Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10238 |
| ensemblid | ENSG00000136485.16 |
| hgncid | 30915 |
| symbol | DCAF7 |
| name | DDB1 and CUL4 associated factor 7 |
| refseq_nuc | NM_005828.5 |
| refseq_prot | NP_005819.3 |
| ensembl_nuc | ENST00000614556.5 |
| ensembl_prot | ENSP00000483236.1 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 63550477 |
| end | 63594266 |
| strand | + |
| ver | v1.2 |
| region | chr17:63550477-63594266 |
| region5000 | chr17:63545477-63599266 |
| regionname0 | DCAF7_chr17_63550477_63594266 |
| regionname5000 | DCAF7_chr17_63545477_63599266 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 342 | 261 | 86 | 48 | 79 | 14 | 32 | 55 | DCAF7_chr17_63545477_63599266 | DCAF7 | MSLHG others(337): Show |
chr17 | 63545477 | 63599266 |
| a0002 | 0/0 | 342 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DCAF7_chr17_63545477_63599266 | DCAF7 | MSLHG others(337): Show |
chr17 | 63545477 | 63599266 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1026 | 246 | 79 | 42 | 77 | 14 | 32 | DCAF7_chr17_63545477_63599266 | DCAF7 | ATGTC others(1021): Show |
chr17 | 63545477 | 63599266 | ||
| a0001c0002 | 0/0 | 1026 | 8 | 7 | 1 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | ATGTC others(1021): Show |
chr17 | 63545477 | 63599266 | ||
| a0001c0003 | 0/0 | 1026 | 7 | 0 | 5 | 2 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | ATGTC others(1021): Show |
chr17 | 63545477 | 63599266 | ||
| a0002c0004 | 0/0 | 1026 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | ATGTC others(1021): Show |
chr17 | 63545477 | 63599266 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 6324 | 187 | 38 | 35 | 73 | 11 | 29 | DCAF7_chr17_63545477_63599266 | DCAF7 | GTCGT others(6319): Show |
chr17 | 63545477 | 63599266 |
| a0001c0001t0003 | 0/0 | 6324 | 6 | 6 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | GTCGT others(6319): Show |
chr17 | 63545477 | 63599266 |
| a0001c0001t0004 | 0/0 | 6324 | 6 | 6 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | GTCGT others(6319): Show |
chr17 | 63545477 | 63599266 |
| a0001c0001t0005 | 0/0 | 6324 | 5 | 4 | 1 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | GTCGT others(6319): Show |
chr17 | 63545477 | 63599266 |
| a0001c0001t0006 | 0/0 | 6325 | 3 | 2 | 1 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | GTCGT others(6320): Show |
chr17 | 63545477 | 63599266 |
| a0001c0001t0007 | 0/1 | 6325 | 3 | 0 | 1 | 0 | 1 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | GTCGT others(6320): Show |
chr17 | 63545477 | 63599266 |
| a0001c0001t0008 | 0/0 | 6324 | 2 | 1 | 1 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | GTCGT others(6319): Show |
chr17 | 63545477 | 63599266 |
| a0001c0001t0009 | 0/0 | 6323 | 2 | 1 | 1 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | GTCGT others(6318): Show |
chr17 | 63545477 | 63599266 |
| a0001c0001t0010 | 0/0 | 6324 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | GTCGT others(6319): Show |
chr17 | 63545477 | 63599266 |
| a0001c0001t0011 | 0/0 | 6324 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | GTCGT others(6319): Show |
chr17 | 63545477 | 63599266 |
| a0001c0001t0012 | 0/0 | 6324 | 2 | 0 | 0 | 0 | 0 | 2 | DCAF7_chr17_63545477_63599266 | DCAF7 | GTCGT others(6319): Show |
chr17 | 63545477 | 63599266 |
| a0001c0001t0013 | 0/0 | 6324 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | GTCGT others(6319): Show |
chr17 | 63545477 | 63599266 |
| a0001c0001t0014 | 0/0 | 6325 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | GTCGT others(6320): Show |
chr17 | 63545477 | 63599266 |
| a0001c0001t0015 | 0/0 | 6325 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | GTCGT others(6320): Show |
chr17 | 63545477 | 63599266 |
| a0001c0001t0016 | 0/0 | 6323 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | GTCGT others(6318): Show |
chr17 | 63545477 | 63599266 |
| a0001c0001t0017 | 0/0 | 6325 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | GTCGT others(6320): Show |
chr17 | 63545477 | 63599266 |
| a0001c0001t0018 | 0/0 | 6324 | 2 | 0 | 2 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | GTCGT others(6319): Show |
chr17 | 63545477 | 63599266 |
| a0001c0001t0019 | 0/0 | 6323 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | GTCGT others(6318): Show |
chr17 | 63545477 | 63599266 |
| a0001c0001t0020 | 0/0 | 6324 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | GTCGT others(6319): Show |
chr17 | 63545477 | 63599266 |
| a0001c0001t0021 | 0/0 | 6325 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | GTCGT others(6320): Show |
chr17 | 63545477 | 63599266 |
| a0001c0001t0022 | 0/0 | 6324 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | GTCGT others(6319): Show |
chr17 | 63545477 | 63599266 |
| a0001c0001t0023 | 0/0 | 6325 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | GTCGT others(6320): Show |
chr17 | 63545477 | 63599266 |
| a0001c0001t0024 | 0/0 | 6324 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | GTCGT others(6319): Show |
chr17 | 63545477 | 63599266 |
| a0001c0001t0025 | 0/0 | 6324 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | GTCGT others(6319): Show |
chr17 | 63545477 | 63599266 |
| a0001c0001t0026 | 0/0 | 6324 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF7_chr17_63545477_63599266 | DCAF7 | GTCGT others(6319): Show |
chr17 | 63545477 | 63599266 |
| a0001c0001t0027 | 0/0 | 6324 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | GTCGT others(6319): Show |
chr17 | 63545477 | 63599266 |
| a0001c0001t0028 | 0/0 | 6324 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | GTCGT others(6319): Show |
chr17 | 63545477 | 63599266 |
| a0001c0001t0029 | 0/0 | 6323 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | GTCGT others(6318): Show |
chr17 | 63545477 | 63599266 |
| a0001c0001t0030 | 0/0 | 6324 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | GTCGT others(6319): Show |
chr17 | 63545477 | 63599266 |
| a0001c0001t0031 | 0/0 | 6325 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | GTCGT others(6320): Show |
chr17 | 63545477 | 63599266 |
| a0001c0001t0032 | 0/0 | 6324 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | GTCGT others(6319): Show |
chr17 | 63545477 | 63599266 |
| a0001c0002t0002 | 0/0 | 6324 | 8 | 7 | 1 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | GTCGT others(6319): Show |
chr17 | 63545477 | 63599266 |
| a0001c0003t0001 | 0/0 | 6324 | 7 | 0 | 5 | 2 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | GTCGT others(6319): Show |
chr17 | 63545477 | 63599266 |
| a0002c0004t0001 | 0/0 | 6324 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | GTCGT others(6319): Show |
chr17 | 63545477 | 63599266 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0002 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0108 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0004g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0004g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0004g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0004g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0004g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0005g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0005g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0005g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0006g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0006g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0006g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0007g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0007g0098 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0007g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0008g0012 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0009g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0009g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0010g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0010g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0011g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0011g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0012g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0012g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0013g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0013g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0014g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0014g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0015g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0015g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0016g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0016g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0017g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0017g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0018g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0018g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0019g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0020g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0021g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0022g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0023g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0024g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0025g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0026g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0027g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0028g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0029g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0030g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0031g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0001t0032g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0002t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0002t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0002t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0002t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0002t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0002t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0002t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0002t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0003t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0003t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0003t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0003t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0001c0003t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| a0002c0004t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0142 | EUR | GBR | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0099 | EUR | GBR | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG00140 | hp1 | a0001 | c0001 | t0007 | g0103 | EUR | GBR | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0123 | EUR | GBR | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0165 | EUR | FIN | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG00280 | hp2 | a0001 | c0001 | t0031 | g0090 | EUR | FIN | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0100 | EUR | FIN | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG00323 | hp2 | a0001 | c0001 | t0030 | g0194 | EUR | FIN | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | CHS | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG00558 | hp2 | a0001 | c0001 | t0027 | g0075 | EAS | CHS | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | CHS | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG00741 | hp2 | a0001 | c0001 | t0008 | g0012 | AMR | PUR | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG01099 | hp2 | a0001 | c0002 | t0002 | g0034 | AMR | PUR | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG01106 | hp1 | a0001 | c0001 | t0018 | g0073 | AMR | PUR | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG01109 | hp2 | a0001 | c0001 | t0009 | g0170 | AMR | PUR | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG01243 | hp1 | a0001 | c0001 | t0006 | g0189 | AMR | PUR | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG01243 | hp2 | a0001 | c0001 | t0007 | g0092 | AMR | PUR | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG01346 | hp1 | a0001 | c0001 | t0005 | g0023 | AMR | CLM | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG01346 | hp2 | a0001 | c0001 | t0018 | g0050 | AMR | CLM | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | CLM | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0068 | EUR | IBS | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0144 | EUR | IBS | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0058 | EUR | IBS | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0044 | EUR | IBS | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG01928 | hp1 | a0001 | c0003 | t0001 | g0006 | AMR | PEL | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG01952 | hp2 | a0001 | c0003 | t0001 | g0006 | AMR | PEL | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG01975 | hp1 | a0001 | c0003 | t0001 | g0185 | AMR | PEL | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02004 | hp1 | a0001 | c0003 | t0001 | g0184 | AMR | PEL | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PEL | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02015 | hp1 | a0001 | c0001 | t0022 | g0217 | EAS | KHV | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0158 | AFR | ACB | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02145 | hp1 | a0001 | c0001 | t0025 | g0087 | AFR | ACB | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02145 | hp2 | a0001 | c0002 | t0002 | g0032 | AFR | ACB | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | CDX | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02257 | hp1 | a0001 | c0001 | t0016 | g0198 | AFR | ACB | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0159 | AFR | ACB | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02280 | hp1 | a0001 | c0001 | t0008 | g0012 | AFR | ACB | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | ACB | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02293 | hp1 | a0001 | c0003 | t0001 | g0043 | AMR | PEL | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02451 | hp1 | a0001 | c0001 | t0010 | g0113 | AFR | ACB | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02572 | hp1 | a0001 | c0002 | t0002 | g0031 | AFR | GWD | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0230 | AFR | GWD | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02622 | hp2 | a0001 | c0001 | t0017 | g0202 | AFR | GWD | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0231 | AFR | GWD | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02630 | hp2 | a0001 | c0001 | t0023 | g0211 | AFR | GWD | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0025 | AFR | GWD | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02723 | hp1 | a0001 | c0001 | t0019 | g0204 | AFR | GWD | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02738 | hp1 | a0001 | c0001 | t0012 | g0035 | SAS | PJL | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02809 | hp1 | a0001 | c0001 | t0006 | g0210 | AFR | GWD | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02818 | hp1 | a0001 | c0001 | t0005 | g0026 | AFR | GWD | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02818 | hp2 | a0001 | c0001 | t0015 | g0235 | AFR | GWD | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | GWD | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0233 | AFR | GWD | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0232 | AFR | GWD | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0174 | AFR | ESN | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ESN | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02965 | hp1 | a0001 | c0001 | t0005 | g0022 | AFR | ESN | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0173 | AFR | ESN | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ESN | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG03041 | hp1 | a0001 | c0001 | t0015 | g0229 | AFR | GWD | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG03041 | hp2 | a0001 | c0001 | t0017 | g0201 | AFR | GWD | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | MSL | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | MSL | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0176 | AFR | ESN | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG03130 | hp2 | a0001 | c0002 | t0002 | g0028 | AFR | ESN | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG03139 | hp1 | a0001 | c0001 | t0011 | g0207 | AFR | ESN | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ESN | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ESN | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG03195 | hp2 | a0001 | c0001 | t0029 | g0169 | AFR | ESN | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG03209 | hp1 | a0001 | c0001 | t0021 | g0209 | AFR | MSL | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG03209 | hp2 | a0001 | c0002 | t0002 | g0033 | AFR | MSL | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | MSL | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | MSL | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG03453 | hp2 | a0001 | c0001 | t0024 | g0077 | AFR | MSL | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG03486 | hp1 | a0001 | c0001 | t0009 | g0224 | AFR | MSL | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG03486 | hp2 | a0001 | c0001 | t0013 | g0086 | AFR | MSL | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG03491 | hp2 | a0001 | c0001 | t0012 | g0009 | SAS | PJL | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | ESN | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | ESN | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0226 | AFR | GWD | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | MSL | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | MSL | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | STU | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | STU | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | BEB | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | BEB | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | BEB | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | BEB | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | BEB | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | BEB | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG04184 | hp2 | a0001 | c0001 | t0026 | g0106 | SAS | BEB | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | STU | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | STU | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | STU | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | STU | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA18522 | hp1 | a0001 | c0001 | t0011 | g0212 | AFR | YRI | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA18522 | hp2 | a0001 | c0001 | t0006 | g0213 | AFR | YRI | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHB | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | CHB | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA18906 | hp1 | a0001 | c0001 | t0013 | g0228 | AFR | YRI | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | YRI | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA18978 | hp2 | a0002 | c0004 | t0001 | g0038 | EAS | JPT | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA19000 | hp2 | a0001 | c0001 | t0020 | g0179 | EAS | JPT | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA19009 | hp1 | a0001 | c0001 | t0028 | g0183 | EAS | JPT | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | LWK | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA19030 | hp2 | a0001 | c0001 | t0014 | g0205 | AFR | LWK | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | LWK | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA19043 | hp2 | a0001 | c0001 | t0014 | g0203 | AFR | LWK | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA19077 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA19087 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA19240 | hp1 | a0001 | c0002 | t0002 | g0027 | AFR | YRI | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | YRI | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0227 | AFR | ASW | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ASW | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02486 | hp1 | a0001 | c0002 | t0002 | g0030 | AFR | ACB | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02559 | hp1 | a0001 | c0001 | t0016 | g0199 | AFR | ACB | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0024 | AFR | ACB | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0175 | AFR | MSL | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG03471 | hp2 | a0001 | c0001 | t0010 | g0192 | AFR | MSL | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | USA | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | USA | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | USA | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA20300 | hp2 | a0001 | c0002 | t0002 | g0029 | AFR | USA | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | LWK | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| NA21309 | hp2 | a0001 | c0001 | t0032 | g0200 | AFR | LWK | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0007 | g0098 | REF | REF | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0108 | REF | REF | DCAF7_chr17_63545477_63599266 | DCAF7 | chr17 | 63545477 | 63599266 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:63578479 | G | A | 1 | a0002 | 1 | NA18978.hp2 | missense_variant | MODERATE | c.148G>A | p.Val50Ile | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 2/7 | 349/6324 | 148/1029 | 50/342 | chr17 | 63578479 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:63578577 | C | T | 1 | a0001c0003 | 7 | HG01928.hp1 HG01952.hp2 HG01975.hp1 others(4): Show |
synonymous_variant | LOW | c.246C>T | p.Gly82Gly | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 2/7 | 447/6324 | 246/1029 | 82/342 | chr17 | 63578577 | |||
| chr17:63579922 | G | A | 1 | a0001c0002 | 8 | HG01099.hp2 HG02145.hp2 HG02486.hp1 others(5): Show |
synonymous_variant | LOW | c.507G>A | p.Gln169Gln | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 4/7 | 708/6324 | 507/1029 | 169/342 | chr17 | 63579922 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:63550546 | C | T | 1 | a0001c0001t0018 | 2 | HG01106.hp1 HG01346.hp2 |
5_prime_UTR_variant | MODIFIER | c.-132C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/7 | 132 | chr17 | 63550546 | ||||||
| chr17:63550656 | G | T | 3 | a0001c0001t0016 a0001c0001t0017 a0001c0001t0032 |
5 | HG02257.hp1 HG02559.hp1 HG02622.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-22G>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/7 | 22 | chr17 | 63550656 | ||||||
| chr17:63589193 | C | T | 3 | a0001c0001t0014 a0001c0001t0015 a0001c0001t0017 |
6 | HG02622.hp2 HG02818.hp2 HG03041.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*21C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 7/7 | 21 | chr17 | 63589193 | ||||||
| chr17:63589233 | C | G | 1 | a0001c0001t0017 | 2 | HG02622.hp2 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*61C>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 7/7 | 61 | chr17 | 63589233 | ||||||
| chr17:63589325 | C | T | 3 | a0001c0001t0007 a0001c0001t0030 a0001c0001t0031 |
4 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*153C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 7/7 | 153 | chr17 | 63589325 | ||||||
| chr17:63589361 | T | C | 1 | a0001c0001t0008 | 2 | HG00741.hp2 HG02280.hp1 |
3_prime_UTR_variant | MODIFIER | c.*189T>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 7/7 | 189 | chr17 | 63589361 | ||||||
| chr17:63589378 | G | C | 1 | a0001c0001t0005 | 5 | HG01346.hp1 HG02559.hp2 HG02717.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*206G>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 7/7 | 206 | chr17 | 63589378 | ||||||
| chr17:63589467 | G | A | 2 | a0001c0001t0009 a0001c0001t0019 |
3 | HG01109.hp2 HG02723.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*295G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 7/7 | 295 | chr17 | 63589467 | ||||||
| chr17:63589489 | G | A | 1 | a0001c0001t0020 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*317G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 7/7 | 317 | chr17 | 63589489 | ||||||
| chr17:63589646 | C | T | 3 | a0001c0001t0007 a0001c0001t0030 a0001c0001t0031 |
4 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*474C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 7/7 | 474 | chr17 | 63589646 | ||||||
| chr17:63589724 | A | G | 1 | a0001c0002t0002 | 8 | HG01099.hp2 HG02145.hp2 HG02486.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*552A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 7/7 | 552 | chr17 | 63589724 | ||||||
| chr17:63589893 | C | T | 1 | a0001c0001t0015 | 2 | HG02818.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*721C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 7/7 | 721 | chr17 | 63589893 | ||||||
| chr17:63589905 | C | T | 2 | a0001c0001t0016 a0001c0001t0029 |
3 | HG02257.hp1 HG02559.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*733C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 7/7 | 733 | chr17 | 63589905 | ||||||
| chr17:63590284 | G | C | 1 | a0001c0001t0021 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1112G>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 7/7 | 1112 | chr17 | 63590284 | ||||||
| chr17:63590481 | C | T | 1 | a0001c0001t0019 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1309C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 7/7 | 1309 | chr17 | 63590481 | ||||||
| chr17:63590513 | A | G | 1 | a0001c0001t0013 | 2 | HG03486.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1341A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 7/7 | 1341 | chr17 | 63590513 | ||||||
| chr17:63590930 | G | C | 1 | a0001c0001t0010 | 2 | HG02451.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1758G>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 7/7 | 1758 | chr17 | 63590930 | ||||||
| chr17:63590933 | C | A | 1 | a0001c0001t0022 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1761C>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 7/7 | 1761 | chr17 | 63590933 | ||||||
| chr17:63591529 | C | G | 1 | a0001c0001t0031 | 1 | HG00280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2357C>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 7/7 | 2357 | chr17 | 63591529 | ||||||
| chr17:63591606 | C | G | 1 | a0001c0001t0032 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2434C>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 7/7 | 2434 | chr17 | 63591606 | ||||||
| chr17:63591869 | G | T | 1 | a0001c0001t0028 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2697G>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 7/7 | 2697 | chr17 | 63591869 | ||||||
| chr17:63591900 | G | A | 1 | a0001c0001t0023 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2728G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 7/7 | 2728 | chr17 | 63591900 | ||||||
| chr17:63591930 | C | G | 1 | a0001c0001t0010 | 2 | HG02451.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2758C>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 7/7 | 2758 | chr17 | 63591930 | ||||||
| chr17:63592104 | AT | A | 5 | a0001c0001t0009 a0001c0001t0016 a0001c0001t0019 others(2): Show |
7 | HG01109.hp2 HG02257.hp1 HG02559.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2935delT | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 7/7 | 2935 | INFO_REALIGN_3_PRIME | chr17 | 63592104 | |||||
| chr17:63592106 | T | C | 1 | a0001c0001t0011 | 2 | HG03139.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2934T>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 7/7 | 2934 | chr17 | 63592106 | ||||||
| chr17:63592322 | G | A | 1 | a0001c0001t0025 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3150G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 7/7 | 3150 | chr17 | 63592322 | ||||||
| chr17:63592383 | C | T | 1 | a0001c0001t0004 | 6 | HG02055.hp1 HG02258.hp1 HG02922.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3211C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 7/7 | 3211 | chr17 | 63592383 | ||||||
| chr17:63592411 | T | A | 1 | a0001c0001t0026 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3239T>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 7/7 | 3239 | chr17 | 63592411 | ||||||
| chr17:63592411 | T | TA | 9 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0014 others(6): Show |
15 | HG00140.hp1 HG00280.hp2 HG01243.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3255dupA | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 7/7 | 3256 | INFO_REALIGN_3_PRIME | chr17 | 63592411 | |||||
| chr17:63592414 | A | T | 4 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0013 others(1): Show |
11 | HG01109.hp2 HG02622.hp1 HG02630.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3242A>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 7/7 | 3242 | chr17 | 63592414 | ||||||
| chr17:63592450 | C | T | 1 | a0001c0001t0012 | 2 | HG02738.hp1 HG03491.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3278C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 7/7 | 3278 | chr17 | 63592450 | ||||||
| chr17:63592630 | G | C | 1 | a0001c0001t0017 | 2 | HG02622.hp2 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3458G>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 7/7 | 3458 | chr17 | 63592630 | ||||||
| chr17:63592669 | G | A | 1 | a0001c0001t0024 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3497G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 7/7 | 3497 | chr17 | 63592669 | ||||||
| chr17:63592991 | T | C | 5 | a0001c0001t0009 a0001c0001t0016 a0001c0001t0019 others(2): Show |
7 | HG01109.hp2 HG02257.hp1 HG02559.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3819T>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 7/7 | 3819 | chr17 | 63592991 | ||||||
| chr17:63593316 | A | G | 1 | a0001c0001t0011 | 2 | HG03139.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4144A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 7/7 | 4144 | chr17 | 63593316 | ||||||
| chr17:63593425 | A | G | 1 | a0001c0001t0005 | 5 | HG01346.hp1 HG02559.hp2 HG02717.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4253A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 7/7 | 4253 | chr17 | 63593425 | ||||||
| chr17:63593765 | A | G | 1 | a0001c0001t0027 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4593A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 7/7 | 4593 | chr17 | 63593765 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:63550868 | C | T | 1 | a0001c0001t0001g0236 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.138+53C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63550868 | |||||||
| chr17:63550932 | G | A | 6 | a0001c0001t0001g0021 a0001c0001t0005g0022 a0001c0001t0005g0023 others(3): Show |
6 | HG01346.hp1 HG02559.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.138+117G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63550932 | |||||||
| chr17:63551177 | G | A | 8 | a0001c0002t0002g0027 a0001c0002t0002g0028 a0001c0002t0002g0029 others(5): Show |
8 | HG01099.hp2 HG02145.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.138+362G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63551177 | |||||||
| chr17:63551242 | C | T | 12 | a0001c0001t0001g0225 a0001c0001t0001g0234 a0001c0001t0003g0226 others(9): Show |
12 | HG02622.hp1 HG02630.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.138+427C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63551242 | |||||||
| chr17:63551294 | G | T | 1 | a0001c0001t0001g0223 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.138+479G>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63551294 | |||||||
| chr17:63551307 | A | ACC | 52 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(49): Show |
60 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.138+499_138+500dup others(2): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63551307 | ||||||
| chr17:63551311 | C | CCT | 10 | a0001c0001t0001g0004 a0001c0001t0001g0214 a0001c0001t0001g0215 others(7): Show |
12 | HG00544.hp2 HG02015.hp1 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.138+497_138+498ins others(2): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63551311 | ||||||
| chr17:63551311 | C | G | 6 | a0001c0001t0001g0021 a0001c0001t0005g0022 a0001c0001t0005g0023 others(3): Show |
6 | HG01346.hp1 HG02559.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.138+496C>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63551311 | |||||||
| chr17:63551320 | A | T | 8 | a0001c0001t0001g0020 a0001c0001t0001g0208 a0001c0001t0006g0210 others(5): Show |
9 | HG02280.hp2 HG02630.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.138+505A>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63551320 | |||||||
| chr17:63551321 | C | T | 6 | a0001c0001t0001g0021 a0001c0001t0005g0022 a0001c0001t0005g0023 others(3): Show |
6 | HG01346.hp1 HG02559.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.138+506C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63551321 | |||||||
| chr17:63551420 | T | C | 1 | a0001c0001t0012g0035 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.138+605T>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63551420 | |||||||
| chr17:63551741 | A | G | 8 | a0001c0001t0001g0020 a0001c0001t0001g0208 a0001c0001t0006g0210 others(5): Show |
9 | HG02280.hp2 HG02630.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.138+926A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63551741 | |||||||
| chr17:63551847 | G | C | 1 | a0001c0001t0001g0014 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.138+1032G>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63551847 | |||||||
| chr17:63551891 | C | CAA | 12 | a0001c0001t0001g0089 a0001c0001t0001g0091 a0001c0001t0001g0093 others(9): Show |
12 | HG00099.hp2 HG00280.hp2 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.138+1115_138+1116d others(4): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63551891 | ||||||
| chr17:63551891 | C | CAAA | 11 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(8): Show |
11 | HG01106.hp2 HG02145.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.138+1114_138+1116d others(5): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63551891 | ||||||
| chr17:63551891 | C | CAAAAAAA others(4): Show |
1 | a0001c0001t0024g0077 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.138+1106_138+1116d others(13): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63551891 | ||||||
| chr17:63551891 | CA | C | 7 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(4): Show |
7 | HG01099.hp2 HG02135.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.138+1116delA | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63551891 | ||||||
| chr17:63551891 | CAA | C | 17 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(14): Show |
21 | HG00140.hp2 HG00597.hp2 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.138+1115_138+1116d others(4): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63551891 | ||||||
| chr17:63551891 | CAAA | C | 32 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(29): Show |
38 | HG00099.hp1 HG00558.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.138+1114_138+1116d others(5): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63551891 | ||||||
| chr17:63551891 | CAAAA | C | 17 | a0001c0001t0001g0002 a0001c0001t0001g0155 a0001c0001t0001g0156 others(14): Show |
20 | HG00280.hp1 HG00741.hp1 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.138+1113_138+1116d others(6): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63551891 | ||||||
| chr17:63551891 | CAAAAA | C | 13 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0177 others(10): Show |
13 | HG01975.hp2 HG02922.hp1 HG02965.hp2 others(10): Show |
intron_variant | MODIFIER | c.138+1112_138+1116d others(7): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63551891 | ||||||
| chr17:63551891 | CAAAAAA | C | 7 | a0001c0001t0001g0036 a0001c0001t0001g0180 a0001c0001t0003g0230 others(4): Show |
7 | HG02622.hp1 HG02630.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.138+1111_138+1116d others(8): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63551891 | ||||||
| chr17:63551891 | CAAAAAAA | C | 7 | a0001c0001t0001g0037 a0001c0001t0001g0039 a0001c0001t0001g0181 others(4): Show |
7 | HG00609.hp1 HG00609.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.138+1110_138+1116d others(9): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63551891 | ||||||
| chr17:63551891 | CAAAAAAA others(1): Show |
C | 32 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0040 others(29): Show |
36 | HG00597.hp1 HG01070.hp1 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.138+1109_138+1116d others(10): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63551891 | ||||||
| chr17:63551891 | CAAAAAAA others(2): Show |
C | 32 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(29): Show |
37 | HG00544.hp2 HG00558.hp2 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.138+1108_138+1116d others(11): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63551891 | ||||||
| chr17:63551891 | CAAAAAAA others(3): Show |
C | 3 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0010g0192 |
3 | HG03471.hp2 NA18965.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.138+1107_138+1116d others(12): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63551891 | ||||||
| chr17:63551891 | CAAAAAAA others(7): Show |
C | 4 | a0001c0001t0001g0193 a0001c0001t0001g0208 a0001c0001t0011g0207 others(1): Show |
4 | HG02027.hp1 HG02280.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.138+1103_138+1116d others(16): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63551891 | ||||||
| chr17:63551891 | CAAAAAAA others(8): Show |
C | 2 | a0001c0001t0006g0210 a0001c0001t0023g0211 |
2 | HG02630.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.138+1102_138+1116d others(17): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63551891 | ||||||
| chr17:63551891 | CAAAAAAA others(9): Show |
C | 1 | a0001c0001t0011g0212 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.138+1101_138+1116d others(18): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63551891 | ||||||
| chr17:63551891 | CAAAAAAA others(10): Show |
C | 2 | a0001c0001t0001g0195 a0001c0001t0030g0194 |
2 | HG00323.hp2 HG00544.hp1 |
intron_variant | MODIFIER | c.138+1100_138+1116d others(19): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63551891 | ||||||
| chr17:63551891 | CAAAAAAA others(12): Show |
C | 2 | a0001c0001t0001g0196 a0001c0001t0001g0197 |
2 | HG02451.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.138+1098_138+1116d others(21): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63551891 | ||||||
| chr17:63551891 | CAAAAAAA others(13): Show |
C | 8 | a0001c0001t0001g0013 a0001c0001t0001g0076 a0001c0001t0006g0213 others(5): Show |
9 | HG00639.hp1 HG02257.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.138+1097_138+1116d others(22): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63551891 | ||||||
| chr17:63551891 | CAAAAAAA others(14): Show |
C | 1 | a0001c0001t0001g0020 | 2 | NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.138+1096_138+1116d others(23): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63551891 | ||||||
| chr17:63551891 | CAAAAAAA others(15): Show |
C | 6 | a0001c0001t0001g0021 a0001c0001t0005g0022 a0001c0001t0005g0023 others(3): Show |
6 | HG01346.hp1 HG02559.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.138+1095_138+1116d others(24): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63551891 | ||||||
| chr17:63551891 | CAAAAAAA others(16): Show |
C | 1 | a0001c0001t0014g0203 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.138+1094_138+1116d others(25): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63551891 | ||||||
| chr17:63551891 | CAAAAAAA others(17): Show |
C | 2 | a0001c0001t0014g0205 a0001c0001t0019g0204 |
2 | HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.138+1093_138+1116d others(26): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63551891 | ||||||
| chr17:63551891 | CAAAAAAA others(18): Show |
C | 1 | a0001c0001t0001g0206 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.138+1092_138+1116d others(27): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63551891 | ||||||
| chr17:63552174 | G | A | 1 | a0001c0001t0022g0217 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.138+1359G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63552174 | |||||||
| chr17:63552317 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.138+1502G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63552317 | |||||||
| chr17:63552326 | CTT | C | 2 | a0001c0001t0001g0020 a0001c0001t0006g0213 |
3 | NA18522.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.138+1513_138+1514d others(4): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63552326 | ||||||
| chr17:63552331 | G | C | 35 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(32): Show |
35 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(32): Show |
intron_variant | MODIFIER | c.138+1516G>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63552331 | |||||||
| chr17:63552430 | A | G | 11 | a0001c0001t0001g0014 a0001c0001t0010g0113 a0001c0001t0014g0203 others(8): Show |
12 | HG01099.hp2 HG02145.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.138+1615A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63552430 | |||||||
| chr17:63552715 | T | C | 80 | a0001c0001t0001g0014 a0001c0001t0001g0020 a0001c0001t0001g0021 others(77): Show |
82 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.138+1900T>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63552715 | |||||||
| chr17:63552756 | GATCAGTG others(10): Show |
G | 6 | a0001c0001t0001g0021 a0001c0001t0005g0022 a0001c0001t0005g0023 others(3): Show |
6 | HG01346.hp1 HG02559.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.138+1943_138+1959d others(19): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63552756 | ||||||
| chr17:63552766 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.138+1951G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63552766 | |||||||
| chr17:63552774 | A | C | 6 | a0001c0001t0001g0021 a0001c0001t0005g0022 a0001c0001t0005g0023 others(3): Show |
6 | HG01346.hp1 HG02559.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.138+1959A>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63552774 | |||||||
| chr17:63552907 | A | C | 3 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0006g0189 |
3 | HG01243.hp1 HG02723.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.138+2092A>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63552907 | |||||||
| chr17:63553252 | C | G | 3 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0006g0189 |
3 | HG01243.hp1 HG02723.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.138+2437C>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63553252 | |||||||
| chr17:63553337 | A | G | 5 | a0001c0001t0016g0198 a0001c0001t0016g0199 a0001c0001t0017g0201 others(2): Show |
5 | HG02257.hp1 HG02559.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.138+2522A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63553337 | |||||||
| chr17:63553739 | G | T | 1 | a0001c0001t0001g0127 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.138+2924G>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63553739 | |||||||
| chr17:63554094 | A | G | 1 | a0001c0001t0010g0192 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.138+3279A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63554094 | |||||||
| chr17:63554340 | T | C | 3 | a0001c0001t0001g0041 a0001c0001t0001g0056 a0001c0001t0001g0057 |
3 | HG02056.hp2 HG02135.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.138+3525T>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63554340 | |||||||
| chr17:63554575 | C | G | 1 | a0001c0001t0014g0205 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.138+3760C>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63554575 | |||||||
| chr17:63554575 | C | T | 2 | a0001c0001t0017g0201 a0001c0001t0017g0202 |
2 | HG02622.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.138+3760C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63554575 | |||||||
| chr17:63554713 | G | A | 1 | a0001c0001t0014g0203 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.138+3898G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63554713 | |||||||
| chr17:63554745 | G | A | 2 | a0001c0001t0001g0078 a0001c0001t0001g0171 |
2 | NA18979.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.138+3930G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63554745 | |||||||
| chr17:63554866 | AAG | A | 8 | a0001c0002t0002g0027 a0001c0002t0002g0028 a0001c0002t0002g0029 others(5): Show |
8 | HG01099.hp2 HG02145.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.138+4054_138+4055d others(4): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63554866 | ||||||
| chr17:63554962 | A | G | 12 | a0001c0001t0001g0225 a0001c0001t0001g0234 a0001c0001t0003g0226 others(9): Show |
12 | HG02622.hp1 HG02630.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.138+4147A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63554962 | |||||||
| chr17:63555077 | G | A | 2 | a0001c0001t0006g0210 a0001c0001t0023g0211 |
2 | HG02630.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.138+4262G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63555077 | |||||||
| chr17:63555143 | T | C | 9 | a0001c0001t0010g0113 a0001c0002t0002g0027 a0001c0002t0002g0028 others(6): Show |
9 | HG01099.hp2 HG02145.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.138+4328T>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63555143 | |||||||
| chr17:63555561 | C | T | 23 | a0001c0001t0001g0225 a0001c0001t0001g0234 a0001c0001t0003g0226 others(20): Show |
23 | HG01099.hp2 HG02145.hp2 HG02451.hp1 others(20): Show |
intron_variant | MODIFIER | c.138+4746C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63555561 | |||||||
| chr17:63555568 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.138+4753G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63555568 | |||||||
| chr17:63555645 | G | A | 1 | a0001c0001t0014g0205 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.138+4830G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63555645 | |||||||
| chr17:63556073 | A | G | 3 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0006g0189 |
3 | HG01243.hp1 HG02723.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.138+5258A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63556073 | |||||||
| chr17:63556296 | G | A | 35 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(32): Show |
35 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(32): Show |
intron_variant | MODIFIER | c.138+5481G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63556296 | |||||||
| chr17:63556344 | C | T | 43 | a0001c0001t0001g0020 a0001c0001t0001g0078 a0001c0001t0001g0079 others(40): Show |
44 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(41): Show |
intron_variant | MODIFIER | c.138+5529C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63556344 | |||||||
| chr17:63556449 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.138+5634A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63556449 | |||||||
| chr17:63556590 | C | T | 1 | a0001c0001t0001g0186 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.138+5775C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63556590 | |||||||
| chr17:63556644 | G | A | 1 | a0001c0001t0017g0201 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.138+5829G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63556644 | |||||||
| chr17:63556922 | G | A | 1 | a0001c0001t0024g0077 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.138+6107G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63556922 | |||||||
| chr17:63556922 | G | C | 5 | a0001c0001t0016g0198 a0001c0001t0016g0199 a0001c0001t0017g0201 others(2): Show |
5 | HG02257.hp1 HG02559.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.138+6107G>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63556922 | |||||||
| chr17:63556998 | C | T | 1 | a0001c0001t0030g0194 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.138+6183C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63556998 | |||||||
| chr17:63557021 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.138+6206G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63557021 | |||||||
| chr17:63557021 | G | C | 73 | a0001c0001t0001g0020 a0001c0001t0001g0078 a0001c0001t0001g0079 others(70): Show |
74 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.138+6206G>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63557021 | |||||||
| chr17:63557147 | C | T | 60 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(57): Show |
60 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.138+6332C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63557147 | |||||||
| chr17:63557177 | C | T | 35 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(32): Show |
35 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(32): Show |
intron_variant | MODIFIER | c.138+6362C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63557177 | |||||||
| chr17:63557364 | C | G | 1 | a0001c0001t0014g0203 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.138+6549C>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63557364 | |||||||
| chr17:63557966 | G | A | 6 | a0001c0001t0001g0021 a0001c0001t0005g0022 a0001c0001t0005g0023 others(3): Show |
6 | HG01346.hp1 HG02559.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.138+7151G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63557966 | |||||||
| chr17:63557992 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.138+7177C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63557992 | |||||||
| chr17:63558000 | A | G | 2 | a0001c0001t0017g0201 a0001c0001t0017g0202 |
2 | HG02622.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.138+7185A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63558000 | |||||||
| chr17:63558169 | C | T | 4 | a0001c0001t0001g0088 a0001c0001t0001g0099 a0001c0001t0025g0087 others(1): Show |
4 | HG00099.hp2 HG01106.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.138+7354C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63558169 | |||||||
| chr17:63558218 | G | A | 23 | a0001c0001t0001g0225 a0001c0001t0001g0234 a0001c0001t0003g0226 others(20): Show |
23 | HG01099.hp2 HG02145.hp2 HG02451.hp1 others(20): Show |
intron_variant | MODIFIER | c.138+7403G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63558218 | |||||||
| chr17:63558219 | G | T | 1 | a0001c0001t0001g0014 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.138+7404G>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63558219 | |||||||
| chr17:63558442 | G | A | 1 | a0001c0001t0019g0204 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.138+7627G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63558442 | |||||||
| chr17:63558470 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.138+7655G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63558470 | |||||||
| chr17:63558587 | G | T | 65 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(62): Show |
75 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.138+7772G>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63558587 | |||||||
| chr17:63558588 | A | G | 1 | a0001c0001t0010g0192 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.138+7773A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63558588 | |||||||
| chr17:63558624 | A | G | 1 | a0001c0001t0013g0086 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.138+7809A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63558624 | |||||||
| chr17:63558626 | C | A | 11 | a0001c0001t0001g0225 a0001c0001t0003g0226 a0001c0001t0003g0227 others(8): Show |
11 | HG02622.hp1 HG02630.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.138+7811C>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63558626 | |||||||
| chr17:63558723 | T | A | 1 | a0001c0001t0001g0218 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.138+7908T>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63558723 | |||||||
| chr17:63558778 | A | C | 12 | a0001c0001t0001g0225 a0001c0001t0001g0234 a0001c0001t0003g0226 others(9): Show |
12 | HG02622.hp1 HG02630.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.138+7963A>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63558778 | |||||||
| chr17:63558833 | A | G | 1 | a0001c0002t0002g0032 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.138+8018A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63558833 | |||||||
| chr17:63558997 | A | G | 11 | a0001c0001t0001g0014 a0001c0001t0010g0113 a0001c0001t0014g0203 others(8): Show |
12 | HG01099.hp2 HG02145.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.138+8182A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63558997 | |||||||
| chr17:63559142 | T | C | 3 | a0001c0003t0001g0005 a0001c0003t0001g0006 a0001c0003t0001g0043 |
5 | HG01928.hp1 HG01952.hp2 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.138+8327T>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63559142 | |||||||
| chr17:63559303 | C | A | 1 | a0001c0001t0010g0192 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.138+8488C>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63559303 | |||||||
| chr17:63559304 | C | CAT | 11 | a0001c0001t0001g0044 a0001c0001t0001g0058 a0001c0001t0001g0059 others(8): Show |
11 | HG01516.hp2 HG01517.hp2 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.138+8504_138+8505d others(4): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63559304 | ||||||
| chr17:63559304 | CAT | C | 11 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0055 others(8): Show |
13 | HG02280.hp2 HG02630.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.138+8504_138+8505d others(4): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63559304 | ||||||
| chr17:63559317 | A | G | 1 | a0001c0001t0020g0179 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.138+8502A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63559317 | |||||||
| chr17:63559320 | T | C | 1 | a0001c0001t0010g0192 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.138+8505T>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63559320 | |||||||
| chr17:63559321 | G | A | 1 | a0001c0001t0010g0192 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.138+8506G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63559321 | |||||||
| chr17:63559323 | A | G | 1 | a0001c0001t0026g0106 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.138+8508A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63559323 | |||||||
| chr17:63559332 | T | C | 1 | a0001c0001t0021g0209 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.138+8517T>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63559332 | |||||||
| chr17:63559334 | C | T | 1 | a0001c0001t0010g0192 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.138+8519C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63559334 | |||||||
| chr17:63559335 | A | ACATATAT others(9): Show |
1 | a0001c0001t0014g0205 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.138+8520_138+8521i others(18): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63559335 | |||||||
| chr17:63559335 | A | G | 63 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(60): Show |
63 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.138+8520A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63559335 | |||||||
| chr17:63559336 | TAC | T | 144 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(141): Show |
155 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.138+8523_138+8524d others(4): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63559336 | ||||||
| chr17:63559338 | C | T | 6 | a0001c0001t0001g0215 a0001c0001t0001g0219 a0001c0001t0001g0220 others(3): Show |
7 | HG03471.hp2 NA18612.hp2 NA19000.hp1 others(4): Show |
intron_variant | MODIFIER | c.138+8523C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63559338 | |||||||
| chr17:63559339 | ATATATAT others(3): Show |
A | 3 | a0001c0001t0001g0215 a0001c0001t0001g0219 a0001c0001t0001g0220 |
3 | NA18612.hp2 NA19000.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.138+8533_138+8542d others(12): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63559339 | ||||||
| chr17:63559346 | T | C | 1 | a0001c0001t0010g0192 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.138+8531T>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63559346 | |||||||
| chr17:63559348 | C | T | 74 | a0001c0001t0001g0014 a0001c0001t0001g0020 a0001c0001t0001g0078 others(71): Show |
77 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.138+8533C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63559348 | |||||||
| chr17:63559349 | G | A | 2 | a0001c0001t0010g0192 a0001c0001t0014g0205 |
2 | HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.138+8534G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63559349 | |||||||
| chr17:63559359 | G | A | 1 | a0001c0003t0001g0005 | 2 | NA19077.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.138+8544G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63559359 | |||||||
| chr17:63559359 | G | GTATGTAT others(29): Show |
1 | a0001c0001t0019g0204 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.138+8553_138+8554i others(38): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63559359 | ||||||
| chr17:63559359 | GTATGTAT others(17): Show |
G | 1 | a0001c0001t0001g0155 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.138+8562_138+8585d others(26): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63559359 | ||||||
| chr17:63559361 | A | ACATATAT others(7): Show |
1 | a0001c0003t0001g0005 | 2 | NA19077.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.138+8546_138+8547i others(16): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63559361 | |||||||
| chr17:63559363 | G | A | 2 | a0001c0001t0014g0205 a0001c0003t0001g0005 |
3 | NA19030.hp2 NA19077.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.138+8548G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63559363 | |||||||
| chr17:63559367 | A | G | 1 | a0001c0001t0010g0192 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.138+8552A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63559367 | |||||||
| chr17:63559367 | ATATATAT others(3): Show |
A | 2 | a0001c0001t0016g0198 a0001c0001t0016g0199 |
2 | HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.138+8560_138+8569d others(12): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63559367 | ||||||
| chr17:63559369 | A | G | 1 | a0001c0001t0014g0205 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.138+8554A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63559369 | |||||||
| chr17:63559371 | A | ATGTATAT others(31): Show |
1 | a0001c0001t0001g0054 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.138+8557_138+8558i others(40): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63559371 | ||||||
| chr17:63559371 | A | G | 1 | a0001c0003t0001g0005 | 2 | NA19077.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.138+8556A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63559371 | |||||||
| chr17:63559373 | A | G | 2 | a0001c0001t0014g0205 a0001c0001t0019g0204 |
2 | HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.138+8558A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63559373 | |||||||
| chr17:63559375 | G | A | 1 | a0001c0001t0014g0205 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.138+8560G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63559375 | |||||||
| chr17:63559375 | GTGTATAT others(3): Show |
G | 1 | a0001c0001t0032g0200 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.138+8572_138+8581d others(12): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63559375 | ||||||
| chr17:63559377 | G | A | 12 | a0001c0001t0001g0020 a0001c0001t0001g0054 a0001c0001t0001g0099 others(9): Show |
14 | HG00099.hp2 HG02280.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.138+8562G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63559377 | |||||||
| chr17:63559377 | G | GTA | 36 | a0001c0001t0001g0014 a0001c0001t0001g0078 a0001c0001t0001g0079 others(33): Show |
37 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.138+8570_138+8571d others(4): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63559377 | ||||||
| chr17:63559377 | GTATATAT others(5): Show |
G | 3 | a0001c0001t0001g0036 a0001c0001t0001g0153 a0002c0004t0001g0038 |
3 | NA18978.hp2 NA19004.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.138+8582_138+8593d others(14): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63559377 | ||||||
| chr17:63559385 | A | G | 1 | a0001c0001t0014g0205 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.138+8570A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63559385 | |||||||
| chr17:63559387 | G | A | 20 | a0001c0001t0001g0225 a0001c0001t0001g0234 a0001c0001t0003g0226 others(17): Show |
20 | HG02451.hp1 HG02486.hp1 HG02572.hp1 others(17): Show |
intron_variant | MODIFIER | c.138+8572G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63559387 | |||||||
| chr17:63559387 | GTA | G | 3 | a0001c0001t0001g0178 a0001c0001t0001g0197 a0001c0001t0009g0170 |
3 | HG01109.hp2 HG02717.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.138+8582_138+8583d others(4): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63559387 | ||||||
| chr17:63559387 | GTATATAT others(31): Show |
G | 8 | a0001c0001t0001g0020 a0001c0001t0001g0208 a0001c0001t0006g0210 others(5): Show |
9 | HG02280.hp2 HG02630.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.138+8580_138+8617d others(40): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63559387 | ||||||
| chr17:63559389 | A | G | 22 | a0001c0001t0001g0054 a0001c0001t0001g0225 a0001c0001t0001g0234 others(19): Show |
23 | HG02451.hp1 HG02486.hp1 HG02572.hp1 others(20): Show |
intron_variant | MODIFIER | c.138+8574A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63559389 | |||||||
| chr17:63559389 | ATATATAT others(3): Show |
A | 1 | a0001c0001t0001g0156 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.138+8594_138+8603d others(12): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63559389 | ||||||
| chr17:63559397 | A | G | 56 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0010 others(53): Show |
64 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.138+8582A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63559397 | |||||||
| chr17:63559399 | G | A | 51 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0010 others(48): Show |
58 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.138+8584G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63559399 | |||||||
| chr17:63559399 | G | GTA | 9 | a0001c0001t0001g0021 a0001c0001t0001g0182 a0001c0001t0005g0022 others(6): Show |
9 | HG01346.hp1 HG02559.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.138+8592_138+8593d others(4): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63559399 | ||||||
| chr17:63559399 | G | GTATATAT others(19): Show |
2 | a0001c0002t0002g0032 a0001c0002t0002g0034 |
2 | HG01099.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.138+8593_138+8594i others(28): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63559399 | ||||||
| chr17:63559399 | G | GTGTA | 14 | a0001c0001t0001g0088 a0001c0001t0001g0225 a0001c0001t0001g0234 others(11): Show |
14 | HG01106.hp2 HG02622.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.138+8585_138+8586i others(6): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63559399 | ||||||
| chr17:63559399 | G | GTGTATAT others(21): Show |
7 | a0001c0001t0010g0113 a0001c0002t0002g0027 a0001c0002t0002g0028 others(4): Show |
7 | HG02451.hp1 HG02486.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.138+8585_138+8586i others(30): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63559399 | ||||||
| chr17:63559399 | GTATATAT others(17): Show |
G | 1 | a0001c0001t0001g0099 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.138+8596_138+8619d others(26): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63559399 | ||||||
| chr17:63559407 | ATGTATAT others(7): Show |
A | 2 | a0001c0001t0016g0198 a0001c0001t0016g0199 |
2 | HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.138+8594_138+8607d others(16): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63559407 | ||||||
| chr17:63559409 | G | A | 35 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(32): Show |
35 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.138+8594G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63559409 | |||||||
| chr17:63559411 | A | G | 35 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(32): Show |
35 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.138+8596A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63559411 | |||||||
| chr17:63559411 | ATATATAT others(3): Show |
A | 39 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0011 others(36): Show |
44 | HG00597.hp1 HG00609.hp1 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.138+8605_138+8614d others(12): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63559411 | ||||||
| chr17:63559413 | ATATATAC others(1): Show |
A | 3 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0027g0075 |
3 | HG00558.hp2 HG01361.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.138+8605_138+8612d others(10): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63559413 | ||||||
| chr17:63559419 | A | G | 25 | a0001c0001t0001g0014 a0001c0001t0001g0064 a0001c0001t0001g0225 others(22): Show |
26 | HG01099.hp2 HG02145.hp2 HG02451.hp1 others(23): Show |
intron_variant | MODIFIER | c.138+8604A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63559419 | |||||||
| chr17:63559419 | ACG | A | 4 | a0001c0001t0013g0086 a0001c0001t0017g0201 a0001c0001t0017g0202 others(1): Show |
4 | HG02622.hp2 HG03041.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.138+8605_138+8606d others(4): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63559419 | |||||||
| chr17:63559420 | C | T | 91 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(88): Show |
97 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.138+8605C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63559420 | |||||||
| chr17:63559421 | G | A | 31 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(28): Show |
31 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(28): Show |
intron_variant | MODIFIER | c.138+8606G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63559421 | |||||||
| chr17:63559423 | A | G | 44 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(41): Show |
44 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.138+8608A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63559423 | |||||||
| chr17:63559425 | A | G | 40 | a0001c0001t0001g0039 a0001c0001t0001g0078 a0001c0001t0001g0079 others(37): Show |
40 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(37): Show |
intron_variant | MODIFIER | c.138+8610A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63559425 | |||||||
| chr17:63559427 | A | G | 47 | a0001c0001t0001g0020 a0001c0001t0001g0078 a0001c0001t0001g0079 others(44): Show |
48 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(45): Show |
intron_variant | MODIFIER | c.138+8612A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63559427 | |||||||
| chr17:63559429 | A | G | 50 | a0001c0001t0001g0020 a0001c0001t0001g0052 a0001c0001t0001g0053 others(47): Show |
51 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.138+8614A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63559429 | |||||||
| chr17:63559431 | A | ATG | 7 | a0001c0001t0001g0013 a0001c0001t0001g0060 a0001c0001t0001g0061 others(4): Show |
8 | HG00639.hp1 HG02486.hp2 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.138+8624_138+8625d others(4): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63559431 | ||||||
| chr17:63559431 | A | ATGTATAT others(15): Show |
1 | a0001c0001t0001g0088 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.138+8619_138+8620i others(24): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63559431 | ||||||
| chr17:63559431 | A | ATGTATAT others(21): Show |
1 | a0001c0001t0001g0014 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.138+8619_138+8620i others(30): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63559431 | ||||||
| chr17:63559431 | A | G | 90 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0011 others(87): Show |
96 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.138+8616A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63559431 | |||||||
| chr17:63559437 | G | A | 3 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0027g0075 |
3 | HG00558.hp2 HG01361.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.138+8622G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63559437 | |||||||
| chr17:63559439 | G | A | 50 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0011 others(47): Show |
56 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.138+8624G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63559439 | |||||||
| chr17:63559439 | G | GTA | 15 | a0001c0001t0001g0004 a0001c0001t0001g0054 a0001c0001t0001g0196 others(12): Show |
18 | HG00544.hp2 HG01109.hp2 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.138+8642_138+8643d others(4): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63559439 | ||||||
| chr17:63559439 | G | GTATA | 3 | a0001c0001t0001g0009 a0001c0001t0012g0009 a0001c0001t0012g0035 |
3 | HG02738.hp1 HG03491.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.138+8640_138+8643d others(6): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63559439 | ||||||
| chr17:63559439 | G | GTGTGTA | 15 | a0001c0001t0001g0021 a0001c0001t0005g0022 a0001c0001t0005g0023 others(12): Show |
15 | HG01099.hp2 HG01346.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.138+8625_138+8626i others(8): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63559439 | ||||||
| chr17:63559439 | G | GTGTGTAT others(3): Show |
1 | a0001c0001t0019g0204 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.138+8625_138+8626i others(12): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63559439 | ||||||
| chr17:63559439 | G | GTGTGTGT others(1): Show |
12 | a0001c0001t0001g0225 a0001c0001t0001g0234 a0001c0001t0003g0226 others(9): Show |
12 | HG02622.hp1 HG02630.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.138+8625_138+8626i others(10): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63559439 | ||||||
| chr17:63559441 | A | G | 6 | a0001c0001t0013g0086 a0001c0001t0016g0198 a0001c0001t0016g0199 others(3): Show |
6 | HG02257.hp1 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.138+8626A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63559441 | |||||||
| chr17:63559457 | A | ATT | 2 | a0001c0001t0001g0008 a0001c0001t0001g0055 |
3 | HG03942.hp1 NA18959.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.138+8646_138+8647d others(4): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63559457 | ||||||
| chr17:63559457 | A | T | 37 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(34): Show |
37 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(34): Show |
intron_variant | MODIFIER | c.138+8642A>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63559457 | |||||||
| chr17:63559459 | T | A | 5 | a0001c0001t0016g0198 a0001c0001t0016g0199 a0001c0001t0017g0201 others(2): Show |
5 | HG02257.hp1 HG02559.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.138+8644T>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63559459 | |||||||
| chr17:63559471 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.138+8656G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63559471 | |||||||
| chr17:63559488 | A | G | 2 | a0001c0001t0001g0051 a0001c0001t0001g0074 |
2 | HG00597.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.138+8673A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63559488 | |||||||
| chr17:63559523 | C | T | 1 | a0001c0001t0019g0204 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.138+8708C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63559523 | |||||||
| chr17:63559773 | G | T | 1 | a0001c0001t0001g0125 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.138+8958G>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63559773 | |||||||
| chr17:63559870 | C | T | 1 | a0001c0001t0014g0205 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.138+9055C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63559870 | |||||||
| chr17:63560060 | G | A | 53 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0010 others(50): Show |
61 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.138+9245G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63560060 | |||||||
| chr17:63560106 | A | G | 1 | a0001c0001t0010g0192 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.138+9291A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63560106 | |||||||
| chr17:63560120 | C | T | 11 | a0001c0001t0001g0014 a0001c0001t0010g0113 a0001c0001t0014g0203 others(8): Show |
12 | HG01099.hp2 HG02145.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.138+9305C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63560120 | |||||||
| chr17:63560144 | GA | G | 7 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0149 others(4): Show |
7 | HG00140.hp2 HG01081.hp2 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.138+9341delA | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63560144 | ||||||
| chr17:63560175 | A | G | 5 | a0001c0001t0016g0198 a0001c0001t0016g0199 a0001c0001t0017g0201 others(2): Show |
5 | HG02257.hp1 HG02559.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.138+9360A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63560175 | |||||||
| chr17:63560322 | CAT | C | 5 | a0001c0001t0016g0198 a0001c0001t0016g0199 a0001c0001t0017g0201 others(2): Show |
5 | HG02257.hp1 HG02559.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.138+9508_138+9509d others(4): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63560322 | |||||||
| chr17:63560553 | A | C | 6 | a0001c0001t0001g0021 a0001c0001t0005g0022 a0001c0001t0005g0023 others(3): Show |
6 | HG01346.hp1 HG02559.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.138+9738A>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63560553 | |||||||
| chr17:63560771 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.138+9956G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63560771 | |||||||
| chr17:63560829 | T | G | 1 | a0001c0001t0009g0224 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.138+10014T>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63560829 | |||||||
| chr17:63560903 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.138+10088C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63560903 | |||||||
| chr17:63561005 | C | T | 2 | a0001c0001t0018g0050 a0001c0001t0018g0073 |
2 | HG01106.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.138+10190C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63561005 | |||||||
| chr17:63561195 | G | A | 1 | a0001c0001t0001g0014 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.138+10380G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63561195 | |||||||
| chr17:63561221 | C | T | 2 | a0001c0001t0006g0210 a0001c0001t0023g0211 |
2 | HG02630.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.138+10406C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63561221 | |||||||
| chr17:63561362 | G | T | 79 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0078 others(76): Show |
80 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.138+10547G>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63561362 | |||||||
| chr17:63561524 | G | T | 2 | a0001c0001t0001g0147 a0001c0001t0001g0148 |
2 | HG01167.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.138+10709G>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63561524 | |||||||
| chr17:63561627 | G | T | 2 | a0001c0001t0006g0210 a0001c0001t0023g0211 |
2 | HG02630.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.138+10812G>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63561627 | |||||||
| chr17:63561711 | C | A | 1 | a0001c0001t0001g0208 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.138+10896C>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63561711 | |||||||
| chr17:63561736 | TTATAAG | T | 5 | a0001c0001t0016g0198 a0001c0001t0016g0199 a0001c0001t0017g0201 others(2): Show |
5 | HG02257.hp1 HG02559.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.138+10926_138+1093 others(10): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63561736 | ||||||
| chr17:63561908 | T | C | 43 | a0001c0001t0001g0020 a0001c0001t0001g0078 a0001c0001t0001g0079 others(40): Show |
44 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(41): Show |
intron_variant | MODIFIER | c.138+11093T>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63561908 | |||||||
| chr17:63561982 | G | A | 9 | a0001c0001t0010g0113 a0001c0002t0002g0027 a0001c0002t0002g0028 others(6): Show |
9 | HG01099.hp2 HG02145.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.138+11167G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63561982 | |||||||
| chr17:63562005 | A | G | 5 | a0001c0001t0016g0198 a0001c0001t0016g0199 a0001c0001t0017g0201 others(2): Show |
5 | HG02257.hp1 HG02559.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.138+11190A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63562005 | |||||||
| chr17:63562010 | C | CA | 56 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(53): Show |
56 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.138+11213dupA | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63562010 | ||||||
| chr17:63562010 | CA | C | 6 | a0001c0001t0014g0205 a0001c0001t0016g0198 a0001c0001t0016g0199 others(3): Show |
6 | HG02257.hp1 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.138+11213delA | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63562010 | ||||||
| chr17:63562333 | T | A | 74 | a0001c0001t0001g0014 a0001c0001t0001g0020 a0001c0001t0001g0078 others(71): Show |
76 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.138+11518T>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63562333 | |||||||
| chr17:63562411 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.138+11596A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63562411 | |||||||
| chr17:63562532 | TTTATTTT others(6): Show |
T | 1 | a0001c0001t0015g0229 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.138+11723_138+1173 others(17): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63562532 | ||||||
| chr17:63562539 | T | A | 1 | a0001c0001t0010g0192 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.138+11724T>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63562539 | |||||||
| chr17:63562539 | TTTATTA | T | 10 | a0001c0001t0001g0225 a0001c0001t0003g0226 a0001c0001t0003g0227 others(7): Show |
10 | HG02622.hp1 HG02630.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.138+11735_138+1174 others(10): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63562539 | ||||||
| chr17:63562677 | A | G | 11 | a0001c0001t0001g0014 a0001c0001t0010g0113 a0001c0001t0014g0203 others(8): Show |
12 | HG01099.hp2 HG02145.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.138+11862A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63562677 | |||||||
| chr17:63562822 | CT | C | 75 | a0001c0001t0001g0014 a0001c0001t0001g0020 a0001c0001t0001g0021 others(72): Show |
77 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.138+12021delT | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63562822 | ||||||
| chr17:63562860 | A | G | 1 | a0001c0001t0001g0040 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.138+12045A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63562860 | |||||||
| chr17:63563147 | A | G | 1 | a0001c0001t0001g0072 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.138+12332A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63563147 | |||||||
| chr17:63563669 | G | C | 1 | a0001c0001t0009g0170 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.138+12854G>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63563669 | |||||||
| chr17:63563814 | C | CAAAT | 7 | a0001c0001t0001g0115 a0001c0001t0001g0133 a0001c0001t0001g0134 others(4): Show |
8 | HG01361.hp1 HG01928.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.138+13030_138+1303 others(8): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63563814 | ||||||
| chr17:63563814 | CAAAT | C | 56 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0078 others(53): Show |
57 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.138+13030_138+1303 others(8): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63563814 | ||||||
| chr17:63563814 | CAAATAAA others(1): Show |
C | 3 | a0001c0001t0001g0049 a0001c0001t0001g0096 a0001c0001t0001g0097 |
3 | HG01081.hp1 HG02300.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.138+13026_138+1303 others(12): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63563814 | ||||||
| chr17:63563814 | CAAATAAA others(5): Show |
C | 24 | a0001c0001t0001g0014 a0001c0001t0001g0225 a0001c0001t0001g0234 others(21): Show |
25 | HG01099.hp2 HG02145.hp2 HG02451.hp1 others(22): Show |
intron_variant | MODIFIER | c.138+13022_138+1303 others(16): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63563814 | ||||||
| chr17:63563814 | CAAATAAA others(9): Show |
C | 1 | a0001c0001t0010g0192 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.138+13018_138+1303 others(20): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63563814 | ||||||
| chr17:63563899 | A | G | 1 | a0001c0001t0001g0191 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.138+13084A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63563899 | |||||||
| chr17:63563950 | G | A | 1 | a0001c0001t0010g0192 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.138+13135G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63563950 | |||||||
| chr17:63564031 | C | G | 1 | a0001c0001t0014g0205 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.138+13216C>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63564031 | |||||||
| chr17:63564108 | G | C | 1 | a0001c0001t0001g0135 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.138+13293G>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63564108 | |||||||
| chr17:63564136 | T | TAC | 12 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0041 others(9): Show |
14 | HG02056.hp2 HG02135.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.138+13347_138+1334 others(6): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63564136 | ||||||
| chr17:63564136 | T | TACAC | 7 | a0001c0001t0001g0020 a0001c0001t0001g0154 a0001c0001t0006g0210 others(4): Show |
8 | HG02622.hp2 HG02630.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.138+13345_138+1334 others(8): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63564136 | ||||||
| chr17:63564136 | T | TACACAC | 4 | a0001c0001t0013g0086 a0001c0001t0016g0198 a0001c0001t0016g0199 others(1): Show |
4 | HG02257.hp1 HG02559.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.138+13343_138+1334 others(10): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63564136 | ||||||
| chr17:63564136 | T | TACACACA others(3): Show |
6 | a0001c0001t0001g0089 a0001c0001t0001g0095 a0001c0001t0001g0097 others(3): Show |
6 | HG00323.hp2 HG02027.hp1 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.138+13339_138+1334 others(14): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63564136 | ||||||
| chr17:63564136 | T | TACACACA others(5): Show |
12 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(9): Show |
12 | HG00099.hp2 HG00140.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.138+13337_138+1334 others(16): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63564136 | ||||||
| chr17:63564136 | T | TACACACA others(7): Show |
5 | a0001c0001t0001g0088 a0001c0001t0001g0096 a0001c0001t0001g0102 others(2): Show |
5 | HG01106.hp2 HG01243.hp2 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.138+13335_138+1334 others(18): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63564136 | ||||||
| chr17:63564136 | T | TACACACA others(9): Show |
4 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0101 others(1): Show |
4 | HG03453.hp2 HG03831.hp2 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.138+13333_138+1334 others(20): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63564136 | ||||||
| chr17:63564136 | T | TACACACA others(11): Show |
4 | a0001c0001t0001g0079 a0001c0001t0001g0091 a0001c0001t0001g0100 others(1): Show |
4 | HG00323.hp1 NA18947.hp2 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.138+13331_138+1334 others(22): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63564136 | ||||||
| chr17:63564136 | T | TACACACA others(13): Show |
2 | a0001c0001t0001g0078 a0001c0001t0031g0090 |
2 | HG00280.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.138+13329_138+1334 others(24): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63564136 | ||||||
| chr17:63564136 | TAC | T | 17 | a0001c0001t0001g0013 a0001c0001t0001g0021 a0001c0001t0001g0061 others(14): Show |
18 | HG00639.hp1 HG01243.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.138+13347_138+1334 others(6): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63564136 | ||||||
| chr17:63564164 | T | C | 43 | a0001c0001t0001g0020 a0001c0001t0001g0078 a0001c0001t0001g0079 others(40): Show |
44 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(41): Show |
intron_variant | MODIFIER | c.138+13349T>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63564164 | |||||||
| chr17:63564170 | T | C | 3 | a0001c0001t0001g0088 a0001c0001t0001g0099 a0001c0001t0025g0087 |
3 | HG00099.hp2 HG01106.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.138+13355T>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63564170 | |||||||
| chr17:63564293 | A | C | 2 | a0001c0001t0011g0207 a0001c0001t0011g0212 |
2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.138+13478A>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63564293 | |||||||
| chr17:63564453 | C | T | 8 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
8 | HG02572.hp2 HG02809.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.138+13638C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63564453 | |||||||
| chr17:63564630 | G | A | 2 | a0001c0001t0006g0210 a0001c0001t0023g0211 |
2 | HG02630.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.138+13815G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63564630 | |||||||
| chr17:63564643 | G | C | 1 | a0001c0001t0001g0190 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.139-13827G>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63564643 | |||||||
| chr17:63565007 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.139-13463A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63565007 | |||||||
| chr17:63565192 | G | C | 5 | a0001c0001t0016g0198 a0001c0001t0016g0199 a0001c0001t0017g0201 others(2): Show |
5 | HG02257.hp1 HG02559.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.139-13278G>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63565192 | |||||||
| chr17:63565230 | C | T | 1 | a0001c0001t0009g0224 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.139-13240C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63565230 | |||||||
| chr17:63565318 | C | T | 1 | a0001c0001t0014g0205 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.139-13152C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63565318 | |||||||
| chr17:63565380 | G | A | 6 | a0001c0001t0001g0021 a0001c0001t0005g0022 a0001c0001t0005g0023 others(3): Show |
6 | HG01346.hp1 HG02559.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.139-13090G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63565380 | |||||||
| chr17:63565515 | A | G | 74 | a0001c0001t0001g0014 a0001c0001t0001g0020 a0001c0001t0001g0078 others(71): Show |
76 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.139-12955A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63565515 | |||||||
| chr17:63565575 | A | T | 1 | a0001c0001t0010g0192 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.139-12895A>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63565575 | |||||||
| chr17:63565997 | A | C | 5 | a0001c0001t0016g0198 a0001c0001t0016g0199 a0001c0001t0017g0201 others(2): Show |
5 | HG02257.hp1 HG02559.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.139-12473A>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63565997 | |||||||
| chr17:63566031 | G | A | 2 | a0001c0001t0006g0210 a0001c0001t0023g0211 |
2 | HG02630.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.139-12439G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63566031 | |||||||
| chr17:63566095 | T | G | 1 | a0001c0001t0001g0037 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.139-12375T>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63566095 | |||||||
| chr17:63566161 | G | C | 3 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0006g0189 |
3 | HG01243.hp1 HG02723.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.139-12309G>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63566161 | |||||||
| chr17:63566327 | C | T | 1 | a0001c0001t0014g0203 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.139-12143C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63566327 | |||||||
| chr17:63566370 | CA | C | 7 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0146 others(4): Show |
7 | HG00140.hp2 HG01081.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.139-12087delA | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63566370 | ||||||
| chr17:63566370 | CAA | C | 150 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(147): Show |
162 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.139-12088_139-1208 others(6): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63566370 | ||||||
| chr17:63566382 | A | C | 1 | a0001c0001t0030g0194 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.139-12088A>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63566382 | |||||||
| chr17:63566463 | T | G | 1 | a0001c0001t0012g0035 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.139-12007T>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63566463 | |||||||
| chr17:63566648 | C | T | 2 | a0001c0001t0001g0096 a0001c0001t0001g0097 |
2 | HG02300.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.139-11822C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63566648 | |||||||
| chr17:63566707 | G | A | 2 | a0001c0001t0001g0116 a0001c0001t0001g0136 |
2 | HG02074.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.139-11763G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63566707 | |||||||
| chr17:63566876 | C | T | 2 | a0001c0001t0001g0215 a0001c0001t0001g0220 |
2 | NA19000.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.139-11594C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63566876 | |||||||
| chr17:63566962 | TTTTC | T | 23 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(20): Show |
23 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(20): Show |
intron_variant | MODIFIER | c.139-11492_139-1148 others(8): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63566962 | ||||||
| chr17:63567006 | G | A | 1 | a0001c0001t0014g0203 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.139-11464G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63567006 | |||||||
| chr17:63567029 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.139-11441A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63567029 | |||||||
| chr17:63567032 | G | A | 9 | a0001c0001t0001g0225 a0001c0001t0001g0234 a0001c0001t0003g0226 others(6): Show |
9 | HG01099.hp2 HG02622.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.139-11438G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63567032 | |||||||
| chr17:63567073 | G | A | 2 | a0001c0001t0001g0196 a0001c0001t0001g0197 |
2 | HG02451.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.139-11397G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63567073 | |||||||
| chr17:63567164 | G | C | 2 | a0001c0001t0009g0170 a0001c0001t0029g0169 |
2 | HG01109.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.139-11306G>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63567164 | |||||||
| chr17:63567271 | T | C | 6 | a0001c0001t0004g0158 a0001c0001t0004g0159 a0001c0001t0004g0173 others(3): Show |
6 | HG02055.hp1 HG02258.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.139-11199T>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63567271 | |||||||
| chr17:63567494 | C | T | 1 | a0001c0001t0010g0192 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.139-10976C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63567494 | |||||||
| chr17:63567753 | G | A | 1 | a0001c0001t0001g0225 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.139-10717G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63567753 | |||||||
| chr17:63567883 | A | C | 3 | a0001c0001t0001g0225 a0001c0001t0006g0210 a0001c0001t0023g0211 |
3 | HG02630.hp2 HG02809.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.139-10587A>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63567883 | |||||||
| chr17:63568059 | T | C | 37 | a0001c0001t0001g0013 a0001c0001t0001g0060 a0001c0001t0001g0061 others(34): Show |
38 | HG00639.hp1 HG01099.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.139-10411T>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63568059 | |||||||
| chr17:63568121 | A | G | 6 | a0001c0001t0009g0224 a0001c0001t0011g0207 a0001c0001t0011g0212 others(3): Show |
6 | HG02622.hp2 HG02723.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.139-10349A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63568121 | |||||||
| chr17:63568309 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.139-10161G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63568309 | |||||||
| chr17:63568360 | G | A | 2 | a0001c0001t0010g0113 a0001c0001t0010g0192 |
2 | HG02451.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.139-10110G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63568360 | |||||||
| chr17:63568378 | C | G | 2 | a0001c0001t0001g0061 a0001c0001t0001g0062 |
2 | HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.139-10092C>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63568378 | |||||||
| chr17:63568492 | T | C | 2 | a0001c0001t0009g0224 a0001c0001t0019g0204 |
2 | HG02723.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.139-9978T>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63568492 | |||||||
| chr17:63568541 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.139-9929C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63568541 | |||||||
| chr17:63568576 | G | C | 2 | a0001c0001t0024g0077 a0001c0001t0032g0200 |
2 | HG03453.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.139-9894G>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63568576 | |||||||
| chr17:63568581 | T | C | 3 | a0001c0001t0001g0225 a0001c0001t0006g0210 a0001c0001t0023g0211 |
3 | HG02630.hp2 HG02809.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.139-9889T>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63568581 | |||||||
| chr17:63568639 | G | A | 41 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(38): Show |
41 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(38): Show |
intron_variant | MODIFIER | c.139-9831G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63568639 | |||||||
| chr17:63568746 | G | C | 3 | a0001c0001t0016g0198 a0001c0001t0016g0199 a0001c0001t0029g0169 |
3 | HG02257.hp1 HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.139-9724G>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63568746 | |||||||
| chr17:63568752 | G | A | 6 | a0001c0001t0001g0013 a0001c0001t0001g0060 a0001c0001t0001g0061 others(3): Show |
7 | HG00639.hp1 HG02486.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.139-9718G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63568752 | |||||||
| chr17:63568779 | C | G | 1 | a0001c0001t0001g0172 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.139-9691C>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63568779 | |||||||
| chr17:63568875 | A | G | 1 | a0001c0001t0008g0012 | 2 | HG00741.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.139-9595A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63568875 | |||||||
| chr17:63568880 | C | T | 2 | a0001c0001t0016g0198 a0001c0001t0016g0199 |
2 | HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.139-9590C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63568880 | |||||||
| chr17:63568883 | T | C | 1 | a0001c0001t0001g0160 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.139-9587T>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63568883 | |||||||
| chr17:63568971 | G | A | 6 | a0001c0001t0001g0013 a0001c0001t0001g0060 a0001c0001t0001g0061 others(3): Show |
7 | HG00639.hp1 HG02486.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.139-9499G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63568971 | |||||||
| chr17:63569383 | GA | G | 12 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0149 others(9): Show |
12 | HG00140.hp2 HG01081.hp2 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.139-9071delA | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63569383 | ||||||
| chr17:63569453 | G | C | 1 | a0001c0001t0001g0117 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.139-9017G>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63569453 | |||||||
| chr17:63569572 | G | T | 1 | a0001c0001t0001g0021 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.139-8898G>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63569572 | |||||||
| chr17:63569649 | A | G | 1 | a0001c0001t0024g0077 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.139-8821A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63569649 | |||||||
| chr17:63569660 | G | A | 3 | a0001c0001t0016g0198 a0001c0001t0016g0199 a0001c0001t0029g0169 |
3 | HG02257.hp1 HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.139-8810G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63569660 | |||||||
| chr17:63570069 | A | G | 2 | a0001c0001t0010g0113 a0001c0001t0010g0192 |
2 | HG02451.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.139-8401A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63570069 | |||||||
| chr17:63570269 | C | T | 6 | a0001c0001t0014g0203 a0001c0001t0014g0205 a0001c0001t0015g0229 others(3): Show |
6 | HG02622.hp2 HG02818.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.139-8201C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63570269 | |||||||
| chr17:63570351 | G | A | 3 | a0001c0001t0016g0198 a0001c0001t0016g0199 a0001c0001t0029g0169 |
3 | HG02257.hp1 HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.139-8119G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63570351 | |||||||
| chr17:63570411 | G | A | 3 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0151 |
3 | HG01167.hp1 HG01433.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.139-8059G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63570411 | |||||||
| chr17:63570447 | G | A | 1 | a0001c0001t0001g0055 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.139-8023G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63570447 | |||||||
| chr17:63570451 | C | CA | 6 | a0001c0001t0003g0226 a0001c0001t0003g0227 a0001c0001t0003g0230 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.139-8010dupA | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63570451 | ||||||
| chr17:63570492 | A | G | 3 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0070 |
3 | HG00642.hp1 HG01070.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.139-7978A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63570492 | |||||||
| chr17:63570516 | C | T | 8 | a0001c0002t0002g0027 a0001c0002t0002g0028 a0001c0002t0002g0029 others(5): Show |
8 | HG01099.hp2 HG02145.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.139-7954C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63570516 | |||||||
| chr17:63570625 | G | T | 22 | a0001c0001t0001g0225 a0001c0001t0006g0210 a0001c0001t0009g0170 others(19): Show |
22 | HG01099.hp2 HG01109.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.139-7845G>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63570625 | |||||||
| chr17:63570730 | T | G | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(173): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.139-7740T>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63570730 | |||||||
| chr17:63570849 | G | A | 2 | a0001c0001t0010g0113 a0001c0001t0010g0192 |
2 | HG02451.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.139-7621G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63570849 | |||||||
| chr17:63571054 | C | T | 18 | a0001c0001t0001g0013 a0001c0001t0001g0060 a0001c0001t0001g0061 others(15): Show |
19 | HG00639.hp1 HG01099.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.139-7416C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63571054 | |||||||
| chr17:63571331 | A | G | 3 | a0001c0001t0009g0170 a0001c0001t0009g0224 a0001c0001t0019g0204 |
3 | HG01109.hp2 HG02723.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.139-7139A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63571331 | |||||||
| chr17:63571371 | G | A | 3 | a0001c0001t0001g0129 a0001c0001t0001g0138 a0001c0001t0001g0221 |
3 | NA18942.hp2 NA18965.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.139-7099G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63571371 | |||||||
| chr17:63571531 | GT | G | 3 | a0001c0001t0016g0198 a0001c0001t0016g0199 a0001c0001t0029g0169 |
3 | HG02257.hp1 HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.139-6938delT | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63571531 | |||||||
| chr17:63571559 | G | A | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(173): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.139-6911G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63571559 | |||||||
| chr17:63571809 | G | A | 2 | a0001c0001t0001g0010 a0001c0001t0001g0046 |
3 | HG01256.hp1 HG01258.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.139-6661G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63571809 | |||||||
| chr17:63571811 | G | A | 1 | a0001c0001t0024g0077 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.139-6659G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63571811 | |||||||
| chr17:63571859 | C | A | 1 | a0001c0001t0001g0112 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.139-6611C>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63571859 | |||||||
| chr17:63572161 | T | C | 1 | a0001c0001t0001g0214 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.139-6309T>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63572161 | |||||||
| chr17:63572222 | A | T | 5 | a0001c0001t0009g0170 a0001c0001t0009g0224 a0001c0001t0011g0207 others(2): Show |
5 | HG01109.hp2 HG02723.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.139-6248A>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63572222 | |||||||
| chr17:63572296 | G | A | 1 | a0001c0001t0009g0170 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.139-6174G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63572296 | |||||||
| chr17:63572799 | G | A | 1 | a0001c0001t0032g0200 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.139-5671G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63572799 | |||||||
| chr17:63572924 | G | A | 1 | a0001c0001t0024g0077 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.139-5546G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63572924 | |||||||
| chr17:63573018 | C | A | 1 | a0001c0001t0001g0083 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.139-5452C>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63573018 | |||||||
| chr17:63573080 | A | T | 3 | a0001c0001t0016g0198 a0001c0001t0016g0199 a0001c0001t0029g0169 |
3 | HG02257.hp1 HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.139-5390A>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63573080 | |||||||
| chr17:63573119 | T | TTTG | 35 | a0001c0001t0001g0013 a0001c0001t0001g0060 a0001c0001t0001g0061 others(32): Show |
36 | HG00639.hp1 HG01099.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.139-5334_139-5332d others(5): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63573119 | ||||||
| chr17:63573313 | T | C | 35 | a0001c0001t0001g0013 a0001c0001t0001g0060 a0001c0001t0001g0061 others(32): Show |
36 | HG00639.hp1 HG01099.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.139-5157T>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63573313 | |||||||
| chr17:63573462 | T | C | 7 | a0001c0001t0001g0190 a0001c0001t0001g0208 a0001c0001t0005g0022 others(4): Show |
7 | HG01346.hp1 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.139-5008T>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63573462 | |||||||
| chr17:63573550 | C | T | 7 | a0001c0001t0001g0013 a0001c0001t0001g0060 a0001c0001t0001g0061 others(4): Show |
8 | HG00639.hp1 HG02486.hp2 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.139-4920C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63573550 | |||||||
| chr17:63573552 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.139-4918C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63573552 | |||||||
| chr17:63573570 | C | CA | 8 | a0001c0002t0002g0027 a0001c0002t0002g0028 a0001c0002t0002g0029 others(5): Show |
8 | HG01099.hp2 HG02145.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.139-4890dupA | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63573570 | ||||||
| chr17:63573705 | G | C | 5 | a0001c0001t0009g0170 a0001c0001t0009g0224 a0001c0001t0011g0207 others(2): Show |
5 | HG01109.hp2 HG02723.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.139-4765G>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63573705 | |||||||
| chr17:63573723 | T | C | 5 | a0001c0001t0005g0022 a0001c0001t0005g0023 a0001c0001t0005g0024 others(2): Show |
5 | HG01346.hp1 HG02559.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.139-4747T>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63573723 | |||||||
| chr17:63573730 | C | CA | 10 | a0001c0001t0001g0054 a0001c0001t0001g0078 a0001c0001t0001g0079 others(7): Show |
10 | HG02165.hp2 HG02738.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.139-4724dupA | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63573730 | ||||||
| chr17:63573730 | CA | C | 19 | a0001c0001t0014g0203 a0001c0001t0015g0229 a0001c0001t0015g0235 others(16): Show |
19 | HG01099.hp2 HG01975.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.139-4724delA | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 63573730 | ||||||
| chr17:63573753 | A | G | 7 | a0001c0001t0001g0190 a0001c0001t0001g0208 a0001c0001t0005g0022 others(4): Show |
7 | HG01346.hp1 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.139-4717A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63573753 | |||||||
| chr17:63574019 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.139-4451G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63574019 | |||||||
| chr17:63574110 | C | T | 1 | a0001c0001t0001g0225 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.139-4360C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63574110 | |||||||
| chr17:63574160 | A | G | 1 | a0001c0001t0001g0040 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.139-4310A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63574160 | |||||||
| chr17:63574200 | A | G | 2 | a0001c0001t0010g0113 a0001c0001t0010g0192 |
2 | HG02451.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.139-4270A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63574200 | |||||||
| chr17:63574297 | C | T | 8 | a0001c0002t0002g0027 a0001c0002t0002g0028 a0001c0002t0002g0029 others(5): Show |
8 | HG01099.hp2 HG02145.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.139-4173C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63574297 | |||||||
| chr17:63574410 | T | G | 1 | a0001c0001t0016g0198 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.139-4060T>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63574410 | |||||||
| chr17:63574595 | A | G | 8 | a0001c0002t0002g0027 a0001c0002t0002g0028 a0001c0002t0002g0029 others(5): Show |
8 | HG01099.hp2 HG02145.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.139-3875A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63574595 | |||||||
| chr17:63574661 | A | G | 6 | a0001c0001t0014g0203 a0001c0001t0014g0205 a0001c0001t0015g0229 others(3): Show |
6 | HG02622.hp2 HG02818.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.139-3809A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63574661 | |||||||
| chr17:63574911 | T | G | 2 | a0001c0001t0001g0190 a0001c0001t0001g0208 |
2 | HG02280.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.139-3559T>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63574911 | |||||||
| chr17:63574962 | A | T | 1 | a0001c0001t0001g0145 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.139-3508A>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63574962 | |||||||
| chr17:63574976 | A | ATAAT | 49 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0020 others(46): Show |
52 | HG00639.hp1 HG01099.hp2 HG01109.hp2 others(49): Show |
intron_variant | MODIFIER | c.139-3494_139-3493i others(6): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63574976 | |||||||
| chr17:63574989 | A | G | 2 | a0001c0001t0010g0113 a0001c0001t0010g0192 |
2 | HG02451.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.139-3481A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63574989 | |||||||
| chr17:63574996 | T | C | 1 | a0001c0001t0001g0001 | 4 | NA18944.hp1 NA18959.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.139-3474T>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63574996 | |||||||
| chr17:63575046 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.139-3424G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63575046 | |||||||
| chr17:63575192 | G | A | 4 | a0001c0001t0016g0198 a0001c0001t0016g0199 a0001c0001t0024g0077 others(1): Show |
4 | HG02257.hp1 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.139-3278G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63575192 | |||||||
| chr17:63575308 | G | T | 2 | a0001c0001t0001g0147 a0001c0001t0001g0148 |
2 | HG01167.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.139-3162G>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63575308 | |||||||
| chr17:63575310 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.139-3160G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63575310 | |||||||
| chr17:63575642 | C | T | 3 | a0001c0001t0016g0198 a0001c0001t0016g0199 a0001c0001t0029g0169 |
3 | HG02257.hp1 HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.139-2828C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63575642 | |||||||
| chr17:63575711 | G | C | 15 | a0001c0001t0009g0170 a0001c0001t0009g0224 a0001c0001t0016g0198 others(12): Show |
15 | HG01099.hp2 HG01109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.139-2759G>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63575711 | |||||||
| chr17:63575773 | G | C | 2 | a0001c0001t0001g0140 a0001c0001t0001g0161 |
2 | HG01256.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.139-2697G>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63575773 | |||||||
| chr17:63575783 | G | A | 15 | a0001c0001t0009g0170 a0001c0001t0009g0224 a0001c0001t0016g0198 others(12): Show |
15 | HG01099.hp2 HG01109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.139-2687G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63575783 | |||||||
| chr17:63575885 | A | G | 1 | a0001c0001t0001g0208 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.139-2585A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63575885 | |||||||
| chr17:63575886 | G | A | 7 | a0001c0001t0001g0190 a0001c0001t0001g0208 a0001c0001t0005g0022 others(4): Show |
7 | HG01346.hp1 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.139-2584G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63575886 | |||||||
| chr17:63576041 | T | C | 2 | a0001c0001t0009g0224 a0001c0001t0019g0204 |
2 | HG02723.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.139-2429T>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63576041 | |||||||
| chr17:63576163 | C | T | 2 | a0001c0003t0001g0184 a0001c0003t0001g0185 |
2 | HG01975.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.139-2307C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63576163 | |||||||
| chr17:63576180 | G | A | 1 | a0001c0001t0029g0169 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.139-2290G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63576180 | |||||||
| chr17:63576301 | G | A | 2 | a0001c0001t0010g0113 a0001c0001t0010g0192 |
2 | HG02451.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.139-2169G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63576301 | |||||||
| chr17:63576518 | T | C | 6 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0063 others(3): Show |
7 | HG02451.hp2 HG02717.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.139-1952T>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63576518 | |||||||
| chr17:63576541 | G | A | 3 | a0001c0001t0009g0170 a0001c0001t0009g0224 a0001c0001t0019g0204 |
3 | HG01109.hp2 HG02723.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.139-1929G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63576541 | |||||||
| chr17:63576651 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.139-1819C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63576651 | |||||||
| chr17:63576864 | C | T | 2 | a0001c0001t0001g0010 a0001c0001t0001g0046 |
3 | HG01256.hp1 HG01258.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.139-1606C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63576864 | |||||||
| chr17:63577040 | C | T | 8 | a0001c0002t0002g0027 a0001c0002t0002g0028 a0001c0002t0002g0029 others(5): Show |
8 | HG01099.hp2 HG02145.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.139-1430C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63577040 | |||||||
| chr17:63577415 | T | C | 49 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0020 others(46): Show |
52 | HG00639.hp1 HG01099.hp2 HG01109.hp2 others(49): Show |
intron_variant | MODIFIER | c.139-1055T>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63577415 | |||||||
| chr17:63577452 | A | G | 6 | a0001c0001t0001g0013 a0001c0001t0001g0060 a0001c0001t0001g0061 others(3): Show |
7 | HG00639.hp1 HG02486.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.139-1018A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63577452 | |||||||
| chr17:63577459 | G | A | 6 | a0001c0001t0001g0013 a0001c0001t0001g0060 a0001c0001t0001g0061 others(3): Show |
7 | HG00639.hp1 HG02486.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.139-1011G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63577459 | |||||||
| chr17:63577522 | G | C | 5 | a0001c0001t0005g0022 a0001c0001t0005g0023 a0001c0001t0005g0024 others(2): Show |
5 | HG01346.hp1 HG02559.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.139-948G>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63577522 | |||||||
| chr17:63577600 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.139-870G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63577600 | |||||||
| chr17:63577613 | A | G | 1 | a0001c0001t0001g0225 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.139-857A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63577613 | |||||||
| chr17:63577823 | A | G | 6 | a0001c0001t0001g0013 a0001c0001t0001g0060 a0001c0001t0001g0061 others(3): Show |
7 | HG00639.hp1 HG02486.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.139-647A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63577823 | |||||||
| chr17:63577993 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.139-477C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63577993 | |||||||
| chr17:63578045 | A | G | 1 | a0001c0001t0020g0179 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.139-425A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63578045 | |||||||
| chr17:63578113 | A | C | 4 | a0001c0001t0014g0203 a0001c0001t0014g0205 a0001c0001t0017g0201 others(1): Show |
4 | HG02622.hp2 HG03041.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.139-357A>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63578113 | |||||||
| chr17:63578207 | G | A | 9 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0085 others(6): Show |
9 | HG02572.hp2 HG02809.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.139-263G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63578207 | |||||||
| chr17:63578431 | T | A | 2 | a0001c0001t0015g0229 a0001c0001t0015g0235 |
2 | HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.139-39T>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 1/6 | chr17 | 63578431 | |||||||
| chr17:63578696 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.297+68G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 2/6 | chr17 | 63578696 | |||||||
| chr17:63579003 | C | T | 2 | a0001c0001t0011g0207 a0001c0001t0011g0212 |
2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.298-334C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 2/6 | chr17 | 63579003 | |||||||
| chr17:63579497 | A | ATTTTC | 5 | a0001c0001t0005g0022 a0001c0001t0005g0023 a0001c0001t0005g0024 others(2): Show |
5 | HG01346.hp1 HG02559.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.409+51_409+55dupTT others(3): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 63579497 | ||||||
| chr17:63579535 | C | T | 2 | a0001c0001t0001g0051 a0001c0001t0001g0074 |
2 | HG00597.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.409+87C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 3/6 | chr17 | 63579535 | |||||||
| chr17:63579629 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.409+181C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 3/6 | chr17 | 63579629 | |||||||
| chr17:63579679 | G | T | 40 | a0001c0001t0001g0013 a0001c0001t0001g0060 a0001c0001t0001g0061 others(37): Show |
41 | HG00639.hp1 HG01099.hp2 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.410-146G>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 3/6 | chr17 | 63579679 | |||||||
| chr17:63579691 | G | A | 1 | a0001c0001t0001g0014 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.410-134G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 3/6 | chr17 | 63579691 | |||||||
| chr17:63579715 | A | G | 6 | a0001c0001t0001g0013 a0001c0001t0001g0060 a0001c0001t0001g0061 others(3): Show |
7 | HG00639.hp1 HG02486.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.410-110A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 3/6 | chr17 | 63579715 | |||||||
| chr17:63579781 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.410-44G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 3/6 | chr17 | 63579781 | |||||||
| chr17:63579994 | G | A | 7 | a0001c0001t0009g0170 a0001c0001t0009g0224 a0001c0001t0016g0198 others(4): Show |
7 | HG01109.hp2 HG02257.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.528+51G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 4/6 | chr17 | 63579994 | |||||||
| chr17:63580507 | C | CT | 31 | a0001c0001t0001g0015 a0001c0001t0001g0049 a0001c0001t0001g0056 others(28): Show |
33 | HG00642.hp1 HG00741.hp1 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.528+592dupT | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 63580507 | ||||||
| chr17:63580507 | C | CTT | 5 | a0001c0001t0011g0207 a0001c0001t0011g0212 a0001c0001t0017g0202 others(2): Show |
5 | HG01346.hp2 HG02622.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.528+591_528+592dup others(2): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 63580507 | ||||||
| chr17:63580507 | CT | C | 45 | a0001c0001t0001g0014 a0001c0001t0001g0018 a0001c0001t0001g0060 others(42): Show |
47 | HG00140.hp2 HG00280.hp1 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.528+592delT | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 63580507 | ||||||
| chr17:63580507 | CTT | C | 33 | a0001c0001t0001g0013 a0001c0001t0001g0061 a0001c0001t0001g0076 others(30): Show |
34 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(31): Show |
intron_variant | MODIFIER | c.528+591_528+592del others(2): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 63580507 | ||||||
| chr17:63580507 | CTTTTTTT others(6): Show |
C | 2 | a0001c0001t0010g0113 a0001c0001t0010g0192 |
2 | HG02451.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.528+580_528+592del others(13): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 63580507 | ||||||
| chr17:63580507 | CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0032g0200 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.528+579_528+592del others(14): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 63580507 | ||||||
| chr17:63580668 | G | A | 2 | a0001c0001t0001g0118 a0001c0001t0001g0126 |
2 | HG02074.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.528+725G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 4/6 | chr17 | 63580668 | |||||||
| chr17:63580740 | G | A | 2 | a0001c0001t0016g0198 a0001c0001t0016g0199 |
2 | HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.528+797G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 4/6 | chr17 | 63580740 | |||||||
| chr17:63580802 | G | A | 1 | a0001c0001t0009g0170 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.528+859G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 4/6 | chr17 | 63580802 | |||||||
| chr17:63581076 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.528+1133G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 4/6 | chr17 | 63581076 | |||||||
| chr17:63581268 | G | A | 2 | a0001c0001t0001g0139 a0001c0001t0001g0143 |
2 | NA18952.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.528+1325G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 4/6 | chr17 | 63581268 | |||||||
| chr17:63581549 | C | G | 1 | a0001c0001t0016g0198 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.528+1606C>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 4/6 | chr17 | 63581549 | |||||||
| chr17:63581844 | T | C | 2 | a0001c0001t0010g0113 a0001c0001t0010g0192 |
2 | HG02451.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.529-1658T>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 4/6 | chr17 | 63581844 | |||||||
| chr17:63581885 | G | A | 2 | a0001c0001t0006g0210 a0001c0001t0023g0211 |
2 | HG02630.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.529-1617G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 4/6 | chr17 | 63581885 | |||||||
| chr17:63582000 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.529-1502C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 4/6 | chr17 | 63582000 | |||||||
| chr17:63582166 | A | T | 1 | a0001c0001t0007g0092 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.529-1336A>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 4/6 | chr17 | 63582166 | |||||||
| chr17:63582293 | C | T | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(231): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.529-1209C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 4/6 | chr17 | 63582293 | |||||||
| chr17:63582336 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.529-1166G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 4/6 | chr17 | 63582336 | |||||||
| chr17:63582356 | C | T | 2 | a0001c0001t0010g0113 a0001c0001t0010g0192 |
2 | HG02451.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.529-1146C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 4/6 | chr17 | 63582356 | |||||||
| chr17:63582471 | C | CT | 6 | a0001c0001t0001g0013 a0001c0001t0001g0060 a0001c0001t0001g0061 others(3): Show |
7 | HG00639.hp1 HG02486.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.529-1018dupT | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 63582471 | ||||||
| chr17:63582531 | T | C | 3 | a0001c0001t0001g0089 a0001c0001t0001g0093 a0001c0001t0001g0095 |
3 | HG02922.hp2 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.529-971T>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 4/6 | chr17 | 63582531 | |||||||
| chr17:63582538 | A | G | 2 | a0001c0001t0010g0113 a0001c0001t0010g0192 |
2 | HG02451.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.529-964A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 4/6 | chr17 | 63582538 | |||||||
| chr17:63582555 | G | A | 6 | a0001c0001t0003g0226 a0001c0001t0003g0227 a0001c0001t0003g0230 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.529-947G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 4/6 | chr17 | 63582555 | |||||||
| chr17:63582564 | G | A | 6 | a0001c0001t0014g0203 a0001c0001t0014g0205 a0001c0001t0015g0229 others(3): Show |
6 | HG02622.hp2 HG02818.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.529-938G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 4/6 | chr17 | 63582564 | |||||||
| chr17:63582586 | A | G | 1 | a0001c0001t0009g0224 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.529-916A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 4/6 | chr17 | 63582586 | |||||||
| chr17:63582611 | G | A | 6 | a0001c0001t0003g0226 a0001c0001t0003g0227 a0001c0001t0003g0230 others(3): Show |
6 | HG02622.hp1 HG02630.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.529-891G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 4/6 | chr17 | 63582611 | |||||||
| chr17:63582716 | G | T | 2 | a0001c0001t0006g0210 a0001c0001t0023g0211 |
2 | HG02630.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.529-786G>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 4/6 | chr17 | 63582716 | |||||||
| chr17:63582717 | C | T | 2 | a0001c0001t0006g0210 a0001c0001t0023g0211 |
2 | HG02630.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.529-785C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 4/6 | chr17 | 63582717 | |||||||
| chr17:63582897 | T | A | 40 | a0001c0001t0001g0013 a0001c0001t0001g0060 a0001c0001t0001g0061 others(37): Show |
41 | HG00639.hp1 HG01099.hp2 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.529-605T>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 4/6 | chr17 | 63582897 | |||||||
| chr17:63582937 | G | A | 1 | a0001c0001t0024g0077 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.529-565G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 4/6 | chr17 | 63582937 | |||||||
| chr17:63583065 | A | G | 1 | a0001c0001t0001g0040 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.529-437A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 4/6 | chr17 | 63583065 | |||||||
| chr17:63583400 | T | A | 1 | a0001c0001t0001g0052 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.529-102T>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 4/6 | chr17 | 63583400 | |||||||
| chr17:63583408 | G | A | 1 | a0001c0001t0003g0227 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.529-94G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 4/6 | chr17 | 63583408 | |||||||
| chr17:63583736 | T | G | 6 | a0001c0001t0001g0013 a0001c0001t0001g0060 a0001c0001t0001g0061 others(3): Show |
7 | HG00639.hp1 HG02486.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.738+25T>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 5/6 | chr17 | 63583736 | |||||||
| chr17:63583798 | G | A | 7 | a0001c0001t0009g0170 a0001c0001t0009g0224 a0001c0001t0016g0198 others(4): Show |
7 | HG01109.hp2 HG02257.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.738+87G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 5/6 | chr17 | 63583798 | |||||||
| chr17:63583886 | G | T | 2 | a0001c0001t0001g0085 a0001c0001t0001g0094 |
2 | HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.738+175G>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 5/6 | chr17 | 63583886 | |||||||
| chr17:63583938 | C | T | 1 | a0001c0001t0024g0077 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.738+227C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 5/6 | chr17 | 63583938 | |||||||
| chr17:63583976 | C | T | 1 | a0001c0001t0029g0169 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.738+265C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 5/6 | chr17 | 63583976 | |||||||
| chr17:63584005 | G | C | 2 | a0001c0001t0001g0040 a0001c0001t0001g0047 |
2 | HG01167.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.738+294G>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 5/6 | chr17 | 63584005 | |||||||
| chr17:63584014 | G | C | 1 | a0001c0001t0001g0206 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.738+303G>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 5/6 | chr17 | 63584014 | |||||||
| chr17:63584052 | C | T | 1 | a0001c0001t0032g0200 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.738+341C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 5/6 | chr17 | 63584052 | |||||||
| chr17:63584192 | G | A | 1 | a0001c0001t0001g0014 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.738+481G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 5/6 | chr17 | 63584192 | |||||||
| chr17:63584195 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.738+484C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 5/6 | chr17 | 63584195 | |||||||
| chr17:63584208 | G | A | 1 | a0001c0001t0009g0224 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.738+497G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 5/6 | chr17 | 63584208 | |||||||
| chr17:63584278 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.738+567G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 5/6 | chr17 | 63584278 | |||||||
| chr17:63584367 | C | T | 6 | a0001c0001t0001g0013 a0001c0001t0001g0060 a0001c0001t0001g0061 others(3): Show |
7 | HG00639.hp1 HG02486.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.738+656C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 5/6 | chr17 | 63584367 | |||||||
| chr17:63584422 | C | T | 2 | a0001c0001t0009g0224 a0001c0001t0019g0204 |
2 | HG02723.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.738+711C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 5/6 | chr17 | 63584422 | |||||||
| chr17:63584449 | T | C | 1 | a0001c0001t0001g0196 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.738+738T>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 5/6 | chr17 | 63584449 | |||||||
| chr17:63584467 | G | A | 49 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0020 others(46): Show |
52 | HG00639.hp1 HG01099.hp2 HG01109.hp2 others(49): Show |
intron_variant | MODIFIER | c.739-744G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 5/6 | chr17 | 63584467 | |||||||
| chr17:63584471 | A | T | 2 | a0001c0001t0016g0198 a0001c0001t0016g0199 |
2 | HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.739-740A>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 5/6 | chr17 | 63584471 | |||||||
| chr17:63584576 | C | T | 33 | a0001c0001t0001g0013 a0001c0001t0001g0060 a0001c0001t0001g0061 others(30): Show |
34 | HG00639.hp1 HG01099.hp2 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.739-635C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 5/6 | chr17 | 63584576 | |||||||
| chr17:63584577 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.739-634G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 5/6 | chr17 | 63584577 | |||||||
| chr17:63584583 | A | G | 5 | a0001c0001t0005g0022 a0001c0001t0005g0023 a0001c0001t0005g0024 others(2): Show |
5 | HG01346.hp1 HG02559.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.739-628A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 5/6 | chr17 | 63584583 | |||||||
| chr17:63584619 | G | A | 3 | a0001c0001t0001g0225 a0001c0001t0006g0210 a0001c0001t0023g0211 |
3 | HG02630.hp2 HG02809.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.739-592G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 5/6 | chr17 | 63584619 | |||||||
| chr17:63584688 | G | A | 2 | a0001c0001t0013g0086 a0001c0001t0013g0228 |
2 | HG03486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.739-523G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 5/6 | chr17 | 63584688 | |||||||
| chr17:63584864 | C | T | 1 | a0001c0001t0001g0120 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.739-347C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 5/6 | chr17 | 63584864 | |||||||
| chr17:63585042 | C | T | 1 | a0001c0001t0011g0212 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.739-169C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 5/6 | chr17 | 63585042 | |||||||
| chr17:63585390 | T | A | 1 | a0001c0001t0001g0151 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.856+62T>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 6/6 | chr17 | 63585390 | |||||||
| chr17:63585567 | G | A | 7 | a0001c0001t0001g0013 a0001c0001t0001g0060 a0001c0001t0001g0061 others(4): Show |
8 | HG00639.hp1 HG02486.hp2 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.856+239G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 6/6 | chr17 | 63585567 | |||||||
| chr17:63585819 | C | T | 7 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(4): Show |
7 | HG02165.hp2 NA18947.hp2 NA18952.hp2 others(4): Show |
intron_variant | MODIFIER | c.856+491C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 6/6 | chr17 | 63585819 | |||||||
| chr17:63586094 | C | T | 3 | a0001c0001t0009g0170 a0001c0001t0009g0224 a0001c0001t0019g0204 |
3 | HG01109.hp2 HG02723.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.856+766C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 6/6 | chr17 | 63586094 | |||||||
| chr17:63586125 | C | CA | 33 | a0001c0001t0001g0059 a0001c0001t0001g0084 a0001c0001t0001g0104 others(30): Show |
33 | HG00099.hp1 HG00642.hp2 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.856+821dupA | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 63586125 | ||||||
| chr17:63586125 | CAAAAAAA others(5): Show |
C | 6 | a0001c0001t0001g0013 a0001c0001t0001g0060 a0001c0001t0001g0061 others(3): Show |
7 | HG00639.hp1 HG02486.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.856+810_856+821del others(12): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 63586125 | ||||||
| chr17:63586142 | A | C | 2 | a0001c0001t0010g0113 a0001c0001t0010g0192 |
2 | HG02451.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.856+814A>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 6/6 | chr17 | 63586142 | |||||||
| chr17:63586178 | C | A | 2 | a0001c0001t0011g0207 a0001c0001t0011g0212 |
2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.856+850C>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 6/6 | chr17 | 63586178 | |||||||
| chr17:63586350 | G | A | 5 | a0001c0001t0005g0022 a0001c0001t0005g0023 a0001c0001t0005g0024 others(2): Show |
5 | HG01346.hp1 HG02559.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.856+1022G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 6/6 | chr17 | 63586350 | |||||||
| chr17:63586532 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.856+1204G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 6/6 | chr17 | 63586532 | |||||||
| chr17:63586548 | G | A | 3 | a0001c0001t0001g0009 a0001c0001t0012g0009 a0001c0001t0012g0035 |
3 | HG02738.hp1 HG03491.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.856+1220G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 6/6 | chr17 | 63586548 | |||||||
| chr17:63586550 | G | A | 1 | a0001c0001t0001g0014 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.856+1222G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 6/6 | chr17 | 63586550 | |||||||
| chr17:63586630 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.856+1302C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 6/6 | chr17 | 63586630 | |||||||
| chr17:63586655 | G | A | 1 | a0001c0002t0002g0028 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.856+1327G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 6/6 | chr17 | 63586655 | |||||||
| chr17:63586914 | C | T | 1 | a0001c0001t0024g0077 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.856+1586C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 6/6 | chr17 | 63586914 | |||||||
| chr17:63586948 | A | G | 1 | a0001c0001t0021g0209 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.856+1620A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 6/6 | chr17 | 63586948 | |||||||
| chr17:63586997 | A | G | 1 | a0001c0001t0001g0068 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.856+1669A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 6/6 | chr17 | 63586997 | |||||||
| chr17:63587109 | C | G | 3 | a0001c0001t0001g0225 a0001c0001t0006g0210 a0001c0001t0023g0211 |
3 | HG02630.hp2 HG02809.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.856+1781C>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 6/6 | chr17 | 63587109 | |||||||
| chr17:63587326 | CT | C | 5 | a0001c0001t0005g0022 a0001c0001t0005g0023 a0001c0001t0005g0024 others(2): Show |
5 | HG01346.hp1 HG02559.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.857-1661delT | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 63587326 | ||||||
| chr17:63587339 | T | C | 1 | a0001c0001t0029g0169 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.857-1661T>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 6/6 | chr17 | 63587339 | |||||||
| chr17:63587378 | A | G | 73 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(70): Show |
85 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.857-1622A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 6/6 | chr17 | 63587378 | |||||||
| chr17:63587398 | T | C | 1 | a0001c0001t0015g0229 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.857-1602T>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 6/6 | chr17 | 63587398 | |||||||
| chr17:63587536 | C | T | 6 | a0001c0001t0014g0203 a0001c0001t0014g0205 a0001c0001t0015g0229 others(3): Show |
6 | HG02622.hp2 HG02818.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.857-1464C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 6/6 | chr17 | 63587536 | |||||||
| chr17:63587561 | TTAGTGCT others(5): Show |
T | 3 | a0001c0001t0001g0225 a0001c0001t0006g0210 a0001c0001t0023g0211 |
3 | HG02630.hp2 HG02809.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.857-1438_857-1427d others(14): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 6/6 | chr17 | 63587561 | |||||||
| chr17:63587574 | G | A | 3 | a0001c0001t0001g0225 a0001c0001t0006g0210 a0001c0001t0023g0211 |
3 | HG02630.hp2 HG02809.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.857-1426G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 6/6 | chr17 | 63587574 | |||||||
| chr17:63587984 | T | TA | 9 | a0001c0001t0001g0036 a0001c0001t0001g0040 a0001c0001t0001g0153 others(6): Show |
9 | HG01167.hp2 HG02055.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.857-996dupA | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 63587984 | ||||||
| chr17:63587984 | TA | T | 18 | a0001c0001t0001g0167 a0001c0001t0004g0174 a0001c0001t0010g0113 others(15): Show |
18 | HG01099.hp2 HG01257.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.857-996delA | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 63587984 | ||||||
| chr17:63587984 | TAA | T | 18 | a0001c0001t0001g0013 a0001c0001t0001g0060 a0001c0001t0001g0061 others(15): Show |
19 | HG00639.hp1 HG01109.hp2 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.857-997_857-996del others(2): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 63587984 | ||||||
| chr17:63588023 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.857-977G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 6/6 | chr17 | 63588023 | |||||||
| chr17:63588023 | G | T | 1 | a0001c0001t0009g0224 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.857-977G>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 6/6 | chr17 | 63588023 | |||||||
| chr17:63588094 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.857-906A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 6/6 | chr17 | 63588094 | |||||||
| chr17:63588098 | T | C | 6 | a0001c0001t0014g0203 a0001c0001t0014g0205 a0001c0001t0015g0229 others(3): Show |
6 | HG02622.hp2 HG02818.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.857-902T>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 6/6 | chr17 | 63588098 | |||||||
| chr17:63588189 | A | AT | 43 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(40): Show |
43 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(40): Show |
intron_variant | MODIFIER | c.857-795dupT | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 63588189 | ||||||
| chr17:63588189 | A | ATTTTTTT others(4): Show |
2 | a0001c0001t0001g0013 a0001c0001t0001g0064 |
3 | HG00639.hp1 HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.857-805_857-795dup others(11): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 63588189 | ||||||
| chr17:63588189 | A | ATTTTTTT others(5): Show |
4 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(1): Show |
4 | HG02486.hp2 HG03139.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.857-806_857-795dup others(12): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 63588189 | ||||||
| chr17:63588189 | A | ATTTTTTT others(6): Show |
1 | a0001c0001t0006g0210 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.857-807_857-795dup others(13): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 63588189 | ||||||
| chr17:63588189 | A | ATTTTTTT others(7): Show |
11 | a0001c0001t0001g0225 a0001c0001t0010g0113 a0001c0001t0015g0229 others(8): Show |
11 | HG01099.hp2 HG02145.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.857-808_857-795dup others(14): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 63588189 | ||||||
| chr17:63588189 | A | ATTTTTTT others(8): Show |
6 | a0001c0001t0015g0235 a0001c0001t0017g0201 a0001c0001t0017g0202 others(3): Show |
6 | HG02572.hp1 HG02622.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.857-809_857-795dup others(15): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 63588189 | ||||||
| chr17:63588189 | A | ATTTTTTT others(10): Show |
3 | a0001c0001t0001g0208 a0001c0001t0010g0192 a0001c0001t0014g0205 |
3 | HG02280.hp2 HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.857-795_857-794ins others(17): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 63588189 | ||||||
| chr17:63588189 | A | ATTTTTTT others(11): Show |
2 | a0001c0001t0001g0190 a0001c0001t0014g0203 |
2 | HG04199.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.857-795_857-794ins others(18): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 63588189 | ||||||
| chr17:63588189 | A | ATTTTTTT others(12): Show |
3 | a0001c0001t0005g0022 a0001c0001t0005g0023 a0001c0001t0016g0198 |
3 | HG01346.hp1 HG02257.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.857-795_857-794ins others(19): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 63588189 | ||||||
| chr17:63588189 | A | ATTTTTTT others(13): Show |
5 | a0001c0001t0005g0024 a0001c0001t0005g0025 a0001c0001t0005g0026 others(2): Show |
5 | HG02559.hp1 HG02559.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.857-795_857-794ins others(20): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 63588189 | ||||||
| chr17:63588296 | T | C | 1 | a0001c0001t0001g0136 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.857-704T>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 6/6 | chr17 | 63588296 | |||||||
| chr17:63588312 | G | A | 5 | a0001c0001t0005g0022 a0001c0001t0005g0023 a0001c0001t0005g0024 others(2): Show |
5 | HG01346.hp1 HG02559.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.857-688G>A | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 6/6 | chr17 | 63588312 | |||||||
| chr17:63588360 | AT | A | 9 | a0001c0001t0014g0205 a0001c0002t0002g0027 a0001c0002t0002g0028 others(6): Show |
9 | HG01099.hp2 HG02145.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.857-624delT | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 63588360 | ||||||
| chr17:63588531 | A | G | 8 | a0001c0002t0002g0027 a0001c0002t0002g0028 a0001c0002t0002g0029 others(5): Show |
8 | HG01099.hp2 HG02145.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.857-469A>G | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 6/6 | chr17 | 63588531 | |||||||
| chr17:63588535 | T | TATCAGTC others(271): Show |
1 | a0001c0001t0032g0200 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.857-454_857-453ins others(278): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 63588535 | ||||||
| chr17:63588535 | T | TATCAGTC others(262): Show |
6 | a0001c0001t0001g0013 a0001c0001t0001g0060 a0001c0001t0001g0061 others(3): Show |
7 | HG00639.hp1 HG02486.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.857-456_857-455ins others(269): Show |
DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 63588535 | ||||||
| chr17:63588653 | T | C | 49 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0020 others(46): Show |
52 | HG00639.hp1 HG01099.hp2 HG01109.hp2 others(49): Show |
intron_variant | MODIFIER | c.857-347T>C | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 6/6 | chr17 | 63588653 | |||||||
| chr17:63588900 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.857-100C>T | DCAF7 | ENSG00000136485.16 | transcript | ENST00000614556.5 | protein_coding | 6/6 | chr17 | 63588900 |