G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37852682 | |||||||
| chr9:37852736 | C | G | 7 | a0001c0001t0002g0001 a0001c0001t0002g0265 a0001c0001t0002g0271 others(4): Show |
10 | HG00558.hp1 HG03239.hp1 HG03490.hp2 others(7): Show |
intron_variant | MODIFIER | c.852-2044C>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37852736 | |||||||
| chr9:37852864 | T | C | 13 | a0001c0001t0001g0009 a0001c0001t0001g0161 a0001c0001t0001g0162 others(10): Show |
14 | HG00438.hp2 HG00735.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.852-1916T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37852864 | |||||||
| chr9:37852930 | T | TTA | 21 | a0001c0001t0001g0072 a0001c0001t0001g0081 a0001c0001t0001g0083 others(18): Show |
21 | HG01099.hp2 HG01516.hp1 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.852-1815_852-1814d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37852930 | ||||||
| chr9:37852930 | T | TTATA | 20 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0078 others(17): Show |
23 | HG00099.hp1 HG00621.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.852-1817_852-1814d others(6): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37852930 | ||||||
| chr9:37852930 | T | TTATATA | 17 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0071 others(14): Show |
17 | HG00558.hp2 HG01261.hp1 HG01993.hp1 others(14): Show |
intron_variant | MODIFIER | c.852-1819_852-1814d others(8): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37852930 | ||||||
| chr9:37852930 | T | TTATATAT others(1): Show |
22 | a0001c0001t0001g0013 a0001c0001t0001g0098 a0001c0001t0001g0101 others(19): Show |
26 | HG00140.hp1 HG00558.hp1 HG00597.hp1 others(23): Show |
intron_variant | MODIFIER | c.852-1821_852-1814d others(10): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37852930 | ||||||
| chr9:37852930 | T | TTATATAT others(3): Show |
39 | a0001c0001t0001g0006 a0001c0001t0001g0066 a0001c0001t0001g0115 others(36): Show |
40 | HG00741.hp2 HG01109.hp1 HG01891.hp2 others(37): Show |
intron_variant | MODIFIER | c.852-1823_852-1814d others(12): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37852930 | ||||||
| chr9:37852930 | T | TTATATAT others(5): Show |
16 | a0001c0001t0001g0069 a0001c0001t0001g0110 a0001c0001t0001g0139 others(13): Show |
16 | HG00642.hp2 HG01074.hp1 HG01981.hp2 others(13): Show |
intron_variant | MODIFIER | c.852-1825_852-1814d others(14): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37852930 | ||||||
| chr9:37852930 | T | TTATATAT others(7): Show |
13 | a0001c0001t0001g0097 a0001c0001t0001g0103 a0001c0001t0001g0107 others(10): Show |
13 | HG02132.hp2 HG02135.hp2 HG02165.hp2 others(10): Show |
intron_variant | MODIFIER | c.852-1827_852-1814d others(16): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37852930 | ||||||
| chr9:37852930 | T | TTATATAT others(9): Show |
2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | HG01257.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.852-1829_852-1814d others(18): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37852930 | ||||||
| chr9:37852930 | T | TTATATAT others(11): Show |
1 | a0001c0001t0002g0298 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.852-1831_852-1814d others(20): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37852930 | ||||||
| chr9:37852930 | T | TTATATAT others(13): Show |
1 | a0001c0001t0024g0141 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.852-1833_852-1814d others(22): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37852930 | ||||||
| chr9:37852930 | TTA | T | 7 | a0001c0001t0001g0282 a0001c0001t0004g0143 a0001c0001t0007g0267 others(4): Show |
7 | HG03195.hp1 NA18947.hp1 NA18952.hp2 others(4): Show |
intron_variant | MODIFIER | c.852-1815_852-1814d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37852930 | ||||||
| chr9:37852930 | TTATA | T | 4 | a0001c0001t0001g0009 a0001c0001t0001g0132 a0001c0001t0001g0162 others(1): Show |
5 | HG03654.hp1 NA18986.hp1 NA19056.hp2 others(2): Show |
intron_variant | MODIFIER | c.852-1817_852-1814d others(6): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37852930 | ||||||
| chr9:37852930 | TTATATAT others(3): Show |
T | 2 | a0001c0001t0002g0283 a0001c0001t0007g0289 |
2 | HG02083.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.852-1823_852-1814d others(12): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37852930 | ||||||
| chr9:37852930 | TTATATAT others(5): Show |
T | 1 | a0001c0001t0006g0262 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.852-1825_852-1814d others(14): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37852930 | ||||||
| chr9:37852930 | TTATATAT others(7): Show |
T | 2 | a0001c0001t0001g0102 a0001c0001t0002g0316 |
2 | HG02055.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.852-1827_852-1814d others(16): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37852930 | ||||||
| chr9:37852930 | TTATATAT others(9): Show |
T | 3 | a0001c0001t0001g0131 a0001c0001t0003g0088 a0001c0001t0003g0089 |
3 | HG00099.hp2 HG00738.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.852-1829_852-1814d others(18): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37852930 | ||||||
| chr9:37852930 | TTATATAT others(11): Show |
T | 102 | a0001c0001t0001g0014 a0001c0001t0001g0122 a0001c0001t0001g0123 others(99): Show |
108 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.852-1831_852-1814d others(20): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37852930 | ||||||
| chr9:37852930 | TTATATAT others(13): Show |
T | 39 | a0001c0001t0001g0334 a0001c0001t0005g0022 a0001c0001t0005g0024 others(36): Show |
41 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(38): Show |
intron_variant | MODIFIER | c.852-1833_852-1814d others(22): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37852930 | ||||||
| chr9:37852950 | A | T | 13 | a0001c0001t0012g0005 a0001c0001t0012g0059 a0001c0001t0012g0060 others(10): Show |
15 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.852-1830A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37852950 | |||||||
| chr9:37852965 | T | A | 51 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(48): Show |
55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.852-1815T>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37852965 | |||||||
| chr9:37852965 | T | TATATATA others(6): Show |
1 | a0001c0001t0002g0290 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.852-1814_852-1813i others(15): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37852965 | ||||||
| chr9:37852966 | A | ATATAT | 3 | a0001c0001t0001g0073 a0001c0001t0002g0258 a0001c0001t0042g0278 |
3 | HG02071.hp2 HG02074.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.852-1814_852-1813i others(7): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37852966 | |||||||
| chr9:37852966 | A | ATATATAT others(6): Show |
2 | a0001c0001t0001g0126 a0001c0001t0001g0245 |
2 | HG02155.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.852-1814_852-1813i others(15): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37852966 | |||||||
| chr9:37853040 | T | G | 26 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(23): Show |
27 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.852-1740T>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37853040 | |||||||
| chr9:37853067 | G | A | 1 | a0001c0003t0030g0045 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.852-1713G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37853067 | |||||||
| chr9:37853108 | C | T | 15 | a0001c0001t0001g0009 a0001c0001t0001g0161 a0001c0001t0001g0162 others(12): Show |
17 | HG00438.hp2 HG00639.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.852-1672C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37853108 | |||||||
| chr9:37853120 | C | G | 1 | a0001c0001t0063g0044 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.852-1660C>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37853120 | |||||||
| chr9:37853144 | C | T | 4 | a0001c0001t0014g0012 a0001c0001t0014g0165 a0001c0001t0014g0237 others(1): Show |
5 | HG03209.hp2 HG03540.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.852-1636C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37853144 | |||||||
| chr9:37853148 | G | A | 29 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(26): Show |
30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.852-1632G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37853148 | |||||||
| chr9:37853152 | C | CA | 12 | a0001c0001t0001g0073 a0001c0001t0001g0146 a0001c0001t0001g0147 others(9): Show |
12 | HG01109.hp1 HG02055.hp2 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.852-1612dupA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37853152 | ||||||
| chr9:37853152 | C | CAA | 30 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(27): Show |
31 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.852-1613_852-1612d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37853152 | ||||||
| chr9:37853152 | C | CAAA | 7 | a0001c0001t0008g0046 a0001c0001t0008g0047 a0001c0001t0008g0048 others(4): Show |
8 | HG02451.hp2 HG02818.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.852-1614_852-1612d others(5): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37853152 | ||||||
| chr9:37853152 | C | CAAAA | 10 | a0001c0001t0008g0050 a0001c0001t0012g0005 a0001c0001t0012g0059 others(7): Show |
12 | HG01243.hp1 HG02486.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.852-1615_852-1612d others(6): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37853152 | ||||||
| chr9:37853284 | G | A | 1 | a0001c0001t0051g0177 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.852-1496G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37853284 | |||||||
| chr9:37853339 | A | G | 51 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(48): Show |
55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.852-1441A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37853339 | |||||||
| chr9:37853356 | CGAGCTGA | C | 8 | a0001c0001t0008g0046 a0001c0001t0008g0047 a0001c0001t0008g0048 others(5): Show |
9 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.852-1421_852-1415d others(9): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37853356 | ||||||
| chr9:37853366 | C | G | 1 | a0001c0003t0030g0045 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.852-1414C>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37853366 | |||||||
| chr9:37853375 | T | G | 1 | a0001c0001t0006g0279 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.852-1405T>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37853375 | |||||||
| chr9:37853413 | CA | C | 260 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(257): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.852-1348delA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37853413 | ||||||
| chr9:37853413 | CAA | C | 7 | a0001c0001t0001g0139 a0001c0001t0001g0334 a0001c0001t0003g0231 others(4): Show |
8 | HG01074.hp1 HG02738.hp2 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.852-1349_852-1348d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37853413 | ||||||
| chr9:37853413 | CAAA | C | 35 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(32): Show |
37 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.852-1350_852-1348d others(5): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37853413 | ||||||
| chr9:37853413 | CAAAA | C | 15 | a0001c0001t0008g0050 a0001c0001t0012g0005 a0001c0001t0012g0059 others(12): Show |
17 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.852-1351_852-1348d others(6): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37853413 | ||||||
| chr9:37853443 | T | C | 1 | a0001c0001t0010g0155 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.852-1337T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37853443 | |||||||
| chr9:37853489 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.852-1291G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37853489 | |||||||
| chr9:37853503 | C | CAAAAAGA others(274): Show |
1 | a0001c0001t0063g0044 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.852-1261_852-1260i others(283): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 37853503 | ||||||
| chr9:37853511 | T | C | 2 | a0001c0001t0004g0240 a0001c0001t0053g0241 |
2 | HG02622.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.852-1269T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37853511 | |||||||
| chr9:37853548 | T | G | 1 | a0001c0001t0006g0261 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.852-1232T>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37853548 | |||||||
| chr9:37853649 | CA | C | 8 | a0001c0001t0008g0046 a0001c0001t0008g0047 a0001c0001t0008g0048 others(5): Show |
9 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.852-1130delA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37853649 | |||||||
| chr9:37853651 | G | T | 8 | a0001c0001t0008g0046 a0001c0001t0008g0047 a0001c0001t0008g0048 others(5): Show |
9 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.852-1129G>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37853651 | |||||||
| chr9:37853815 | C | T | 38 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(35): Show |
40 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.852-965C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37853815 | |||||||
| chr9:37853903 | C | T | 4 | a0001c0001t0001g0101 a0001c0001t0001g0116 a0001c0001t0001g0119 others(1): Show |
4 | HG02129.hp2 NA18950.hp2 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.852-877C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37853903 | |||||||
| chr9:37854277 | T | C | 51 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(48): Show |
55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.852-503T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37854277 | |||||||
| chr9:37854459 | A | G | 1 | a0001c0001t0002g0277 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.852-321A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37854459 | |||||||
| chr9:37854551 | G | A | 1 | a0001c0001t0015g0038 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.852-229G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37854551 | |||||||
| chr9:37854588 | A | G | 1 | a0001c0001t0001g0122 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.852-192A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 3/6 | chr9 | 37854588 | |||||||
| chr9:37855006 | A | G | 51 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(48): Show |
55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.1054+24A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | chr9 | 37855006 | |||||||
| chr9:37855041 | G | A | 51 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(48): Show |
55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.1054+59G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | chr9 | 37855041 | |||||||
| chr9:37855086 | G | A | 51 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(48): Show |
55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.1054+104G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | chr9 | 37855086 | |||||||
| chr9:37855124 | G | A | 1 | a0001c0003t0030g0045 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1054+142G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | chr9 | 37855124 | |||||||
| chr9:37855133 | T | C | 1 | a0002c0007t0008g0052 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1054+151T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | chr9 | 37855133 | |||||||
| chr9:37855158 | A | G | 1 | a0001c0001t0009g0028 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1054+176A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | chr9 | 37855158 | |||||||
| chr9:37855313 | A | C | 1 | a0001c0001t0001g0242 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1054+331A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | chr9 | 37855313 | |||||||
| chr9:37855389 | G | A | 1 | a0002c0007t0008g0052 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1054+407G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | chr9 | 37855389 | |||||||
| chr9:37855536 | C | T | 4 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0004g0150 others(1): Show |
4 | HG02572.hp2 HG02630.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1054+554C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | chr9 | 37855536 | |||||||
| chr9:37855537 | G | A | 8 | a0001c0001t0008g0046 a0001c0001t0008g0047 a0001c0001t0008g0048 others(5): Show |
9 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.1054+555G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | chr9 | 37855537 | |||||||
| chr9:37855555 | A | G | 30 | a0001c0001t0004g0091 a0001c0001t0005g0022 a0001c0001t0005g0024 others(27): Show |
31 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.1054+573A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | chr9 | 37855555 | |||||||
| chr9:37855699 | G | T | 89 | a0001c0001t0001g0014 a0001c0001t0001g0122 a0001c0001t0001g0123 others(86): Show |
93 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.1054+717G>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | chr9 | 37855699 | |||||||
| chr9:37855700 | C | T | 90 | a0001c0001t0001g0014 a0001c0001t0001g0122 a0001c0001t0001g0123 others(87): Show |
94 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.1054+718C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | chr9 | 37855700 | |||||||
| chr9:37855738 | G | A | 4 | a0001c0001t0012g0005 a0001c0001t0012g0059 a0001c0001t0012g0060 others(1): Show |
5 | HG02647.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1054+756G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | chr9 | 37855738 | |||||||
| chr9:37855750 | C | T | 48 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0094 others(45): Show |
49 | HG00558.hp2 HG00597.hp1 HG01069.hp2 others(46): Show |
intron_variant | MODIFIER | c.1054+768C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | chr9 | 37855750 | |||||||
| chr9:37855767 | T | C | 1 | a0001c0001t0003g0182 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1054+785T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | chr9 | 37855767 | |||||||
| chr9:37855827 | C | A | 2 | a0001c0001t0045g0264 a0001c0004t0047g0288 |
2 | HG02074.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.1054+845C>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | chr9 | 37855827 | |||||||
| chr9:37855844 | A | C | 1 | a0001c0001t0001g0111 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1054+862A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | chr9 | 37855844 | |||||||
| chr9:37855991 | A | C | 8 | a0001c0001t0008g0046 a0001c0001t0008g0047 a0001c0001t0008g0048 others(5): Show |
9 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.1054+1009A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | chr9 | 37855991 | |||||||
| chr9:37856003 | T | C | 3 | a0001c0001t0022g0335 a0001c0001t0022g0336 a0001c0001t0031g0337 |
3 | HG02257.hp2 HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1054+1021T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | chr9 | 37856003 | |||||||
| chr9:37856183 | A | T | 1 | a0001c0001t0008g0050 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1055-1058A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | chr9 | 37856183 | |||||||
| chr9:37856237 | G | T | 1 | a0001c0001t0001g0002 | 3 | HG02735.hp2 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1055-1004G>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | chr9 | 37856237 | |||||||
| chr9:37856471 | G | GT | 51 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(48): Show |
55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.1055-769dupT | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr9 | 37856471 | ||||||
| chr9:37856514 | A | C | 1 | a0001c0001t0001g0138 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1055-727A>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | chr9 | 37856514 | |||||||
| chr9:37856636 | TTA | T | 3 | a0001c0001t0003g0173 a0001c0001t0003g0174 a0001c0001t0003g0175 |
3 | NA18960.hp1 NA18980.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1055-603_1055-602d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr9 | 37856636 | ||||||
| chr9:37856685 | C | T | 2 | a0001c0001t0006g0261 a0001c0001t0006g0262 |
2 | NA18995.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1055-556C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | chr9 | 37856685 | |||||||
| chr9:37856783 | G | A | 29 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(26): Show |
30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.1055-458G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | chr9 | 37856783 | |||||||
| chr9:37856787 | C | CA | 12 | a0001c0001t0002g0290 a0001c0001t0002g0292 a0001c0001t0002g0298 others(9): Show |
12 | HG02132.hp1 HG02148.hp1 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.1055-445dupA | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr9 | 37856787 | ||||||
| chr9:37857070 | G | C | 13 | a0001c0001t0012g0005 a0001c0001t0012g0059 a0001c0001t0012g0060 others(10): Show |
15 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.1055-171G>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | chr9 | 37857070 | |||||||
| chr9:37857131 | G | A | 1 | a0001c0001t0008g0050 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1055-110G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 4/6 | chr9 | 37857131 | |||||||
| chr9:37857428 | C | A | 2 | a0001c0001t0004g0240 a0001c0001t0053g0241 |
2 | HG02622.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1165+77C>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 5/6 | chr9 | 37857428 | |||||||
| chr9:37857606 | G | A | 9 | a0001c0001t0019g0055 a0001c0001t0019g0057 a0001c0001t0020g0053 others(6): Show |
10 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1165+255G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 5/6 | chr9 | 37857606 | |||||||
| chr9:37857669 | C | T | 9 | a0001c0001t0019g0055 a0001c0001t0019g0057 a0001c0001t0020g0053 others(6): Show |
10 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1165+318C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 5/6 | chr9 | 37857669 | |||||||
| chr9:37857681 | GTATAAA | G | 4 | a0001c0001t0008g0046 a0001c0001t0008g0047 a0001c0001t0008g0048 others(1): Show |
4 | HG02451.hp2 HG02818.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1165+336_1165+341d others(8): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr9 | 37857681 | ||||||
| chr9:37857708 | G | A | 1 | a0002c0007t0008g0052 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1165+357G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 5/6 | chr9 | 37857708 | |||||||
| chr9:37857964 | G | C | 51 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(48): Show |
55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.1165+613G>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 5/6 | chr9 | 37857964 | |||||||
| chr9:37858037 | C | CT | 16 | a0001c0001t0001g0204 a0001c0001t0008g0046 a0001c0001t0008g0047 others(13): Show |
18 | HG02257.hp2 HG02451.hp2 HG02647.hp2 others(15): Show |
intron_variant | MODIFIER | c.1165+696dupT | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr9 | 37858037 | ||||||
| chr9:37858037 | C | CTT | 7 | a0001c0001t0019g0055 a0001c0001t0019g0057 a0001c0001t0020g0053 others(4): Show |
8 | HG01243.hp1 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1165+695_1165+696d others(4): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr9 | 37858037 | ||||||
| chr9:37858299 | T | G | 1 | a0002c0007t0008g0052 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1165+948T>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 5/6 | chr9 | 37858299 | |||||||
| chr9:37858399 | A | G | 28 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(25): Show |
29 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.1165+1048A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 5/6 | chr9 | 37858399 | |||||||
| chr9:37858425 | TG | T | 1 | a0001c0001t0001g0002 | 3 | HG02735.hp2 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1165+1075delG | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 5/6 | chr9 | 37858425 | |||||||
| chr9:37858488 | A | G | 1 | a0001c0001t0001g0081 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1165+1137A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 5/6 | chr9 | 37858488 | |||||||
| chr9:37858655 | G | T | 1 | a0001c0001t0018g0016 | 2 | HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1165+1304G>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 5/6 | chr9 | 37858655 | |||||||
| chr9:37858864 | C | G | 51 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(48): Show |
55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.1166-1184C>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 5/6 | chr9 | 37858864 | |||||||
| chr9:37858930 | G | A | 1 | a0001c0001t0001g0239 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1166-1118G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 5/6 | chr9 | 37858930 | |||||||
| chr9:37858963 | C | T | 4 | a0001c0001t0001g0139 a0001c0001t0024g0140 a0001c0001t0024g0141 others(1): Show |
4 | HG00140.hp1 HG01074.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.1166-1085C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 5/6 | chr9 | 37858963 | |||||||
| chr9:37859124 | T | C | 1 | a0001c0001t0001g0252 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1166-924T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 5/6 | chr9 | 37859124 | |||||||
| chr9:37859149 | G | C | 1 | a0001c0003t0030g0045 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1166-899G>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 5/6 | chr9 | 37859149 | |||||||
| chr9:37859397 | C | A | 1 | a0002c0007t0008g0052 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1166-651C>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 5/6 | chr9 | 37859397 | |||||||
| chr9:37859734 | G | A | 29 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(26): Show |
30 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.1166-314G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 5/6 | chr9 | 37859734 | |||||||
| chr9:37859883 | C | T | 1 | a0001c0001t0058g0096 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1166-165C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 5/6 | chr9 | 37859883 | |||||||
| chr9:37859894 | T | C | 8 | a0001c0001t0008g0046 a0001c0001t0008g0047 a0001c0001t0008g0048 others(5): Show |
9 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.1166-154T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 5/6 | chr9 | 37859894 | |||||||
| chr9:37859953 | G | A | 3 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0003c0005t0001g0074 |
3 | NA18945.hp2 NA18957.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1166-95G>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 5/6 | chr9 | 37859953 | |||||||
| chr9:37860208 | A | G | 1 | a0001c0001t0016g0195 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1311+15A>G | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 6/6 | chr9 | 37860208 | |||||||
| chr9:37860230 | T | C | 1 | a0001c0001t0040g0235 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1311+37T>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 6/6 | chr9 | 37860230 | |||||||
| chr9:37860261 | G | C | 51 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(48): Show |
55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.1311+68G>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 6/6 | chr9 | 37860261 | |||||||
| chr9:37860269 | C | T | 1 | a0001c0001t0001g0238 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1311+76C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 6/6 | chr9 | 37860269 | |||||||
| chr9:37860377 | C | A | 1 | a0001c0001t0014g0165 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1311+184C>A | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 6/6 | chr9 | 37860377 | |||||||
| chr9:37860395 | C | T | 1 | a0001c0001t0002g0283 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1311+202C>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 6/6 | chr9 | 37860395 | |||||||
| chr9:37860492 | T | TAAAC | 5 | a0001c0001t0001g0015 a0001c0001t0001g0132 a0001c0001t0001g0133 others(2): Show |
6 | HG00642.hp1 HG01099.hp2 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.1311+323_1311+326d others(6): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr9 | 37860492 | ||||||
| chr9:37860492 | TAAAC | T | 26 | a0001c0001t0005g0026 a0001c0001t0005g0027 a0001c0001t0005g0029 others(23): Show |
29 | HG01243.hp1 HG02257.hp2 HG02451.hp2 others(26): Show |
intron_variant | MODIFIER | c.1311+323_1311+326d others(6): Show |
DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr9 | 37860492 | ||||||
| chr9:37860902 | A | T | 3 | a0001c0001t0003g0088 a0001c0001t0003g0089 a0001c0001t0037g0223 |
3 | HG00099.hp2 HG00738.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.1312-238A>T | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 6/6 | chr9 | 37860902 | |||||||
| chr9:37860973 | G | C | 51 | a0001c0001t0005g0022 a0001c0001t0005g0024 a0001c0001t0005g0026 others(48): Show |
55 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.1312-167G>C | DCAF10 | ENSG00000122741.16 | transcript | ENST00000377724.8 | protein_coding | 6/6 | chr9 | 37860973 |