Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 25879 |
| ensemblid | ENSG00000164934.15 |
| hgncid | 24535 |
| symbol | DCAF13 |
| name | DDB1 and CUL4 associated factor 13 |
| refseq_nuc | NM_015420.7 |
| refseq_prot | NP_056235.5 |
| ensembl_nuc | ENST00000612750.5 |
| ensembl_prot | ENSP00000484962.1 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 103415386 |
| end | 103443453 |
| strand | + |
| ver | v1.2 |
| region | chr8:103415386-103443453 |
| region5000 | chr8:103410386-103448453 |
| regionname0 | DCAF13_chr8_103415386_103443453 |
| regionname5000 | DCAF13_chr8_103410386_103448453 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 445 | 230 | 75 | 42 | 77 | 11 | 24 | 58 | DCAF13_chr8_103410386_103448453 | DCAF13 | MKVKM others(440): Show |
chr8 | 103410386 | 103448453 |
| a0002 | 0/1 | 445 | 111 | 17 | 25 | 55 | 5 | 8 | 48 | DCAF13_chr8_103410386_103448453 | DCAF13 | MKVKM others(440): Show |
chr8 | 103410386 | 103448453 |
| a0003 | 0/0 | 445 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | MKVKM others(440): Show |
chr8 | 103410386 | 103448453 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1335 | 225 | 71 | 41 | 77 | 11 | 24 | DCAF13_chr8_103410386_103448453 | DCAF13 | ATGAA others(1330): Show |
chr8 | 103410386 | 103448453 | ||
| a0001c0004 | 0/0 | 1335 | 3 | 3 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | ATGAA others(1330): Show |
chr8 | 103410386 | 103448453 | ||
| a0001c0005 | 0/0 | 1335 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | ATGAA others(1330): Show |
chr8 | 103410386 | 103448453 | ||
| a0001c0006 | 0/0 | 1335 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | ATGAA others(1330): Show |
chr8 | 103410386 | 103448453 | ||
| a0002c0002 | 0/1 | 1335 | 103 | 15 | 22 | 54 | 3 | 8 | DCAF13_chr8_103410386_103448453 | DCAF13 | ATGAA others(1330): Show |
chr8 | 103410386 | 103448453 | ||
| a0002c0003 | 0/0 | 1335 | 7 | 1 | 3 | 1 | 2 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | ATGAA others(1330): Show |
chr8 | 103410386 | 103448453 | ||
| a0002c0007 | 0/0 | 1335 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | ATGAA others(1330): Show |
chr8 | 103410386 | 103448453 | ||
| a0003c0008 | 0/0 | 1335 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | ATGAA others(1330): Show |
chr8 | 103410386 | 103448453 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 1970 | 222 | 71 | 38 | 77 | 11 | 24 | DCAF13_chr8_103410386_103448453 | DCAF13 | GTGGC others(1965): Show |
chr8 | 103410386 | 103448453 |
| a0001c0001t0002 | 0/0 | 1970 | 2 | 0 | 2 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | GTGGC others(1965): Show |
chr8 | 103410386 | 103448453 |
| a0001c0001t0004 | 0/0 | 1970 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | GTGGC others(1965): Show |
chr8 | 103410386 | 103448453 |
| a0001c0004t0001 | 0/0 | 1970 | 3 | 3 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | GTGGC others(1965): Show |
chr8 | 103410386 | 103448453 |
| a0001c0005t0001 | 0/0 | 1970 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | GTGGC others(1965): Show |
chr8 | 103410386 | 103448453 |
| a0001c0006t0001 | 0/0 | 1970 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | GTGGC others(1965): Show |
chr8 | 103410386 | 103448453 |
| a0002c0002t0001 | 0/1 | 1970 | 102 | 15 | 22 | 53 | 3 | 8 | DCAF13_chr8_103410386_103448453 | DCAF13 | GTGGC others(1965): Show |
chr8 | 103410386 | 103448453 |
| a0002c0002t0003 | 0/0 | 1970 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | GTGGC others(1965): Show |
chr8 | 103410386 | 103448453 |
| a0002c0003t0001 | 0/0 | 1970 | 7 | 1 | 3 | 1 | 2 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | GTGGC others(1965): Show |
chr8 | 103410386 | 103448453 |
| a0002c0007t0001 | 0/0 | 1970 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | GTGGC others(1965): Show |
chr8 | 103410386 | 103448453 |
| a0003c0008t0001 | 0/0 | 1970 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | GTGGC others(1965): Show |
chr8 | 103410386 | 103448453 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/0 | 29 | 2 | 5 | 16 | 1 | 4 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0002 | 0/0 | 8 | 1 | 0 | 2 | 2 | 3 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0006 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0007 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0017 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0021 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0037 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0051 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0002g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0001t0004g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0004t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0005t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0001c0006t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0004 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0005 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0008 | 0/0 | 4 | 0 | 0 | 1 | 1 | 2 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0028 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0105 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0002t0003g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0003t0001g0054 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0003t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0003t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0003t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0003t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0002c0007t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| a0003c0008t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0148 | EUR | GBR | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0104 | EUR | GBR | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0132 | EUR | GBR | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0167 | EUR | FIN | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG00280 | hp2 | a0002 | c0002 | t0001 | g0069 | EUR | FIN | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG00323 | hp2 | a0002 | c0003 | t0001 | g0207 | EUR | FIN | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG00423 | hp1 | a0002 | c0002 | t0001 | g0080 | EAS | CHS | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0097 | EAS | CHS | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0013 | EAS | CHS | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | CHS | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | CHS | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0030 | EAS | CHS | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG00639 | hp1 | a0002 | c0003 | t0001 | g0206 | AMR | PUR | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | CHS | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0108 | EAS | CHS | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0084 | AMR | PUR | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0083 | AMR | PUR | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0031 | AMR | PUR | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01070 | hp1 | a0002 | c0003 | t0001 | g0054 | AMR | PUR | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0031 | AMR | PUR | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01167 | hp2 | a0001 | c0005 | t0001 | g0006 | AMR | PUR | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | PUR | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | PUR | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0098 | AMR | PUR | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0045 | AMR | CLM | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | CLM | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0045 | AMR | CLM | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01257 | hp1 | a0001 | c0001 | t0004 | g0002 | AMR | CLM | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | CLM | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | CLM | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | CLM | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | CLM | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | CLM | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01361 | hp1 | a0002 | c0003 | t0001 | g0054 | AMR | CLM | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0034 | AMR | CLM | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0077 | AMR | CLM | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0034 | AMR | CLM | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0128 | EUR | IBS | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0130 | EUR | IBS | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0043 | EUR | IBS | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01928 | hp2 | a0002 | c0002 | t0001 | g0099 | AMR | PEL | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01952 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | PEL | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01975 | hp1 | a0003 | c0008 | t0001 | g0003 | AMR | PEL | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | PEL | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0030 | AMR | PEL | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | KHV | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | CDX | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | ACB | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02647 | hp2 | a0002 | c0002 | t0001 | g0091 | AFR | GWD | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02698 | hp2 | a0002 | c0002 | t0001 | g0074 | SAS | PJL | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02717 | hp2 | a0002 | c0002 | t0001 | g0028 | AFR | GWD | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0092 | AFR | GWD | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0111 | AFR | GWD | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0016 | AFR | GWD | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ESN | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | ESN | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | MSL | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG03098 | hp2 | a0002 | c0002 | t0001 | g0016 | AFR | MSL | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG03195 | hp2 | a0001 | c0004 | t0001 | g0018 | AFR | ESN | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | MSL | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG03209 | hp2 | a0002 | c0007 | t0001 | g0135 | AFR | MSL | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | MSL | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG03453 | hp2 | a0002 | c0002 | t0001 | g0016 | AFR | MSL | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | MSL | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0008 | SAS | PJL | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0008 | SAS | PJL | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0056 | AFR | ESN | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG03540 | hp1 | a0001 | c0004 | t0001 | g0018 | AFR | GWD | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | MSL | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | MSL | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0065 | SAS | STU | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0100 | SAS | BEB | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | BEB | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | BEB | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | BEB | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | BEB | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0085 | SAS | BEB | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | STU | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | STU | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | STU | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG04199 | hp2 | a0002 | c0002 | t0001 | g0090 | SAS | STU | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0102 | SAS | STU | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | YRI | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | CHB | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | CHB | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | YRI | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0032 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0106 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18956 | hp2 | a0002 | c0002 | t0001 | g0081 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18959 | hp1 | a0002 | c0002 | t0001 | g0071 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18959 | hp2 | a0002 | c0002 | t0001 | g0072 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18961 | hp2 | a0002 | c0002 | t0001 | g0079 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18963 | hp2 | a0002 | c0002 | t0001 | g0082 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0073 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18964 | hp2 | a0002 | c0002 | t0001 | g0086 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18967 | hp1 | a0002 | c0002 | t0001 | g0075 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18968 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18980 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18988 | hp1 | a0002 | c0002 | t0001 | g0093 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18989 | hp2 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18990 | hp2 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18991 | hp1 | a0002 | c0002 | t0001 | g0101 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0032 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18997 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18999 | hp1 | a0002 | c0002 | t0003 | g0014 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA19000 | hp1 | a0002 | c0003 | t0001 | g0204 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0096 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA19003 | hp1 | a0002 | c0002 | t0001 | g0095 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0087 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA19006 | hp1 | a0002 | c0002 | t0001 | g0089 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA19007 | hp2 | a0002 | c0002 | t0001 | g0088 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0029 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA19010 | hp1 | a0002 | c0002 | t0001 | g0029 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA19012 | hp1 | a0002 | c0002 | t0001 | g0067 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | LWK | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA19030 | hp2 | a0002 | c0002 | t0001 | g0035 | AFR | LWK | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA19043 | hp1 | a0002 | c0002 | t0001 | g0058 | AFR | LWK | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0110 | AFR | LWK | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA19060 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA19064 | hp2 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0094 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA19067 | hp1 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA19075 | hp1 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA19076 | hp1 | a0002 | c0002 | t0001 | g0066 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA19077 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA19078 | hp1 | a0002 | c0002 | t0001 | g0068 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0070 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA19082 | hp2 | a0002 | c0002 | t0001 | g0076 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA19086 | hp2 | a0002 | c0002 | t0001 | g0078 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0107 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA19088 | hp2 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA19089 | hp2 | a0002 | c0002 | t0001 | g0103 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA19240 | hp1 | a0002 | c0003 | t0001 | g0059 | AFR | YRI | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | YRI | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ASW | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ASW | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA20752 | hp1 | a0002 | c0003 | t0001 | g0205 | EUR | TSI | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0179 | EUR | TSI | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0008 | EUR | TSI | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | GIH | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02109 | hp1 | a0001 | c0004 | t0001 | g0018 | AFR | ACB | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG03471 | hp1 | a0001 | c0006 | t0001 | g0001 | AFR | MSL | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG03471 | hp2 | a0002 | c0002 | t0001 | g0061 | AFR | MSL | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | USA | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | USA | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA18955 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0057 | AFR | USA | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | USA | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0035 | AFR | LWK | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| NA21309 | hp2 | a0002 | c0002 | t0001 | g0055 | AFR | LWK | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0105 | REF | REF | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | DCAF13_chr8_103410386_103448453 | DCAF13 | chr8 | 103410386 | 103448453 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:103420317 | A | G | 2 | a0002 a0003 |
111 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(108): Show |
missense_variant | MODERATE | c.124A>G | p.Ile42Val | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 2/11 | 185/1970 | 124/1338 | 42/445 | chr8 | 103420317 | |||
| chr8:103432741 | A | C | 1 | a0003 | 1 | HG01975.hp1 | missense_variant&splice_region_variant | MODERATE | c.785A>C | p.Asn262Thr | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 7/11 | 846/1970 | 785/1338 | 262/445 | chr8 | 103432741 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:103420403 | T | C | 1 | a0002c0003 | 7 | HG00323.hp2 HG00639.hp1 HG01070.hp1 others(4): Show |
synonymous_variant | LOW | c.210T>C | p.Asn70Asn | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 2/11 | 271/1970 | 210/1338 | 70/445 | chr8 | 103420403 | |||
| chr8:103420442 | T | C | 1 | a0001c0005 | 1 | HG01167.hp2 | synonymous_variant | LOW | c.249T>C | p.Leu83Leu | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 2/11 | 310/1970 | 249/1338 | 83/445 | chr8 | 103420442 | |||
| chr8:103426112 | C | T | 1 | a0001c0004 | 3 | HG02109.hp1 HG03195.hp2 HG03540.hp1 |
synonymous_variant | LOW | c.435C>T | p.Asp145Asp | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 4/11 | 496/1970 | 435/1338 | 145/445 | chr8 | 103426112 | |||
| chr8:103426118 | A | G | 1 | a0001c0006 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.441A>G | p.Glu147Glu | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 4/11 | 502/1970 | 441/1338 | 147/445 | chr8 | 103426118 | |||
| chr8:103441460 | A | G | 1 | a0002c0007 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.1092A>G | p.Thr364Thr | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 10/11 | 1153/1970 | 1092/1338 | 364/445 | chr8 | 103441460 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:103443145 | T | C | 1 | a0002c0002t0003 | 1 | NA18999.hp1 | 3_prime_UTR_variant | MODIFIER | c.*263T>C | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 11/11 | 263 | chr8 | 103443145 | ||||||
| chr8:103443160 | T | A | 1 | a0001c0001t0004 | 1 | HG01257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*278T>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 11/11 | 278 | chr8 | 103443160 | ||||||
| chr8:103443443 | C | G | 1 | a0001c0001t0002 | 2 | HG01255.hp1 HG01256.hp2 |
3_prime_UTR_variant | MODIFIER | c.*561C>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 11/11 | 561 | chr8 | 103443443 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:103415642 | T | A | 4 | a0002c0002t0001g0055 a0002c0002t0001g0056 a0002c0002t0001g0057 others(1): Show |
4 | HG03516.hp2 NA19043.hp1 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.70+126T>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103415642 | |||||||
| chr8:103415686 | A | G | 1 | a0001c0001t0001g0209 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.70+170A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103415686 | |||||||
| chr8:103415702 | G | A | 1 | a0002c0003t0001g0059 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.70+186G>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103415702 | |||||||
| chr8:103415773 | C | A | 1 | a0001c0001t0001g0060 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.70+257C>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103415773 | |||||||
| chr8:103415938 | G | C | 4 | a0002c0002t0001g0055 a0002c0002t0001g0056 a0002c0002t0001g0057 others(1): Show |
4 | HG03516.hp2 NA19043.hp1 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.70+422G>C | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103415938 | |||||||
| chr8:103415952 | T | C | 1 | a0002c0002t0001g0061 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.70+436T>C | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103415952 | |||||||
| chr8:103416064 | T | C | 4 | a0001c0001t0001g0060 a0001c0001t0001g0062 a0001c0001t0001g0063 others(1): Show |
4 | NA18947.hp1 NA18950.hp2 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.70+548T>C | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103416064 | |||||||
| chr8:103416088 | A | G | 2 | a0001c0001t0001g0027 a0001c0001t0001g0208 |
4 | HG02622.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.70+572A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103416088 | |||||||
| chr8:103416301 | A | G | 4 | a0002c0003t0001g0054 a0002c0003t0001g0205 a0002c0003t0001g0206 others(1): Show |
5 | HG00323.hp2 HG00639.hp1 HG01070.hp1 others(2): Show |
intron_variant | MODIFIER | c.70+785A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103416301 | |||||||
| chr8:103416302 | T | C | 61 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(58): Show |
93 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.70+786T>C | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103416302 | |||||||
| chr8:103416462 | G | A | 1 | a0002c0002t0001g0065 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.70+946G>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103416462 | |||||||
| chr8:103416596 | C | A | 1 | a0001c0001t0001g0109 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.70+1080C>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103416596 | |||||||
| chr8:103416628 | C | T | 6 | a0002c0003t0001g0054 a0002c0003t0001g0059 a0002c0003t0001g0204 others(3): Show |
7 | HG00323.hp2 HG00639.hp1 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.70+1112C>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103416628 | |||||||
| chr8:103416811 | A | G | 8 | a0001c0001t0001g0012 a0001c0001t0001g0026 a0001c0001t0001g0052 others(5): Show |
15 | HG01891.hp2 HG02451.hp2 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.70+1295A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103416811 | |||||||
| chr8:103416846 | G | T | 1 | a0002c0002t0001g0061 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.70+1330G>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103416846 | |||||||
| chr8:103416943 | G | C | 1 | a0002c0002t0001g0055 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.70+1427G>C | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103416943 | |||||||
| chr8:103417051 | G | A | 4 | a0002c0002t0001g0055 a0002c0002t0001g0056 a0002c0002t0001g0057 others(1): Show |
4 | HG03516.hp2 NA19043.hp1 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.70+1535G>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103417051 | |||||||
| chr8:103417101 | A | G | 8 | a0001c0001t0001g0012 a0001c0001t0001g0026 a0001c0001t0001g0052 others(5): Show |
15 | HG01891.hp2 HG02451.hp2 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.70+1585A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103417101 | |||||||
| chr8:103417164 | C | T | 1 | a0002c0003t0001g0059 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.70+1648C>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103417164 | |||||||
| chr8:103417199 | G | A | 2 | a0002c0002t0001g0110 a0002c0002t0001g0111 |
2 | HG02809.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.70+1683G>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103417199 | |||||||
| chr8:103417343 | T | TA | 74 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(71): Show |
109 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.70+1836dupA | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103417343 | ||||||
| chr8:103417363 | T | A | 1 | a0001c0001t0001g0112 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.70+1847T>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103417363 | |||||||
| chr8:103417368 | G | C | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | NA19058.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.70+1852G>C | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103417368 | |||||||
| chr8:103417546 | G | A | 1 | a0001c0001t0001g0037 | 2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.70+2030G>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103417546 | |||||||
| chr8:103417596 | T | C | 111 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(108): Show |
174 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.70+2080T>C | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103417596 | |||||||
| chr8:103417631 | G | C | 1 | a0001c0001t0001g0136 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.70+2115G>C | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103417631 | |||||||
| chr8:103417641 | C | CA | 21 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0017 others(18): Show |
34 | HG00741.hp1 HG01074.hp1 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.70+2144dupA | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103417641 | ||||||
| chr8:103417641 | CA | C | 75 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0196 others(72): Show |
111 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.70+2144delA | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103417641 | ||||||
| chr8:103417658 | A | G | 2 | a0001c0001t0001g0199 a0001c0001t0001g0209 |
2 | HG00673.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.70+2142A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103417658 | |||||||
| chr8:103417815 | C | G | 1 | a0002c0003t0001g0059 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.70+2299C>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103417815 | |||||||
| chr8:103417845 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.70+2329C>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103417845 | |||||||
| chr8:103417997 | G | A | 74 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(71): Show |
109 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.71-2267G>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103417997 | |||||||
| chr8:103418021 | G | C | 12 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0038 others(9): Show |
20 | HG01074.hp1 HG01074.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.71-2243G>C | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103418021 | |||||||
| chr8:103418072 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.71-2192G>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103418072 | |||||||
| chr8:103418127 | C | CA | 7 | a0002c0002t0001g0061 a0002c0003t0001g0054 a0002c0003t0001g0204 others(4): Show |
8 | HG00323.hp2 HG00639.hp1 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.71-2127dupA | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418127 | ||||||
| chr8:103418195 | A | G | 1 | a0002c0002t0001g0108 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.71-2069A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103418195 | |||||||
| chr8:103418525 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.71-1739C>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103418525 | |||||||
| chr8:103418709 | A | G | 3 | a0002c0002t0001g0015 a0002c0002t0001g0106 a0002c0002t0001g0107 |
5 | NA18947.hp2 NA18951.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.71-1555A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103418709 | |||||||
| chr8:103418796 | C | T | 1 | a0001c0001t0001g0193 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.71-1468C>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103418796 | |||||||
| chr8:103418824 | T | TTA | 4 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(1): Show |
4 | HG01981.hp1 HG02071.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.71-1398_71-1397dup others(2): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418824 | ||||||
| chr8:103418824 | T | TTATA | 4 | a0001c0001t0001g0021 a0001c0001t0001g0142 a0001c0001t0001g0146 others(1): Show |
6 | HG00280.hp2 HG01891.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.71-1400_71-1397dup others(4): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418824 | ||||||
| chr8:103418824 | TTA | T | 6 | a0001c0001t0001g0025 a0001c0001t0001g0176 a0001c0001t0001g0177 others(3): Show |
8 | HG02698.hp1 HG03834.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.71-1398_71-1397del others(2): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418824 | ||||||
| chr8:103418824 | TTATA | T | 6 | a0001c0001t0001g0060 a0001c0001t0001g0063 a0001c0001t0001g0064 others(3): Show |
6 | HG00099.hp2 HG02280.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.71-1400_71-1397del others(4): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418824 | ||||||
| chr8:103418824 | TTATATA | T | 5 | a0001c0001t0001g0133 a0001c0001t0001g0182 a0001c0001t0001g0183 others(2): Show |
5 | HG03669.hp2 HG04115.hp1 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-1402_71-1397del others(6): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418824 | ||||||
| chr8:103418824 | TTATATAT others(1): Show |
T | 3 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0209 |
3 | HG01099.hp2 HG01928.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.71-1404_71-1397del others(8): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418824 | ||||||
| chr8:103418824 | TTATATAT others(5): Show |
T | 1 | a0001c0001t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.71-1408_71-1397del others(12): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418824 | ||||||
| chr8:103418824 | TTATATAT others(11): Show |
T | 2 | a0001c0001t0001g0121 a0001c0001t0001g0190 |
2 | HG02976.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.71-1414_71-1397del others(18): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418824 | ||||||
| chr8:103418828 | A | T | 1 | a0001c0001t0001g0192 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.71-1436A>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103418828 | |||||||
| chr8:103418835 | TATATATA others(18): Show |
T | 1 | a0001c0001t0001g0191 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.71-1428_71-1404del others(25): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103418835 | |||||||
| chr8:103418840 | ATATATAT others(21): Show |
A | 1 | a0001c0001t0001g0012 | 3 | HG01891.hp2 NA18522.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.71-1422_71-1395del others(28): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418840 | ||||||
| chr8:103418840 | ATATATAT others(23): Show |
A | 4 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0202 others(1): Show |
6 | HG02451.hp2 HG02647.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.71-1422_71-1393del others(30): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418840 | ||||||
| chr8:103418840 | ATATATAT others(24): Show |
A | 1 | a0001c0001t0001g0026 | 3 | HG02976.hp2 HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.71-1422_71-1392del others(31): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418840 | ||||||
| chr8:103418842 | ATATATAT others(23): Show |
A | 1 | a0001c0001t0001g0201 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.71-1420_71-1391del others(30): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418842 | ||||||
| chr8:103418844 | ATATATAT others(18): Show |
A | 1 | a0001c0001t0001g0012 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.71-1418_71-1394del others(25): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418844 | ||||||
| chr8:103418844 | ATATATAT others(26): Show |
A | 1 | a0001c0001t0001g0200 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.71-1418_71-1386del others(33): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418844 | ||||||
| chr8:103418846 | ATATATAT others(14): Show |
A | 2 | a0001c0001t0001g0006 a0001c0001t0001g0007 |
4 | HG01074.hp2 HG02895.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-1416_71-1396del others(21): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418846 | ||||||
| chr8:103418846 | ATATATAT others(15): Show |
A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0118 |
3 | HG01099.hp1 HG02615.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.71-1416_71-1395del others(22): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418846 | ||||||
| chr8:103418846 | ATATATAT others(16): Show |
A | 1 | a0001c0001t0001g0116 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.71-1416_71-1394del others(23): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418846 | ||||||
| chr8:103418846 | ATATATAT others(18): Show |
A | 1 | a0001c0001t0001g0208 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.71-1416_71-1392del others(25): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418846 | ||||||
| chr8:103418848 | ATATATAT others(13): Show |
A | 3 | a0001c0001t0001g0006 a0001c0001t0001g0117 a0001c0005t0001g0006 |
3 | HG01167.hp2 HG01358.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.71-1414_71-1395del others(20): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418848 | ||||||
| chr8:103418848 | ATATATAT others(14): Show |
A | 2 | a0001c0001t0001g0006 a0001c0001t0001g0115 |
3 | HG01074.hp1 HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.71-1414_71-1394del others(21): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418848 | ||||||
| chr8:103418848 | ATATATAT others(15): Show |
A | 2 | a0001c0001t0001g0038 a0001c0001t0001g0120 |
3 | HG01884.hp1 HG02055.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.71-1414_71-1393del others(22): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418848 | ||||||
| chr8:103418848 | ATATATAT others(16): Show |
A | 2 | a0001c0001t0001g0027 a0001c0001t0001g0126 |
2 | HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.71-1414_71-1392del others(23): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418848 | ||||||
| chr8:103418848 | ATATATAT others(17): Show |
A | 1 | a0001c0001t0001g0027 | 2 | HG02622.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.71-1414_71-1391del others(24): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418848 | ||||||
| chr8:103418849 | TATATATA others(10): Show |
T | 2 | a0001c0001t0001g0001 a0001c0001t0001g0119 |
2 | HG01243.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.71-1414_71-1398del others(17): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103418849 | |||||||
| chr8:103418850 | A | T | 3 | a0002c0002t0001g0103 a0002c0002t0001g0111 a0002c0003t0001g0204 |
3 | HG02809.hp1 NA19000.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.71-1414A>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103418850 | |||||||
| chr8:103418850 | ATATATAT others(14): Show |
A | 1 | a0001c0001t0001g0001 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.71-1412_71-1392del others(21): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418850 | ||||||
| chr8:103418850 | ATATATAT others(20): Show |
A | 1 | a0001c0001t0001g0158 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.71-1412_71-1386del others(27): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418850 | ||||||
| chr8:103418850 | ATATATAT others(22): Show |
A | 1 | a0002c0007t0001g0135 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.71-1412_71-1384del others(29): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418850 | ||||||
| chr8:103418852 | A | T | 3 | a0002c0002t0001g0100 a0002c0002t0001g0101 a0002c0002t0001g0102 |
3 | HG03831.hp1 HG04228.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.71-1412A>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103418852 | |||||||
| chr8:103418852 | ATATATAT others(8): Show |
A | 1 | a0001c0001t0001g0001 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.71-1410_71-1396del others(15): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418852 | ||||||
| chr8:103418852 | ATATATAT others(14): Show |
A | 1 | a0002c0002t0001g0061 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.71-1410_71-1390del others(21): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418852 | ||||||
| chr8:103418854 | A | T | 19 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(16): Show |
38 | HG00423.hp2 HG00642.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.71-1410A>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103418854 | |||||||
| chr8:103418854 | ATATATAT others(7): Show |
A | 1 | a0001c0001t0001g0010 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.71-1408_71-1395del others(14): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418854 | ||||||
| chr8:103418854 | ATATATAT others(10): Show |
A | 1 | a0001c0001t0001g0160 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.71-1408_71-1392del others(17): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418854 | ||||||
| chr8:103418856 | A | T | 13 | a0002c0002t0001g0014 a0002c0002t0001g0034 a0002c0002t0001g0035 others(10): Show |
13 | HG00558.hp2 HG00735.hp1 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.71-1408A>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103418856 | |||||||
| chr8:103418856 | ATATATAT others(8): Show |
A | 1 | a0001c0001t0001g0157 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.71-1406_71-1392del others(15): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418856 | ||||||
| chr8:103418856 | ATATATAT others(15): Show |
A | 1 | a0001c0001t0001g0023 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.71-1406_71-1385del others(22): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418856 | ||||||
| chr8:103418858 | A | T | 10 | a0001c0001t0001g0123 a0002c0002t0001g0014 a0002c0002t0001g0035 others(7): Show |
10 | HG00639.hp1 HG01070.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.71-1406A>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103418858 | |||||||
| chr8:103418858 | ATATATAT others(11): Show |
A | 1 | a0001c0001t0001g0172 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.71-1404_71-1387del others(18): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418858 | ||||||
| chr8:103418860 | A | T | 11 | a0001c0001t0001g0024 a0001c0001t0001g0123 a0001c0001t0001g0180 others(8): Show |
11 | HG00323.hp2 HG01109.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.71-1404A>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103418860 | |||||||
| chr8:103418860 | ATATATAT others(2): Show |
A | 4 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0041 others(1): Show |
6 | HG01169.hp2 HG02258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.71-1402_71-1394del others(9): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418860 | ||||||
| chr8:103418860 | ATATATAT others(3): Show |
A | 2 | a0001c0001t0001g0041 a0001c0004t0001g0018 |
3 | HG01167.hp1 HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.71-1402_71-1393del others(10): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418860 | ||||||
| chr8:103418860 | ATATATAT others(7): Show |
A | 1 | a0001c0001t0001g0124 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.71-1402_71-1389del others(14): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418860 | ||||||
| chr8:103418860 | ATATATAT others(21): Show |
A | 1 | a0002c0003t0001g0204 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.71-1402_71-1375del others(28): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418860 | ||||||
| chr8:103418861 | TA | T | 3 | a0001c0001t0001g0050 a0001c0001t0001g0125 a0001c0001t0001g0181 |
4 | HG02809.hp2 HG03139.hp1 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.71-1402delA | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103418861 | |||||||
| chr8:103418861 | TATATA | T | 3 | a0001c0001t0001g0051 a0001c0001t0001g0134 a0001c0001t0001g0186 |
4 | HG00639.hp2 HG02129.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.71-1402_71-1398del others(5): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103418861 | |||||||
| chr8:103418862 | A | T | 35 | a0001c0001t0001g0017 a0001c0001t0001g0024 a0001c0001t0001g0025 others(32): Show |
58 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.71-1402A>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103418862 | |||||||
| chr8:103418862 | ATATATT | A | 9 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0002c0002t0001g0013 others(6): Show |
12 | HG00544.hp2 HG00733.hp2 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.71-1400_71-1395del others(6): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418862 | ||||||
| chr8:103418862 | ATATATTT others(2): Show |
A | 5 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0020 others(2): Show |
6 | HG00323.hp1 HG02886.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.71-1400_71-1392del others(9): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418862 | ||||||
| chr8:103418862 | ATATATTT others(3): Show |
A | 1 | a0001c0004t0001g0018 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.71-1400_71-1391del others(10): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418862 | ||||||
| chr8:103418862 | ATATATTT others(4): Show |
A | 1 | a0001c0001t0001g0019 | 2 | HG00738.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.71-1400_71-1390del others(11): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418862 | ||||||
| chr8:103418862 | ATATATTT others(5): Show |
A | 1 | a0001c0001t0001g0017 | 2 | HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.71-1400_71-1389del others(12): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418862 | ||||||
| chr8:103418862 | ATATATTT others(6): Show |
A | 5 | a0002c0002t0001g0081 a0002c0002t0001g0082 a0002c0002t0001g0083 others(2): Show |
5 | HG00735.hp1 HG00735.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.71-1400_71-1388del others(13): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418862 | ||||||
| chr8:103418862 | ATATATTT others(7): Show |
A | 8 | a0002c0002t0001g0014 a0002c0002t0001g0034 a0002c0002t0001g0035 others(5): Show |
8 | HG00558.hp2 HG01496.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.71-1400_71-1387del others(14): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418862 | ||||||
| chr8:103418862 | ATATATTT others(9): Show |
A | 1 | a0002c0003t0001g0059 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.71-1400_71-1385del others(16): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418862 | ||||||
| chr8:103418864 | A | ATT | 3 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0042 |
4 | HG01106.hp2 HG01243.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-1399_71-1398ins others(2): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418864 | ||||||
| chr8:103418864 | A | T | 17 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(14): Show |
19 | HG00558.hp1 HG01109.hp1 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.71-1400A>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103418864 | |||||||
| chr8:103418864 | ATATT | A | 8 | a0001c0001t0001g0171 a0001c0001t0001g0195 a0002c0002t0001g0013 others(5): Show |
9 | HG01069.hp1 HG01071.hp2 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.71-1398_71-1395del others(4): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418864 | ||||||
| chr8:103418864 | ATATTTTT others(5): Show |
A | 4 | a0002c0002t0001g0014 a0002c0002t0001g0035 a0002c0002t0001g0057 others(1): Show |
4 | NA18968.hp1 NA19006.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-1398_71-1387del others(12): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418864 | ||||||
| chr8:103418864 | ATATTTTT others(6): Show |
A | 1 | a0002c0002t0001g0055 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.71-1398_71-1386del others(13): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418864 | ||||||
| chr8:103418864 | ATATTTTT others(16): Show |
A | 1 | a0002c0003t0001g0054 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.71-1398_71-1376del others(23): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418864 | ||||||
| chr8:103418865 | TA | T | 3 | a0001c0001t0001g0001 a0001c0001t0001g0165 a0001c0001t0001g0168 |
4 | HG01346.hp2 HG02602.hp1 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-1398delA | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103418865 | |||||||
| chr8:103418866 | A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0022 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.71-1397_71-1396ins others(11): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418866 | ||||||
| chr8:103418866 | A | ATATATAT others(5): Show |
1 | a0001c0001t0001g0022 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.71-1397_71-1396ins others(12): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418866 | ||||||
| chr8:103418866 | A | ATATATAT others(3): Show |
1 | a0001c0001t0001g0001 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.71-1397_71-1396ins others(10): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418866 | ||||||
| chr8:103418866 | A | ATATATAT others(5): Show |
1 | a0001c0001t0001g0001 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.71-1397_71-1396ins others(12): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418866 | ||||||
| chr8:103418866 | A | ATATATTT others(3): Show |
1 | a0001c0001t0001g0049 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.71-1397_71-1396ins others(10): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418866 | ||||||
| chr8:103418866 | A | T | 25 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(22): Show |
36 | HG00280.hp1 HG00558.hp1 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.71-1398A>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103418866 | |||||||
| chr8:103418866 | AT | A | 6 | a0001c0001t0001g0001 a0001c0001t0001g0128 a0001c0001t0001g0152 others(3): Show |
6 | HG00673.hp1 HG01106.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.71-1363delT | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418866 | ||||||
| chr8:103418866 | ATTTTTTT others(1): Show |
A | 7 | a0002c0002t0001g0015 a0002c0002t0001g0032 a0002c0002t0001g0033 others(4): Show |
11 | HG01433.hp2 NA18943.hp1 NA18947.hp2 others(8): Show |
intron_variant | MODIFIER | c.71-1370_71-1363del others(8): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418866 | ||||||
| chr8:103418866 | ATTTTTTT others(3): Show |
A | 5 | a0001c0001t0004g0002 a0002c0002t0001g0034 a0002c0002t0001g0088 others(2): Show |
5 | HG01257.hp1 HG01433.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.71-1372_71-1363del others(10): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418866 | ||||||
| chr8:103418866 | ATTTTTTT others(8): Show |
A | 7 | a0002c0002t0001g0003 a0002c0002t0001g0036 a0002c0002t0001g0094 others(4): Show |
13 | HG00673.hp2 HG01975.hp1 HG02129.hp2 others(10): Show |
intron_variant | MODIFIER | c.71-1377_71-1363del others(15): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418866 | ||||||
| chr8:103418866 | ATTTTTTT others(9): Show |
A | 11 | a0002c0002t0001g0004 a0002c0002t0001g0005 a0002c0002t0001g0008 others(8): Show |
24 | HG00423.hp2 HG00642.hp2 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.71-1378_71-1363del others(16): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418866 | ||||||
| chr8:103418866 | ATTTTTTT others(10): Show |
A | 2 | a0002c0002t0001g0100 a0002c0002t0001g0110 |
2 | HG03831.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.71-1379_71-1363del others(17): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418866 | ||||||
| chr8:103418866 | ATTTTTTT others(11): Show |
A | 2 | a0002c0002t0001g0101 a0002c0002t0001g0102 |
2 | HG04228.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.71-1380_71-1363del others(18): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418866 | ||||||
| chr8:103418866 | ATTTTTTT others(12): Show |
A | 2 | a0002c0003t0001g0205 a0002c0003t0001g0207 |
2 | HG00323.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.71-1381_71-1363del others(19): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418866 | ||||||
| chr8:103418866 | ATTTTTTT others(13): Show |
A | 1 | a0002c0002t0001g0103 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.71-1382_71-1363del others(20): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418866 | ||||||
| chr8:103418866 | ATTTTTTT others(14): Show |
A | 3 | a0002c0002t0001g0111 a0002c0003t0001g0054 a0002c0003t0001g0206 |
3 | HG00639.hp1 HG01070.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.71-1383_71-1363del others(21): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103418866 | ||||||
| chr8:103418867 | T | TA | 3 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0148 |
3 | HG00099.hp1 HG01175.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.71-1397_71-1396ins others(1): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103418867 | |||||||
| chr8:103418867 | T | TATA | 2 | a0001c0001t0001g0044 a0001c0001t0001g0136 |
3 | HG02071.hp1 NA18990.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.71-1397_71-1396ins others(3): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103418867 | |||||||
| chr8:103418867 | T | TATATATA | 4 | a0001c0001t0001g0109 a0001c0001t0001g0139 a0001c0001t0001g0140 others(1): Show |
4 | HG01952.hp2 HG02145.hp2 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.71-1397_71-1396ins others(7): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103418867 | |||||||
| chr8:103418867 | T | TATATATA others(6): Show |
1 | a0001c0001t0001g0194 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.71-1397_71-1396ins others(13): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103418867 | |||||||
| chr8:103418868 | T | A | 8 | a0001c0001t0001g0021 a0001c0001t0001g0043 a0001c0001t0001g0127 others(5): Show |
11 | HG00280.hp2 HG00544.hp1 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.71-1396T>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103418868 | |||||||
| chr8:103418869 | T | A | 6 | a0001c0001t0001g0128 a0001c0001t0001g0144 a0001c0001t0001g0145 others(3): Show |
6 | HG01106.hp1 HG01175.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.71-1395T>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103418869 | |||||||
| chr8:103418870 | T | A | 4 | a0001c0001t0001g0043 a0001c0001t0001g0127 a0001c0001t0001g0143 others(1): Show |
5 | HG00099.hp2 HG00544.hp1 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-1394T>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103418870 | |||||||
| chr8:103418871 | T | A | 3 | a0001c0001t0001g0128 a0001c0001t0001g0152 a0001c0001t0001g0155 |
3 | HG01106.hp1 HG01515.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.71-1393T>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103418871 | |||||||
| chr8:103418872 | T | A | 18 | a0001c0001t0001g0043 a0001c0001t0001g0127 a0001c0001t0001g0129 others(15): Show |
25 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.71-1392T>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103418872 | |||||||
| chr8:103418873 | T | A | 3 | a0001c0001t0001g0128 a0001c0001t0001g0152 a0002c0002t0001g0016 |
5 | HG01106.hp1 HG01515.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-1391T>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103418873 | |||||||
| chr8:103418874 | T | A | 15 | a0002c0002t0001g0013 a0002c0002t0001g0028 a0002c0002t0001g0029 others(12): Show |
21 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(18): Show |
intron_variant | MODIFIER | c.71-1390T>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103418874 | |||||||
| chr8:103418875 | T | A | 4 | a0001c0001t0001g0152 a0001c0001t0001g0156 a0002c0002t0001g0016 others(1): Show |
6 | HG01106.hp1 HG02083.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.71-1389T>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103418875 | |||||||
| chr8:103418876 | T | A | 21 | a0002c0002t0001g0013 a0002c0002t0001g0015 a0002c0002t0001g0028 others(18): Show |
31 | HG00280.hp2 HG00544.hp2 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.71-1388T>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103418876 | |||||||
| chr8:103418877 | T | A | 3 | a0001c0001t0001g0152 a0002c0002t0001g0016 a0002c0002t0001g0080 |
5 | HG00423.hp1 HG01106.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-1387T>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103418877 | |||||||
| chr8:103418878 | T | A | 1 | a0002c0002t0001g0104 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.71-1386T>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103418878 | |||||||
| chr8:103418879 | T | A | 7 | a0002c0002t0001g0080 a0002c0002t0001g0081 a0002c0002t0001g0082 others(4): Show |
7 | HG00423.hp1 HG00735.hp1 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.71-1385T>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103418879 | |||||||
| chr8:103418880 | T | A | 35 | a0002c0002t0001g0013 a0002c0002t0001g0014 a0002c0002t0001g0015 others(32): Show |
48 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.71-1384T>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103418880 | |||||||
| chr8:103418881 | T | A | 9 | a0002c0002t0001g0016 a0002c0002t0001g0055 a0002c0002t0001g0080 others(6): Show |
11 | HG00423.hp1 HG00735.hp1 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.71-1383T>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103418881 | |||||||
| chr8:103418882 | T | A | 36 | a0002c0002t0001g0013 a0002c0002t0001g0014 a0002c0002t0001g0015 others(33): Show |
49 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.71-1382T>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103418882 | |||||||
| chr8:103418883 | T | A | 16 | a0002c0002t0001g0003 a0002c0002t0001g0016 a0002c0002t0001g0036 others(13): Show |
24 | HG00423.hp1 HG00673.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.71-1381T>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103418883 | |||||||
| chr8:103418884 | T | A | 47 | a0002c0002t0001g0004 a0002c0002t0001g0005 a0002c0002t0001g0008 others(44): Show |
73 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.71-1380T>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103418884 | |||||||
| chr8:103418885 | T | A | 18 | a0002c0002t0001g0003 a0002c0002t0001g0016 a0002c0002t0001g0036 others(15): Show |
26 | HG00423.hp1 HG00673.hp2 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.71-1379T>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103418885 | |||||||
| chr8:103418886 | T | A | 48 | a0002c0002t0001g0004 a0002c0002t0001g0005 a0002c0002t0001g0008 others(45): Show |
74 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.71-1378T>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103418886 | |||||||
| chr8:103418887 | T | A | 18 | a0002c0002t0001g0003 a0002c0002t0001g0016 a0002c0002t0001g0036 others(15): Show |
26 | HG00323.hp2 HG00423.hp1 HG00673.hp2 others(23): Show |
intron_variant | MODIFIER | c.71-1377T>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103418887 | |||||||
| chr8:103418888 | T | A | 6 | a0002c0002t0001g0056 a0002c0002t0001g0058 a0002c0002t0001g0065 others(3): Show |
6 | HG03516.hp2 HG03688.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.71-1376T>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103418888 | |||||||
| chr8:103418889 | T | A | 5 | a0002c0002t0001g0036 a0002c0002t0001g0080 a0002c0002t0001g0081 others(2): Show |
6 | HG00423.hp1 HG00673.hp2 NA18956.hp2 others(3): Show |
intron_variant | MODIFIER | c.71-1375T>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103418889 | |||||||
| chr8:103418890 | T | A | 1 | a0002c0003t0001g0059 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.71-1374T>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103418890 | |||||||
| chr8:103418970 | A | G | 76 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(73): Show |
111 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.71-1294A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103418970 | |||||||
| chr8:103418999 | T | A | 1 | a0002c0003t0001g0204 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.71-1265T>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103418999 | |||||||
| chr8:103419018 | G | T | 8 | a0001c0001t0001g0020 a0001c0001t0001g0040 a0001c0001t0001g0041 others(5): Show |
14 | HG00140.hp2 HG00639.hp2 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.71-1246G>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103419018 | |||||||
| chr8:103419085 | T | C | 1 | a0002c0007t0001g0135 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.71-1179T>C | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103419085 | |||||||
| chr8:103419127 | G | C | 1 | a0002c0003t0001g0204 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.71-1137G>C | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103419127 | |||||||
| chr8:103419141 | C | G | 1 | a0002c0003t0001g0205 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.71-1123C>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103419141 | |||||||
| chr8:103419142 | C | G | 1 | a0001c0001t0001g0126 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.71-1122C>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103419142 | |||||||
| chr8:103419149 | G | T | 1 | a0001c0001t0001g0120 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.71-1115G>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103419149 | |||||||
| chr8:103419175 | C | T | 5 | a0002c0003t0001g0054 a0002c0003t0001g0204 a0002c0003t0001g0205 others(2): Show |
6 | HG00323.hp2 HG00639.hp1 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.71-1089C>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103419175 | |||||||
| chr8:103419177 | C | T | 68 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(65): Show |
102 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.71-1087C>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103419177 | |||||||
| chr8:103419184 | C | T | 1 | a0002c0002t0001g0035 | 2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.71-1080C>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103419184 | |||||||
| chr8:103419408 | A | G | 2 | a0002c0002t0001g0110 a0002c0002t0001g0111 |
2 | HG02809.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.71-856A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103419408 | |||||||
| chr8:103419517 | G | A | 5 | a0002c0003t0001g0054 a0002c0003t0001g0204 a0002c0003t0001g0205 others(2): Show |
6 | HG00323.hp2 HG00639.hp1 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.71-747G>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103419517 | |||||||
| chr8:103419588 | C | G | 1 | a0002c0003t0001g0059 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.71-676C>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103419588 | |||||||
| chr8:103419770 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.71-494G>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103419770 | |||||||
| chr8:103419877 | C | G | 68 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(65): Show |
102 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.71-387C>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103419877 | |||||||
| chr8:103419988 | A | G | 4 | a0001c0001t0001g0024 a0001c0001t0001g0174 a0001c0001t0001g0175 others(1): Show |
6 | HG02280.hp1 HG02451.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.71-276A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103419988 | |||||||
| chr8:103419989 | C | T | 1 | a0001c0001t0001g0173 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.71-275C>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | chr8 | 103419989 | |||||||
| chr8:103420007 | C | CA | 68 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(65): Show |
101 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.71-241dupA | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 103420007 | ||||||
| chr8:103420699 | A | C | 2 | a0002c0002t0001g0061 a0002c0007t0001g0135 |
2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.270+236A>C | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 2/10 | chr8 | 103420699 | |||||||
| chr8:103420707 | A | G | 2 | a0002c0002t0001g0061 a0002c0007t0001g0135 |
2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.270+244A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 2/10 | chr8 | 103420707 | |||||||
| chr8:103420709 | G | C | 2 | a0001c0001t0001g0176 a0001c0001t0001g0182 |
2 | NA18953.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.270+246G>C | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 2/10 | chr8 | 103420709 | |||||||
| chr8:103420780 | G | C | 1 | a0001c0001t0001g0113 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.271-195G>C | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 2/10 | chr8 | 103420780 | |||||||
| chr8:103420906 | A | G | 2 | a0001c0001t0001g0176 a0001c0001t0001g0182 |
2 | NA18953.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.271-69A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 2/10 | chr8 | 103420906 | |||||||
| chr8:103421298 | A | G | 1 | a0001c0001t0001g0172 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.378+216A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 3/10 | chr8 | 103421298 | |||||||
| chr8:103421445 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.378+363G>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 3/10 | chr8 | 103421445 | |||||||
| chr8:103421462 | C | G | 1 | a0002c0003t0001g0205 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.378+380C>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 3/10 | chr8 | 103421462 | |||||||
| chr8:103421597 | C | T | 6 | a0001c0001t0001g0026 a0001c0001t0001g0052 a0001c0001t0001g0053 others(3): Show |
10 | HG02451.hp2 HG02647.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.378+515C>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 3/10 | chr8 | 103421597 | |||||||
| chr8:103421860 | C | A | 2 | a0002c0002t0001g0110 a0002c0002t0001g0111 |
2 | HG02809.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.378+778C>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 3/10 | chr8 | 103421860 | |||||||
| chr8:103422120 | T | C | 120 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(117): Show |
190 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.378+1038T>C | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 3/10 | chr8 | 103422120 | |||||||
| chr8:103422365 | A | G | 4 | a0002c0002t0001g0004 a0002c0002t0001g0034 a0002c0002t0001g0098 others(1): Show |
11 | HG00642.hp2 HG01109.hp2 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.378+1283A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 3/10 | chr8 | 103422365 | |||||||
| chr8:103422455 | G | A | 2 | a0001c0001t0001g0027 a0001c0001t0001g0208 |
4 | HG02622.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.378+1373G>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 3/10 | chr8 | 103422455 | |||||||
| chr8:103422611 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.378+1529A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 3/10 | chr8 | 103422611 | |||||||
| chr8:103422794 | A | C | 76 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(73): Show |
111 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.378+1712A>C | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 3/10 | chr8 | 103422794 | |||||||
| chr8:103422796 | T | C | 1 | a0001c0001t0001g0201 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.378+1714T>C | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 3/10 | chr8 | 103422796 | |||||||
| chr8:103422909 | T | A | 30 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(27): Show |
56 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.378+1827T>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 3/10 | chr8 | 103422909 | |||||||
| chr8:103422973 | A | C | 4 | a0002c0003t0001g0054 a0002c0003t0001g0205 a0002c0003t0001g0206 others(1): Show |
5 | HG00323.hp2 HG00639.hp1 HG01070.hp1 others(2): Show |
intron_variant | MODIFIER | c.378+1891A>C | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 3/10 | chr8 | 103422973 | |||||||
| chr8:103422974 | G | C | 5 | a0002c0003t0001g0054 a0002c0003t0001g0204 a0002c0003t0001g0205 others(2): Show |
6 | HG00323.hp2 HG00639.hp1 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.378+1892G>C | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 3/10 | chr8 | 103422974 | |||||||
| chr8:103423006 | A | G | 8 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0039 others(5): Show |
18 | HG00323.hp1 HG00609.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.378+1924A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 3/10 | chr8 | 103423006 | |||||||
| chr8:103423125 | T | G | 1 | a0002c0002t0001g0055 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.378+2043T>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 3/10 | chr8 | 103423125 | |||||||
| chr8:103423221 | A | AT | 6 | a0001c0001t0001g0017 a0001c0001t0001g0122 a0001c0001t0001g0123 others(3): Show |
8 | HG00741.hp1 HG01109.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.378+2148dupT | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 103423221 | ||||||
| chr8:103423303 | G | A | 2 | a0002c0002t0001g0110 a0002c0002t0001g0111 |
2 | HG02809.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.378+2221G>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 3/10 | chr8 | 103423303 | |||||||
| chr8:103423309 | C | A | 6 | a0002c0003t0001g0054 a0002c0003t0001g0059 a0002c0003t0001g0204 others(3): Show |
7 | HG00323.hp2 HG00639.hp1 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.378+2227C>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 3/10 | chr8 | 103423309 | |||||||
| chr8:103423323 | A | AT | 11 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0038 others(8): Show |
19 | HG01074.hp1 HG01074.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.378+2245dupT | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 103423323 | ||||||
| chr8:103423328 | A | T | 8 | a0001c0001t0001g0020 a0001c0001t0001g0040 a0001c0001t0001g0041 others(5): Show |
12 | HG00140.hp2 HG00639.hp2 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.378+2246A>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 3/10 | chr8 | 103423328 | |||||||
| chr8:103423468 | C | T | 2 | a0002c0002t0001g0061 a0002c0007t0001g0135 |
2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.378+2386C>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 3/10 | chr8 | 103423468 | |||||||
| chr8:103423506 | T | G | 74 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(71): Show |
109 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.378+2424T>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 3/10 | chr8 | 103423506 | |||||||
| chr8:103423516 | T | C | 1 | a0001c0001t0001g0022 | 3 | NA18960.hp2 NA19077.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.378+2434T>C | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 3/10 | chr8 | 103423516 | |||||||
| chr8:103423677 | C | A | 6 | a0002c0003t0001g0054 a0002c0003t0001g0059 a0002c0003t0001g0204 others(3): Show |
7 | HG00323.hp2 HG00639.hp1 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.379-2379C>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 3/10 | chr8 | 103423677 | |||||||
| chr8:103423748 | G | A | 7 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0159 others(4): Show |
11 | HG02280.hp1 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.379-2308G>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 3/10 | chr8 | 103423748 | |||||||
| chr8:103423905 | G | A | 1 | a0002c0002t0001g0107 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.379-2151G>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 3/10 | chr8 | 103423905 | |||||||
| chr8:103423916 | C | T | 1 | a0002c0002t0001g0072 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.379-2140C>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 3/10 | chr8 | 103423916 | |||||||
| chr8:103423982 | G | A | 1 | a0002c0002t0001g0085 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.379-2074G>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 3/10 | chr8 | 103423982 | |||||||
| chr8:103423989 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.379-2067T>C | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 3/10 | chr8 | 103423989 | |||||||
| chr8:103424179 | C | T | 1 | a0001c0001t0001g0064 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.379-1877C>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 3/10 | chr8 | 103424179 | |||||||
| chr8:103424549 | A | G | 1 | a0001c0001t0001g0176 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.379-1507A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 3/10 | chr8 | 103424549 | |||||||
| chr8:103424650 | C | T | 5 | a0002c0003t0001g0054 a0002c0003t0001g0204 a0002c0003t0001g0205 others(2): Show |
6 | HG00323.hp2 HG00639.hp1 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.379-1406C>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 3/10 | chr8 | 103424650 | |||||||
| chr8:103424674 | A | C | 1 | a0001c0001t0001g0203 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.379-1382A>C | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 3/10 | chr8 | 103424674 | |||||||
| chr8:103424746 | T | C | 1 | a0001c0001t0001g0160 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.379-1310T>C | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 3/10 | chr8 | 103424746 | |||||||
| chr8:103424964 | C | T | 2 | a0002c0002t0001g0110 a0002c0002t0001g0111 |
2 | HG02809.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.379-1092C>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 3/10 | chr8 | 103424964 | |||||||
| chr8:103424976 | CAA | C | 5 | a0001c0001t0001g0017 a0001c0001t0001g0122 a0001c0001t0001g0123 others(2): Show |
7 | HG00741.hp1 HG01109.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.379-1077_379-1076d others(4): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 103424976 | ||||||
| chr8:103425162 | T | C | 2 | a0002c0002t0001g0086 a0002c0002t0001g0101 |
2 | NA18964.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.379-894T>C | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 3/10 | chr8 | 103425162 | |||||||
| chr8:103425167 | A | G | 7 | a0002c0002t0001g0030 a0002c0002t0001g0031 a0002c0002t0001g0032 others(4): Show |
10 | HG00423.hp1 HG00609.hp2 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.379-889A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 3/10 | chr8 | 103425167 | |||||||
| chr8:103425554 | A | G | 2 | a0002c0002t0001g0035 a0002c0002t0001g0092 |
3 | HG02723.hp2 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.379-502A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 3/10 | chr8 | 103425554 | |||||||
| chr8:103425669 | A | G | 1 | a0002c0002t0001g0085 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.379-387A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 3/10 | chr8 | 103425669 | |||||||
| chr8:103425728 | T | G | 2 | a0002c0002t0001g0081 a0002c0002t0001g0082 |
2 | NA18956.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.379-328T>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 3/10 | chr8 | 103425728 | |||||||
| chr8:103425877 | G | A | 1 | a0002c0003t0001g0205 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.379-179G>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 3/10 | chr8 | 103425877 | |||||||
| chr8:103425925 | A | G | 2 | a0002c0002t0001g0061 a0002c0007t0001g0135 |
2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.379-131A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 3/10 | chr8 | 103425925 | |||||||
| chr8:103426269 | A | G | 35 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(32): Show |
63 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.468+124A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 4/10 | chr8 | 103426269 | |||||||
| chr8:103426335 | G | A | 74 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(71): Show |
109 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.468+190G>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 4/10 | chr8 | 103426335 | |||||||
| chr8:103426335 | G | T | 2 | a0002c0002t0001g0061 a0002c0007t0001g0135 |
2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.468+190G>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 4/10 | chr8 | 103426335 | |||||||
| chr8:103426425 | C | T | 76 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(73): Show |
111 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.468+280C>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 4/10 | chr8 | 103426425 | |||||||
| chr8:103426491 | A | G | 2 | a0001c0001t0001g0148 a0001c0001t0001g0152 |
2 | HG00099.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.468+346A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 4/10 | chr8 | 103426491 | |||||||
| chr8:103426856 | G | A | 2 | a0002c0002t0001g0055 a0002c0002t0001g0057 |
2 | NA20300.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.469-241G>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 4/10 | chr8 | 103426856 | |||||||
| chr8:103426877 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.469-220G>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 4/10 | chr8 | 103426877 | |||||||
| chr8:103426881 | C | A | 30 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(27): Show |
56 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.469-216C>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 4/10 | chr8 | 103426881 | |||||||
| chr8:103426883 | C | T | 2 | a0002c0002t0001g0061 a0002c0007t0001g0135 |
2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.469-214C>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 4/10 | chr8 | 103426883 | |||||||
| chr8:103426940 | G | A | 62 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(59): Show |
96 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.469-157G>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 4/10 | chr8 | 103426940 | |||||||
| chr8:103427401 | T | C | 1 | a0001c0001t0002g0045 | 2 | HG01255.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.624+149T>C | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 5/10 | chr8 | 103427401 | |||||||
| chr8:103427642 | A | G | 1 | a0002c0002t0001g0035 | 2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.624+390A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 5/10 | chr8 | 103427642 | |||||||
| chr8:103427761 | A | G | 2 | a0002c0002t0001g0005 a0002c0002t0001g0084 |
6 | HG00735.hp1 HG01168.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.624+509A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 5/10 | chr8 | 103427761 | |||||||
| chr8:103427820 | C | T | 5 | a0001c0001t0001g0017 a0001c0001t0001g0122 a0001c0001t0001g0123 others(2): Show |
7 | HG00741.hp1 HG01109.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.624+568C>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 5/10 | chr8 | 103427820 | |||||||
| chr8:103427853 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.624+601T>C | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 5/10 | chr8 | 103427853 | |||||||
| chr8:103427965 | C | T | 1 | a0001c0001t0001g0012 | 4 | HG01891.hp2 HG03516.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.624+713C>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 5/10 | chr8 | 103427965 | |||||||
| chr8:103428048 | G | A | 1 | a0002c0003t0001g0204 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.624+796G>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 5/10 | chr8 | 103428048 | |||||||
| chr8:103428114 | T | C | 2 | a0001c0001t0001g0162 a0001c0001t0001g0177 |
2 | HG03017.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.624+862T>C | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 5/10 | chr8 | 103428114 | |||||||
| chr8:103428158 | T | C | 2 | a0002c0002t0001g0110 a0002c0002t0001g0111 |
2 | HG02809.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.624+906T>C | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 5/10 | chr8 | 103428158 | |||||||
| chr8:103428380 | A | G | 1 | a0002c0002t0001g0096 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.624+1128A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 5/10 | chr8 | 103428380 | |||||||
| chr8:103428523 | C | T | 72 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(69): Show |
107 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.624+1271C>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 5/10 | chr8 | 103428523 | |||||||
| chr8:103428657 | A | G | 1 | a0002c0002t0001g0091 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.624+1405A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 5/10 | chr8 | 103428657 | |||||||
| chr8:103428815 | C | T | 111 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(108): Show |
174 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.624+1563C>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 5/10 | chr8 | 103428815 | |||||||
| chr8:103428833 | T | G | 1 | a0001c0001t0001g0187 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.624+1581T>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 5/10 | chr8 | 103428833 | |||||||
| chr8:103428834 | C | T | 6 | a0002c0003t0001g0054 a0002c0003t0001g0059 a0002c0003t0001g0204 others(3): Show |
7 | HG00323.hp2 HG00639.hp1 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.624+1582C>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 5/10 | chr8 | 103428834 | |||||||
| chr8:103428883 | A | G | 1 | a0002c0002t0001g0090 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.624+1631A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 5/10 | chr8 | 103428883 | |||||||
| chr8:103428906 | GT | G | 79 | a0001c0001t0001g0017 a0001c0001t0001g0122 a0001c0001t0001g0123 others(76): Show |
116 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.624+1665delT | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 103428906 | ||||||
| chr8:103429127 | C | T | 1 | a0001c0001t0001g0179 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.625-1485C>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 5/10 | chr8 | 103429127 | |||||||
| chr8:103429230 | C | T | 1 | a0001c0001t0002g0045 | 2 | HG01255.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.625-1382C>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 5/10 | chr8 | 103429230 | |||||||
| chr8:103429273 | G | C | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0125 |
3 | HG01109.hp1 HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.625-1339G>C | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 5/10 | chr8 | 103429273 | |||||||
| chr8:103429667 | G | C | 1 | a0001c0001t0001g0116 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.625-945G>C | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 5/10 | chr8 | 103429667 | |||||||
| chr8:103429686 | TAAC | T | 32 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(29): Show |
58 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.625-921_625-919del others(3): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 103429686 | ||||||
| chr8:103429695 | G | A | 74 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(71): Show |
109 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.625-917G>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 5/10 | chr8 | 103429695 | |||||||
| chr8:103429761 | A | C | 1 | a0001c0001t0001g0026 | 3 | HG02976.hp2 HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.625-851A>C | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 5/10 | chr8 | 103429761 | |||||||
| chr8:103429863 | T | A | 1 | a0002c0002t0001g0073 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.625-749T>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 5/10 | chr8 | 103429863 | |||||||
| chr8:103429965 | C | T | 1 | a0002c0002t0001g0111 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.625-647C>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 5/10 | chr8 | 103429965 | |||||||
| chr8:103430000 | A | G | 1 | a0001c0001t0001g0171 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.625-612A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 5/10 | chr8 | 103430000 | |||||||
| chr8:103430052 | A | G | 8 | a0001c0001t0001g0012 a0001c0001t0001g0026 a0001c0001t0001g0052 others(5): Show |
15 | HG01891.hp2 HG02451.hp2 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.625-560A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 5/10 | chr8 | 103430052 | |||||||
| chr8:103430368 | G | C | 1 | a0001c0001t0001g0147 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.625-244G>C | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 5/10 | chr8 | 103430368 | |||||||
| chr8:103430377 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.625-235G>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 5/10 | chr8 | 103430377 | |||||||
| chr8:103430391 | CTAAA | C | 111 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(108): Show |
174 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.625-200_625-197del others(4): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 103430391 | ||||||
| chr8:103430412 | T | A | 1 | a0001c0001t0001g0149 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.625-200T>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 5/10 | chr8 | 103430412 | |||||||
| chr8:103430438 | G | A | 74 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(71): Show |
109 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.625-174G>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 5/10 | chr8 | 103430438 | |||||||
| chr8:103431055 | G | A | 74 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(71): Show |
109 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.702+366G>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 6/10 | chr8 | 103431055 | |||||||
| chr8:103431243 | A | G | 1 | a0001c0001t0001g0118 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.702+554A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 6/10 | chr8 | 103431243 | |||||||
| chr8:103431269 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.702+580A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 6/10 | chr8 | 103431269 | |||||||
| chr8:103431381 | A | T | 1 | a0001c0001t0001g0158 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.702+692A>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 6/10 | chr8 | 103431381 | |||||||
| chr8:103431535 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.702+846A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 6/10 | chr8 | 103431535 | |||||||
| chr8:103431597 | G | A | 2 | a0002c0002t0001g0056 a0002c0002t0001g0058 |
2 | HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.702+908G>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 6/10 | chr8 | 103431597 | |||||||
| chr8:103431617 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.702+928G>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 6/10 | chr8 | 103431617 | |||||||
| chr8:103431638 | C | T | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG00733.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.702+949C>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 6/10 | chr8 | 103431638 | |||||||
| chr8:103431797 | T | A | 2 | a0002c0002t0001g0061 a0002c0007t0001g0135 |
2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.703-862T>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 6/10 | chr8 | 103431797 | |||||||
| chr8:103431904 | G | A | 7 | a0001c0001t0001g0009 a0001c0001t0001g0046 a0001c0001t0001g0163 others(4): Show |
11 | HG01099.hp2 HG01261.hp2 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.703-755G>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 6/10 | chr8 | 103431904 | |||||||
| chr8:103431929 | G | A | 2 | a0001c0001t0001g0164 a0001c0001t0001g0190 |
2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.703-730G>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 6/10 | chr8 | 103431929 | |||||||
| chr8:103432039 | T | G | 37 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(34): Show |
65 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.703-620T>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 6/10 | chr8 | 103432039 | |||||||
| chr8:103432126 | C | T | 1 | a0002c0003t0001g0059 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.703-533C>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 6/10 | chr8 | 103432126 | |||||||
| chr8:103432133 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.703-526G>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 6/10 | chr8 | 103432133 | |||||||
| chr8:103432195 | A | G | 2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | HG02647.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.703-464A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 6/10 | chr8 | 103432195 | |||||||
| chr8:103432434 | A | G | 1 | a0001c0001t0001g0153 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.703-225A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 6/10 | chr8 | 103432434 | |||||||
| chr8:103432478 | T | G | 2 | a0001c0001t0001g0044 a0001c0001t0001g0047 |
4 | NA18953.hp2 NA18990.hp1 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.703-181T>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 6/10 | chr8 | 103432478 | |||||||
| chr8:103432521 | A | G | 2 | a0002c0002t0001g0061 a0002c0007t0001g0135 |
2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.703-138A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 6/10 | chr8 | 103432521 | |||||||
| chr8:103432781 | T | G | 76 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(73): Show |
111 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.785+40T>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 7/10 | chr8 | 103432781 | |||||||
| chr8:103432790 | T | A | 1 | a0001c0001t0001g0048 | 2 | NA18957.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.785+49T>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 7/10 | chr8 | 103432790 | |||||||
| chr8:103432803 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.785+62C>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 7/10 | chr8 | 103432803 | |||||||
| chr8:103432841 | A | G | 1 | a0001c0001t0001g0169 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.785+100A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 7/10 | chr8 | 103432841 | |||||||
| chr8:103432931 | T | A | 1 | a0001c0001t0001g0160 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.785+190T>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 7/10 | chr8 | 103432931 | |||||||
| chr8:103433132 | A | G | 111 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(108): Show |
174 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.785+391A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 7/10 | chr8 | 103433132 | |||||||
| chr8:103433133 | T | C | 5 | a0001c0001t0001g0017 a0001c0001t0001g0122 a0001c0001t0001g0123 others(2): Show |
7 | HG00741.hp1 HG01109.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.785+392T>C | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 7/10 | chr8 | 103433133 | |||||||
| chr8:103433161 | A | G | 2 | a0002c0002t0001g0110 a0002c0002t0001g0111 |
2 | HG02809.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.785+420A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 7/10 | chr8 | 103433161 | |||||||
| chr8:103433347 | G | A | 1 | a0002c0007t0001g0135 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.785+606G>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 7/10 | chr8 | 103433347 | |||||||
| chr8:103433487 | A | G | 37 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(34): Show |
65 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.785+746A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 7/10 | chr8 | 103433487 | |||||||
| chr8:103433569 | T | C | 1 | a0002c0002t0001g0074 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.785+828T>C | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 7/10 | chr8 | 103433569 | |||||||
| chr8:103433635 | C | G | 1 | a0001c0001t0001g0158 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.785+894C>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 7/10 | chr8 | 103433635 | |||||||
| chr8:103434049 | G | T | 1 | a0002c0002t0001g0108 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.785+1308G>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 7/10 | chr8 | 103434049 | |||||||
| chr8:103434210 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.786-1416C>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 7/10 | chr8 | 103434210 | |||||||
| chr8:103434337 | T | G | 1 | a0002c0002t0001g0066 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.786-1289T>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 7/10 | chr8 | 103434337 | |||||||
| chr8:103434353 | A | G | 1 | a0002c0003t0001g0206 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.786-1273A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 7/10 | chr8 | 103434353 | |||||||
| chr8:103434354 | T | C | 1 | a0001c0001t0001g0131 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.786-1272T>C | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 7/10 | chr8 | 103434354 | |||||||
| chr8:103434416 | C | T | 1 | a0002c0002t0001g0055 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.786-1210C>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 7/10 | chr8 | 103434416 | |||||||
| chr8:103434448 | G | A | 74 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(71): Show |
109 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.786-1178G>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 7/10 | chr8 | 103434448 | |||||||
| chr8:103434468 | C | T | 74 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(71): Show |
109 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.786-1158C>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 7/10 | chr8 | 103434468 | |||||||
| chr8:103434502 | A | G | 2 | a0002c0002t0001g0061 a0002c0007t0001g0135 |
2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.786-1124A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 7/10 | chr8 | 103434502 | |||||||
| chr8:103434547 | G | A | 3 | a0002c0002t0001g0065 a0002c0002t0001g0077 a0002c0002t0001g0091 |
3 | HG01433.hp2 HG02647.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.786-1079G>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 7/10 | chr8 | 103434547 | |||||||
| chr8:103434575 | G | C | 1 | a0001c0001t0001g0165 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.786-1051G>C | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 7/10 | chr8 | 103434575 | |||||||
| chr8:103434641 | T | C | 74 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(71): Show |
109 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.786-985T>C | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 7/10 | chr8 | 103434641 | |||||||
| chr8:103434644 | T | C | 1 | a0001c0001t0001g0166 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.786-982T>C | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 7/10 | chr8 | 103434644 | |||||||
| chr8:103434877 | A | G | 119 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(116): Show |
189 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.786-749A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 7/10 | chr8 | 103434877 | |||||||
| chr8:103435279 | A | T | 2 | a0002c0002t0001g0061 a0002c0007t0001g0135 |
2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.786-347A>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 7/10 | chr8 | 103435279 | |||||||
| chr8:103435357 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.786-269G>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 7/10 | chr8 | 103435357 | |||||||
| chr8:103435425 | A | G | 74 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(71): Show |
109 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.786-201A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 7/10 | chr8 | 103435425 | |||||||
| chr8:103435904 | A | C | 1 | a0001c0001t0001g0039 | 2 | HG00609.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.950+114A>C | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 8/10 | chr8 | 103435904 | |||||||
| chr8:103435961 | A | G | 120 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(117): Show |
190 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.950+171A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 8/10 | chr8 | 103435961 | |||||||
| chr8:103436007 | G | A | 1 | a0001c0001t0001g0116 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.950+217G>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 8/10 | chr8 | 103436007 | |||||||
| chr8:103436257 | T | C | 8 | a0001c0001t0001g0020 a0001c0001t0001g0040 a0001c0001t0001g0041 others(5): Show |
14 | HG00140.hp2 HG00639.hp2 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.950+467T>C | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 8/10 | chr8 | 103436257 | |||||||
| chr8:103436390 | G | T | 1 | a0001c0001t0001g0168 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.950+600G>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 8/10 | chr8 | 103436390 | |||||||
| chr8:103436449 | A | T | 1 | a0001c0001t0001g0132 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.950+659A>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 8/10 | chr8 | 103436449 | |||||||
| chr8:103436495 | T | C | 34 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(31): Show |
56 | HG00423.hp2 HG00558.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.950+705T>C | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 8/10 | chr8 | 103436495 | |||||||
| chr8:103436564 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.950+774C>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 8/10 | chr8 | 103436564 | |||||||
| chr8:103436736 | G | A | 2 | a0002c0002t0001g0055 a0002c0002t0001g0057 |
2 | NA20300.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.950+946G>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 8/10 | chr8 | 103436736 | |||||||
| chr8:103436854 | A | G | 6 | a0002c0003t0001g0054 a0002c0003t0001g0059 a0002c0003t0001g0204 others(3): Show |
7 | HG00323.hp2 HG00639.hp1 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.950+1064A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 8/10 | chr8 | 103436854 | |||||||
| chr8:103436870 | C | T | 111 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(108): Show |
174 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.950+1080C>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 8/10 | chr8 | 103436870 | |||||||
| chr8:103436884 | A | G | 1 | a0001c0001t0001g0178 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.950+1094A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 8/10 | chr8 | 103436884 | |||||||
| chr8:103437131 | A | G | 1 | a0001c0001t0001g0053 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.950+1341A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 8/10 | chr8 | 103437131 | |||||||
| chr8:103437372 | A | G | 1 | a0001c0001t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.950+1582A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 8/10 | chr8 | 103437372 | |||||||
| chr8:103437443 | A | G | 2 | a0001c0001t0001g0020 a0001c0001t0001g0131 |
4 | HG02258.hp1 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.950+1653A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 8/10 | chr8 | 103437443 | |||||||
| chr8:103437458 | G | C | 5 | a0001c0001t0001g0017 a0001c0001t0001g0122 a0001c0001t0001g0123 others(2): Show |
7 | HG00741.hp1 HG01109.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.950+1668G>C | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 8/10 | chr8 | 103437458 | |||||||
| chr8:103437480 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.950+1690A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 8/10 | chr8 | 103437480 | |||||||
| chr8:103437533 | G | T | 1 | a0002c0003t0001g0204 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.950+1743G>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 8/10 | chr8 | 103437533 | |||||||
| chr8:103437591 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.950+1801C>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 8/10 | chr8 | 103437591 | |||||||
| chr8:103437600 | G | T | 3 | a0002c0002t0001g0014 a0002c0002t0001g0097 a0002c0002t0003g0014 |
4 | HG00423.hp2 HG00558.hp2 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.950+1810G>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 8/10 | chr8 | 103437600 | |||||||
| chr8:103437893 | A | G | 1 | a0001c0001t0001g0202 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.950+2103A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 8/10 | chr8 | 103437893 | |||||||
| chr8:103437988 | A | G | 1 | a0002c0003t0001g0059 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.951-2148A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 8/10 | chr8 | 103437988 | |||||||
| chr8:103438129 | G | C | 1 | a0001c0001t0001g0180 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.951-2007G>C | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 8/10 | chr8 | 103438129 | |||||||
| chr8:103438254 | C | A | 2 | a0002c0002t0001g0067 a0002c0002t0001g0068 |
2 | NA19012.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.951-1882C>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 8/10 | chr8 | 103438254 | |||||||
| chr8:103438254 | C | G | 109 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(106): Show |
172 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.951-1882C>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 8/10 | chr8 | 103438254 | |||||||
| chr8:103438277 | C | T | 1 | a0001c0001t0001g0012 | 4 | HG01891.hp2 HG03516.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.951-1859C>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 8/10 | chr8 | 103438277 | |||||||
| chr8:103438307 | C | T | 2 | a0001c0001t0001g0142 a0001c0001t0001g0160 |
2 | HG02818.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.951-1829C>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 8/10 | chr8 | 103438307 | |||||||
| chr8:103438421 | A | AT | 63 | a0001c0001t0001g0145 a0001c0001t0001g0151 a0001c0001t0001g0197 others(60): Show |
94 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.951-1698dupT | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr8 | 103438421 | ||||||
| chr8:103438421 | A | ATT | 6 | a0002c0002t0001g0068 a0002c0002t0001g0089 a0002c0002t0001g0096 others(3): Show |
6 | HG02809.hp1 HG03831.hp1 NA19000.hp2 others(3): Show |
intron_variant | MODIFIER | c.951-1699_951-1698d others(4): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr8 | 103438421 | ||||||
| chr8:103438421 | A | T | 1 | a0002c0002t0001g0016 | 3 | HG02818.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.951-1715A>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 8/10 | chr8 | 103438421 | |||||||
| chr8:103438917 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.951-1219A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 8/10 | chr8 | 103438917 | |||||||
| chr8:103439213 | G | C | 76 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(73): Show |
111 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.951-923G>C | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 8/10 | chr8 | 103439213 | |||||||
| chr8:103439226 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.951-910C>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 8/10 | chr8 | 103439226 | |||||||
| chr8:103439306 | T | A | 72 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(69): Show |
107 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.951-830T>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 8/10 | chr8 | 103439306 | |||||||
| chr8:103439309 | C | T | 72 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(69): Show |
107 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.951-827C>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 8/10 | chr8 | 103439309 | |||||||
| chr8:103439329 | T | G | 2 | a0002c0002t0001g0061 a0002c0007t0001g0135 |
2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.951-807T>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 8/10 | chr8 | 103439329 | |||||||
| chr8:103439383 | C | CT | 81 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(78): Show |
132 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.951-730dupT | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr8 | 103439383 | ||||||
| chr8:103439383 | C | CTT | 19 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0117 others(16): Show |
26 | HG00423.hp2 HG00738.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.951-731_951-730dup others(2): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr8 | 103439383 | ||||||
| chr8:103439433 | C | T | 1 | a0002c0007t0001g0135 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.951-703C>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 8/10 | chr8 | 103439433 | |||||||
| chr8:103439590 | T | C | 1 | a0001c0001t0001g0121 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.951-546T>C | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 8/10 | chr8 | 103439590 | |||||||
| chr8:103439731 | A | C | 1 | a0002c0002t0001g0016 | 3 | HG02818.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.951-405A>C | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 8/10 | chr8 | 103439731 | |||||||
| chr8:103439813 | T | C | 111 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(108): Show |
174 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.951-323T>C | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 8/10 | chr8 | 103439813 | |||||||
| chr8:103439918 | G | T | 2 | a0002c0002t0001g0061 a0002c0007t0001g0135 |
2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.951-218G>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 8/10 | chr8 | 103439918 | |||||||
| chr8:103439970 | C | A | 1 | a0002c0002t0001g0094 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.951-166C>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 8/10 | chr8 | 103439970 | |||||||
| chr8:103439971 | G | A | 113 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(110): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.951-165G>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 8/10 | chr8 | 103439971 | |||||||
| chr8:103440053 | A | G | 74 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(71): Show |
109 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.951-83A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 8/10 | chr8 | 103440053 | |||||||
| chr8:103440070 | T | C | 1 | a0001c0001t0001g0168 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.951-66T>C | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 8/10 | chr8 | 103440070 | |||||||
| chr8:103440085 | C | CAAAG | 111 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(108): Show |
174 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.951-48_951-47insGA others(2): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr8 | 103440085 | ||||||
| chr8:103440102 | T | A | 1 | a0001c0001t0001g0012 | 4 | HG01891.hp2 HG03516.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.951-34T>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 8/10 | chr8 | 103440102 | |||||||
| chr8:103440105 | A | C | 1 | a0001c0001t0001g0012 | 4 | HG01891.hp2 HG03516.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.951-31A>C | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 8/10 | chr8 | 103440105 | |||||||
| chr8:103440110 | G | A | 1 | a0001c0001t0001g0166 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.951-26G>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 8/10 | chr8 | 103440110 | |||||||
| chr8:103440125 | G | A | 1 | a0002c0003t0001g0204 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.951-11G>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 8/10 | chr8 | 103440125 | |||||||
| chr8:103440289 | C | A | 1 | a0001c0001t0001g0184 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1086+18C>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 9/10 | chr8 | 103440289 | |||||||
| chr8:103440326 | A | ATAT | 111 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(108): Show |
174 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.1086+58_1086+60dup others(3): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr8 | 103440326 | ||||||
| chr8:103440393 | TAAAA | T | 66 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(63): Show |
100 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.1086+126_1086+129d others(6): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr8 | 103440393 | ||||||
| chr8:103440541 | G | C | 2 | a0002c0002t0001g0061 a0002c0007t0001g0135 |
2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1086+270G>C | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 9/10 | chr8 | 103440541 | |||||||
| chr8:103440733 | A | G | 1 | a0002c0002t0001g0061 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1086+462A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 9/10 | chr8 | 103440733 | |||||||
| chr8:103440851 | CAG | C | 5 | a0001c0001t0001g0017 a0001c0001t0001g0122 a0001c0001t0001g0123 others(2): Show |
7 | HG00741.hp1 HG01109.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.1086+583_1086+584d others(4): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr8 | 103440851 | ||||||
| chr8:103441051 | A | T | 1 | a0001c0001t0001g0137 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1087-404A>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 9/10 | chr8 | 103441051 | |||||||
| chr8:103441139 | T | C | 1 | a0001c0001t0001g0163 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1087-316T>C | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 9/10 | chr8 | 103441139 | |||||||
| chr8:103441375 | G | A | 74 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0005 others(71): Show |
109 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.1087-80G>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 9/10 | chr8 | 103441375 | |||||||
| chr8:103441416 | A | G | 1 | a0001c0001t0001g0175 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1087-39A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 9/10 | chr8 | 103441416 | |||||||
| chr8:103441432 | G | T | 1 | a0001c0001t0001g0007 | 5 | HG02615.hp1 HG02895.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1087-23G>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 9/10 | chr8 | 103441432 | |||||||
| chr8:103441781 | C | CT | 64 | a0001c0001t0001g0167 a0002c0002t0001g0003 a0002c0002t0001g0004 others(61): Show |
98 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.1250+177dupT | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 103441781 | ||||||
| chr8:103441859 | G | T | 1 | a0002c0002t0001g0078 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1250+241G>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 10/10 | chr8 | 103441859 | |||||||
| chr8:103441913 | G | C | 120 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(117): Show |
190 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1250+295G>C | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 10/10 | chr8 | 103441913 | |||||||
| chr8:103441959 | G | T | 2 | a0001c0001t0001g0176 a0001c0001t0001g0182 |
2 | NA18953.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.1250+341G>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 10/10 | chr8 | 103441959 | |||||||
| chr8:103441988 | A | G | 1 | a0002c0002t0001g0031 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1250+370A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 10/10 | chr8 | 103441988 | |||||||
| chr8:103442047 | A | C | 1 | a0001c0001t0001g0186 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1250+429A>C | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 10/10 | chr8 | 103442047 | |||||||
| chr8:103442058 | C | T | 1 | a0001c0001t0001g0026 | 3 | HG02976.hp2 HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1250+440C>T | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 10/10 | chr8 | 103442058 | |||||||
| chr8:103442060 | C | CGCCCAGA others(15): Show |
1 | a0001c0001t0001g0174 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1250+443_1250+464d others(24): Show |
DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 103442060 | ||||||
| chr8:103442084 | T | C | 119 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(116): Show |
189 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.1250+466T>C | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 10/10 | chr8 | 103442084 | |||||||
| chr8:103442253 | A | G | 1 | a0001c0001t0001g0010 | 4 | HG00642.hp1 HG00733.hp2 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.1251-542A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 10/10 | chr8 | 103442253 | |||||||
| chr8:103442287 | C | A | 2 | a0002c0002t0001g0055 a0002c0002t0001g0057 |
2 | NA20300.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1251-508C>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 10/10 | chr8 | 103442287 | |||||||
| chr8:103442566 | A | C | 111 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(108): Show |
174 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.1251-229A>C | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 10/10 | chr8 | 103442566 | |||||||
| chr8:103442583 | T | TA | 1 | a0001c0004t0001g0018 | 3 | HG02109.hp1 HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1251-209dupA | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 103442583 | ||||||
| chr8:103442629 | A | G | 1 | a0001c0001t0001g0115 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1251-166A>G | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 10/10 | chr8 | 103442629 | |||||||
| chr8:103442718 | G | A | 4 | a0001c0001t0001g0049 a0001c0001t0001g0139 a0001c0001t0001g0146 others(1): Show |
5 | HG00558.hp1 HG01952.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.1251-77G>A | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 10/10 | chr8 | 103442718 | |||||||
| chr8:103442771 | A | C | 1 | a0002c0003t0001g0059 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1251-24A>C | DCAF13 | ENSG00000164934.15 | transcript | ENST00000612750.5 | protein_coding | 10/10 | chr8 | 103442771 |