Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8816 |
| ensemblid | ENSG00000139990.18 |
| hgncid | 20224 |
| symbol | DCAF5 |
| name | DDB1 and CUL4 associated factor 5 |
| refseq_nuc | NM_003861.3 |
| refseq_prot | NP_003852.1 |
| ensembl_nuc | ENST00000341516.10 |
| ensembl_prot | ENSP00000341351.5 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 69050881 |
| end | 69153119 |
| strand | - |
| ver | v1.2 |
| region | chr14:69050881-69153119 |
| region5000 | chr14:69045881-69158119 |
| regionname0 | DCAF5_chr14_69050881_69153119 |
| regionname5000 | DCAF5_chr14_69045881_69158119 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 942 | 241 | 91 | 55 | 41 | 14 | 38 | 29 | DCAF5_chr14_69045881_69158119 | DCAF5 | MKRRA others(937): Show |
chr14 | 69045881 | 69158119 |
| a0002 | 0/0 | 942 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | MKRRA others(937): Show |
chr14 | 69045881 | 69158119 |
| a0003 | 0/0 | 942 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | MKRRA others(937): Show |
chr14 | 69045881 | 69158119 |
| a0004 | 0/0 | 942 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | MKRRA others(937): Show |
chr14 | 69045881 | 69158119 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2826 | 188 | 64 | 42 | 38 | 9 | 33 | DCAF5_chr14_69045881_69158119 | DCAF5 | ATGAA others(2821): Show |
chr14 | 69045881 | 69158119 | ||
| a0001c0002 | 0/0 | 2826 | 25 | 4 | 11 | 0 | 5 | 5 | DCAF5_chr14_69045881_69158119 | DCAF5 | ATGAA others(2821): Show |
chr14 | 69045881 | 69158119 | ||
| a0001c0003 | 0/0 | 2826 | 22 | 21 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | ATGAA others(2821): Show |
chr14 | 69045881 | 69158119 | ||
| a0001c0004 | 0/0 | 2826 | 3 | 0 | 0 | 3 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | ATGAA others(2821): Show |
chr14 | 69045881 | 69158119 | ||
| a0001c0005 | 0/0 | 2826 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | ATGAA others(2821): Show |
chr14 | 69045881 | 69158119 | ||
| a0001c0006 | 0/0 | 2826 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | ATGAA others(2821): Show |
chr14 | 69045881 | 69158119 | ||
| a0001c0010 | 0/0 | 2826 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | ATGAA others(2821): Show |
chr14 | 69045881 | 69158119 | ||
| a0002c0009 | 0/0 | 2826 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | ATGAA others(2821): Show |
chr14 | 69045881 | 69158119 | ||
| a0003c0007 | 0/0 | 2826 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | ATGAA others(2821): Show |
chr14 | 69045881 | 69158119 | ||
| a0004c0008 | 0/0 | 2826 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | ATGAA others(2821): Show |
chr14 | 69045881 | 69158119 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 5946 | 66 | 22 | 14 | 7 | 5 | 17 | DCAF5_chr14_69045881_69158119 | DCAF5 | ACACC others(5941): Show |
chr14 | 69045881 | 69158119 |
| a0001c0001t0002 | 0/0 | 5945 | 46 | 13 | 13 | 16 | 2 | 2 | DCAF5_chr14_69045881_69158119 | DCAF5 | ACACC others(5940): Show |
chr14 | 69045881 | 69158119 |
| a0001c0001t0003 | 0/1 | 5944 | 36 | 1 | 9 | 11 | 1 | 13 | DCAF5_chr14_69045881_69158119 | DCAF5 | ACACC others(5939): Show |
chr14 | 69045881 | 69158119 |
| a0001c0001t0004 | 0/0 | 5946 | 13 | 9 | 3 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | ACACC others(5941): Show |
chr14 | 69045881 | 69158119 |
| a0001c0001t0005 | 0/0 | 5945 | 4 | 4 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | ACACC others(5940): Show |
chr14 | 69045881 | 69158119 |
| a0001c0001t0006 | 0/0 | 5946 | 4 | 4 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | ACACC others(5941): Show |
chr14 | 69045881 | 69158119 |
| a0001c0001t0007 | 0/0 | 5945 | 3 | 2 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | ACACC others(5940): Show |
chr14 | 69045881 | 69158119 |
| a0001c0001t0008 | 0/0 | 5944 | 3 | 0 | 2 | 0 | 1 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | ACACC others(5939): Show |
chr14 | 69045881 | 69158119 |
| a0001c0001t0009 | 0/0 | 5945 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | ACACC others(5940): Show |
chr14 | 69045881 | 69158119 |
| a0001c0001t0010 | 0/0 | 5946 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | ACACC others(5941): Show |
chr14 | 69045881 | 69158119 |
| a0001c0001t0011 | 0/0 | 5957 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | ACACC others(5952): Show |
chr14 | 69045881 | 69158119 |
| a0001c0001t0013 | 0/0 | 5945 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | ACACC others(5940): Show |
chr14 | 69045881 | 69158119 |
| a0001c0001t0014 | 0/0 | 5945 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | ACACC others(5940): Show |
chr14 | 69045881 | 69158119 |
| a0001c0001t0015 | 0/0 | 5945 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | ACACC others(5940): Show |
chr14 | 69045881 | 69158119 |
| a0001c0001t0017 | 0/0 | 5945 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | ACACC others(5940): Show |
chr14 | 69045881 | 69158119 |
| a0001c0001t0018 | 0/0 | 5945 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | ACACC others(5940): Show |
chr14 | 69045881 | 69158119 |
| a0001c0001t0019 | 0/0 | 5946 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | ACACC others(5941): Show |
chr14 | 69045881 | 69158119 |
| a0001c0001t0020 | 0/0 | 5944 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | ACACC others(5939): Show |
chr14 | 69045881 | 69158119 |
| a0001c0002t0001 | 0/0 | 5946 | 24 | 4 | 11 | 0 | 4 | 5 | DCAF5_chr14_69045881_69158119 | DCAF5 | ACACC others(5941): Show |
chr14 | 69045881 | 69158119 |
| a0001c0002t0016 | 0/0 | 5945 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | ACACC others(5940): Show |
chr14 | 69045881 | 69158119 |
| a0001c0003t0002 | 0/0 | 5945 | 22 | 21 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | ACACC others(5940): Show |
chr14 | 69045881 | 69158119 |
| a0001c0004t0003 | 0/0 | 5944 | 3 | 0 | 0 | 3 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | ACACC others(5939): Show |
chr14 | 69045881 | 69158119 |
| a0001c0005t0002 | 0/0 | 5945 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | ACACC others(5940): Show |
chr14 | 69045881 | 69158119 |
| a0001c0006t0003 | 0/0 | 5944 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | ACACC others(5939): Show |
chr14 | 69045881 | 69158119 |
| a0001c0010t0001 | 0/0 | 5946 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | ACACC others(5941): Show |
chr14 | 69045881 | 69158119 |
| a0002c0009t0002 | 0/0 | 5945 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | ACACC others(5940): Show |
chr14 | 69045881 | 69158119 |
| a0003c0007t0012 | 0/0 | 5945 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | ACACC others(5940): Show |
chr14 | 69045881 | 69158119 |
| a0004c0008t0003 | 0/0 | 5944 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | ACACC others(5939): Show |
chr14 | 69045881 | 69158119 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0215 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0002g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0003g0036 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0004g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0004g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0004g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0004g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0004g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0004g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0004g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0004g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0005g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0005g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0005g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0005g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0006g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0006g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0006g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0007g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0007g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0007g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0008g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0008g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0008g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0009g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0009g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0010g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0010g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0011g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0011g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0013g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0014g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0015g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0017g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0018g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0019g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0001t0020g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0002t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0002t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0002t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0002t0016g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0003t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0003t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0003t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0003t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0003t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0003t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0003t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0003t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0003t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0003t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0003t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0003t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0003t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0003t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0003t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0003t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0003t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0003t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0003t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0003t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0003t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0003t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0004t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0004t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0004t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0005t0002g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0006t0003g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0001c0010t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0002c0009t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0003c0007t0012g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| a0004c0008t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0088 | EUR | GBR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG00099 | hp2 | a0001 | c0002 | t0016 | g0146 | EUR | GBR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0228 | EUR | GBR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0066 | EUR | GBR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0155 | EUR | FIN | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0137 | EUR | FIN | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0167 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0032 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0163 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0048 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG00741 | hp2 | a0001 | c0006 | t0003 | g0006 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0164 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG01069 | hp2 | a0001 | c0001 | t0004 | g0010 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0156 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0082 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG01074 | hp2 | a0001 | c0001 | t0007 | g0097 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0090 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0151 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0149 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0074 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0029 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0035 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG01175 | hp2 | a0001 | c0001 | t0004 | g0187 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG01192 | hp1 | a0001 | c0001 | t0004 | g0009 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0123 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG01243 | hp2 | a0001 | c0003 | t0002 | g0115 | AMR | PUR | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0028 | AMR | CLM | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | CLM | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0147 | AMR | CLM | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0153 | AMR | CLM | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0065 | AMR | CLM | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0037 | AMR | CLM | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0075 | AMR | CLM | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | CLM | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0027 | AMR | CLM | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG01433 | hp2 | a0002 | c0009 | t0002 | g0107 | AMR | CLM | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0091 | AMR | CLM | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0038 | AMR | CLM | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0159 | EUR | IBS | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0136 | EUR | IBS | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0135 | EUR | IBS | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0165 | EUR | IBS | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG01891 | hp2 | a0001 | c0003 | t0002 | g0105 | AFR | ACB | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0069 | AMR | PEL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0039 | AMR | PEL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0154 | AMR | PEL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG01934 | hp2 | a0001 | c0001 | t0008 | g0060 | AMR | PEL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0073 | AMR | PEL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0034 | AMR | PEL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02004 | hp1 | a0001 | c0001 | t0008 | g0061 | AMR | PEL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0080 | AMR | PEL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0127 | AFR | ACB | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0150 | AFR | ACB | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02056 | hp1 | a0001 | c0001 | t0015 | g0014 | EAS | KHV | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | KHV | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | KHV | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | KHV | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0053 | EAS | KHV | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | KHV | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02135 | hp1 | a0001 | c0004 | t0003 | g0047 | EAS | KHV | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02145 | hp1 | a0001 | c0001 | t0005 | g0172 | AFR | ACB | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02145 | hp2 | a0001 | c0003 | t0002 | g0112 | AFR | ACB | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | CDX | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0068 | EAS | CDX | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | CDX | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | CDX | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | ACB | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0051 | AFR | ACB | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0182 | AFR | ACB | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02258 | hp2 | a0001 | c0005 | t0002 | g0005 | AFR | ACB | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02280 | hp1 | a0001 | c0001 | t0006 | g0169 | AFR | ACB | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02280 | hp2 | a0001 | c0003 | t0002 | g0106 | AFR | ACB | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02451 | hp1 | a0001 | c0001 | t0006 | g0003 | AFR | ACB | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0176 | AFR | ACB | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02572 | hp1 | a0003 | c0007 | t0012 | g0128 | AFR | GWD | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0044 | SAS | PJL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0177 | AFR | GWD | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02622 | hp2 | a0001 | c0003 | t0002 | g0114 | AFR | GWD | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02630 | hp1 | a0001 | c0001 | t0005 | g0173 | AFR | GWD | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02630 | hp2 | a0001 | c0001 | t0018 | g0238 | AFR | GWD | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02647 | hp1 | a0001 | c0003 | t0002 | g0118 | AFR | GWD | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02717 | hp1 | a0001 | c0003 | t0002 | g0113 | AFR | GWD | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0180 | AFR | GWD | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02723 | hp2 | a0001 | c0003 | t0002 | g0116 | AFR | GWD | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0052 | SAS | PJL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02818 | hp1 | a0001 | c0003 | t0002 | g0102 | AFR | GWD | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0126 | AFR | GWD | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02886 | hp2 | a0001 | c0001 | t0006 | g0168 | AFR | GWD | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0101 | AFR | GWD | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0185 | AFR | GWD | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0171 | AFR | GWD | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02896 | hp2 | a0001 | c0003 | t0002 | g0120 | AFR | GWD | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0100 | AFR | GWD | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0170 | AFR | GWD | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | ESN | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02922 | hp2 | a0001 | c0003 | t0002 | g0110 | AFR | ESN | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02965 | hp1 | a0001 | c0003 | t0002 | g0104 | AFR | ESN | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0235 | AFR | ESN | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | ESN | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02970 | hp2 | a0001 | c0003 | t0002 | g0108 | AFR | ESN | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0063 | SAS | PJL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0184 | AFR | GWD | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG03041 | hp2 | a0001 | c0001 | t0006 | g0003 | AFR | GWD | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG03098 | hp1 | a0001 | c0001 | t0017 | g0098 | AFR | MSL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0072 | AFR | MSL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG03130 | hp1 | a0001 | c0001 | t0010 | g0210 | AFR | ESN | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | ESN | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ESN | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG03195 | hp1 | a0001 | c0001 | t0007 | g0096 | AFR | ESN | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG03195 | hp2 | a0001 | c0003 | t0002 | g0125 | AFR | ESN | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG03209 | hp2 | a0001 | c0003 | t0002 | g0117 | AFR | MSL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | MSL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0178 | AFR | MSL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0092 | SAS | PJL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0181 | AFR | MSL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG03453 | hp2 | a0001 | c0001 | t0014 | g0094 | AFR | MSL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG03486 | hp1 | a0001 | c0001 | t0011 | g0236 | AFR | MSL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG03486 | hp2 | a0001 | c0003 | t0002 | g0103 | AFR | MSL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0160 | SAS | PJL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0031 | SAS | PJL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0158 | SAS | PJL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG03516 | hp1 | a0001 | c0001 | t0013 | g0099 | AFR | ESN | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG03516 | hp2 | a0001 | c0003 | t0002 | g0111 | AFR | ESN | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0076 | AFR | GWD | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG03540 | hp2 | a0001 | c0003 | t0002 | g0121 | AFR | GWD | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | MSL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG03579 | hp2 | a0001 | c0010 | t0001 | g0218 | AFR | MSL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0062 | SAS | PJL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0148 | SAS | PJL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0015 | SAS | STU | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0049 | SAS | STU | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0152 | SAS | PJL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0064 | SAS | PJL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0033 | SAS | BEB | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | BEB | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0043 | SAS | BEB | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0162 | SAS | BEB | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG04115 | hp1 | a0001 | c0001 | t0004 | g0008 | SAS | STU | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | STU | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | STU | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0025 | SAS | STU | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | STU | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0050 | SAS | STU | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0041 | SAS | STU | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0093 | SAS | STU | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | YRI | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| NA18522 | hp2 | a0001 | c0001 | t0019 | g0239 | AFR | YRI | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | YRI | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0188 | AFR | YRI | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| NA18940 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| NA18945 | hp2 | a0001 | c0004 | t0003 | g0030 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| NA19002 | hp1 | a0001 | c0001 | t0009 | g0016 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | LWK | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| NA19030 | hp2 | a0001 | c0003 | t0002 | g0119 | AFR | LWK | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0179 | AFR | LWK | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0086 | AFR | LWK | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| NA19055 | hp1 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| NA19055 | hp2 | a0001 | c0001 | t0020 | g0240 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| NA19081 | hp1 | a0001 | c0004 | t0003 | g0055 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| NA19081 | hp2 | a0001 | c0001 | t0009 | g0022 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| NA19090 | hp2 | a0004 | c0008 | t0003 | g0067 | EAS | JPT | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0174 | AFR | YRI | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| NA19240 | hp2 | a0001 | c0001 | t0007 | g0095 | AFR | YRI | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| NA20129 | hp1 | a0001 | c0001 | t0011 | g0237 | AFR | ASW | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0161 | AFR | ASW | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0157 | EUR | TSI | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| NA20752 | hp2 | a0001 | c0001 | t0008 | g0045 | EUR | TSI | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0234 | EUR | TSI | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0077 | EUR | TSI | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | GIH | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | GIH | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | ACB | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02109 | hp2 | a0001 | c0003 | t0002 | g0124 | AFR | ACB | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | ACB | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02486 | hp2 | a0001 | c0003 | t0002 | g0122 | AFR | ACB | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0175 | AFR | ACB | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG02559 | hp2 | a0001 | c0003 | t0002 | g0109 | AFR | ACB | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0183 | AFR | MSL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG03471 | hp2 | a0001 | c0001 | t0010 | g0209 | AFR | MSL | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0186 | AFR | USA | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | USA | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0070 | AFR | USA | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | USA | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | LWK | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0083 | AFR | LWK | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0036 | REF | REF | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0215 | REF | REF | DCAF5_chr14_69045881_69158119 | DCAF5 | chr14 | 69045881 | 69158119 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:69054179 | C | T | 1 | a0002 | 1 | HG01433.hp2 | missense_variant | MODERATE | c.2507G>A | p.Arg836His | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 9/9 | 2648/5946 | 2507/2829 | 836/942 | chr14 | 69054179 | |||
| chr14:69054621 | C | A | 1 | a0003 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.2065G>T | p.Ala689Ser | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 9/9 | 2206/5946 | 2065/2829 | 689/942 | chr14 | 69054621 | |||
| chr14:69054920 | C | T | 1 | a0004 | 1 | NA19090.hp2 | missense_variant | MODERATE | c.1766G>A | p.Arg589His | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 9/9 | 1907/5946 | 1766/2829 | 589/942 | chr14 | 69054920 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:69054628 | G | A | 1 | a0001c0002 | 25 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(22): Show |
synonymous_variant | LOW | c.2058C>T | p.Thr686Thr | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 9/9 | 2199/5946 | 2058/2829 | 686/942 | chr14 | 69054628 | |||
| chr14:69055300 | C | T | 1 | a0003c0007 | 1 | HG02572.hp1 | synonymous_variant | LOW | c.1386G>A | p.Ser462Ser | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 9/9 | 1527/5946 | 1386/2829 | 462/942 | chr14 | 69055300 | |||
| chr14:69055345 | G | A | 3 | a0001c0003 a0001c0005 a0002c0009 |
24 | HG01243.hp2 HG01433.hp2 HG01891.hp2 others(21): Show |
synonymous_variant | LOW | c.1341C>T | p.His447His | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 9/9 | 1482/5946 | 1341/2829 | 447/942 | chr14 | 69055345 | |||
| chr14:69055462 | C | G | 1 | a0001c0004 | 3 | HG02135.hp1 NA18945.hp2 NA19081.hp1 |
synonymous_variant | LOW | c.1224G>C | p.Ser408Ser | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 9/9 | 1365/5946 | 1224/2829 | 408/942 | chr14 | 69055462 | |||
| chr14:69055552 | G | A | 1 | a0001c0010 | 1 | HG03579.hp2 | synonymous_variant | LOW | c.1134C>T | p.Asp378Asp | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 9/9 | 1275/5946 | 1134/2829 | 378/942 | chr14 | 69055552 | |||
| chr14:69152838 | C | T | 1 | a0001c0006 | 1 | HG00741.hp2 | synonymous_variant | LOW | c.141G>A | p.Lys47Lys | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/9 | 282/5946 | 141/2829 | 47/942 | chr14 | 69152838 | |||
| chr14:69152880 | A | G | 1 | a0001c0005 | 1 | HG02258.hp2 | synonymous_variant | LOW | c.99T>C | p.Phe33Phe | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/9 | 240/5946 | 99/2829 | 33/942 | chr14 | 69152880 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:69051281 | A | G | 1 | a0001c0001t0008 | 3 | HG01934.hp2 HG02004.hp1 NA20752.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2576T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 9/9 | 2576 | chr14 | 69051281 | ||||||
| chr14:69051940 | C | A | 1 | a0001c0001t0006 | 4 | HG02280.hp1 HG02451.hp1 HG02886.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1917G>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 9/9 | 1917 | chr14 | 69051940 | ||||||
| chr14:69052242 | C | G | 1 | a0001c0001t0010 | 2 | HG03130.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1615G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 9/9 | 1615 | chr14 | 69052242 | ||||||
| chr14:69052252 | A | T | 1 | a0001c0001t0013 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1605T>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 9/9 | 1605 | chr14 | 69052252 | ||||||
| chr14:69052257 | T | C | 2 | a0001c0001t0007 a0001c0001t0017 |
4 | HG01074.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1600A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 9/9 | 1600 | chr14 | 69052257 | ||||||
| chr14:69052379 | C | G | 1 | a0001c0001t0009 | 2 | NA19002.hp1 NA19081.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1478G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 9/9 | 1478 | chr14 | 69052379 | ||||||
| chr14:69052566 | C | T | 1 | a0003c0007t0012 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1291G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 9/9 | 1291 | chr14 | 69052566 | ||||||
| chr14:69052587 | T | C | 1 | a0001c0001t0014 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1270A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 9/9 | 1270 | chr14 | 69052587 | ||||||
| chr14:69052607 | T | C | 2 | a0001c0001t0004 a0001c0001t0019 |
14 | HG01069.hp2 HG01175.hp2 HG01192.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1250A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 9/9 | 1250 | chr14 | 69052607 | ||||||
| chr14:69052609 | C | G | 1 | a0001c0001t0005 | 4 | HG02145.hp1 HG02559.hp1 HG02630.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1248G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 9/9 | 1248 | chr14 | 69052609 | ||||||
| chr14:69052712 | T | C | 1 | a0001c0001t0015 | 1 | HG02056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1145A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 9/9 | 1145 | chr14 | 69052712 | ||||||
| chr14:69053643 | TC | T | 20 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(17): Show |
131 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*213delG | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 9/9 | 213 | chr14 | 69053643 | ||||||
| chr14:69053644 | C | T | 1 | a0001c0001t0001 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*213G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 9/9 | 213 | chr14 | 69053644 | ||||||
| chr14:69053801 | AT | A | 7 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0020 others(4): Show |
45 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*55delA | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 9/9 | 55 | chr14 | 69053801 | ||||||
| chr14:69053814 | T | G | 1 | a0001c0001t0017 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*43A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 9/9 | 43 | chr14 | 69053814 | ||||||
| chr14:69153002 | T | TCGCGCCG others(5): Show |
1 | a0001c0001t0011 | 2 | HG03486.hp1 NA20129.hp1 |
5_prime_UTR_variant | MODIFIER | c.-36_-25dupGGCGGCGG others(4): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/9 | 25 | chr14 | 69153002 | ||||||
| chr14:69153056 | G | A | 2 | a0001c0001t0018 a0001c0001t0019 |
2 | HG02630.hp2 NA18522.hp2 |
5_prime_UTR_variant | MODIFIER | c.-78C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/9 | 78 | chr14 | 69153056 | ||||||
| chr14:69153109 | G | A | 1 | a0001c0001t0020 | 1 | NA19055.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-131C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/9 | chr14 | 69153109 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:69055661 | TC | T | 5 | a0001c0001t0002g0123 a0001c0001t0007g0095 a0001c0001t0007g0096 others(2): Show |
5 | HG01074.hp2 HG01192.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1075-51delG | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69055661 | |||||||
| chr14:69055692 | G | A | 26 | a0001c0001t0002g0100 a0001c0001t0002g0101 a0001c0003t0002g0102 others(23): Show |
26 | HG01243.hp2 HG01433.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.1075-81C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69055692 | |||||||
| chr14:69055729 | G | A | 14 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0002g0018 others(11): Show |
14 | HG01361.hp1 HG02055.hp1 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.1075-118C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69055729 | |||||||
| chr14:69056164 | A | C | 1 | a0003c0007t0012g0128 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1075-553T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69056164 | |||||||
| chr14:69056311 | G | A | 2 | a0001c0001t0003g0092 a0001c0001t0003g0093 |
2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1075-700C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69056311 | |||||||
| chr14:69056332 | A | G | 2 | a0001c0001t0013g0099 a0001c0001t0014g0094 |
2 | HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1075-721T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69056332 | |||||||
| chr14:69056414 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1075-803C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69056414 | |||||||
| chr14:69056436 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1075-825C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69056436 | |||||||
| chr14:69056506 | C | G | 17 | a0001c0003t0002g0108 a0001c0003t0002g0109 a0001c0003t0002g0111 others(14): Show |
17 | HG01243.hp2 HG01433.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1075-895G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69056506 | |||||||
| chr14:69056685 | C | T | 23 | a0001c0001t0001g0004 a0001c0001t0001g0190 a0001c0001t0001g0191 others(20): Show |
24 | HG00642.hp1 HG00741.hp1 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.1075-1074G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69056685 | |||||||
| chr14:69056706 | C | T | 3 | a0001c0001t0002g0176 a0001c0001t0002g0177 a0001c0001t0002g0178 |
3 | HG02451.hp2 HG02622.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1075-1095G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69056706 | |||||||
| chr14:69056829 | A | AT | 5 | a0001c0001t0002g0090 a0001c0001t0002g0091 a0001c0001t0002g0176 others(2): Show |
5 | HG01081.hp1 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1075-1219dupA | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69056829 | |||||||
| chr14:69057101 | C | T | 5 | a0001c0003t0002g0113 a0001c0003t0002g0121 a0001c0003t0002g0124 others(2): Show |
5 | HG02109.hp2 HG02258.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1075-1490G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69057101 | |||||||
| chr14:69057348 | A | AT | 83 | a0001c0001t0001g0081 a0001c0001t0001g0134 a0001c0001t0001g0135 others(80): Show |
83 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.1075-1738dupA | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69057348 | |||||||
| chr14:69057348 | AT | A | 8 | a0001c0001t0001g0207 a0001c0001t0001g0229 a0001c0001t0001g0232 others(5): Show |
8 | HG01081.hp1 HG01496.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1075-1738delA | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69057348 | |||||||
| chr14:69057429 | C | G | 1 | a0001c0001t0001g0081 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1075-1818G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69057429 | |||||||
| chr14:69057874 | G | A | 3 | a0001c0004t0003g0030 a0001c0004t0003g0047 a0001c0004t0003g0055 |
3 | HG02135.hp1 NA18945.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1075-2263C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69057874 | |||||||
| chr14:69057959 | T | C | 1 | a0001c0002t0001g0157 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1075-2348A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69057959 | |||||||
| chr14:69058092 | G | A | 71 | a0001c0001t0001g0081 a0001c0001t0002g0011 a0001c0001t0002g0012 others(68): Show |
71 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.1075-2481C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69058092 | |||||||
| chr14:69058166 | T | C | 71 | a0001c0001t0001g0081 a0001c0001t0002g0011 a0001c0001t0002g0012 others(68): Show |
71 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.1075-2555A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69058166 | |||||||
| chr14:69058285 | G | A | 5 | a0001c0001t0002g0090 a0001c0001t0002g0091 a0001c0001t0002g0176 others(2): Show |
5 | HG01081.hp1 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1075-2674C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69058285 | |||||||
| chr14:69058427 | G | A | 27 | a0001c0001t0002g0100 a0001c0001t0002g0101 a0001c0001t0002g0123 others(24): Show |
27 | HG01192.hp2 HG01243.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.1075-2816C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69058427 | |||||||
| chr14:69058537 | C | CAT | 70 | a0001c0001t0001g0081 a0001c0001t0002g0011 a0001c0001t0002g0012 others(67): Show |
70 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.1075-2928_1075-292 others(6): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69058537 | |||||||
| chr14:69058571 | T | C | 9 | a0001c0001t0002g0090 a0001c0001t0002g0091 a0001c0001t0002g0176 others(6): Show |
9 | HG01081.hp1 HG01496.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1075-2960A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69058571 | |||||||
| chr14:69058802 | A | T | 9 | a0001c0001t0002g0090 a0001c0001t0002g0091 a0001c0001t0002g0176 others(6): Show |
9 | HG01081.hp1 HG01496.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1075-3191T>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69058802 | |||||||
| chr14:69058876 | C | CA | 10 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0001g0213 others(7): Show |
10 | HG01192.hp2 HG02257.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1075-3266dupT | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69058876 | |||||||
| chr14:69058876 | CA | C | 7 | a0001c0001t0002g0029 a0001c0001t0002g0074 a0001c0001t0003g0032 others(4): Show |
7 | HG00735.hp1 HG01169.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.1075-3266delT | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69058876 | |||||||
| chr14:69058894 | GAAAGAAA others(7): Show |
G | 1 | a0001c0001t0002g0072 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1075-3297_1075-328 others(18): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69058894 | |||||||
| chr14:69058955 | T | C | 1 | a0001c0001t0002g0235 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1075-3344A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69058955 | |||||||
| chr14:69059191 | C | A | 1 | a0003c0007t0012g0128 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1074+3193G>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69059191 | |||||||
| chr14:69059208 | C | T | 1 | a0001c0001t0002g0235 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1074+3176G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69059208 | |||||||
| chr14:69059210 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1074+3174C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69059210 | |||||||
| chr14:69059219 | A | G | 107 | a0001c0001t0001g0081 a0001c0001t0002g0011 a0001c0001t0002g0012 others(104): Show |
107 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(104): Show |
intron_variant | MODIFIER | c.1074+3165T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69059219 | |||||||
| chr14:69059319 | C | G | 1 | a0001c0001t0002g0235 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1074+3065G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69059319 | |||||||
| chr14:69059367 | G | A | 1 | a0001c0001t0002g0235 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1074+3017C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69059367 | |||||||
| chr14:69059394 | C | T | 1 | a0001c0001t0002g0085 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1074+2990G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69059394 | |||||||
| chr14:69059508 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1074+2876C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69059508 | |||||||
| chr14:69059590 | C | T | 122 | a0001c0001t0001g0081 a0001c0001t0002g0011 a0001c0001t0002g0012 others(119): Show |
122 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(119): Show |
intron_variant | MODIFIER | c.1074+2794G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69059590 | |||||||
| chr14:69059850 | C | T | 28 | a0001c0001t0001g0166 a0001c0001t0006g0003 a0001c0001t0006g0168 others(25): Show |
30 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.1074+2534G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69059850 | |||||||
| chr14:69060307 | A | G | 14 | a0001c0001t0004g0008 a0001c0001t0004g0009 a0001c0001t0004g0010 others(11): Show |
14 | HG01069.hp2 HG01175.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.1074+2077T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69060307 | |||||||
| chr14:69060310 | C | T | 2 | a0001c0001t0001g0207 a0001c0001t0001g0229 |
2 | HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1074+2074G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69060310 | |||||||
| chr14:69060396 | T | C | 1 | a0001c0002t0016g0146 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1074+1988A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69060396 | |||||||
| chr14:69060418 | C | T | 27 | a0001c0001t0002g0100 a0001c0001t0002g0101 a0001c0001t0002g0123 others(24): Show |
27 | HG01192.hp2 HG01243.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.1074+1966G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69060418 | |||||||
| chr14:69060537 | C | CT | 31 | a0001c0001t0001g0004 a0001c0001t0001g0190 a0001c0001t0001g0191 others(28): Show |
32 | HG00642.hp1 HG00741.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.1074+1846dupA | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69060537 | |||||||
| chr14:69060644 | G | A | 1 | a0001c0001t0001g0226 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1074+1740C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69060644 | |||||||
| chr14:69060693 | G | A | 4 | a0001c0001t0007g0095 a0001c0001t0007g0096 a0001c0001t0007g0097 others(1): Show |
4 | HG01074.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1074+1691C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69060693 | |||||||
| chr14:69060757 | C | T | 1 | a0003c0007t0012g0128 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1074+1627G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69060757 | |||||||
| chr14:69060783 | C | G | 4 | a0001c0001t0007g0095 a0001c0001t0007g0096 a0001c0001t0007g0097 others(1): Show |
4 | HG01074.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1074+1601G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69060783 | |||||||
| chr14:69060946 | C | CAAGTT | 189 | a0001c0001t0001g0001 a0001c0001t0001g0081 a0001c0001t0001g0129 others(186): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.1074+1437_1074+143 others(9): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69060946 | |||||||
| chr14:69060997 | T | TA | 4 | a0001c0001t0005g0172 a0001c0001t0005g0173 a0001c0001t0005g0174 others(1): Show |
4 | HG02145.hp1 HG02559.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1074+1386dupT | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69060997 | |||||||
| chr14:69061155 | C | T | 1 | a0001c0001t0002g0235 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1074+1229G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69061155 | |||||||
| chr14:69061328 | C | A | 2 | a0001c0002t0001g0158 a0001c0002t0001g0160 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1074+1056G>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69061328 | |||||||
| chr14:69061480 | T | G | 1 | a0001c0001t0002g0021 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1074+904A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69061480 | |||||||
| chr14:69061538 | A | G | 1 | a0001c0001t0003g0046 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1074+846T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69061538 | |||||||
| chr14:69061669 | C | T | 1 | a0001c0001t0003g0059 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1074+715G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69061669 | |||||||
| chr14:69061828 | C | T | 2 | a0001c0002t0001g0170 a0001c0002t0001g0171 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1074+556G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69061828 | |||||||
| chr14:69061864 | T | C | 1 | a0001c0001t0002g0235 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1074+520A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69061864 | |||||||
| chr14:69061934 | C | T | 1 | a0001c0001t0001g0224 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1074+450G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69061934 | |||||||
| chr14:69062314 | T | C | 23 | a0001c0001t0001g0004 a0001c0001t0001g0190 a0001c0001t0001g0191 others(20): Show |
24 | HG00642.hp1 HG00741.hp1 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.1074+70A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 8/8 | chr14 | 69062314 | |||||||
| chr14:69062665 | AAG | A | 27 | a0001c0001t0002g0100 a0001c0001t0002g0101 a0001c0001t0002g0123 others(24): Show |
27 | HG01192.hp2 HG01243.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.947-156_947-155del others(2): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69062665 | |||||||
| chr14:69062775 | A | G | 9 | a0001c0001t0002g0090 a0001c0001t0002g0091 a0001c0001t0002g0176 others(6): Show |
9 | HG01081.hp1 HG01496.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.947-264T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69062775 | |||||||
| chr14:69062779 | C | G | 23 | a0001c0001t0001g0081 a0001c0001t0002g0029 a0001c0001t0002g0069 others(20): Show |
23 | HG00099.hp1 HG01071.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.947-268G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69062779 | |||||||
| chr14:69062963 | G | A | 1 | a0003c0007t0012g0128 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.947-452C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69062963 | |||||||
| chr14:69063021 | C | A | 1 | a0001c0001t0001g0208 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.947-510G>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69063021 | |||||||
| chr14:69063108 | G | C | 14 | a0001c0001t0004g0008 a0001c0001t0004g0009 a0001c0001t0004g0010 others(11): Show |
14 | HG01069.hp2 HG01175.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.947-597C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69063108 | |||||||
| chr14:69063532 | C | G | 2 | a0001c0001t0003g0092 a0001c0001t0003g0093 |
2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.947-1021G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69063532 | |||||||
| chr14:69063547 | C | T | 1 | a0001c0001t0001g0189 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.947-1036G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69063547 | |||||||
| chr14:69063601 | C | T | 2 | a0001c0001t0003g0092 a0001c0001t0003g0093 |
2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.947-1090G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69063601 | |||||||
| chr14:69063676 | C | T | 1 | a0001c0001t0003g0053 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.947-1165G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69063676 | |||||||
| chr14:69064042 | A | G | 2 | a0001c0001t0003g0092 a0001c0001t0003g0093 |
2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.947-1531T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69064042 | |||||||
| chr14:69064129 | A | T | 14 | a0001c0001t0004g0008 a0001c0001t0004g0009 a0001c0001t0004g0010 others(11): Show |
14 | HG01069.hp2 HG01175.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.947-1618T>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69064129 | |||||||
| chr14:69064332 | C | T | 17 | a0001c0003t0002g0108 a0001c0003t0002g0109 a0001c0003t0002g0111 others(14): Show |
17 | HG01243.hp2 HG01433.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.947-1821G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69064332 | |||||||
| chr14:69064361 | A | T | 1 | a0001c0001t0003g0038 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.947-1850T>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69064361 | |||||||
| chr14:69064918 | G | A | 1 | a0001c0001t0003g0049 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.947-2407C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69064918 | |||||||
| chr14:69065021 | A | G | 4 | a0001c0001t0001g0001 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
5 | HG02647.hp2 HG03130.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.947-2510T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69065021 | |||||||
| chr14:69065022 | T | C | 1 | a0001c0001t0003g0054 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.947-2511A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69065022 | |||||||
| chr14:69065096 | C | CT | 158 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0081 others(155): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.947-2586dupA | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69065096 | |||||||
| chr14:69065096 | C | CTT | 9 | a0001c0001t0001g0192 a0001c0001t0001g0205 a0001c0001t0003g0033 others(6): Show |
9 | HG02602.hp1 HG02896.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.947-2587_947-2586d others(4): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69065096 | |||||||
| chr14:69065096 | C | CTTT | 21 | a0001c0001t0001g0195 a0001c0001t0002g0011 a0001c0001t0002g0012 others(18): Show |
21 | HG01074.hp2 HG01361.hp1 HG02056.hp1 others(18): Show |
intron_variant | MODIFIER | c.947-2588_947-2586d others(5): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69065096 | |||||||
| chr14:69065229 | T | C | 4 | a0001c0001t0004g0183 a0001c0001t0004g0184 a0001c0001t0004g0186 others(1): Show |
4 | HG03041.hp1 HG03471.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.947-2718A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69065229 | |||||||
| chr14:69065253 | T | C | 33 | a0001c0001t0001g0001 a0001c0001t0001g0129 a0001c0001t0001g0130 others(30): Show |
34 | HG01192.hp2 HG01243.hp2 HG01433.hp2 others(31): Show |
intron_variant | MODIFIER | c.947-2742A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69065253 | |||||||
| chr14:69065347 | G | C | 2 | a0001c0001t0003g0092 a0001c0001t0003g0093 |
2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.947-2836C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69065347 | |||||||
| chr14:69065374 | C | T | 12 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(9): Show |
12 | HG00280.hp2 HG00738.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.947-2863G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69065374 | |||||||
| chr14:69065522 | A | C | 1 | a0001c0001t0001g0226 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.947-3011T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69065522 | |||||||
| chr14:69065674 | G | A | 43 | a0001c0001t0002g0035 a0001c0001t0002g0074 a0001c0001t0003g0026 others(40): Show |
43 | HG00140.hp2 HG00735.hp1 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.947-3163C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69065674 | |||||||
| chr14:69065823 | T | C | 1 | a0001c0001t0014g0094 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.947-3312A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69065823 | |||||||
| chr14:69066259 | C | T | 2 | a0001c0001t0003g0092 a0001c0001t0003g0093 |
2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.947-3748G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69066259 | |||||||
| chr14:69066292 | G | A | 4 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(1): Show |
4 | HG00733.hp2 HG01106.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.947-3781C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69066292 | |||||||
| chr14:69066368 | C | T | 1 | a0001c0001t0002g0178 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.947-3857G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69066368 | |||||||
| chr14:69066417 | G | C | 1 | a0001c0001t0001g0132 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.947-3906C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69066417 | |||||||
| chr14:69066625 | G | A | 19 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(16): Show |
19 | HG01361.hp1 HG02055.hp1 HG02056.hp1 others(16): Show |
intron_variant | MODIFIER | c.947-4114C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69066625 | |||||||
| chr14:69066668 | T | C | 3 | a0001c0001t0002g0075 a0001c0001t0002g0076 a0001c0001t0002g0077 |
3 | HG01346.hp1 HG03540.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.947-4157A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69066668 | |||||||
| chr14:69066910 | C | T | 2 | a0001c0001t0003g0092 a0001c0001t0003g0093 |
2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.947-4399G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69066910 | |||||||
| chr14:69067093 | C | G | 6 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(3): Show |
6 | HG00733.hp2 HG01106.hp2 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.947-4582G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69067093 | |||||||
| chr14:69067097 | G | A | 1 | a0001c0003t0002g0124 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.947-4586C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69067097 | |||||||
| chr14:69067120 | T | C | 82 | a0001c0001t0001g0081 a0001c0001t0001g0190 a0001c0001t0001g0191 others(79): Show |
82 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.947-4609A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69067120 | |||||||
| chr14:69067156 | A | T | 5 | a0001c0001t0007g0095 a0001c0001t0007g0097 a0001c0003t0002g0102 others(2): Show |
5 | HG01074.hp2 HG02818.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.947-4645T>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69067156 | |||||||
| chr14:69067222 | G | T | 1 | a0001c0002t0001g0155 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.947-4711C>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69067222 | |||||||
| chr14:69067337 | C | CT | 30 | a0001c0001t0001g0134 a0001c0001t0001g0202 a0001c0001t0001g0226 others(27): Show |
30 | HG01069.hp2 HG01081.hp1 HG01258.hp1 others(27): Show |
intron_variant | MODIFIER | c.947-4827dupA | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69067337 | |||||||
| chr14:69067337 | C | CTT | 14 | a0001c0001t0004g0008 a0001c0001t0004g0009 a0001c0001t0004g0179 others(11): Show |
14 | HG01175.hp2 HG01192.hp1 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.947-4828_947-4827d others(4): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69067337 | |||||||
| chr14:69067337 | CT | C | 21 | a0001c0001t0001g0004 a0001c0001t0001g0190 a0001c0001t0001g0191 others(18): Show |
22 | HG00642.hp1 HG00741.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.947-4827delA | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69067337 | |||||||
| chr14:69067337 | CTTTTTTT others(1): Show |
C | 28 | a0001c0001t0002g0100 a0001c0001t0002g0101 a0001c0001t0002g0123 others(25): Show |
28 | HG01192.hp2 HG01243.hp2 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.947-4834_947-4827d others(10): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69067337 | |||||||
| chr14:69067337 | CTTTTTTT others(3): Show |
C | 67 | a0001c0001t0001g0081 a0001c0001t0002g0020 a0001c0001t0002g0029 others(64): Show |
67 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.947-4836_947-4827d others(12): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69067337 | |||||||
| chr14:69067337 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0002g0085 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.947-4837_947-4827d others(13): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69067337 | |||||||
| chr14:69067582 | C | T | 2 | a0001c0001t0003g0092 a0001c0001t0003g0093 |
2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.947-5071G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69067582 | |||||||
| chr14:69067656 | T | C | 4 | a0001c0001t0007g0095 a0001c0001t0007g0096 a0001c0001t0007g0097 others(1): Show |
4 | HG01074.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.947-5145A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69067656 | |||||||
| chr14:69067706 | G | A | 2 | a0001c0001t0003g0092 a0001c0001t0003g0093 |
2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.947-5195C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69067706 | |||||||
| chr14:69067739 | C | T | 1 | a0001c0001t0013g0099 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.947-5228G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69067739 | |||||||
| chr14:69067829 | G | A | 1 | a0003c0007t0012g0128 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.947-5318C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69067829 | |||||||
| chr14:69068126 | C | G | 1 | a0001c0001t0014g0094 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.947-5615G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69068126 | |||||||
| chr14:69068265 | T | A | 67 | a0001c0001t0001g0081 a0001c0001t0002g0029 a0001c0001t0002g0035 others(64): Show |
67 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.947-5754A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69068265 | |||||||
| chr14:69068344 | G | A | 3 | a0001c0001t0006g0003 a0001c0001t0006g0168 a0001c0001t0006g0169 |
4 | HG02280.hp1 HG02451.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.947-5833C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69068344 | |||||||
| chr14:69068388 | C | A | 1 | a0001c0001t0002g0235 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.947-5877G>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69068388 | |||||||
| chr14:69068405 | G | A | 2 | a0001c0001t0002g0035 a0001c0006t0003g0006 |
2 | HG00741.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.947-5894C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69068405 | |||||||
| chr14:69068639 | G | A | 1 | a0001c0001t0002g0235 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.947-6128C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69068639 | |||||||
| chr14:69068647 | G | A | 1 | a0001c0003t0002g0113 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.947-6136C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69068647 | |||||||
| chr14:69068698 | C | CA | 18 | a0001c0001t0001g0214 a0001c0001t0002g0035 a0001c0001t0002g0087 others(15): Show |
18 | HG00735.hp2 HG01074.hp2 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.947-6188dupT | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69068698 | |||||||
| chr14:69068698 | C | CAA | 43 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(40): Show |
44 | HG01243.hp2 HG01361.hp1 HG01433.hp2 others(41): Show |
intron_variant | MODIFIER | c.947-6189_947-6188d others(4): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69068698 | |||||||
| chr14:69068773 | A | T | 1 | a0001c0001t0013g0099 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.947-6262T>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69068773 | |||||||
| chr14:69068835 | A | G | 4 | a0001c0001t0007g0095 a0001c0001t0007g0096 a0001c0001t0007g0097 others(1): Show |
4 | HG01074.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.947-6324T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69068835 | |||||||
| chr14:69068882 | T | G | 1 | a0001c0001t0011g0236 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.947-6371A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69068882 | |||||||
| chr14:69068952 | A | C | 2 | a0001c0001t0011g0236 a0001c0001t0011g0237 |
2 | HG03486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.946+6393T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69068952 | |||||||
| chr14:69069098 | T | C | 12 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(9): Show |
12 | HG00280.hp2 HG00738.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.946+6247A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69069098 | |||||||
| chr14:69069242 | T | C | 1 | a0001c0001t0001g0194 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.946+6103A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69069242 | |||||||
| chr14:69069721 | C | T | 2 | a0001c0001t0003g0092 a0001c0001t0003g0093 |
2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.946+5624G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69069721 | |||||||
| chr14:69070050 | G | C | 27 | a0001c0001t0002g0100 a0001c0001t0002g0101 a0001c0001t0002g0123 others(24): Show |
27 | HG01192.hp2 HG01243.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.946+5295C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69070050 | |||||||
| chr14:69070053 | A | G | 27 | a0001c0001t0002g0100 a0001c0001t0002g0101 a0001c0001t0002g0123 others(24): Show |
27 | HG01192.hp2 HG01243.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.946+5292T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69070053 | |||||||
| chr14:69070238 | A | C | 4 | a0001c0001t0003g0042 a0001c0001t0003g0044 a0001c0001t0003g0046 others(1): Show |
4 | HG02602.hp2 HG02735.hp2 NA18940.hp2 others(1): Show |
intron_variant | MODIFIER | c.946+5107T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69070238 | |||||||
| chr14:69070492 | G | A | 72 | a0001c0001t0001g0081 a0001c0001t0002g0011 a0001c0001t0002g0012 others(69): Show |
72 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.946+4853C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69070492 | |||||||
| chr14:69070790 | CT | C | 26 | a0001c0001t0001g0166 a0001c0001t0002g0071 a0001c0001t0006g0003 others(23): Show |
28 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.946+4554delA | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69070790 | |||||||
| chr14:69070856 | G | A | 1 | a0001c0001t0002g0235 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.946+4489C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69070856 | |||||||
| chr14:69070922 | C | T | 2 | a0001c0002t0001g0162 a0001c0002t0001g0163 |
2 | HG00735.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.946+4423G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69070922 | |||||||
| chr14:69070939 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.946+4406C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69070939 | |||||||
| chr14:69071061 | G | A | 1 | a0001c0001t0014g0094 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.946+4284C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69071061 | |||||||
| chr14:69072005 | T | C | 1 | a0001c0001t0002g0078 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.946+3340A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69072005 | |||||||
| chr14:69072009 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.946+3336G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69072009 | |||||||
| chr14:69072093 | C | A | 2 | a0001c0001t0002g0100 a0001c0001t0002g0101 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.946+3252G>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69072093 | |||||||
| chr14:69072288 | T | C | 1 | a0001c0001t0001g0166 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.946+3057A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69072288 | |||||||
| chr14:69072335 | T | C | 1 | a0001c0001t0002g0025 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.946+3010A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69072335 | |||||||
| chr14:69072426 | A | G | 27 | a0001c0001t0002g0100 a0001c0001t0002g0101 a0001c0001t0002g0123 others(24): Show |
27 | HG01192.hp2 HG01243.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.946+2919T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69072426 | |||||||
| chr14:69072550 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.946+2795A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69072550 | |||||||
| chr14:69072623 | TA | T | 68 | a0001c0001t0001g0004 a0001c0001t0001g0132 a0001c0001t0001g0134 others(65): Show |
69 | HG00280.hp2 HG00642.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.946+2721delT | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69072623 | |||||||
| chr14:69072623 | TAA | T | 40 | a0001c0001t0001g0001 a0001c0001t0001g0081 a0001c0001t0001g0129 others(37): Show |
41 | HG00099.hp1 HG01069.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.946+2720_946+2721d others(4): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69072623 | |||||||
| chr14:69072623 | TAAA | T | 72 | a0001c0001t0001g0166 a0001c0001t0001g0204 a0001c0001t0001g0205 others(69): Show |
74 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.946+2719_946+2721d others(5): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69072623 | |||||||
| chr14:69072623 | TAAAA | T | 30 | a0001c0001t0002g0100 a0001c0001t0002g0101 a0001c0001t0002g0123 others(27): Show |
30 | HG01192.hp2 HG01243.hp2 HG01433.hp2 others(27): Show |
intron_variant | MODIFIER | c.946+2718_946+2721d others(6): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69072623 | |||||||
| chr14:69072636 | A | C | 21 | a0001c0001t0001g0004 a0001c0001t0001g0190 a0001c0001t0001g0191 others(18): Show |
22 | HG00642.hp1 HG00741.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.946+2709T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69072636 | |||||||
| chr14:69072723 | C | T | 6 | a0001c0002t0001g0151 a0001c0002t0001g0155 a0001c0002t0001g0158 others(3): Show |
6 | HG00280.hp1 HG01081.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.946+2622G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69072723 | |||||||
| chr14:69072800 | A | T | 4 | a0001c0001t0007g0095 a0001c0001t0007g0096 a0001c0001t0007g0097 others(1): Show |
4 | HG01074.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.946+2545T>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69072800 | |||||||
| chr14:69073331 | A | G | 2 | a0001c0001t0003g0092 a0001c0001t0003g0093 |
2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.946+2014T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69073331 | |||||||
| chr14:69073481 | T | G | 1 | a0001c0001t0001g0197 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.946+1864A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69073481 | |||||||
| chr14:69073667 | AAGAAAGC others(7): Show |
A | 1 | a0001c0001t0002g0123 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.946+1664_946+1677d others(16): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69073667 | |||||||
| chr14:69073763 | C | T | 6 | a0001c0001t0002g0074 a0001c0001t0003g0032 a0001c0001t0003g0034 others(3): Show |
6 | HG00735.hp1 HG01169.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.946+1582G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69073763 | |||||||
| chr14:69073771 | G | A | 4 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0002t0001g0162 others(1): Show |
4 | HG00735.hp2 HG03942.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.946+1574C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69073771 | |||||||
| chr14:69074034 | C | T | 12 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(9): Show |
12 | HG00280.hp2 HG00738.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.946+1311G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69074034 | |||||||
| chr14:69074090 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.946+1255C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69074090 | |||||||
| chr14:69074091 | T | G | 1 | a0001c0003t0002g0110 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.946+1254A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69074091 | |||||||
| chr14:69074478 | T | A | 5 | a0001c0001t0002g0090 a0001c0001t0002g0091 a0001c0001t0002g0176 others(2): Show |
5 | HG01081.hp1 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.946+867A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69074478 | |||||||
| chr14:69074620 | T | C | 2 | a0001c0001t0001g0194 a0001c0001t0001g0196 |
2 | HG00741.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.946+725A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69074620 | |||||||
| chr14:69074837 | C | T | 4 | a0001c0001t0001g0001 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
5 | HG02647.hp2 HG03130.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.946+508G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69074837 | |||||||
| chr14:69074844 | G | C | 1 | a0001c0001t0014g0094 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.946+501C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69074844 | |||||||
| chr14:69075034 | C | CA | 55 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(52): Show |
55 | HG00140.hp2 HG01074.hp2 HG01192.hp2 others(52): Show |
intron_variant | MODIFIER | c.946+310dupT | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69075034 | |||||||
| chr14:69075114 | A | C | 1 | a0001c0001t0002g0235 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.946+231T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69075114 | |||||||
| chr14:69075239 | A | G | 50 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(47): Show |
50 | HG01074.hp2 HG01192.hp2 HG01243.hp2 others(47): Show |
intron_variant | MODIFIER | c.946+106T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69075239 | |||||||
| chr14:69075288 | T | C | 2 | a0001c0001t0003g0092 a0001c0001t0003g0093 |
2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.946+57A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 7/8 | chr14 | 69075288 | |||||||
| chr14:69075443 | A | C | 5 | a0001c0003t0002g0102 a0001c0003t0002g0103 a0001c0003t0002g0104 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.880-32T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69075443 | |||||||
| chr14:69075449 | T | C | 1 | a0001c0001t0002g0235 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.880-38A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69075449 | |||||||
| chr14:69075644 | G | C | 1 | a0001c0001t0001g0201 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.880-233C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69075644 | |||||||
| chr14:69076025 | G | T | 68 | a0001c0001t0001g0081 a0001c0001t0002g0029 a0001c0001t0002g0035 others(65): Show |
68 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.880-614C>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69076025 | |||||||
| chr14:69076116 | C | CA | 20 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(17): Show |
20 | HG01361.hp1 HG02055.hp1 HG02056.hp1 others(17): Show |
intron_variant | MODIFIER | c.880-706dupT | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69076116 | |||||||
| chr14:69076183 | G | C | 23 | a0001c0001t0001g0004 a0001c0001t0001g0190 a0001c0001t0001g0191 others(20): Show |
24 | HG00642.hp1 HG00741.hp1 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.880-772C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69076183 | |||||||
| chr14:69076187 | G | T | 2 | a0001c0001t0001g0131 a0001c0001t0001g0211 |
2 | HG02572.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.880-776C>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69076187 | |||||||
| chr14:69076265 | A | G | 17 | a0001c0003t0002g0108 a0001c0003t0002g0109 a0001c0003t0002g0111 others(14): Show |
17 | HG01243.hp2 HG01433.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.880-854T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69076265 | |||||||
| chr14:69076349 | G | C | 1 | a0001c0001t0002g0126 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.880-938C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69076349 | |||||||
| chr14:69076365 | T | C | 2 | a0001c0001t0003g0027 a0001c0001t0003g0051 |
2 | HG01433.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.880-954A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69076365 | |||||||
| chr14:69076401 | T | C | 2 | a0001c0001t0003g0092 a0001c0001t0003g0093 |
2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.880-990A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69076401 | |||||||
| chr14:69076467 | T | C | 74 | a0001c0001t0001g0081 a0001c0001t0002g0011 a0001c0001t0002g0012 others(71): Show |
74 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.880-1056A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69076467 | |||||||
| chr14:69076507 | G | A | 70 | a0001c0001t0001g0081 a0001c0001t0002g0029 a0001c0001t0002g0035 others(67): Show |
70 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.880-1096C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69076507 | |||||||
| chr14:69076550 | G | T | 1 | a0001c0001t0003g0033 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.880-1139C>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69076550 | |||||||
| chr14:69076726 | T | C | 2 | a0001c0001t0001g0216 a0001c0001t0001g0217 |
2 | HG02109.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.880-1315A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69076726 | |||||||
| chr14:69076771 | G | T | 4 | a0001c0001t0001g0001 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
5 | HG02647.hp2 HG03130.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.880-1360C>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69076771 | |||||||
| chr14:69076899 | A | G | 1 | a0001c0001t0002g0126 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.880-1488T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69076899 | |||||||
| chr14:69077011 | G | A | 1 | a0001c0001t0002g0127 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.880-1600C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69077011 | |||||||
| chr14:69077336 | G | A | 3 | a0001c0001t0001g0131 a0001c0001t0001g0189 a0001c0001t0001g0211 |
3 | HG02572.hp2 HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.880-1925C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69077336 | |||||||
| chr14:69077365 | C | CTTAT | 46 | a0001c0001t0001g0001 a0001c0001t0001g0129 a0001c0001t0001g0130 others(43): Show |
47 | HG00733.hp1 HG00741.hp1 HG01192.hp2 others(44): Show |
intron_variant | MODIFIER | c.880-1958_880-1955d others(6): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69077365 | |||||||
| chr14:69077365 | C | CTTATTTA others(1): Show |
56 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(53): Show |
58 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.880-1962_880-1955d others(10): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69077365 | |||||||
| chr14:69077365 | C | CTTATTTA others(5): Show |
17 | a0001c0001t0001g0166 a0001c0001t0001g0197 a0001c0001t0002g0015 others(14): Show |
17 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.880-1966_880-1955d others(14): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69077365 | |||||||
| chr14:69077365 | C | CTTATTTA others(9): Show |
10 | a0001c0001t0001g0134 a0001c0001t0002g0090 a0001c0001t0002g0091 others(7): Show |
10 | HG01081.hp1 HG01496.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.880-1970_880-1955d others(18): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69077365 | |||||||
| chr14:69077365 | C | CTTATTTA others(13): Show |
2 | a0001c0001t0004g0183 a0001c0001t0004g0186 |
2 | HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.880-1974_880-1955d others(22): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69077365 | |||||||
| chr14:69077365 | CTTAT | C | 13 | a0001c0001t0001g0004 a0001c0001t0001g0191 a0001c0001t0001g0199 others(10): Show |
14 | HG00642.hp1 HG01074.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.880-1958_880-1955d others(6): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69077365 | |||||||
| chr14:69077365 | CTTATTTA others(1): Show |
C | 72 | a0001c0001t0001g0081 a0001c0001t0002g0011 a0001c0001t0002g0012 others(69): Show |
72 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.880-1962_880-1955d others(10): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69077365 | |||||||
| chr14:69077556 | T | G | 23 | a0001c0001t0001g0004 a0001c0001t0001g0190 a0001c0001t0001g0191 others(20): Show |
24 | HG00642.hp1 HG00741.hp1 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.880-2145A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69077556 | |||||||
| chr14:69078084 | A | G | 1 | a0001c0001t0002g0235 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.880-2673T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69078084 | |||||||
| chr14:69078152 | A | G | 1 | a0001c0001t0003g0041 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.880-2741T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69078152 | |||||||
| chr14:69078315 | T | G | 2 | a0001c0001t0003g0027 a0001c0001t0003g0051 |
2 | HG01433.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.880-2904A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69078315 | |||||||
| chr14:69078351 | T | A | 4 | a0001c0001t0007g0095 a0001c0001t0007g0096 a0001c0001t0007g0097 others(1): Show |
4 | HG01074.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.880-2940A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69078351 | |||||||
| chr14:69078950 | C | T | 2 | a0001c0001t0003g0092 a0001c0001t0003g0093 |
2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.880-3539G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69078950 | |||||||
| chr14:69078976 | C | G | 23 | a0001c0001t0001g0004 a0001c0001t0001g0190 a0001c0001t0001g0191 others(20): Show |
24 | HG00642.hp1 HG00741.hp1 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.880-3565G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69078976 | |||||||
| chr14:69079049 | C | T | 12 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(9): Show |
12 | HG00280.hp2 HG00738.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.880-3638G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69079049 | |||||||
| chr14:69079081 | GC | G | 40 | a0001c0001t0001g0166 a0001c0001t0004g0008 a0001c0001t0004g0009 others(37): Show |
42 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.880-3671delG | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69079081 | |||||||
| chr14:69079354 | A | T | 2 | a0001c0001t0003g0092 a0001c0001t0003g0093 |
2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.880-3943T>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69079354 | |||||||
| chr14:69079450 | T | C | 2 | a0001c0002t0001g0170 a0001c0002t0001g0171 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.880-4039A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69079450 | |||||||
| chr14:69079786 | T | C | 2 | a0001c0001t0002g0079 a0001c0001t0002g0087 |
2 | NA18949.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.880-4375A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69079786 | |||||||
| chr14:69079900 | G | T | 5 | a0001c0001t0002g0090 a0001c0001t0002g0091 a0001c0001t0002g0176 others(2): Show |
5 | HG01081.hp1 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.880-4489C>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69079900 | |||||||
| chr14:69079905 | C | T | 5 | a0001c0001t0002g0090 a0001c0001t0002g0091 a0001c0001t0002g0176 others(2): Show |
5 | HG01081.hp1 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.880-4494G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69079905 | |||||||
| chr14:69079944 | G | A | 7 | a0001c0001t0004g0008 a0001c0001t0004g0009 a0001c0001t0004g0010 others(4): Show |
7 | HG01069.hp2 HG01192.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.880-4533C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69079944 | |||||||
| chr14:69079970 | C | T | 1 | a0001c0001t0014g0094 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.880-4559G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69079970 | |||||||
| chr14:69080095 | T | C | 9 | a0001c0001t0002g0090 a0001c0001t0002g0091 a0001c0001t0002g0176 others(6): Show |
9 | HG01081.hp1 HG01496.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.880-4684A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69080095 | |||||||
| chr14:69080331 | C | T | 12 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(9): Show |
12 | HG00280.hp2 HG00738.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.880-4920G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69080331 | |||||||
| chr14:69080421 | C | T | 1 | a0001c0001t0013g0099 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.880-5010G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69080421 | |||||||
| chr14:69080502 | A | G | 5 | a0001c0001t0002g0090 a0001c0001t0002g0091 a0001c0001t0002g0176 others(2): Show |
5 | HG01081.hp1 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.880-5091T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69080502 | |||||||
| chr14:69080561 | C | T | 1 | a0001c0001t0013g0099 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.880-5150G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69080561 | |||||||
| chr14:69080562 | T | C | 4 | a0001c0001t0005g0172 a0001c0001t0005g0173 a0001c0001t0005g0174 others(1): Show |
4 | HG02145.hp1 HG02559.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.880-5151A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69080562 | |||||||
| chr14:69081050 | AAAT | A | 9 | a0001c0001t0002g0090 a0001c0001t0002g0091 a0001c0001t0002g0176 others(6): Show |
9 | HG01081.hp1 HG01496.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.880-5642_880-5640d others(5): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69081050 | |||||||
| chr14:69081068 | GA | G | 25 | a0001c0001t0002g0123 a0001c0003t0002g0102 a0001c0003t0002g0103 others(22): Show |
25 | HG01192.hp2 HG01243.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.880-5658delT | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69081068 | |||||||
| chr14:69081113 | C | T | 1 | a0001c0003t0002g0108 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.880-5702G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69081113 | |||||||
| chr14:69081468 | G | A | 3 | a0001c0001t0006g0003 a0001c0001t0006g0168 a0001c0001t0006g0169 |
4 | HG02280.hp1 HG02451.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.880-6057C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69081468 | |||||||
| chr14:69081746 | T | C | 1 | a0001c0001t0001g0233 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.880-6335A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69081746 | |||||||
| chr14:69081752 | ATGTG | A | 67 | a0001c0001t0001g0081 a0001c0001t0002g0029 a0001c0001t0002g0035 others(64): Show |
67 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.880-6345_880-6342d others(6): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69081752 | |||||||
| chr14:69081920 | T | C | 1 | a0001c0001t0013g0099 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.880-6509A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69081920 | |||||||
| chr14:69082168 | T | G | 67 | a0001c0001t0001g0081 a0001c0001t0002g0029 a0001c0001t0002g0035 others(64): Show |
67 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.880-6757A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69082168 | |||||||
| chr14:69082287 | C | T | 159 | a0001c0001t0001g0081 a0001c0001t0001g0166 a0001c0001t0002g0011 others(156): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.880-6876G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69082287 | |||||||
| chr14:69082465 | T | TATTA | 212 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0081 others(209): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.880-7058_880-7055d others(6): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69082465 | |||||||
| chr14:69082722 | T | C | 1 | a0001c0001t0002g0235 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.880-7311A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69082722 | |||||||
| chr14:69082892 | T | C | 18 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(15): Show |
18 | HG01361.hp1 HG02055.hp1 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.880-7481A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69082892 | |||||||
| chr14:69082988 | C | T | 9 | a0001c0001t0002g0090 a0001c0001t0002g0091 a0001c0001t0002g0176 others(6): Show |
9 | HG01081.hp1 HG01496.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.880-7577G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69082988 | |||||||
| chr14:69083023 | T | C | 44 | a0001c0001t0002g0035 a0001c0001t0002g0056 a0001c0001t0002g0074 others(41): Show |
44 | HG00140.hp2 HG00735.hp1 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.880-7612A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69083023 | |||||||
| chr14:69083045 | C | T | 159 | a0001c0001t0001g0081 a0001c0001t0001g0166 a0001c0001t0002g0011 others(156): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.880-7634G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69083045 | |||||||
| chr14:69083247 | C | T | 67 | a0001c0001t0001g0081 a0001c0001t0002g0029 a0001c0001t0002g0035 others(64): Show |
67 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.880-7836G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69083247 | |||||||
| chr14:69083299 | A | G | 4 | a0001c0001t0001g0001 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
5 | HG02647.hp2 HG03130.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.880-7888T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69083299 | |||||||
| chr14:69083343 | C | T | 1 | a0001c0001t0013g0099 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.880-7932G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69083343 | |||||||
| chr14:69083463 | G | A | 2 | a0001c0001t0003g0092 a0001c0001t0003g0093 |
2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.880-8052C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69083463 | |||||||
| chr14:69083610 | T | C | 231 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0081 others(228): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.879+8064A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69083610 | |||||||
| chr14:69083634 | T | C | 1 | a0001c0001t0013g0099 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.879+8040A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69083634 | |||||||
| chr14:69084070 | C | T | 1 | a0001c0001t0002g0088 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.879+7604G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69084070 | |||||||
| chr14:69084234 | T | C | 1 | a0001c0001t0002g0235 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.879+7440A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69084234 | |||||||
| chr14:69084395 | G | T | 2 | a0001c0001t0003g0092 a0001c0001t0003g0093 |
2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.879+7279C>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69084395 | |||||||
| chr14:69084544 | T | A | 5 | a0001c0003t0002g0102 a0001c0003t0002g0103 a0001c0003t0002g0104 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.879+7130A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69084544 | |||||||
| chr14:69084614 | T | C | 1 | a0001c0001t0002g0075 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.879+7060A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69084614 | |||||||
| chr14:69085314 | C | T | 1 | a0001c0001t0014g0094 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.879+6360G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69085314 | |||||||
| chr14:69085433 | A | C | 2 | a0001c0002t0001g0151 a0001c0002t0001g0159 |
2 | HG01081.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.879+6241T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69085433 | |||||||
| chr14:69085640 | T | C | 7 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(4): Show |
7 | HG00140.hp1 HG02135.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.879+6034A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69085640 | |||||||
| chr14:69085889 | A | G | 2 | a0001c0001t0002g0075 a0001c0001t0002g0076 |
2 | HG01346.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.879+5785T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69085889 | |||||||
| chr14:69086069 | A | G | 1 | a0001c0001t0002g0069 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.879+5605T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69086069 | |||||||
| chr14:69086251 | C | T | 1 | a0001c0001t0001g0226 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.879+5423G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69086251 | |||||||
| chr14:69086339 | T | C | 2 | a0001c0001t0003g0092 a0001c0001t0003g0093 |
2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.879+5335A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69086339 | |||||||
| chr14:69086410 | A | G | 173 | a0001c0001t0001g0081 a0001c0001t0001g0166 a0001c0001t0002g0011 others(170): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.879+5264T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69086410 | |||||||
| chr14:69086474 | A | G | 1 | a0001c0001t0014g0094 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.879+5200T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69086474 | |||||||
| chr14:69086483 | T | C | 1 | a0001c0001t0009g0016 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.879+5191A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69086483 | |||||||
| chr14:69086504 | G | T | 3 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 |
3 | HG00140.hp2 HG01258.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.879+5170C>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69086504 | |||||||
| chr14:69086517 | G | A | 1 | a0001c0001t0003g0049 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.879+5157C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69086517 | |||||||
| chr14:69086564 | G | A | 1 | a0001c0002t0016g0146 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.879+5110C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69086564 | |||||||
| chr14:69086605 | C | T | 1 | a0001c0001t0002g0084 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.879+5069G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69086605 | |||||||
| chr14:69086606 | G | A | 12 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(9): Show |
12 | HG00280.hp2 HG00738.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.879+5068C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69086606 | |||||||
| chr14:69086620 | T | TA | 5 | a0001c0001t0002g0090 a0001c0001t0002g0091 a0001c0001t0002g0176 others(2): Show |
5 | HG01081.hp1 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.879+5053dupT | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69086620 | |||||||
| chr14:69086620 | TA | T | 116 | a0001c0001t0001g0081 a0001c0001t0001g0192 a0001c0001t0002g0007 others(113): Show |
116 | HG00140.hp2 HG00735.hp1 HG00738.hp1 others(113): Show |
intron_variant | MODIFIER | c.879+5053delT | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69086620 | |||||||
| chr14:69086620 | TAA | T | 6 | a0001c0001t0002g0073 a0001c0001t0002g0100 a0001c0001t0002g0101 others(3): Show |
6 | HG01943.hp1 HG02886.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.879+5052_879+5053d others(4): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69086620 | |||||||
| chr14:69086621 | A | T | 1 | a0001c0001t0002g0088 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.879+5053T>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69086621 | |||||||
| chr14:69086622 | A | T | 69 | a0001c0001t0001g0081 a0001c0001t0002g0011 a0001c0001t0002g0012 others(66): Show |
69 | HG00140.hp2 HG00735.hp1 HG00738.hp1 others(66): Show |
intron_variant | MODIFIER | c.879+5052T>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69086622 | |||||||
| chr14:69086623 | A | T | 1 | a0001c0001t0002g0073 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.879+5051T>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69086623 | |||||||
| chr14:69086688 | C | G | 164 | a0001c0001t0001g0081 a0001c0001t0001g0166 a0001c0001t0002g0011 others(161): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.879+4986G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69086688 | |||||||
| chr14:69086703 | T | C | 173 | a0001c0001t0001g0081 a0001c0001t0001g0166 a0001c0001t0002g0011 others(170): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.879+4971A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69086703 | |||||||
| chr14:69086721 | G | A | 159 | a0001c0001t0001g0081 a0001c0001t0001g0166 a0001c0001t0002g0011 others(156): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.879+4953C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69086721 | |||||||
| chr14:69086766 | C | A | 1 | a0003c0007t0012g0128 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.879+4908G>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69086766 | |||||||
| chr14:69086960 | C | A | 1 | a0001c0001t0001g0228 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.879+4714G>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69086960 | |||||||
| chr14:69087266 | C | A | 1 | a0001c0001t0002g0088 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.879+4408G>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69087266 | |||||||
| chr14:69087456 | G | C | 14 | a0001c0001t0004g0008 a0001c0001t0004g0009 a0001c0001t0004g0010 others(11): Show |
14 | HG01069.hp2 HG01175.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.879+4218C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69087456 | |||||||
| chr14:69087518 | T | C | 7 | a0001c0001t0004g0008 a0001c0001t0004g0009 a0001c0001t0004g0010 others(4): Show |
7 | HG01069.hp2 HG01192.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.879+4156A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69087518 | |||||||
| chr14:69087617 | G | T | 1 | a0001c0001t0001g0228 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.879+4057C>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69087617 | |||||||
| chr14:69087776 | G | A | 2 | a0001c0002t0001g0148 a0001c0002t0001g0152 |
2 | HG03669.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.879+3898C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69087776 | |||||||
| chr14:69087807 | C | G | 2 | a0001c0001t0003g0092 a0001c0001t0003g0093 |
2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.879+3867G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69087807 | |||||||
| chr14:69088144 | T | A | 42 | a0001c0001t0001g0166 a0001c0001t0004g0008 a0001c0001t0004g0009 others(39): Show |
44 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.879+3530A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69088144 | |||||||
| chr14:69088275 | G | T | 4 | a0001c0001t0007g0095 a0001c0001t0007g0096 a0001c0001t0007g0097 others(1): Show |
4 | HG01074.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.879+3399C>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69088275 | |||||||
| chr14:69088336 | GAAAGA | G | 5 | a0001c0003t0002g0102 a0001c0003t0002g0103 a0001c0003t0002g0104 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.879+3333_879+3337d others(7): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69088336 | |||||||
| chr14:69088989 | C | CA | 212 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0081 others(209): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.879+2684dupT | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69088989 | |||||||
| chr14:69089145 | G | A | 1 | a0001c0001t0017g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.879+2529C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69089145 | |||||||
| chr14:69089149 | G | C | 71 | a0001c0001t0001g0081 a0001c0001t0002g0011 a0001c0001t0002g0012 others(68): Show |
71 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.879+2525C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69089149 | |||||||
| chr14:69089157 | T | G | 1 | a0001c0001t0001g0134 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.879+2517A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69089157 | |||||||
| chr14:69089224 | T | C | 71 | a0001c0001t0001g0081 a0001c0001t0002g0011 a0001c0001t0002g0012 others(68): Show |
71 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.879+2450A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69089224 | |||||||
| chr14:69089276 | T | C | 1 | a0001c0001t0006g0169 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.879+2398A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69089276 | |||||||
| chr14:69089319 | A | C | 1 | a0001c0001t0003g0026 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.879+2355T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69089319 | |||||||
| chr14:69089466 | TTGTC | T | 14 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0002g0018 others(11): Show |
14 | HG01361.hp1 HG02055.hp1 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.879+2204_879+2207d others(6): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69089466 | |||||||
| chr14:69089469 | T | C | 4 | a0001c0001t0005g0172 a0001c0001t0005g0173 a0001c0001t0005g0174 others(1): Show |
4 | HG02145.hp1 HG02559.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.879+2205A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69089469 | |||||||
| chr14:69089548 | G | A | 1 | a0001c0001t0002g0035 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.879+2126C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69089548 | |||||||
| chr14:69089937 | T | C | 4 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(1): Show |
4 | HG02083.hp1 HG02165.hp1 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.879+1737A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69089937 | |||||||
| chr14:69089988 | A | G | 1 | a0001c0003t0002g0122 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.879+1686T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69089988 | |||||||
| chr14:69090033 | T | G | 1 | a0001c0001t0002g0127 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.879+1641A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69090033 | |||||||
| chr14:69090070 | T | A | 1 | a0001c0001t0002g0127 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.879+1604A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69090070 | |||||||
| chr14:69090151 | A | G | 2 | a0001c0001t0003g0092 a0001c0001t0003g0093 |
2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.879+1523T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69090151 | |||||||
| chr14:69090447 | G | T | 1 | a0001c0001t0014g0094 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.879+1227C>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69090447 | |||||||
| chr14:69090668 | G | A | 2 | a0001c0001t0003g0058 a0001c0001t0003g0059 |
2 | NA19070.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.879+1006C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69090668 | |||||||
| chr14:69090885 | G | C | 1 | a0001c0002t0001g0002 | 2 | HG00642.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.879+789C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69090885 | |||||||
| chr14:69091639 | A | G | 1 | a0001c0001t0003g0044 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.879+35T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 6/8 | chr14 | 69091639 | |||||||
| chr14:69091961 | T | C | 230 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0081 others(227): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.666-74A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69091961 | |||||||
| chr14:69092012 | T | C | 1 | a0001c0001t0013g0099 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.666-125A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69092012 | |||||||
| chr14:69092165 | T | C | 1 | a0001c0001t0001g0166 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.666-278A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69092165 | |||||||
| chr14:69092229 | C | G | 1 | a0001c0001t0001g0081 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.666-342G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69092229 | |||||||
| chr14:69092255 | A | C | 4 | a0001c0001t0007g0095 a0001c0001t0007g0096 a0001c0001t0007g0097 others(1): Show |
4 | HG01074.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.666-368T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69092255 | |||||||
| chr14:69092463 | A | T | 1 | a0001c0001t0003g0068 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.666-576T>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69092463 | |||||||
| chr14:69092716 | T | G | 1 | a0001c0001t0003g0040 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.666-829A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69092716 | |||||||
| chr14:69092801 | G | T | 68 | a0001c0001t0001g0081 a0001c0001t0002g0029 a0001c0001t0002g0035 others(65): Show |
68 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.666-914C>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69092801 | |||||||
| chr14:69092813 | G | C | 14 | a0001c0001t0004g0008 a0001c0001t0004g0009 a0001c0001t0004g0010 others(11): Show |
14 | HG01069.hp2 HG01175.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.666-926C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69092813 | |||||||
| chr14:69092844 | T | C | 4 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(1): Show |
4 | HG00733.hp2 HG01106.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.666-957A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69092844 | |||||||
| chr14:69092926 | T | G | 1 | a0001c0001t0003g0058 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.666-1039A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69092926 | |||||||
| chr14:69092963 | T | A | 3 | a0001c0001t0002g0100 a0001c0001t0002g0101 a0001c0001t0004g0183 |
3 | HG02895.hp1 HG02897.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.666-1076A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69092963 | |||||||
| chr14:69093702 | T | C | 1 | a0001c0001t0001g0191 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.666-1815A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69093702 | |||||||
| chr14:69093899 | C | G | 1 | a0001c0002t0001g0155 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.666-2012G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69093899 | |||||||
| chr14:69094044 | T | C | 1 | a0001c0001t0001g0134 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.666-2157A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69094044 | |||||||
| chr14:69094476 | A | G | 150 | a0001c0001t0001g0081 a0001c0001t0001g0166 a0001c0001t0002g0011 others(147): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.666-2589T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69094476 | |||||||
| chr14:69094787 | T | TA | 12 | a0001c0003t0002g0108 a0001c0003t0002g0109 a0001c0003t0002g0111 others(9): Show |
12 | HG01243.hp2 HG01433.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.666-2901dupT | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69094787 | |||||||
| chr14:69094888 | A | AG | 4 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(1): Show |
4 | HG02083.hp1 HG02165.hp1 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.666-3002dupC | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69094888 | |||||||
| chr14:69094983 | A | G | 14 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0002g0018 others(11): Show |
14 | HG01361.hp1 HG02055.hp1 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.666-3096T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69094983 | |||||||
| chr14:69095269 | C | T | 1 | a0003c0007t0012g0128 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.666-3382G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69095269 | |||||||
| chr14:69095537 | T | C | 1 | a0003c0007t0012g0128 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.666-3650A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69095537 | |||||||
| chr14:69095550 | T | TAC | 71 | a0001c0001t0001g0081 a0001c0001t0002g0011 a0001c0001t0002g0012 others(68): Show |
71 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.666-3665_666-3664d others(4): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69095550 | |||||||
| chr14:69095556 | C | A | 1 | a0001c0010t0001g0218 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.666-3669G>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69095556 | |||||||
| chr14:69095670 | A | C | 1 | a0001c0001t0013g0099 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.666-3783T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69095670 | |||||||
| chr14:69095695 | G | A | 1 | a0001c0001t0013g0099 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.666-3808C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69095695 | |||||||
| chr14:69095748 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.666-3861C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69095748 | |||||||
| chr14:69095862 | C | T | 1 | a0001c0001t0013g0099 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.666-3975G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69095862 | |||||||
| chr14:69095884 | T | C | 1 | a0001c0001t0001g0208 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.666-3997A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69095884 | |||||||
| chr14:69095978 | T | C | 1 | a0001c0001t0002g0126 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.666-4091A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69095978 | |||||||
| chr14:69096208 | T | C | 4 | a0001c0001t0001g0001 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
5 | HG02647.hp2 HG03130.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.666-4321A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69096208 | |||||||
| chr14:69096250 | C | G | 14 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0002g0018 others(11): Show |
14 | HG01361.hp1 HG02055.hp1 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.666-4363G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69096250 | |||||||
| chr14:69096282 | T | C | 1 | a0001c0001t0013g0099 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.666-4395A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69096282 | |||||||
| chr14:69096296 | G | A | 2 | a0001c0001t0002g0017 a0001c0001t0002g0023 |
2 | HG02155.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.666-4409C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69096296 | |||||||
| chr14:69096354 | A | G | 1 | a0001c0001t0003g0026 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.666-4467T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69096354 | |||||||
| chr14:69096380 | C | T | 25 | a0001c0001t0002g0123 a0001c0003t0002g0102 a0001c0003t0002g0103 others(22): Show |
25 | HG01192.hp2 HG01243.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.666-4493G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69096380 | |||||||
| chr14:69096415 | T | C | 1 | a0001c0001t0007g0097 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.666-4528A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69096415 | |||||||
| chr14:69096578 | A | G | 99 | a0001c0001t0001g0081 a0001c0001t0002g0011 a0001c0001t0002g0012 others(96): Show |
99 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(96): Show |
intron_variant | MODIFIER | c.666-4691T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69096578 | |||||||
| chr14:69096622 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.666-4735G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69096622 | |||||||
| chr14:69097029 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.666-5142G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69097029 | |||||||
| chr14:69097040 | A | AGACAAGA others(29): Show |
1 | a0001c0001t0003g0089 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.666-5189_666-5154d others(38): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69097040 | |||||||
| chr14:69097148 | G | A | 1 | a0001c0001t0002g0235 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.666-5261C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69097148 | |||||||
| chr14:69097211 | G | A | 2 | a0001c0001t0010g0209 a0001c0001t0010g0210 |
2 | HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.666-5324C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69097211 | |||||||
| chr14:69097582 | A | T | 1 | a0001c0001t0001g0004 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.666-5695T>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69097582 | |||||||
| chr14:69097582 | AT | A | 32 | a0001c0001t0001g0145 a0001c0001t0002g0100 a0001c0001t0002g0101 others(29): Show |
32 | HG00738.hp2 HG00741.hp2 HG01192.hp2 others(29): Show |
intron_variant | MODIFIER | c.666-5696delA | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69097582 | |||||||
| chr14:69097582 | ATT | A | 60 | a0001c0001t0001g0081 a0001c0001t0002g0029 a0001c0001t0002g0035 others(57): Show |
60 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.666-5697_666-5696d others(4): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69097582 | |||||||
| chr14:69097584 | T | TA | 5 | a0001c0001t0003g0028 a0001c0001t0005g0172 a0001c0001t0005g0173 others(2): Show |
5 | HG01255.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.666-5698_666-5697i others(3): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69097584 | |||||||
| chr14:69097585 | T | A | 129 | a0001c0001t0001g0001 a0001c0001t0001g0129 a0001c0001t0001g0130 others(126): Show |
132 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.666-5698A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69097585 | |||||||
| chr14:69097586 | T | A | 27 | a0001c0001t0001g0145 a0001c0001t0002g0100 a0001c0001t0002g0101 others(24): Show |
27 | HG00738.hp2 HG01243.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.666-5699A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69097586 | |||||||
| chr14:69097587 | T | A | 58 | a0001c0001t0001g0081 a0001c0001t0002g0029 a0001c0001t0002g0056 others(55): Show |
58 | HG00099.hp1 HG00140.hp2 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.666-5700A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69097587 | |||||||
| chr14:69097588 | T | A | 65 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0133 others(62): Show |
67 | HG00140.hp1 HG00642.hp1 HG00735.hp2 others(64): Show |
intron_variant | MODIFIER | c.666-5701A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69097588 | |||||||
| chr14:69097589 | T | A | 8 | a0001c0001t0002g0100 a0001c0001t0002g0101 a0001c0001t0013g0099 others(5): Show |
8 | HG01891.hp2 HG02280.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.666-5702A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69097589 | |||||||
| chr14:69097590 | T | A | 17 | a0001c0001t0001g0081 a0001c0001t0002g0029 a0001c0001t0002g0069 others(14): Show |
17 | HG01071.hp2 HG01169.hp2 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.666-5703A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69097590 | |||||||
| chr14:69097591 | T | A | 5 | a0001c0001t0001g0208 a0001c0001t0001g0214 a0001c0001t0001g0224 others(2): Show |
5 | HG00140.hp1 HG02135.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.666-5704A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69097591 | |||||||
| chr14:69097593 | T | A | 1 | a0001c0001t0002g0077 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.666-5706A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69097593 | |||||||
| chr14:69097966 | A | G | 23 | a0001c0001t0001g0004 a0001c0001t0001g0190 a0001c0001t0001g0191 others(20): Show |
24 | HG00642.hp1 HG00741.hp1 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.666-6079T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69097966 | |||||||
| chr14:69098145 | C | CTCT | 172 | a0001c0001t0001g0081 a0001c0001t0001g0166 a0001c0001t0002g0011 others(169): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.666-6261_666-6259d others(5): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69098145 | |||||||
| chr14:69098145 | C | T | 1 | a0001c0001t0014g0094 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.666-6258G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69098145 | |||||||
| chr14:69098476 | T | G | 145 | a0001c0001t0001g0081 a0001c0001t0001g0166 a0001c0001t0002g0011 others(142): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.666-6589A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69098476 | |||||||
| chr14:69098612 | G | A | 1 | a0001c0001t0001g0220 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.666-6725C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69098612 | |||||||
| chr14:69098727 | C | CA | 96 | a0001c0001t0001g0081 a0001c0001t0002g0025 a0001c0001t0002g0029 others(93): Show |
96 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(93): Show |
intron_variant | MODIFIER | c.666-6841dupT | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69098727 | |||||||
| chr14:69098727 | C | CAA | 10 | a0001c0001t0002g0083 a0001c0001t0003g0066 a0001c0001t0003g0089 others(7): Show |
10 | HG00140.hp2 HG02559.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.666-6842_666-6841d others(4): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69098727 | |||||||
| chr14:69098727 | CA | C | 66 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0129 others(63): Show |
68 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.666-6841delT | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69098727 | |||||||
| chr14:69098759 | G | A | 1 | a0001c0001t0002g0088 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.666-6872C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69098759 | |||||||
| chr14:69098879 | C | T | 1 | a0001c0001t0002g0056 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.666-6992G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69098879 | |||||||
| chr14:69098893 | C | CA | 21 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(18): Show |
21 | HG00280.hp2 HG01257.hp2 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.666-7007dupT | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69098893 | |||||||
| chr14:69098893 | CA | C | 171 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0081 others(168): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.666-7007delT | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69098893 | |||||||
| chr14:69098911 | A | G | 95 | a0001c0001t0001g0081 a0001c0001t0002g0029 a0001c0001t0002g0035 others(92): Show |
95 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(92): Show |
intron_variant | MODIFIER | c.666-7024T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69098911 | |||||||
| chr14:69098912 | A | G | 4 | a0001c0001t0001g0001 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
5 | HG02647.hp2 HG03130.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.666-7025T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69098912 | |||||||
| chr14:69098980 | C | T | 2 | a0001c0001t0002g0100 a0001c0001t0002g0101 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.666-7093G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69098980 | |||||||
| chr14:69099048 | C | T | 2 | a0001c0003t0002g0113 a0001c0005t0002g0005 |
2 | HG02258.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.666-7161G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69099048 | |||||||
| chr14:69099082 | C | T | 1 | a0001c0001t0013g0099 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.666-7195G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69099082 | |||||||
| chr14:69099174 | C | T | 3 | a0001c0001t0006g0003 a0001c0001t0006g0168 a0001c0001t0006g0169 |
4 | HG02280.hp1 HG02451.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.666-7287G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69099174 | |||||||
| chr14:69099251 | A | AAC | 45 | a0001c0001t0001g0081 a0001c0001t0002g0069 a0001c0001t0002g0072 others(42): Show |
45 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(42): Show |
intron_variant | MODIFIER | c.666-7366_666-7365d others(4): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69099251 | |||||||
| chr14:69099251 | A | AACAC | 28 | a0001c0001t0002g0011 a0001c0001t0002g0013 a0001c0001t0002g0015 others(25): Show |
28 | HG00735.hp1 HG01433.hp1 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.666-7368_666-7365d others(6): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69099251 | |||||||
| chr14:69099251 | A | AACACAC | 20 | a0001c0001t0002g0012 a0001c0001t0002g0024 a0001c0001t0002g0056 others(17): Show |
21 | HG00642.hp2 HG00741.hp2 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.666-7370_666-7365d others(8): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69099251 | |||||||
| chr14:69099251 | A | AACACACA others(1): Show |
4 | a0001c0001t0002g0126 a0001c0001t0003g0041 a0001c0001t0003g0049 others(1): Show |
4 | HG02886.hp1 HG03688.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.666-7372_666-7365d others(10): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69099251 | |||||||
| chr14:69099251 | A | AACACACA others(3): Show |
2 | a0001c0001t0002g0035 a0001c0001t0011g0237 |
2 | HG01175.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.666-7374_666-7365d others(12): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69099251 | |||||||
| chr14:69099251 | AAC | A | 22 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(19): Show |
22 | HG00280.hp2 HG00733.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.666-7366_666-7365d others(4): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69099251 | |||||||
| chr14:69099251 | AACAC | A | 17 | a0001c0001t0001g0001 a0001c0001t0001g0129 a0001c0001t0001g0130 others(14): Show |
17 | HG01069.hp2 HG01192.hp1 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.666-7368_666-7365d others(6): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69099251 | |||||||
| chr14:69099251 | AACACAC | A | 12 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0166 others(9): Show |
12 | HG01891.hp1 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.666-7370_666-7365d others(8): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69099251 | |||||||
| chr14:69099251 | AACACACA others(1): Show |
A | 8 | a0001c0001t0001g0198 a0001c0001t0001g0201 a0001c0001t0002g0071 others(5): Show |
8 | HG01943.hp2 HG01981.hp1 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.666-7372_666-7365d others(10): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69099251 | |||||||
| chr14:69099251 | AACACACA others(3): Show |
A | 41 | a0001c0001t0001g0004 a0001c0001t0001g0131 a0001c0001t0001g0189 others(38): Show |
42 | HG00140.hp1 HG00642.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.666-7374_666-7365d others(12): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69099251 | |||||||
| chr14:69099251 | AACACACA others(5): Show |
A | 2 | a0001c0001t0001g0194 a0001c0001t0001g0196 |
2 | HG00741.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.666-7376_666-7365d others(14): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69099251 | |||||||
| chr14:69099251 | AACACACA others(9): Show |
A | 1 | a0001c0001t0003g0063 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.666-7380_666-7365d others(18): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69099251 | |||||||
| chr14:69099376 | G | A | 67 | a0001c0001t0001g0081 a0001c0001t0002g0029 a0001c0001t0002g0035 others(64): Show |
67 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.666-7489C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69099376 | |||||||
| chr14:69099536 | A | G | 1 | a0001c0002t0001g0152 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.666-7649T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69099536 | |||||||
| chr14:69099594 | T | A | 67 | a0001c0001t0001g0081 a0001c0001t0002g0029 a0001c0001t0002g0035 others(64): Show |
67 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.666-7707A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69099594 | |||||||
| chr14:69099787 | A | AC | 167 | a0001c0001t0001g0081 a0001c0001t0001g0166 a0001c0001t0001g0207 others(164): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.666-7901_666-7900i others(3): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69099787 | |||||||
| chr14:69099985 | G | A | 2 | a0001c0001t0003g0092 a0001c0001t0003g0093 |
2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.666-8098C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69099985 | |||||||
| chr14:69099999 | C | A | 1 | a0001c0001t0001g0134 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.666-8112G>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69099999 | |||||||
| chr14:69100146 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.666-8259G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69100146 | |||||||
| chr14:69100472 | T | A | 173 | a0001c0001t0001g0081 a0001c0001t0001g0166 a0001c0001t0002g0011 others(170): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.666-8585A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69100472 | |||||||
| chr14:69100560 | C | A | 67 | a0001c0001t0001g0081 a0001c0001t0002g0029 a0001c0001t0002g0035 others(64): Show |
67 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.666-8673G>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69100560 | |||||||
| chr14:69100986 | T | G | 1 | a0001c0001t0014g0094 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.666-9099A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69100986 | |||||||
| chr14:69101135 | A | C | 71 | a0001c0001t0001g0081 a0001c0001t0002g0011 a0001c0001t0002g0012 others(68): Show |
71 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.666-9248T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69101135 | |||||||
| chr14:69101245 | T | C | 1 | a0001c0001t0002g0235 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.666-9358A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69101245 | |||||||
| chr14:69101377 | T | C | 2 | a0001c0001t0003g0092 a0001c0001t0003g0093 |
2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.666-9490A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69101377 | |||||||
| chr14:69101439 | C | G | 189 | a0001c0001t0001g0001 a0001c0001t0001g0081 a0001c0001t0001g0129 others(186): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.666-9552G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69101439 | |||||||
| chr14:69101682 | T | C | 1 | a0001c0001t0002g0021 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.666-9795A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69101682 | |||||||
| chr14:69101825 | G | A | 1 | a0001c0001t0002g0088 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.666-9938C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69101825 | |||||||
| chr14:69101911 | G | T | 2 | a0001c0001t0009g0016 a0001c0001t0009g0022 |
2 | NA19002.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.666-10024C>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69101911 | |||||||
| chr14:69102025 | A | G | 99 | a0001c0001t0001g0081 a0001c0001t0002g0011 a0001c0001t0002g0012 others(96): Show |
99 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(96): Show |
intron_variant | MODIFIER | c.666-10138T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69102025 | |||||||
| chr14:69102087 | T | C | 1 | a0001c0001t0014g0094 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.666-10200A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69102087 | |||||||
| chr14:69102107 | C | CT | 48 | a0001c0001t0001g0166 a0001c0001t0001g0211 a0001c0001t0002g0021 others(45): Show |
49 | HG00099.hp2 HG00280.hp1 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.666-10221dupA | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69102107 | |||||||
| chr14:69102107 | CT | C | 6 | a0001c0001t0002g0007 a0001c0001t0002g0015 a0001c0001t0002g0025 others(3): Show |
6 | HG01257.hp2 HG02056.hp2 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.666-10221delA | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69102107 | |||||||
| chr14:69102107 | CTTT | C | 16 | a0001c0003t0002g0108 a0001c0003t0002g0109 a0001c0003t0002g0111 others(13): Show |
16 | HG01243.hp2 HG01433.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.666-10223_666-1022 others(7): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69102107 | |||||||
| chr14:69102246 | T | C | 27 | a0001c0001t0002g0100 a0001c0001t0002g0101 a0001c0001t0002g0123 others(24): Show |
27 | HG01192.hp2 HG01243.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.666-10359A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69102246 | |||||||
| chr14:69102313 | T | C | 12 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(9): Show |
12 | HG00280.hp2 HG00738.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.666-10426A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69102313 | |||||||
| chr14:69102397 | G | A | 7 | a0001c0001t0004g0008 a0001c0001t0004g0009 a0001c0001t0004g0010 others(4): Show |
7 | HG01069.hp2 HG01192.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.666-10510C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69102397 | |||||||
| chr14:69102542 | C | CT | 29 | a0001c0001t0002g0100 a0001c0001t0002g0101 a0001c0001t0002g0123 others(26): Show |
29 | HG01192.hp2 HG01243.hp2 HG01433.hp2 others(26): Show |
intron_variant | MODIFIER | c.666-10656dupA | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69102542 | |||||||
| chr14:69102591 | G | GAC | 18 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0002g0018 others(15): Show |
18 | HG01192.hp2 HG01361.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.666-10706_666-1070 others(6): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69102591 | |||||||
| chr14:69102591 | G | GACAC | 16 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(13): Show |
16 | HG01074.hp2 HG01081.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.666-10708_666-1070 others(8): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69102591 | |||||||
| chr14:69102591 | G | GACACAC | 3 | a0001c0001t0002g0078 a0001c0001t0007g0096 a0001c0003t0002g0110 |
3 | HG02129.hp2 HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.666-10710_666-1070 others(10): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69102591 | |||||||
| chr14:69102591 | G | GACACACA others(1): Show |
23 | a0001c0001t0006g0003 a0001c0001t0006g0168 a0001c0001t0006g0169 others(20): Show |
24 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.666-10712_666-1070 others(12): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69102591 | |||||||
| chr14:69102591 | G | GACACACA others(3): Show |
6 | a0001c0001t0001g0166 a0001c0001t0003g0092 a0001c0002t0001g0002 others(3): Show |
7 | HG00280.hp1 HG00642.hp2 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.666-10714_666-1070 others(14): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69102591 | |||||||
| chr14:69102591 | G | GACACACA others(5): Show |
5 | a0001c0001t0002g0085 a0001c0001t0004g0181 a0001c0001t0004g0182 others(2): Show |
5 | HG02258.hp1 HG02895.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.666-10716_666-1070 others(16): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69102591 | |||||||
| chr14:69102591 | G | GACACACA others(7): Show |
5 | a0001c0001t0002g0235 a0001c0001t0003g0027 a0001c0001t0003g0093 others(2): Show |
5 | HG01175.hp2 HG01433.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.666-10718_666-1070 others(18): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69102591 | |||||||
| chr14:69102591 | G | GACACACA others(9): Show |
8 | a0001c0001t0002g0079 a0001c0001t0003g0049 a0001c0001t0003g0051 others(5): Show |
8 | HG01069.hp2 HG01192.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.666-10720_666-1070 others(20): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69102591 | |||||||
| chr14:69102591 | G | GACACACA others(11): Show |
11 | a0001c0001t0002g0087 a0001c0001t0002g0088 a0001c0001t0003g0028 others(8): Show |
11 | HG00099.hp1 HG01255.hp1 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.666-10722_666-1070 others(22): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69102591 | |||||||
| chr14:69102591 | G | GACACACA others(13): Show |
29 | a0001c0001t0002g0029 a0001c0001t0002g0035 a0001c0001t0002g0056 others(26): Show |
29 | HG00140.hp2 HG00738.hp1 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.666-10724_666-1070 others(24): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69102591 | |||||||
| chr14:69102591 | G | GACACACA others(15): Show |
17 | a0001c0001t0002g0069 a0001c0001t0002g0070 a0001c0001t0002g0073 others(14): Show |
17 | HG00735.hp1 HG00741.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.666-10726_666-1070 others(26): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69102591 | |||||||
| chr14:69102591 | G | GACACACA others(17): Show |
4 | a0001c0001t0001g0081 a0001c0001t0002g0076 a0001c0001t0002g0077 others(1): Show |
4 | HG01071.hp2 HG02683.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.666-10728_666-1070 others(28): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69102591 | |||||||
| chr14:69102591 | G | GACACACA others(19): Show |
2 | a0001c0001t0002g0075 a0001c0001t0003g0054 |
2 | HG01346.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.666-10730_666-1070 others(30): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69102591 | |||||||
| chr14:69102591 | G | GACACACA others(21): Show |
1 | a0001c0001t0003g0050 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.666-10732_666-1070 others(32): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69102591 | |||||||
| chr14:69102591 | GAC | G | 23 | a0001c0001t0001g0004 a0001c0001t0001g0190 a0001c0001t0001g0191 others(20): Show |
24 | HG00642.hp1 HG00741.hp1 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.666-10706_666-1070 others(6): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69102591 | |||||||
| chr14:69102621 | T | C | 42 | a0001c0001t0001g0166 a0001c0001t0004g0008 a0001c0001t0004g0009 others(39): Show |
44 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.666-10734A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69102621 | |||||||
| chr14:69102657 | T | A | 1 | a0001c0001t0002g0123 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.666-10770A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69102657 | |||||||
| chr14:69103189 | T | A | 1 | a0001c0001t0001g0191 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.666-11302A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69103189 | |||||||
| chr14:69103253 | T | C | 2 | a0001c0001t0003g0092 a0001c0001t0003g0093 |
2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.666-11366A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69103253 | |||||||
| chr14:69103303 | A | T | 3 | a0001c0001t0006g0003 a0001c0001t0006g0168 a0001c0001t0006g0169 |
4 | HG02280.hp1 HG02451.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.666-11416T>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69103303 | |||||||
| chr14:69103400 | G | C | 1 | a0001c0010t0001g0218 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.666-11513C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69103400 | |||||||
| chr14:69103745 | C | G | 28 | a0001c0001t0001g0166 a0001c0001t0006g0003 a0001c0001t0006g0168 others(25): Show |
30 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.666-11858G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69103745 | |||||||
| chr14:69103946 | C | G | 1 | a0001c0001t0013g0099 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.666-12059G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69103946 | |||||||
| chr14:69104199 | C | T | 2 | a0001c0001t0003g0092 a0001c0001t0003g0093 |
2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.665+12167G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69104199 | |||||||
| chr14:69104455 | G | C | 1 | a0001c0001t0014g0094 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.665+11911C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69104455 | |||||||
| chr14:69104515 | G | A | 1 | a0001c0001t0014g0094 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.665+11851C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69104515 | |||||||
| chr14:69104640 | G | C | 4 | a0001c0001t0001g0001 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
5 | HG02647.hp2 HG03130.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.665+11726C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69104640 | |||||||
| chr14:69104713 | C | T | 1 | a0001c0006t0003g0006 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.665+11653G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69104713 | |||||||
| chr14:69104734 | G | A | 7 | a0001c0002t0001g0148 a0001c0002t0001g0149 a0001c0002t0001g0150 others(4): Show |
7 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.665+11632C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69104734 | |||||||
| chr14:69104793 | G | T | 17 | a0001c0003t0002g0108 a0001c0003t0002g0109 a0001c0003t0002g0111 others(14): Show |
17 | HG01243.hp2 HG01433.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.665+11573C>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69104793 | |||||||
| chr14:69104818 | T | C | 12 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(9): Show |
12 | HG00280.hp2 HG00738.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.665+11548A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69104818 | |||||||
| chr14:69104821 | C | T | 1 | a0001c0001t0003g0042 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.665+11545G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69104821 | |||||||
| chr14:69104881 | A | G | 4 | a0001c0001t0007g0095 a0001c0001t0007g0096 a0001c0001t0007g0097 others(1): Show |
4 | HG01074.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.665+11485T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69104881 | |||||||
| chr14:69104889 | C | G | 1 | a0003c0007t0012g0128 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.665+11477G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69104889 | |||||||
| chr14:69105034 | T | C | 2 | a0001c0001t0003g0092 a0001c0001t0003g0093 |
2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.665+11332A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105034 | |||||||
| chr14:69105039 | T | G | 19 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(16): Show |
19 | HG01361.hp1 HG02055.hp1 HG02056.hp1 others(16): Show |
intron_variant | MODIFIER | c.665+11327A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105039 | |||||||
| chr14:69105048 | T | A | 127 | a0001c0001t0001g0081 a0001c0001t0001g0166 a0001c0001t0002g0029 others(124): Show |
129 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.665+11318A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105048 | |||||||
| chr14:69105188 | G | A | 5 | a0001c0003t0002g0102 a0001c0003t0002g0103 a0001c0003t0002g0104 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.665+11178C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105188 | |||||||
| chr14:69105204 | A | G | 1 | a0001c0001t0013g0099 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.665+11162T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105204 | |||||||
| chr14:69105240 | C | T | 1 | a0001c0001t0014g0094 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.665+11126G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105240 | |||||||
| chr14:69105286 | A | C | 159 | a0001c0001t0001g0081 a0001c0001t0001g0166 a0001c0001t0002g0011 others(156): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.665+11080T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105286 | |||||||
| chr14:69105765 | C | G | 14 | a0001c0001t0004g0008 a0001c0001t0004g0009 a0001c0001t0004g0010 others(11): Show |
14 | HG01069.hp2 HG01175.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.665+10601G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105765 | |||||||
| chr14:69105910 | C | T | 2 | a0001c0003t0002g0115 a0001c0003t0002g0119 |
2 | HG01243.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.665+10456G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105910 | |||||||
| chr14:69105914 | C | CAT | 3 | a0001c0001t0001g0194 a0001c0001t0001g0231 a0001c0001t0002g0127 |
3 | HG02055.hp1 HG02970.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.665+10450_665+1045 others(6): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105914 | |||||||
| chr14:69105914 | C | CATATATA others(1): Show |
3 | a0001c0001t0001g0134 a0001c0001t0002g0075 a0001c0001t0011g0237 |
3 | HG01346.hp1 NA18967.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.665+10444_665+1045 others(12): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105914 | |||||||
| chr14:69105914 | C | CATATATA others(3): Show |
3 | a0001c0001t0001g0141 a0001c0001t0002g0235 a0001c0001t0007g0097 |
3 | HG01074.hp2 HG02965.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.665+10442_665+1045 others(14): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105914 | |||||||
| chr14:69105914 | C | CATATATA others(5): Show |
5 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0144 others(2): Show |
5 | HG03492.hp1 NA18940.hp1 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.665+10440_665+1045 others(16): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105914 | |||||||
| chr14:69105914 | C | CATATATA others(7): Show |
2 | a0001c0001t0001g0140 a0001c0001t0007g0095 |
2 | NA19070.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.665+10438_665+1045 others(18): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105914 | |||||||
| chr14:69105914 | C | CATATATA others(9): Show |
4 | a0001c0001t0001g0081 a0001c0001t0001g0145 a0001c0004t0003g0047 others(1): Show |
4 | HG00738.hp2 HG02135.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.665+10436_665+1045 others(20): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105914 | |||||||
| chr14:69105914 | C | CATATATA others(11): Show |
4 | a0001c0001t0001g0137 a0001c0001t0002g0084 a0001c0001t0003g0058 others(1): Show |
4 | HG00280.hp2 HG02165.hp2 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.665+10434_665+1045 others(22): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105914 | |||||||
| chr14:69105914 | C | CATATATA others(13): Show |
8 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0142 others(5): Show |
8 | HG01361.hp2 HG01515.hp2 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.665+10432_665+1045 others(24): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105914 | |||||||
| chr14:69105914 | C | CATATATA others(15): Show |
14 | a0001c0001t0002g0029 a0001c0001t0002g0074 a0001c0001t0002g0078 others(11): Show |
14 | HG00140.hp2 HG01081.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.665+10430_665+1045 others(26): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105914 | |||||||
| chr14:69105914 | C | CATATATA others(17): Show |
4 | a0001c0001t0002g0072 a0001c0001t0002g0080 a0001c0001t0003g0092 others(1): Show |
4 | HG02004.hp1 HG02004.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.665+10428_665+1045 others(28): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105914 | |||||||
| chr14:69105914 | C | CATATATA others(19): Show |
12 | a0001c0001t0002g0011 a0001c0001t0002g0071 a0001c0001t0003g0028 others(9): Show |
12 | HG00738.hp1 HG01255.hp1 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.665+10426_665+1045 others(30): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105914 | |||||||
| chr14:69105914 | C | CATATATA others(21): Show |
11 | a0001c0001t0002g0012 a0001c0001t0002g0056 a0001c0001t0002g0069 others(8): Show |
11 | HG00735.hp1 HG01496.hp2 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.665+10424_665+1045 others(32): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105914 | |||||||
| chr14:69105914 | C | CATATATA others(23): Show |
6 | a0001c0001t0002g0070 a0001c0001t0003g0037 a0001c0001t0003g0051 others(3): Show |
6 | HG01261.hp1 HG02257.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.665+10422_665+1045 others(34): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105914 | |||||||
| chr14:69105914 | C | CATATATA others(25): Show |
2 | a0001c0001t0002g0013 a0001c0001t0003g0050 |
2 | HG04204.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.665+10420_665+1045 others(36): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105914 | |||||||
| chr14:69105914 | C | CATATATA others(27): Show |
2 | a0001c0001t0003g0040 a0001c0001t0003g0043 |
2 | HG03942.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.665+10451_665+1045 others(38): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105914 | |||||||
| chr14:69105914 | C | CATATATA others(29): Show |
1 | a0001c0001t0003g0033 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.665+10451_665+1045 others(40): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105914 | |||||||
| chr14:69105914 | C | CATATATA others(31): Show |
1 | a0001c0001t0002g0085 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.665+10451_665+1045 others(42): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105914 | |||||||
| chr14:69105914 | C | CATATATA others(41): Show |
1 | a0001c0001t0002g0073 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.665+10451_665+1045 others(52): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105914 | |||||||
| chr14:69105914 | C | CTATATAT others(20): Show |
1 | a0001c0001t0002g0079 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.665+10451_665+1045 others(31): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105914 | |||||||
| chr14:69105914 | C | CTATATAT others(22): Show |
1 | a0001c0001t0002g0087 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.665+10451_665+1045 others(33): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105914 | |||||||
| chr14:69105914 | CAT | C | 33 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0189 others(30): Show |
34 | HG00733.hp2 HG00741.hp2 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.665+10450_665+1045 others(6): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105914 | |||||||
| chr14:69105914 | CATAT | C | 24 | a0001c0001t0001g0004 a0001c0001t0001g0129 a0001c0001t0001g0190 others(21): Show |
25 | HG00140.hp1 HG00642.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.665+10448_665+1045 others(8): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105914 | |||||||
| chr14:69105914 | CATATATA others(1): Show |
C | 3 | a0001c0001t0001g0131 a0001c0001t0001g0211 a0001c0001t0002g0077 |
3 | HG02572.hp2 HG03579.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.665+10444_665+1045 others(12): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105914 | |||||||
| chr14:69105914 | CATATATA others(5): Show |
C | 2 | a0001c0001t0003g0041 a0001c0001t0014g0094 |
2 | HG03453.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.665+10440_665+1045 others(16): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105914 | |||||||
| chr14:69105914 | CATATATA others(7): Show |
C | 27 | a0001c0001t0002g0100 a0001c0001t0002g0101 a0001c0001t0002g0123 others(24): Show |
27 | HG01192.hp2 HG01243.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.665+10438_665+1045 others(18): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105914 | |||||||
| chr14:69105914 | CATATATA others(11): Show |
C | 1 | a0001c0001t0017g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.665+10434_665+1045 others(22): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105914 | |||||||
| chr14:69105919 | A | T | 4 | a0001c0001t0005g0172 a0001c0001t0005g0173 a0001c0001t0005g0174 others(1): Show |
4 | HG02145.hp1 HG02559.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.665+10447T>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105919 | |||||||
| chr14:69105920 | T | C | 4 | a0001c0001t0005g0172 a0001c0001t0005g0173 a0001c0001t0005g0174 others(1): Show |
4 | HG02145.hp1 HG02559.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.665+10446A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105920 | |||||||
| chr14:69105929 | A | ATATATAT others(15): Show |
1 | a0001c0001t0002g0088 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.665+10436_665+1043 others(26): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105929 | |||||||
| chr14:69105939 | A | ATCTATCT others(3): Show |
1 | a0001c0001t0013g0099 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.665+10426_665+1042 others(14): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105939 | |||||||
| chr14:69105943 | A | C | 1 | a0001c0001t0013g0099 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.665+10423T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105943 | |||||||
| chr14:69105944 | T | TATATATA others(8): Show |
1 | a0001c0001t0001g0166 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.665+10421_665+1042 others(19): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105944 | |||||||
| chr14:69105944 | T | TATATATA others(12): Show |
1 | a0001c0002t0001g0161 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.665+10421_665+1042 others(23): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105944 | |||||||
| chr14:69105944 | T | TATATATA others(14): Show |
5 | a0001c0001t0004g0009 a0001c0001t0004g0186 a0001c0002t0001g0155 others(2): Show |
5 | HG00280.hp1 HG00733.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.665+10421_665+1042 others(25): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105944 | |||||||
| chr14:69105944 | T | TATATATA others(16): Show |
3 | a0001c0001t0004g0183 a0001c0001t0004g0188 a0001c0002t0001g0002 |
4 | HG00642.hp2 HG01099.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.665+10421_665+1042 others(27): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105944 | |||||||
| chr14:69105944 | T | TATATATA others(24): Show |
1 | a0001c0002t0001g0165 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.665+10421_665+1042 others(35): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105944 | |||||||
| chr14:69105944 | T | TATATATA others(18): Show |
7 | a0001c0001t0004g0010 a0001c0001t0004g0184 a0001c0001t0004g0185 others(4): Show |
7 | HG01069.hp2 HG02055.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.665+10421_665+1042 others(29): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105944 | |||||||
| chr14:69105944 | T | TATATATA others(20): Show |
7 | a0001c0001t0004g0181 a0001c0002t0001g0149 a0001c0002t0001g0151 others(4): Show |
7 | HG00099.hp2 HG01081.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.665+10421_665+1042 others(31): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105944 | |||||||
| chr14:69105944 | T | TATATATA others(22): Show |
8 | a0001c0001t0004g0008 a0001c0001t0004g0179 a0001c0001t0004g0180 others(5): Show |
9 | HG01175.hp2 HG02451.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.665+10421_665+1042 others(33): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105944 | |||||||
| chr14:69105944 | T | TATATATA others(24): Show |
4 | a0001c0001t0004g0182 a0001c0002t0001g0154 a0001c0002t0001g0157 others(1): Show |
4 | HG00735.hp2 HG01934.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.665+10421_665+1042 others(35): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105944 | |||||||
| chr14:69105944 | T | TATATATA others(26): Show |
2 | a0001c0002t0001g0156 a0001c0002t0001g0164 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.665+10421_665+1042 others(37): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105944 | |||||||
| chr14:69105944 | T | TATATATA others(28): Show |
1 | a0001c0002t0001g0153 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.665+10421_665+1042 others(39): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105944 | |||||||
| chr14:69105944 | T | TATATATA others(30): Show |
1 | a0001c0002t0001g0147 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.665+10421_665+1042 others(41): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69105944 | |||||||
| chr14:69106214 | G | A | 2 | a0001c0001t0002g0090 a0001c0001t0002g0091 |
2 | HG01081.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.665+10152C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69106214 | |||||||
| chr14:69106378 | T | A | 71 | a0001c0001t0001g0081 a0001c0001t0002g0011 a0001c0001t0002g0012 others(68): Show |
71 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.665+9988A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69106378 | |||||||
| chr14:69106767 | C | T | 1 | a0001c0001t0013g0099 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.665+9599G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69106767 | |||||||
| chr14:69106821 | C | T | 4 | a0001c0001t0007g0095 a0001c0001t0007g0096 a0001c0001t0007g0097 others(1): Show |
4 | HG01074.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.665+9545G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69106821 | |||||||
| chr14:69107064 | T | TAATTAAA others(1): Show |
140 | a0001c0001t0001g0081 a0001c0001t0001g0166 a0001c0001t0002g0029 others(137): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.665+9301_665+9302i others(10): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69107064 | |||||||
| chr14:69107179 | C | T | 1 | a0001c0001t0010g0209 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.665+9187G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69107179 | |||||||
| chr14:69107274 | C | A | 1 | a0003c0007t0012g0128 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.665+9092G>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69107274 | |||||||
| chr14:69107319 | G | A | 1 | a0001c0001t0014g0094 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.665+9047C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69107319 | |||||||
| chr14:69107346 | T | C | 3 | a0001c0003t0002g0102 a0001c0003t0002g0103 a0001c0003t0002g0104 |
3 | HG02818.hp1 HG02965.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.665+9020A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69107346 | |||||||
| chr14:69107439 | A | T | 2 | a0001c0001t0003g0092 a0001c0001t0003g0093 |
2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.665+8927T>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69107439 | |||||||
| chr14:69107561 | C | T | 4 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(1): Show |
4 | HG00733.hp2 HG01106.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.665+8805G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69107561 | |||||||
| chr14:69107633 | C | T | 1 | a0001c0001t0002g0012 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.665+8733G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69107633 | |||||||
| chr14:69107637 | GCT | G | 3 | a0001c0001t0006g0003 a0001c0001t0006g0168 a0001c0001t0006g0169 |
4 | HG02280.hp1 HG02451.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.665+8727_665+8728d others(4): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69107637 | |||||||
| chr14:69107653 | C | T | 1 | a0001c0001t0003g0027 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.665+8713G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69107653 | |||||||
| chr14:69107717 | G | A | 2 | a0001c0001t0010g0209 a0001c0001t0010g0210 |
2 | HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.665+8649C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69107717 | |||||||
| chr14:69107926 | C | T | 1 | a0001c0001t0014g0094 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.665+8440G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69107926 | |||||||
| chr14:69107927 | G | A | 1 | a0001c0001t0002g0021 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.665+8439C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69107927 | |||||||
| chr14:69107995 | T | C | 24 | a0001c0002t0001g0002 a0001c0002t0001g0147 a0001c0002t0001g0148 others(21): Show |
25 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.665+8371A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69107995 | |||||||
| chr14:69108134 | T | G | 4 | a0001c0001t0007g0095 a0001c0001t0007g0096 a0001c0001t0007g0097 others(1): Show |
4 | HG01074.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.665+8232A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69108134 | |||||||
| chr14:69108231 | T | A | 1 | a0001c0002t0001g0167 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.665+8135A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69108231 | |||||||
| chr14:69108282 | A | G | 71 | a0001c0001t0001g0081 a0001c0001t0002g0011 a0001c0001t0002g0012 others(68): Show |
71 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.665+8084T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69108282 | |||||||
| chr14:69108337 | A | G | 163 | a0001c0001t0001g0081 a0001c0001t0001g0166 a0001c0001t0002g0011 others(160): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.665+8029T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69108337 | |||||||
| chr14:69108338 | T | A | 1 | a0001c0001t0001g0225 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.665+8028A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69108338 | |||||||
| chr14:69108344 | C | T | 6 | a0001c0002t0001g0002 a0001c0002t0001g0147 a0001c0002t0001g0153 others(3): Show |
7 | HG00642.hp2 HG00733.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.665+8022G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69108344 | |||||||
| chr14:69108398 | G | A | 1 | a0001c0001t0013g0099 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.665+7968C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69108398 | |||||||
| chr14:69108400 | G | C | 23 | a0001c0001t0001g0004 a0001c0001t0001g0190 a0001c0001t0001g0191 others(20): Show |
24 | HG00642.hp1 HG00741.hp1 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.665+7966C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69108400 | |||||||
| chr14:69108434 | G | T | 1 | a0001c0001t0017g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.665+7932C>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69108434 | |||||||
| chr14:69108454 | C | G | 18 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(15): Show |
18 | HG01361.hp1 HG02055.hp1 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.665+7912G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69108454 | |||||||
| chr14:69108535 | A | C | 2 | a0001c0001t0003g0092 a0001c0001t0003g0093 |
2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.665+7831T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69108535 | |||||||
| chr14:69108800 | C | A | 2 | a0001c0003t0002g0124 a0001c0003t0002g0125 |
2 | HG02109.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.665+7566G>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69108800 | |||||||
| chr14:69108911 | T | C | 1 | a0001c0001t0003g0063 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.665+7455A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69108911 | |||||||
| chr14:69109137 | T | C | 212 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0081 others(209): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.665+7229A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69109137 | |||||||
| chr14:69109169 | A | G | 1 | a0001c0001t0013g0099 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.665+7197T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69109169 | |||||||
| chr14:69109299 | G | A | 1 | a0001c0003t0002g0121 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.665+7067C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69109299 | |||||||
| chr14:69109312 | C | T | 14 | a0001c0001t0001g0004 a0001c0001t0001g0191 a0001c0001t0001g0199 others(11): Show |
15 | HG00642.hp1 HG01074.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.665+7054G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69109312 | |||||||
| chr14:69109374 | C | A | 1 | a0001c0001t0002g0018 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.665+6992G>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69109374 | |||||||
| chr14:69109502 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.665+6864G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69109502 | |||||||
| chr14:69109611 | C | T | 1 | a0001c0001t0015g0014 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.665+6755G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69109611 | |||||||
| chr14:69109955 | T | C | 1 | a0001c0001t0002g0235 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.665+6411A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69109955 | |||||||
| chr14:69110058 | A | G | 1 | a0001c0002t0016g0146 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.665+6308T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69110058 | |||||||
| chr14:69110155 | T | C | 1 | a0001c0010t0001g0218 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.665+6211A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69110155 | |||||||
| chr14:69110228 | CT | C | 28 | a0001c0001t0001g0166 a0001c0001t0006g0003 a0001c0001t0006g0168 others(25): Show |
30 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.665+6137delA | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69110228 | |||||||
| chr14:69110270 | C | CT | 80 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0129 others(77): Show |
84 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(81): Show |
intron_variant | MODIFIER | c.665+6095dupA | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69110270 | |||||||
| chr14:69110270 | C | CTT | 7 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(4): Show |
7 | HG00280.hp2 HG00738.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.665+6094_665+6095d others(4): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69110270 | |||||||
| chr14:69110357 | C | G | 42 | a0001c0001t0001g0166 a0001c0001t0004g0008 a0001c0001t0004g0009 others(39): Show |
44 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.665+6009G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69110357 | |||||||
| chr14:69110423 | G | A | 24 | a0001c0002t0001g0002 a0001c0002t0001g0147 a0001c0002t0001g0148 others(21): Show |
25 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.665+5943C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69110423 | |||||||
| chr14:69110440 | A | AT | 27 | a0001c0001t0001g0208 a0001c0001t0002g0123 a0001c0001t0003g0089 others(24): Show |
27 | HG01192.hp2 HG01243.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.665+5925dupA | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69110440 | |||||||
| chr14:69110503 | T | C | 212 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0081 others(209): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.665+5863A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69110503 | |||||||
| chr14:69110701 | C | T | 1 | a0001c0001t0003g0049 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.665+5665G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69110701 | |||||||
| chr14:69110876 | C | CA | 41 | a0001c0001t0001g0138 a0001c0001t0001g0140 a0001c0001t0001g0166 others(38): Show |
42 | HG00735.hp2 HG01069.hp2 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.665+5489dupT | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69110876 | |||||||
| chr14:69110876 | C | CAA | 8 | a0001c0001t0005g0172 a0001c0001t0006g0168 a0001c0001t0006g0169 others(5): Show |
8 | HG02145.hp1 HG02280.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.665+5488_665+5489d others(4): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69110876 | |||||||
| chr14:69110876 | CA | C | 50 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0129 others(47): Show |
52 | HG00140.hp1 HG00642.hp1 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.665+5489delT | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69110876 | |||||||
| chr14:69110876 | CAAA | C | 11 | a0001c0001t0002g0070 a0001c0001t0002g0071 a0001c0001t0002g0079 others(8): Show |
11 | HG02083.hp2 HG02630.hp2 HG03927.hp1 others(8): Show |
intron_variant | MODIFIER | c.665+5487_665+5489d others(5): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69110876 | |||||||
| chr14:69110876 | CAAAA | C | 56 | a0001c0001t0001g0081 a0001c0001t0002g0029 a0001c0001t0002g0035 others(53): Show |
56 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.665+5486_665+5489d others(6): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69110876 | |||||||
| chr14:69110876 | CAAAAAAA others(8): Show |
C | 5 | a0001c0003t0002g0102 a0001c0003t0002g0103 a0001c0003t0002g0104 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.665+5475_665+5489d others(17): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69110876 | |||||||
| chr14:69110946 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.665+5420G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69110946 | |||||||
| chr14:69111122 | C | T | 4 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(1): Show |
4 | HG00733.hp2 HG01106.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.665+5244G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69111122 | |||||||
| chr14:69111132 | C | T | 1 | a0001c0001t0002g0235 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.665+5234G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69111132 | |||||||
| chr14:69111279 | T | C | 68 | a0001c0001t0001g0081 a0001c0001t0002g0029 a0001c0001t0002g0035 others(65): Show |
68 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.665+5087A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69111279 | |||||||
| chr14:69111805 | C | G | 1 | a0001c0001t0002g0127 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.665+4561G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69111805 | |||||||
| chr14:69111965 | A | G | 4 | a0001c0001t0001g0131 a0001c0001t0001g0189 a0001c0001t0001g0211 others(1): Show |
4 | HG02257.hp1 HG02572.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.665+4401T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69111965 | |||||||
| chr14:69112005 | G | A | 1 | a0001c0002t0001g0161 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.665+4361C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69112005 | |||||||
| chr14:69112119 | A | G | 1 | a0001c0001t0002g0079 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.665+4247T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69112119 | |||||||
| chr14:69112134 | A | G | 3 | a0001c0003t0002g0102 a0001c0003t0002g0103 a0001c0003t0002g0104 |
3 | HG02818.hp1 HG02965.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.665+4232T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69112134 | |||||||
| chr14:69112442 | G | T | 1 | a0001c0001t0007g0097 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.665+3924C>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69112442 | |||||||
| chr14:69112594 | T | TAC | 23 | a0001c0001t0001g0130 a0001c0001t0001g0230 a0001c0001t0002g0072 others(20): Show |
23 | HG00099.hp1 HG00140.hp2 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.665+3770_665+3771d others(4): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69112594 | |||||||
| chr14:69112594 | T | TACAC | 6 | a0001c0001t0001g0001 a0001c0001t0001g0129 a0001c0001t0001g0143 others(3): Show |
7 | HG02258.hp1 HG03130.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.665+3768_665+3771d others(6): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69112594 | |||||||
| chr14:69112594 | T | TACACAC | 6 | a0001c0001t0002g0007 a0001c0001t0002g0015 a0001c0001t0002g0021 others(3): Show |
6 | HG01257.hp2 HG03195.hp2 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.665+3766_665+3771d others(8): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69112594 | |||||||
| chr14:69112594 | T | TACACACA others(1): Show |
18 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(15): Show |
18 | HG00280.hp2 HG01074.hp2 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.665+3764_665+3771d others(10): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69112594 | |||||||
| chr14:69112594 | T | TACACACA others(3): Show |
19 | a0001c0001t0001g0134 a0001c0001t0001g0138 a0001c0001t0001g0139 others(16): Show |
19 | HG00738.hp2 HG01192.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.665+3762_665+3771d others(12): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69112594 | |||||||
| chr14:69112594 | T | TACACACA others(5): Show |
1 | a0001c0003t0002g0106 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.665+3760_665+3771d others(14): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69112594 | |||||||
| chr14:69112594 | T | TACACACA others(7): Show |
6 | a0001c0001t0017g0098 a0001c0003t0002g0102 a0001c0003t0002g0103 others(3): Show |
6 | HG02622.hp2 HG02818.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.665+3758_665+3771d others(16): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69112594 | |||||||
| chr14:69112594 | T | TACACACA others(9): Show |
9 | a0001c0003t0002g0104 a0001c0003t0002g0108 a0001c0003t0002g0109 others(6): Show |
9 | HG01243.hp2 HG01433.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.665+3756_665+3771d others(18): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69112594 | |||||||
| chr14:69112594 | T | TACACACA others(11): Show |
2 | a0001c0003t0002g0112 a0001c0003t0002g0120 |
2 | HG02145.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.665+3754_665+3771d others(20): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69112594 | |||||||
| chr14:69112594 | TAC | T | 25 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0192 others(22): Show |
25 | HG00735.hp1 HG00738.hp1 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.665+3770_665+3771d others(4): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69112594 | |||||||
| chr14:69112594 | TACAC | T | 29 | a0001c0001t0001g0166 a0001c0001t0006g0003 a0001c0001t0006g0168 others(26): Show |
31 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.665+3768_665+3771d others(6): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69112594 | |||||||
| chr14:69112594 | TACACACA others(5): Show |
T | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG04115.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.665+3760_665+3771d others(14): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69112594 | |||||||
| chr14:69112594 | TACACACA others(7): Show |
T | 4 | a0001c0001t0001g0004 a0001c0001t0001g0200 a0001c0001t0001g0203 others(1): Show |
5 | HG00642.hp1 HG01074.hp1 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.665+3758_665+3771d others(16): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69112594 | |||||||
| chr14:69112756 | G | A | 1 | a0001c0001t0014g0094 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.665+3610C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69112756 | |||||||
| chr14:69112840 | T | C | 1 | a0001c0001t0002g0088 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.665+3526A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69112840 | |||||||
| chr14:69112902 | C | T | 68 | a0001c0001t0001g0081 a0001c0001t0002g0029 a0001c0001t0002g0035 others(65): Show |
68 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.665+3464G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69112902 | |||||||
| chr14:69113023 | AT | A | 8 | a0001c0001t0004g0008 a0001c0001t0004g0009 a0001c0001t0004g0010 others(5): Show |
8 | HG01069.hp2 HG01192.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.665+3342delA | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69113023 | |||||||
| chr14:69113051 | A | C | 42 | a0001c0001t0001g0166 a0001c0001t0004g0008 a0001c0001t0004g0009 others(39): Show |
44 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.665+3315T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69113051 | |||||||
| chr14:69113098 | T | C | 17 | a0001c0003t0002g0108 a0001c0003t0002g0109 a0001c0003t0002g0111 others(14): Show |
17 | HG01243.hp2 HG01433.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.665+3268A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69113098 | |||||||
| chr14:69113102 | C | T | 1 | a0001c0004t0003g0047 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.665+3264G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69113102 | |||||||
| chr14:69113197 | G | A | 5 | a0001c0003t0002g0102 a0001c0003t0002g0103 a0001c0003t0002g0104 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.665+3169C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69113197 | |||||||
| chr14:69113447 | CAT | C | 4 | a0001c0001t0001g0001 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
5 | HG02647.hp2 HG03130.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.665+2917_665+2918d others(4): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69113447 | |||||||
| chr14:69113692 | G | T | 1 | a0001c0001t0003g0028 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.665+2674C>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69113692 | |||||||
| chr14:69113988 | G | A | 1 | a0001c0001t0002g0235 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.665+2378C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69113988 | |||||||
| chr14:69113989 | T | C | 2 | a0001c0001t0003g0092 a0001c0001t0003g0093 |
2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.665+2377A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69113989 | |||||||
| chr14:69113991 | G | A | 2 | a0001c0002t0001g0162 a0001c0002t0001g0163 |
2 | HG00735.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.665+2375C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69113991 | |||||||
| chr14:69114047 | A | G | 1 | a0001c0001t0002g0235 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.665+2319T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69114047 | |||||||
| chr14:69114267 | T | C | 1 | a0001c0001t0014g0094 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.665+2099A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69114267 | |||||||
| chr14:69114519 | C | A | 149 | a0001c0001t0001g0081 a0001c0001t0001g0166 a0001c0001t0002g0011 others(146): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.665+1847G>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69114519 | |||||||
| chr14:69114643 | A | C | 1 | a0003c0007t0012g0128 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.665+1723T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69114643 | |||||||
| chr14:69114726 | A | G | 2 | a0001c0001t0003g0092 a0001c0001t0003g0093 |
2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.665+1640T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69114726 | |||||||
| chr14:69115060 | T | C | 2 | a0001c0001t0001g0138 a0001c0001t0001g0144 |
2 | NA18956.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.665+1306A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69115060 | |||||||
| chr14:69115122 | G | C | 1 | a0001c0001t0001g0166 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.665+1244C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69115122 | |||||||
| chr14:69115181 | C | G | 42 | a0001c0001t0001g0166 a0001c0001t0004g0008 a0001c0001t0004g0009 others(39): Show |
44 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.665+1185G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69115181 | |||||||
| chr14:69115862 | G | C | 2 | a0001c0003t0002g0124 a0001c0003t0002g0125 |
2 | HG02109.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.665+504C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69115862 | |||||||
| chr14:69116134 | C | T | 1 | a0001c0002t0001g0167 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.665+232G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69116134 | |||||||
| chr14:69116184 | G | A | 1 | a0001c0001t0008g0061 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.665+182C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69116184 | |||||||
| chr14:69116232 | G | C | 1 | a0001c0001t0002g0013 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.665+134C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 5/8 | chr14 | 69116232 | |||||||
| chr14:69116546 | T | C | 4 | a0001c0001t0007g0095 a0001c0001t0007g0096 a0001c0001t0007g0097 others(1): Show |
4 | HG01074.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.536-51A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 4/8 | chr14 | 69116546 | |||||||
| chr14:69116608 | G | A | 1 | a0001c0001t0003g0063 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.536-113C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 4/8 | chr14 | 69116608 | |||||||
| chr14:69116827 | G | A | 1 | a0001c0003t0002g0121 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.536-332C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 4/8 | chr14 | 69116827 | |||||||
| chr14:69116959 | G | T | 1 | a0001c0001t0002g0126 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.536-464C>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 4/8 | chr14 | 69116959 | |||||||
| chr14:69117245 | C | T | 1 | a0001c0001t0002g0126 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.536-750G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 4/8 | chr14 | 69117245 | |||||||
| chr14:69117487 | G | A | 1 | a0001c0001t0002g0127 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.535+652C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 4/8 | chr14 | 69117487 | |||||||
| chr14:69117929 | G | C | 12 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(9): Show |
12 | HG00280.hp2 HG00738.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.535+210C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 4/8 | chr14 | 69117929 | |||||||
| chr14:69118453 | A | G | 2 | a0001c0001t0003g0092 a0001c0001t0003g0093 |
2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.396-175T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 3/8 | chr14 | 69118453 | |||||||
| chr14:69118690 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.396-412C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 3/8 | chr14 | 69118690 | |||||||
| chr14:69118937 | C | T | 22 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(19): Show |
22 | HG01074.hp2 HG01361.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.395+257G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 3/8 | chr14 | 69118937 | |||||||
| chr14:69118939 | T | C | 1 | a0001c0001t0007g0097 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.395+255A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 3/8 | chr14 | 69118939 | |||||||
| chr14:69119423 | T | A | 4 | a0001c0001t0001g0001 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
5 | HG02647.hp2 HG03130.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.359-193A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69119423 | |||||||
| chr14:69119490 | T | TA | 6 | a0001c0001t0002g0078 a0001c0001t0002g0126 a0001c0001t0007g0095 others(3): Show |
6 | HG01074.hp2 HG02129.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.359-261dupT | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69119490 | |||||||
| chr14:69119590 | T | C | 2 | a0001c0001t0001g0194 a0001c0001t0001g0196 |
2 | HG00741.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.359-360A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69119590 | |||||||
| chr14:69119669 | C | T | 1 | a0001c0001t0002g0078 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.359-439G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69119669 | |||||||
| chr14:69119678 | G | T | 1 | a0001c0001t0002g0123 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.359-448C>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69119678 | |||||||
| chr14:69119704 | C | G | 2 | a0001c0001t0003g0092 a0001c0001t0003g0093 |
2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.359-474G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69119704 | |||||||
| chr14:69119704 | CA | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0129 a0001c0001t0001g0130 others(115): Show |
121 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.359-475delT | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69119704 | |||||||
| chr14:69119704 | CAA | C | 69 | a0001c0001t0001g0081 a0001c0001t0002g0029 a0001c0001t0002g0035 others(66): Show |
69 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.359-476_359-475del others(2): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69119704 | |||||||
| chr14:69119724 | G | T | 2 | a0001c0001t0003g0092 a0001c0001t0003g0093 |
2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.359-494C>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69119724 | |||||||
| chr14:69119862 | G | A | 212 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0081 others(209): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.359-632C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69119862 | |||||||
| chr14:69119880 | T | A | 50 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(47): Show |
50 | HG01074.hp2 HG01192.hp2 HG01243.hp2 others(47): Show |
intron_variant | MODIFIER | c.359-650A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69119880 | |||||||
| chr14:69120066 | T | G | 1 | a0001c0001t0001g0197 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.359-836A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69120066 | |||||||
| chr14:69120224 | C | T | 12 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(9): Show |
12 | HG00280.hp2 HG00738.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.359-994G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69120224 | |||||||
| chr14:69120276 | G | C | 1 | a0001c0001t0014g0094 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.359-1046C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69120276 | |||||||
| chr14:69120450 | A | G | 2 | a0001c0001t0003g0092 a0001c0001t0003g0093 |
2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.359-1220T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69120450 | |||||||
| chr14:69120493 | G | A | 14 | a0001c0001t0004g0008 a0001c0001t0004g0009 a0001c0001t0004g0010 others(11): Show |
14 | HG01069.hp2 HG01175.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.359-1263C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69120493 | |||||||
| chr14:69120516 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.359-1286C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69120516 | |||||||
| chr14:69121106 | T | C | 1 | a0001c0001t0002g0088 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.358+1111A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69121106 | |||||||
| chr14:69121168 | G | T | 3 | a0001c0001t0007g0095 a0001c0001t0007g0096 a0001c0001t0007g0097 |
3 | HG01074.hp2 HG03195.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.358+1049C>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69121168 | |||||||
| chr14:69121327 | C | T | 1 | a0001c0001t0002g0025 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.358+890G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69121327 | |||||||
| chr14:69121328 | G | A | 28 | a0001c0001t0001g0166 a0001c0001t0006g0003 a0001c0001t0006g0168 others(25): Show |
30 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.358+889C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69121328 | |||||||
| chr14:69121455 | C | T | 2 | a0001c0001t0003g0092 a0001c0001t0003g0093 |
2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.358+762G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69121455 | |||||||
| chr14:69121596 | T | G | 2 | a0001c0001t0002g0035 a0001c0006t0003g0006 |
2 | HG00741.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.358+621A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69121596 | |||||||
| chr14:69121651 | T | A | 1 | a0001c0001t0018g0238 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.358+566A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69121651 | |||||||
| chr14:69121798 | G | C | 2 | a0001c0001t0002g0019 a0001c0001t0002g0024 |
2 | NA19080.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.358+419C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69121798 | |||||||
| chr14:69121829 | G | A | 13 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0002g0018 others(10): Show |
13 | HG01361.hp1 HG02056.hp1 HG02155.hp1 others(10): Show |
intron_variant | MODIFIER | c.358+388C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69121829 | |||||||
| chr14:69121880 | C | T | 132 | a0001c0001t0001g0081 a0001c0001t0001g0166 a0001c0001t0002g0011 others(129): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.358+337G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69121880 | |||||||
| chr14:69121935 | C | G | 1 | a0001c0001t0013g0099 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.358+282G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69121935 | |||||||
| chr14:69121993 | A | G | 2 | a0001c0002t0001g0170 a0001c0002t0001g0171 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.358+224T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69121993 | |||||||
| chr14:69122192 | C | T | 1 | a0001c0001t0005g0172 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.358+25G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 2/8 | chr14 | 69122192 | |||||||
| chr14:69122532 | G | A | 218 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0081 others(215): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.215-172C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69122532 | |||||||
| chr14:69122620 | T | G | 1 | a0001c0001t0007g0097 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.215-260A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69122620 | |||||||
| chr14:69122872 | T | TA | 100 | a0001c0001t0001g0081 a0001c0001t0002g0011 a0001c0001t0002g0012 others(97): Show |
100 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(97): Show |
intron_variant | MODIFIER | c.215-513dupT | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69122872 | |||||||
| chr14:69122941 | T | G | 24 | a0001c0002t0001g0002 a0001c0002t0001g0147 a0001c0002t0001g0148 others(21): Show |
25 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.215-581A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69122941 | |||||||
| chr14:69123204 | C | T | 1 | a0001c0003t0002g0110 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.215-844G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69123204 | |||||||
| chr14:69123336 | T | G | 2 | a0001c0001t0002g0072 a0001c0001t0018g0238 |
2 | HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.215-976A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69123336 | |||||||
| chr14:69123443 | G | C | 2 | a0001c0001t0002g0100 a0001c0001t0002g0101 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.215-1083C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69123443 | |||||||
| chr14:69123714 | C | T | 1 | a0001c0001t0002g0035 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.215-1354G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69123714 | |||||||
| chr14:69123768 | G | A | 2 | a0001c0001t0003g0092 a0001c0001t0003g0093 |
2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.215-1408C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69123768 | |||||||
| chr14:69123889 | G | A | 6 | a0001c0001t0002g0077 a0001c0003t0002g0102 a0001c0003t0002g0103 others(3): Show |
6 | HG01891.hp2 HG02280.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.215-1529C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69123889 | |||||||
| chr14:69123935 | T | C | 28 | a0001c0001t0002g0100 a0001c0001t0002g0101 a0001c0001t0002g0123 others(25): Show |
28 | HG01192.hp2 HG01243.hp2 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.215-1575A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69123935 | |||||||
| chr14:69124212 | T | C | 1 | a0001c0002t0001g0002 | 2 | HG00642.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.215-1852A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69124212 | |||||||
| chr14:69124432 | C | G | 1 | a0001c0001t0002g0235 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.215-2072G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69124432 | |||||||
| chr14:69124795 | C | T | 4 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(1): Show |
4 | HG00733.hp2 HG01106.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.215-2435G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69124795 | |||||||
| chr14:69124999 | A | C | 1 | a0001c0001t0002g0235 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.215-2639T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69124999 | |||||||
| chr14:69125095 | A | C | 2 | a0001c0001t0003g0092 a0001c0001t0003g0093 |
2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.215-2735T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69125095 | |||||||
| chr14:69125237 | G | A | 1 | a0001c0001t0002g0127 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.215-2877C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69125237 | |||||||
| chr14:69125492 | A | G | 28 | a0001c0001t0001g0166 a0001c0001t0006g0003 a0001c0001t0006g0168 others(25): Show |
30 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.215-3132T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69125492 | |||||||
| chr14:69125984 | A | G | 1 | a0001c0001t0001g0129 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.215-3624T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69125984 | |||||||
| chr14:69125999 | A | C | 18 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(15): Show |
18 | HG01361.hp1 HG02055.hp1 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.215-3639T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69125999 | |||||||
| chr14:69126022 | G | A | 189 | a0001c0001t0001g0001 a0001c0001t0001g0081 a0001c0001t0001g0129 others(186): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.215-3662C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69126022 | |||||||
| chr14:69126064 | T | C | 71 | a0001c0001t0001g0081 a0001c0001t0002g0011 a0001c0001t0002g0012 others(68): Show |
71 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.215-3704A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69126064 | |||||||
| chr14:69126074 | A | G | 1 | a0001c0001t0004g0185 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.215-3714T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69126074 | |||||||
| chr14:69126155 | C | CT | 14 | a0001c0001t0001g0001 a0001c0001t0001g0129 a0001c0001t0001g0130 others(11): Show |
16 | HG01934.hp2 HG02145.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.215-3796dupA | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69126155 | |||||||
| chr14:69126295 | T | G | 1 | a0001c0001t0001g0231 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.215-3935A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69126295 | |||||||
| chr14:69126442 | C | A | 1 | a0001c0001t0013g0099 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.215-4082G>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69126442 | |||||||
| chr14:69126485 | C | T | 1 | a0001c0001t0017g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.215-4125G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69126485 | |||||||
| chr14:69126523 | C | G | 4 | a0001c0001t0007g0095 a0001c0001t0007g0096 a0001c0001t0007g0097 others(1): Show |
4 | HG01074.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.215-4163G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69126523 | |||||||
| chr14:69126567 | C | A | 2 | a0001c0001t0003g0042 a0001c0001t0003g0046 |
2 | NA18940.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.215-4207G>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69126567 | |||||||
| chr14:69126735 | G | A | 128 | a0001c0001t0001g0081 a0001c0001t0001g0166 a0001c0001t0002g0029 others(125): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.215-4375C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69126735 | |||||||
| chr14:69126866 | G | C | 1 | a0001c0001t0003g0068 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.215-4506C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69126866 | |||||||
| chr14:69127152 | T | C | 1 | a0001c0001t0001g0220 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.215-4792A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69127152 | |||||||
| chr14:69127194 | T | C | 3 | a0001c0001t0006g0003 a0001c0001t0006g0168 a0001c0001t0006g0169 |
4 | HG02280.hp1 HG02451.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.215-4834A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69127194 | |||||||
| chr14:69127259 | T | C | 1 | a0001c0003t0002g0122 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.215-4899A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69127259 | |||||||
| chr14:69127276 | G | A | 21 | a0001c0001t0001g0081 a0001c0001t0002g0069 a0001c0001t0002g0070 others(18): Show |
21 | HG00099.hp1 HG01071.hp2 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.215-4916C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69127276 | |||||||
| chr14:69127304 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.215-4944C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69127304 | |||||||
| chr14:69127395 | C | T | 1 | a0001c0001t0013g0099 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.215-5035G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69127395 | |||||||
| chr14:69127465 | A | G | 28 | a0001c0001t0001g0166 a0001c0001t0006g0003 a0001c0001t0006g0168 others(25): Show |
30 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.215-5105T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69127465 | |||||||
| chr14:69127480 | T | A | 28 | a0001c0001t0001g0166 a0001c0001t0006g0003 a0001c0001t0006g0168 others(25): Show |
30 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.215-5120A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69127480 | |||||||
| chr14:69127486 | G | A | 1 | a0001c0001t0004g0185 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.215-5126C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69127486 | |||||||
| chr14:69127738 | T | G | 1 | a0001c0001t0001g0225 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.215-5378A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69127738 | |||||||
| chr14:69127814 | C | T | 28 | a0001c0001t0001g0166 a0001c0001t0006g0003 a0001c0001t0006g0168 others(25): Show |
30 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.215-5454G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69127814 | |||||||
| chr14:69128085 | T | G | 2 | a0001c0001t0003g0092 a0001c0001t0003g0093 |
2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.215-5725A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69128085 | |||||||
| chr14:69128087 | T | C | 1 | a0001c0001t0013g0099 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.215-5727A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69128087 | |||||||
| chr14:69128116 | T | C | 1 | a0001c0003t0002g0122 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.215-5756A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69128116 | |||||||
| chr14:69128122 | T | C | 1 | a0001c0001t0001g0134 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.215-5762A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69128122 | |||||||
| chr14:69128193 | C | CT | 37 | a0001c0001t0001g0001 a0001c0001t0001g0129 a0001c0001t0001g0130 others(34): Show |
38 | HG01192.hp2 HG01243.hp2 HG01433.hp2 others(35): Show |
intron_variant | MODIFIER | c.215-5834dupA | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69128193 | |||||||
| chr14:69128196 | T | C | 28 | a0001c0001t0001g0166 a0001c0001t0006g0003 a0001c0001t0006g0168 others(25): Show |
30 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.215-5836A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69128196 | |||||||
| chr14:69128234 | C | T | 28 | a0001c0001t0001g0166 a0001c0001t0006g0003 a0001c0001t0006g0168 others(25): Show |
30 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.215-5874G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69128234 | |||||||
| chr14:69128378 | A | G | 159 | a0001c0001t0001g0081 a0001c0001t0001g0166 a0001c0001t0002g0011 others(156): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.215-6018T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69128378 | |||||||
| chr14:69128432 | C | T | 14 | a0001c0001t0001g0081 a0001c0001t0002g0069 a0001c0001t0002g0070 others(11): Show |
14 | HG00099.hp1 HG01071.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.215-6072G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69128432 | |||||||
| chr14:69128646 | T | C | 2 | a0001c0001t0003g0043 a0001c0001t0003g0062 |
2 | HG03654.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.215-6286A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69128646 | |||||||
| chr14:69128670 | A | T | 1 | a0001c0001t0013g0099 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.215-6310T>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69128670 | |||||||
| chr14:69128671 | G | T | 1 | a0001c0001t0013g0099 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.215-6311C>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69128671 | |||||||
| chr14:69128679 | A | G | 1 | a0001c0001t0013g0099 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.215-6319T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69128679 | |||||||
| chr14:69128680 | A | T | 1 | a0001c0001t0013g0099 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.215-6320T>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69128680 | |||||||
| chr14:69128681 | T | C | 1 | a0001c0001t0013g0099 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.215-6321A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69128681 | |||||||
| chr14:69128710 | G | A | 99 | a0001c0001t0001g0081 a0001c0001t0002g0011 a0001c0001t0002g0012 others(96): Show |
99 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(96): Show |
intron_variant | MODIFIER | c.215-6350C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69128710 | |||||||
| chr14:69128790 | C | A | 1 | a0001c0001t0002g0020 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.215-6430G>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69128790 | |||||||
| chr14:69128790 | C | T | 4 | a0001c0001t0005g0172 a0001c0001t0005g0173 a0001c0001t0005g0174 others(1): Show |
4 | HG02145.hp1 HG02559.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.215-6430G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69128790 | |||||||
| chr14:69128814 | C | T | 4 | a0001c0001t0007g0095 a0001c0001t0007g0096 a0001c0001t0007g0097 others(1): Show |
4 | HG01074.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.215-6454G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69128814 | |||||||
| chr14:69129366 | A | G | 14 | a0001c0001t0004g0008 a0001c0001t0004g0009 a0001c0001t0004g0010 others(11): Show |
14 | HG01069.hp2 HG01175.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.215-7006T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69129366 | |||||||
| chr14:69129382 | T | C | 1 | a0001c0003t0002g0110 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.215-7022A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69129382 | |||||||
| chr14:69129652 | G | A | 14 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0002g0018 others(11): Show |
14 | HG01361.hp1 HG02055.hp1 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.215-7292C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69129652 | |||||||
| chr14:69129824 | C | A | 1 | a0001c0001t0001g0190 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.215-7464G>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69129824 | |||||||
| chr14:69129853 | T | C | 1 | a0001c0001t0002g0021 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.215-7493A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69129853 | |||||||
| chr14:69129898 | A | G | 12 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(9): Show |
12 | HG00280.hp2 HG00738.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.215-7538T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69129898 | |||||||
| chr14:69130173 | G | A | 1 | a0001c0001t0001g0004 | 2 | HG01074.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.215-7813C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69130173 | |||||||
| chr14:69130213 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.215-7853C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69130213 | |||||||
| chr14:69130230 | G | A | 1 | a0001c0001t0004g0184 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.215-7870C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69130230 | |||||||
| chr14:69130313 | T | G | 1 | a0003c0007t0012g0128 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.215-7953A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69130313 | |||||||
| chr14:69131052 | G | C | 128 | a0001c0001t0001g0081 a0001c0001t0001g0166 a0001c0001t0002g0029 others(125): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.215-8692C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69131052 | |||||||
| chr14:69131532 | T | C | 1 | a0001c0001t0001g0226 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.215-9172A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69131532 | |||||||
| chr14:69131759 | C | CT | 27 | a0001c0001t0001g0166 a0001c0001t0002g0075 a0001c0001t0002g0076 others(24): Show |
28 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.215-9400dupA | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69131759 | |||||||
| chr14:69131759 | CT | C | 9 | a0001c0001t0001g0136 a0001c0001t0001g0200 a0001c0001t0002g0023 others(6): Show |
9 | HG01515.hp2 HG02145.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.215-9400delA | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69131759 | |||||||
| chr14:69132163 | T | C | 1 | a0001c0001t0002g0235 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.215-9803A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69132163 | |||||||
| chr14:69132171 | C | T | 1 | a0001c0001t0008g0045 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.215-9811G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69132171 | |||||||
| chr14:69132204 | T | C | 6 | a0001c0001t0001g0134 a0001c0001t0001g0138 a0001c0001t0001g0139 others(3): Show |
6 | NA18940.hp1 NA18956.hp2 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.215-9844A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69132204 | |||||||
| chr14:69132429 | T | C | 9 | a0001c0001t0002g0090 a0001c0001t0002g0091 a0001c0001t0002g0176 others(6): Show |
9 | HG01081.hp1 HG01496.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.215-10069A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69132429 | |||||||
| chr14:69132722 | TAGCAC | T | 20 | a0001c0001t0002g0123 a0001c0003t0002g0108 a0001c0003t0002g0109 others(17): Show |
20 | HG01192.hp2 HG01243.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.215-10367_215-1036 others(9): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69132722 | |||||||
| chr14:69132766 | G | T | 42 | a0001c0001t0002g0029 a0001c0001t0002g0035 a0001c0001t0003g0026 others(39): Show |
42 | HG00140.hp2 HG00735.hp1 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.215-10406C>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69132766 | |||||||
| chr14:69132853 | T | C | 98 | a0001c0001t0001g0081 a0001c0001t0002g0029 a0001c0001t0002g0035 others(95): Show |
98 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(95): Show |
intron_variant | MODIFIER | c.215-10493A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69132853 | |||||||
| chr14:69132973 | T | A | 1 | a0001c0002t0001g0165 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.215-10613A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69132973 | |||||||
| chr14:69133000 | T | C | 4 | a0001c0001t0001g0001 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
5 | HG02647.hp2 HG03130.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.215-10640A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69133000 | |||||||
| chr14:69133049 | G | GA | 14 | a0001c0001t0004g0008 a0001c0001t0004g0009 a0001c0001t0004g0010 others(11): Show |
14 | HG01069.hp2 HG01175.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.215-10690dupT | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69133049 | |||||||
| chr14:69133530 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.215-11170G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69133530 | |||||||
| chr14:69133539 | T | A | 3 | a0001c0001t0007g0095 a0001c0001t0007g0096 a0001c0001t0007g0097 |
3 | HG01074.hp2 HG03195.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.215-11179A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69133539 | |||||||
| chr14:69133551 | A | AG | 3 | a0001c0003t0002g0102 a0001c0003t0002g0103 a0001c0003t0002g0104 |
3 | HG02818.hp1 HG02965.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.215-11192dupC | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69133551 | |||||||
| chr14:69133554 | C | G | 98 | a0001c0001t0001g0081 a0001c0001t0002g0029 a0001c0001t0002g0035 others(95): Show |
98 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(95): Show |
intron_variant | MODIFIER | c.215-11194G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69133554 | |||||||
| chr14:69133556 | G | C | 2 | a0001c0001t0003g0092 a0001c0001t0003g0093 |
2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.215-11196C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69133556 | |||||||
| chr14:69133602 | A | C | 1 | a0001c0001t0004g0185 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.215-11242T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69133602 | |||||||
| chr14:69133723 | T | C | 4 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(1): Show |
4 | HG00733.hp2 HG01106.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.215-11363A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69133723 | |||||||
| chr14:69133872 | T | G | 1 | a0001c0001t0001g0202 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.215-11512A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69133872 | |||||||
| chr14:69133918 | A | G | 2 | a0001c0001t0008g0060 a0001c0001t0008g0061 |
2 | HG01934.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.215-11558T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69133918 | |||||||
| chr14:69134177 | G | A | 1 | a0001c0001t0014g0094 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.215-11817C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69134177 | |||||||
| chr14:69134370 | G | A | 12 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(9): Show |
12 | HG00280.hp2 HG00738.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.215-12010C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69134370 | |||||||
| chr14:69134492 | C | T | 12 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(9): Show |
12 | HG00280.hp2 HG00738.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.215-12132G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69134492 | |||||||
| chr14:69134500 | T | A | 1 | a0001c0001t0002g0235 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.215-12140A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69134500 | |||||||
| chr14:69134823 | T | G | 1 | a0001c0001t0001g0198 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.215-12463A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69134823 | |||||||
| chr14:69135033 | G | C | 1 | a0001c0001t0001g0202 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.215-12673C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69135033 | |||||||
| chr14:69135056 | A | G | 2 | a0001c0001t0003g0092 a0001c0001t0003g0093 |
2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.215-12696T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69135056 | |||||||
| chr14:69135168 | T | C | 3 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0020g0240 |
3 | HG02083.hp1 HG02165.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.215-12808A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69135168 | |||||||
| chr14:69135170 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.215-12810G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69135170 | |||||||
| chr14:69135408 | C | T | 1 | a0001c0001t0003g0044 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.215-13048G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69135408 | |||||||
| chr14:69135458 | G | A | 2 | a0001c0001t0003g0092 a0001c0001t0003g0093 |
2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.215-13098C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69135458 | |||||||
| chr14:69135491 | A | G | 1 | a0001c0001t0014g0094 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.215-13131T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69135491 | |||||||
| chr14:69135649 | G | T | 1 | a0001c0001t0002g0126 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.215-13289C>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69135649 | |||||||
| chr14:69135686 | A | G | 2 | a0001c0001t0002g0123 a0001c0003t0002g0110 |
2 | HG01192.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.215-13326T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69135686 | |||||||
| chr14:69135712 | T | C | 2 | a0001c0001t0001g0139 a0001c0001t0001g0140 |
2 | NA18940.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.215-13352A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69135712 | |||||||
| chr14:69135938 | A | G | 5 | a0001c0001t0002g0090 a0001c0001t0002g0091 a0001c0001t0002g0176 others(2): Show |
5 | HG01081.hp1 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.215-13578T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69135938 | |||||||
| chr14:69136113 | C | CT | 58 | a0001c0001t0001g0132 a0001c0001t0001g0141 a0001c0001t0001g0166 others(55): Show |
60 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.215-13754dupA | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69136113 | |||||||
| chr14:69136113 | C | CTT | 108 | a0001c0001t0001g0081 a0001c0001t0002g0011 a0001c0001t0002g0012 others(105): Show |
108 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(105): Show |
intron_variant | MODIFIER | c.215-13755_215-1375 others(6): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69136113 | |||||||
| chr14:69136113 | C | CTTT | 6 | a0001c0001t0002g0123 a0001c0001t0003g0034 a0001c0001t0003g0042 others(3): Show |
6 | HG01192.hp2 HG01981.hp2 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.215-13756_215-1375 others(7): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69136113 | |||||||
| chr14:69136289 | T | C | 1 | a0001c0001t0001g0224 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.215-13929A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69136289 | |||||||
| chr14:69136314 | C | T | 1 | a0001c0001t0002g0126 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.215-13954G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69136314 | |||||||
| chr14:69136601 | A | G | 4 | a0001c0001t0005g0172 a0001c0001t0005g0173 a0001c0001t0005g0174 others(1): Show |
4 | HG02145.hp1 HG02559.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.215-14241T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69136601 | |||||||
| chr14:69136771 | T | C | 1 | a0001c0003t0002g0122 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.215-14411A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69136771 | |||||||
| chr14:69136793 | C | G | 12 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(9): Show |
12 | HG00280.hp2 HG00738.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.215-14433G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69136793 | |||||||
| chr14:69136824 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.215-14464C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69136824 | |||||||
| chr14:69136848 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.215-14488A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69136848 | |||||||
| chr14:69136979 | A | G | 4 | a0001c0001t0001g0001 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
5 | HG02647.hp2 HG03130.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.215-14619T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69136979 | |||||||
| chr14:69137256 | G | A | 4 | a0001c0001t0001g0001 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
5 | HG02647.hp2 HG03130.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.215-14896C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69137256 | |||||||
| chr14:69137296 | T | C | 2 | a0001c0001t0003g0092 a0001c0001t0003g0093 |
2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.215-14936A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69137296 | |||||||
| chr14:69137385 | C | G | 2 | a0001c0001t0010g0209 a0001c0001t0010g0210 |
2 | HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.215-15025G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69137385 | |||||||
| chr14:69137527 | A | C | 50 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(47): Show |
50 | HG01074.hp2 HG01192.hp2 HG01243.hp2 others(47): Show |
intron_variant | MODIFIER | c.215-15167T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69137527 | |||||||
| chr14:69138308 | G | A | 2 | a0001c0001t0003g0058 a0001c0001t0003g0059 |
2 | NA19070.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.214+14457C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69138308 | |||||||
| chr14:69138554 | G | A | 1 | a0001c0001t0002g0084 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.214+14211C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69138554 | |||||||
| chr14:69138555 | C | A | 1 | a0001c0001t0002g0084 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.214+14210G>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69138555 | |||||||
| chr14:69138702 | T | C | 2 | a0001c0001t0003g0092 a0001c0001t0003g0093 |
2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.214+14063A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69138702 | |||||||
| chr14:69138834 | A | T | 1 | a0001c0001t0013g0099 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.214+13931T>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69138834 | |||||||
| chr14:69138965 | G | A | 1 | a0001c0001t0014g0094 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.214+13800C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69138965 | |||||||
| chr14:69139049 | G | A | 4 | a0001c0001t0005g0172 a0001c0001t0005g0173 a0001c0001t0005g0174 others(1): Show |
4 | HG02145.hp1 HG02559.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.214+13716C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69139049 | |||||||
| chr14:69139411 | G | C | 1 | a0001c0001t0002g0235 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.214+13354C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69139411 | |||||||
| chr14:69139537 | G | C | 1 | a0001c0001t0001g0166 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.214+13228C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69139537 | |||||||
| chr14:69139582 | G | A | 1 | a0001c0001t0002g0085 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.214+13183C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69139582 | |||||||
| chr14:69139750 | C | T | 3 | a0001c0001t0002g0100 a0001c0001t0002g0101 a0003c0007t0012g0128 |
3 | HG02572.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.214+13015G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69139750 | |||||||
| chr14:69140079 | G | A | 150 | a0001c0001t0001g0081 a0001c0001t0001g0166 a0001c0001t0002g0011 others(147): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.214+12686C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69140079 | |||||||
| chr14:69140191 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.214+12574G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69140191 | |||||||
| chr14:69140192 | G | A | 1 | a0001c0002t0001g0151 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.214+12573C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69140192 | |||||||
| chr14:69140286 | G | C | 71 | a0001c0001t0001g0081 a0001c0001t0002g0011 a0001c0001t0002g0012 others(68): Show |
71 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.214+12479C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69140286 | |||||||
| chr14:69140415 | C | A | 1 | a0001c0001t0020g0240 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.214+12350G>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69140415 | |||||||
| chr14:69140536 | T | G | 1 | a0001c0001t0001g0201 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.214+12229A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69140536 | |||||||
| chr14:69140753 | T | C | 1 | a0001c0001t0002g0126 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.214+12012A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69140753 | |||||||
| chr14:69140832 | G | A | 1 | a0003c0007t0012g0128 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.214+11933C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69140832 | |||||||
| chr14:69140845 | G | A | 4 | a0001c0001t0001g0001 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
5 | HG02647.hp2 HG03130.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.214+11920C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69140845 | |||||||
| chr14:69140956 | A | G | 1 | a0001c0001t0003g0041 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.214+11809T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69140956 | |||||||
| chr14:69140973 | A | G | 17 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(14): Show |
17 | HG01361.hp1 HG02056.hp1 HG02083.hp1 others(14): Show |
intron_variant | MODIFIER | c.214+11792T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69140973 | |||||||
| chr14:69141139 | T | A | 4 | a0001c0001t0007g0095 a0001c0001t0007g0096 a0001c0001t0007g0097 others(1): Show |
4 | HG01074.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.214+11626A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69141139 | |||||||
| chr14:69141139 | T | TA | 33 | a0001c0001t0001g0134 a0001c0001t0001g0141 a0001c0001t0001g0166 others(30): Show |
35 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.214+11625dupT | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69141139 | |||||||
| chr14:69141139 | TA | T | 18 | a0001c0001t0001g0191 a0001c0001t0001g0193 a0001c0001t0001g0199 others(15): Show |
18 | HG00099.hp1 HG01069.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.214+11625delT | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69141139 | |||||||
| chr14:69141139 | TAAAAAAA | T | 12 | a0001c0003t0002g0108 a0001c0003t0002g0109 a0001c0003t0002g0111 others(9): Show |
12 | HG01243.hp2 HG01433.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.214+11619_214+1162 others(11): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69141139 | |||||||
| chr14:69141139 | TAAAAAAA others(1): Show |
T | 5 | a0001c0001t0001g0001 a0001c0001t0001g0129 a0001c0001t0001g0130 others(2): Show |
6 | HG02647.hp2 HG02922.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.214+11618_214+1162 others(12): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69141139 | |||||||
| chr14:69141139 | TAAAAAAA others(3): Show |
T | 1 | a0001c0001t0002g0235 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.214+11616_214+1162 others(14): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69141139 | |||||||
| chr14:69141139 | TAAAAAAA others(6): Show |
T | 1 | a0001c0001t0013g0099 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.214+11613_214+1162 others(17): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69141139 | |||||||
| chr14:69141236 | T | C | 3 | a0001c0001t0004g0183 a0001c0001t0004g0184 a0001c0001t0004g0188 |
3 | HG03041.hp1 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.214+11529A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69141236 | |||||||
| chr14:69141343 | CTT | C | 67 | a0001c0001t0001g0081 a0001c0001t0002g0029 a0001c0001t0002g0035 others(64): Show |
67 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.214+11420_214+1142 others(6): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69141343 | |||||||
| chr14:69141354 | TTTTTC | T | 9 | a0001c0001t0001g0190 a0001c0001t0001g0192 a0001c0001t0001g0193 others(6): Show |
9 | HG00741.hp1 HG01346.hp2 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.214+11406_214+1141 others(9): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69141354 | |||||||
| chr14:69141401 | C | T | 1 | a0001c0001t0003g0033 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.214+11364G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69141401 | |||||||
| chr14:69141812 | C | T | 1 | a0001c0001t0013g0099 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.214+10953G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69141812 | |||||||
| chr14:69141881 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.214+10884G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69141881 | |||||||
| chr14:69142070 | G | A | 1 | a0001c0003t0002g0106 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.214+10695C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69142070 | |||||||
| chr14:69142106 | G | A | 5 | a0001c0001t0002g0090 a0001c0001t0002g0091 a0001c0001t0002g0176 others(2): Show |
5 | HG01081.hp1 HG01496.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.214+10659C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69142106 | |||||||
| chr14:69142127 | T | C | 28 | a0001c0001t0002g0100 a0001c0001t0002g0101 a0001c0001t0002g0123 others(25): Show |
28 | HG01192.hp2 HG01243.hp2 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.214+10638A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69142127 | |||||||
| chr14:69142141 | T | A | 15 | a0001c0001t0004g0008 a0001c0001t0004g0009 a0001c0001t0004g0010 others(12): Show |
15 | HG01069.hp2 HG01175.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.214+10624A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69142141 | |||||||
| chr14:69142446 | G | A | 2 | a0001c0001t0003g0092 a0001c0001t0003g0093 |
2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.214+10319C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69142446 | |||||||
| chr14:69142494 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.214+10271G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69142494 | |||||||
| chr14:69142780 | G | C | 4 | a0001c0001t0001g0166 a0001c0001t0006g0003 a0001c0001t0006g0168 others(1): Show |
5 | HG02280.hp1 HG02451.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.214+9985C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69142780 | |||||||
| chr14:69142781 | T | C | 28 | a0001c0001t0001g0166 a0001c0001t0006g0003 a0001c0001t0006g0168 others(25): Show |
30 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.214+9984A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69142781 | |||||||
| chr14:69142899 | A | G | 1 | a0001c0001t0013g0099 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.214+9866T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69142899 | |||||||
| chr14:69143135 | A | C | 71 | a0001c0001t0001g0081 a0001c0001t0002g0011 a0001c0001t0002g0012 others(68): Show |
71 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.214+9630T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69143135 | |||||||
| chr14:69143412 | T | G | 1 | a0001c0001t0002g0123 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.214+9353A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69143412 | |||||||
| chr14:69143484 | G | A | 2 | a0001c0001t0008g0060 a0001c0001t0008g0061 |
2 | HG01934.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.214+9281C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69143484 | |||||||
| chr14:69143553 | C | CT | 99 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0081 others(96): Show |
101 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.214+9211dupA | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69143553 | |||||||
| chr14:69143553 | C | CTT | 23 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0232 others(20): Show |
23 | HG01175.hp1 HG01192.hp2 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.214+9210_214+9211d others(4): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69143553 | |||||||
| chr14:69143553 | C | CTTT | 12 | a0001c0001t0003g0032 a0001c0001t0003g0092 a0001c0001t0003g0093 others(9): Show |
12 | HG00735.hp1 HG01243.hp2 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.214+9209_214+9211d others(5): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69143553 | |||||||
| chr14:69143553 | C | CTTTT | 7 | a0001c0001t0002g0235 a0001c0003t0002g0111 a0001c0003t0002g0112 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.214+9208_214+9211d others(6): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69143553 | |||||||
| chr14:69143553 | CT | C | 9 | a0001c0001t0001g0132 a0001c0001t0001g0228 a0001c0001t0004g0010 others(6): Show |
9 | HG00140.hp1 HG01069.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.214+9211delA | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69143553 | |||||||
| chr14:69143635 | G | A | 2 | a0001c0001t0003g0092 a0001c0001t0003g0093 |
2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.214+9130C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69143635 | |||||||
| chr14:69143637 | C | T | 1 | a0001c0001t0003g0031 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.214+9128G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69143637 | |||||||
| chr14:69143651 | G | C | 12 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(9): Show |
12 | HG00280.hp2 HG00738.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.214+9114C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69143651 | |||||||
| chr14:69143761 | A | G | 71 | a0001c0001t0001g0081 a0001c0001t0002g0011 a0001c0001t0002g0012 others(68): Show |
71 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.214+9004T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69143761 | |||||||
| chr14:69144007 | A | C | 18 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0002g0018 others(15): Show |
18 | HG01074.hp2 HG01361.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.214+8758T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69144007 | |||||||
| chr14:69144008 | T | C | 100 | a0001c0001t0001g0081 a0001c0001t0002g0011 a0001c0001t0002g0012 others(97): Show |
100 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(97): Show |
intron_variant | MODIFIER | c.214+8757A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69144008 | |||||||
| chr14:69144100 | A | G | 1 | a0001c0003t0002g0110 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.214+8665T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69144100 | |||||||
| chr14:69144293 | C | A | 1 | a0001c0001t0003g0028 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.214+8472G>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69144293 | |||||||
| chr14:69144294 | C | T | 1 | a0001c0001t0003g0028 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.214+8471G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69144294 | |||||||
| chr14:69144302 | G | A | 1 | a0001c0001t0003g0028 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.214+8463C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69144302 | |||||||
| chr14:69144303 | T | A | 1 | a0001c0001t0003g0028 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.214+8462A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69144303 | |||||||
| chr14:69144304 | G | A | 1 | a0001c0001t0003g0028 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.214+8461C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69144304 | |||||||
| chr14:69144424 | T | A | 1 | a0001c0001t0001g0229 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.214+8341A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69144424 | |||||||
| chr14:69144504 | G | A | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.214+8261C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69144504 | |||||||
| chr14:69144533 | C | T | 1 | a0001c0004t0003g0030 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.214+8232G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69144533 | |||||||
| chr14:69144545 | C | G | 2 | a0001c0001t0003g0092 a0001c0001t0003g0093 |
2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.214+8220G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69144545 | |||||||
| chr14:69144563 | C | T | 1 | a0001c0001t0002g0235 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.214+8202G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69144563 | |||||||
| chr14:69144571 | C | T | 3 | a0001c0003t0002g0102 a0001c0003t0002g0103 a0001c0003t0002g0104 |
3 | HG02818.hp1 HG02965.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.214+8194G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69144571 | |||||||
| chr14:69144993 | C | T | 132 | a0001c0001t0001g0081 a0001c0001t0001g0166 a0001c0001t0002g0011 others(129): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.214+7772G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69144993 | |||||||
| chr14:69145043 | A | C | 1 | a0001c0001t0014g0094 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.214+7722T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69145043 | |||||||
| chr14:69145171 | C | A | 1 | a0001c0001t0013g0099 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.214+7594G>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69145171 | |||||||
| chr14:69145245 | G | A | 1 | a0001c0001t0005g0175 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.214+7520C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69145245 | |||||||
| chr14:69145300 | G | A | 1 | a0001c0001t0013g0099 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.214+7465C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69145300 | |||||||
| chr14:69145388 | A | G | 100 | a0001c0001t0001g0081 a0001c0001t0002g0011 a0001c0001t0002g0012 others(97): Show |
100 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(97): Show |
intron_variant | MODIFIER | c.214+7377T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69145388 | |||||||
| chr14:69145523 | A | T | 4 | a0001c0001t0001g0001 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
5 | HG02647.hp2 HG03130.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.214+7242T>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69145523 | |||||||
| chr14:69145524 | A | T | 182 | a0001c0001t0001g0001 a0001c0001t0001g0081 a0001c0001t0001g0129 others(179): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.214+7241T>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69145524 | |||||||
| chr14:69145667 | AT | A | 102 | a0001c0001t0001g0081 a0001c0001t0002g0011 a0001c0001t0002g0012 others(99): Show |
102 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(99): Show |
intron_variant | MODIFIER | c.214+7097delA | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69145667 | |||||||
| chr14:69145691 | C | T | 2 | a0001c0001t0003g0092 a0001c0001t0003g0093 |
2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.214+7074G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69145691 | |||||||
| chr14:69146010 | T | C | 2 | a0001c0001t0001g0142 a0001c0001t0001g0145 |
2 | HG00738.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.214+6755A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69146010 | |||||||
| chr14:69146093 | C | T | 1 | a0001c0001t0002g0029 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.214+6672G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69146093 | |||||||
| chr14:69146234 | T | C | 100 | a0001c0001t0001g0081 a0001c0001t0002g0011 a0001c0001t0002g0012 others(97): Show |
100 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(97): Show |
intron_variant | MODIFIER | c.214+6531A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69146234 | |||||||
| chr14:69146262 | T | A | 12 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0002g0018 others(9): Show |
12 | HG01361.hp1 HG02056.hp1 HG02155.hp1 others(9): Show |
intron_variant | MODIFIER | c.214+6503A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69146262 | |||||||
| chr14:69146409 | T | G | 1 | a0001c0001t0001g0134 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.214+6356A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69146409 | |||||||
| chr14:69146411 | A | T | 1 | a0001c0001t0001g0134 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.214+6354T>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69146411 | |||||||
| chr14:69146412 | T | C | 1 | a0001c0001t0001g0134 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.214+6353A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69146412 | |||||||
| chr14:69146414 | T | C | 1 | a0001c0001t0001g0134 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.214+6351A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69146414 | |||||||
| chr14:69146415 | G | A | 1 | a0001c0001t0002g0024 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.214+6350C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69146415 | |||||||
| chr14:69146417 | A | G | 1 | a0001c0001t0001g0134 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.214+6348T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69146417 | |||||||
| chr14:69146419 | C | A | 1 | a0001c0001t0013g0099 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.214+6346G>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69146419 | |||||||
| chr14:69146543 | T | C | 2 | a0001c0001t0003g0092 a0001c0001t0003g0093 |
2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.214+6222A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69146543 | |||||||
| chr14:69146544 | T | G | 14 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0002g0018 others(11): Show |
14 | HG01361.hp1 HG02055.hp1 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.214+6221A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69146544 | |||||||
| chr14:69146757 | G | T | 1 | a0001c0001t0001g0189 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.214+6008C>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69146757 | |||||||
| chr14:69146758 | T | C | 1 | a0001c0001t0014g0094 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.214+6007A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69146758 | |||||||
| chr14:69146766 | A | G | 1 | a0001c0003t0002g0124 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.214+5999T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69146766 | |||||||
| chr14:69147048 | T | C | 3 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0066 |
3 | HG00140.hp2 HG01258.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.214+5717A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69147048 | |||||||
| chr14:69147085 | C | T | 3 | a0001c0003t0002g0108 a0001c0003t0002g0109 a0002c0009t0002g0107 |
3 | HG01433.hp2 HG02559.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.214+5680G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69147085 | |||||||
| chr14:69147750 | A | G | 4 | a0001c0001t0007g0095 a0001c0001t0007g0096 a0001c0001t0007g0097 others(1): Show |
4 | HG01074.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.214+5015T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69147750 | |||||||
| chr14:69147910 | G | A | 1 | a0001c0001t0002g0127 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.214+4855C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69147910 | |||||||
| chr14:69148102 | C | CA | 9 | a0001c0001t0001g0133 a0001c0001t0001g0232 a0001c0001t0004g0187 others(6): Show |
11 | HG00642.hp2 HG00733.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.214+4662dupT | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69148102 | |||||||
| chr14:69148102 | CA | C | 59 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(56): Show |
59 | HG00741.hp2 HG01074.hp2 HG01192.hp2 others(56): Show |
intron_variant | MODIFIER | c.214+4662delT | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69148102 | |||||||
| chr14:69148102 | CAA | C | 64 | a0001c0001t0001g0081 a0001c0001t0002g0029 a0001c0001t0002g0035 others(61): Show |
64 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.214+4661_214+4662d others(4): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69148102 | |||||||
| chr14:69148160 | A | C | 1 | a0001c0001t0001g0134 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.214+4605T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69148160 | |||||||
| chr14:69148161 | G | A | 1 | a0001c0001t0001g0134 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.214+4604C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69148161 | |||||||
| chr14:69148162 | G | C | 1 | a0001c0001t0001g0134 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.214+4603C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69148162 | |||||||
| chr14:69148163 | A | T | 1 | a0001c0001t0001g0134 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.214+4602T>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69148163 | |||||||
| chr14:69148165 | A | G | 1 | a0001c0001t0001g0134 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.214+4600T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69148165 | |||||||
| chr14:69148167 | G | C | 2 | a0001c0001t0003g0092 a0001c0001t0003g0093 |
2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.214+4598C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69148167 | |||||||
| chr14:69148167 | G | T | 1 | a0001c0001t0001g0134 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.214+4598C>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69148167 | |||||||
| chr14:69148169 | A | G | 1 | a0001c0001t0001g0134 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.214+4596T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69148169 | |||||||
| chr14:69148170 | T | C | 1 | a0001c0001t0001g0134 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.214+4595A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69148170 | |||||||
| chr14:69148171 | A | G | 1 | a0001c0001t0001g0134 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.214+4594T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69148171 | |||||||
| chr14:69148172 | A | T | 1 | a0001c0001t0001g0134 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.214+4593T>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69148172 | |||||||
| chr14:69148174 | A | T | 1 | a0001c0001t0001g0134 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.214+4591T>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69148174 | |||||||
| chr14:69148176 | G | T | 1 | a0001c0001t0001g0134 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.214+4589C>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69148176 | |||||||
| chr14:69148218 | C | A | 1 | a0001c0001t0001g0234 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.214+4547G>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69148218 | |||||||
| chr14:69148262 | G | A | 28 | a0001c0001t0001g0166 a0001c0001t0006g0003 a0001c0001t0006g0168 others(25): Show |
30 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.214+4503C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69148262 | |||||||
| chr14:69148338 | C | T | 4 | a0001c0001t0001g0001 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
5 | HG02647.hp2 HG03130.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.214+4427G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69148338 | |||||||
| chr14:69148378 | A | T | 1 | a0001c0001t0002g0235 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.214+4387T>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69148378 | |||||||
| chr14:69148503 | T | G | 1 | a0001c0001t0002g0178 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.214+4262A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69148503 | |||||||
| chr14:69148549 | G | A | 1 | a0001c0001t0002g0088 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.214+4216C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69148549 | |||||||
| chr14:69148589 | G | A | 2 | a0001c0001t0003g0092 a0001c0001t0003g0093 |
2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.214+4176C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69148589 | |||||||
| chr14:69148819 | T | C | 2 | a0001c0003t0002g0124 a0001c0003t0002g0125 |
2 | HG02109.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.214+3946A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69148819 | |||||||
| chr14:69149084 | T | C | 1 | a0001c0001t0001g0143 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.214+3681A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69149084 | |||||||
| chr14:69149124 | T | C | 12 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(9): Show |
12 | HG00280.hp2 HG00738.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.214+3641A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69149124 | |||||||
| chr14:69149139 | A | G | 1 | a0001c0001t0003g0028 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.214+3626T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69149139 | |||||||
| chr14:69149586 | T | C | 1 | a0001c0001t0001g0233 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.214+3179A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69149586 | |||||||
| chr14:69149606 | C | T | 5 | a0001c0003t0002g0102 a0001c0003t0002g0103 a0001c0003t0002g0104 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.214+3159G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69149606 | |||||||
| chr14:69149737 | A | C | 2 | a0001c0001t0002g0100 a0001c0001t0002g0101 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.214+3028T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69149737 | |||||||
| chr14:69149870 | A | C | 1 | a0001c0001t0014g0094 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.214+2895T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69149870 | |||||||
| chr14:69149916 | T | A | 4 | a0001c0001t0005g0172 a0001c0001t0005g0173 a0001c0001t0005g0174 others(1): Show |
4 | HG02145.hp1 HG02559.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.214+2849A>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69149916 | |||||||
| chr14:69149923 | C | A | 1 | a0001c0001t0003g0068 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.214+2842G>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69149923 | |||||||
| chr14:69150055 | G | A | 2 | a0001c0002t0001g0170 a0001c0002t0001g0171 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.214+2710C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69150055 | |||||||
| chr14:69150129 | G | A | 3 | a0001c0001t0003g0092 a0001c0001t0003g0093 a0001c0001t0013g0099 |
3 | HG03239.hp1 HG03516.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.214+2636C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69150129 | |||||||
| chr14:69150243 | T | TG | 18 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(15): Show |
18 | HG01361.hp1 HG02055.hp1 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.214+2521dupC | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69150243 | |||||||
| chr14:69150285 | C | G | 1 | a0001c0001t0003g0027 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.214+2480G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69150285 | |||||||
| chr14:69150357 | T | C | 1 | a0001c0001t0001g0234 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.214+2408A>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69150357 | |||||||
| chr14:69150445 | AAT | A | 23 | a0001c0001t0001g0081 a0001c0001t0002g0069 a0001c0001t0002g0070 others(20): Show |
23 | HG00099.hp1 HG01071.hp2 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.214+2318_214+2319d others(4): Show |
DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69150445 | |||||||
| chr14:69150520 | G | A | 1 | a0003c0007t0012g0128 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.214+2245C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69150520 | |||||||
| chr14:69150597 | A | T | 1 | a0001c0001t0003g0053 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.214+2168T>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69150597 | |||||||
| chr14:69150698 | C | A | 46 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(43): Show |
46 | HG01192.hp2 HG01243.hp2 HG01361.hp1 others(43): Show |
intron_variant | MODIFIER | c.214+2067G>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69150698 | |||||||
| chr14:69150722 | C | CA | 90 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0166 others(87): Show |
92 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(89): Show |
intron_variant | MODIFIER | c.214+2042dupT | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69150722 | |||||||
| chr14:69150722 | CA | C | 11 | a0001c0001t0002g0090 a0001c0001t0002g0091 a0001c0001t0002g0176 others(8): Show |
11 | HG01081.hp1 HG01496.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.214+2042delT | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69150722 | |||||||
| chr14:69150746 | C | G | 11 | a0001c0001t0002g0090 a0001c0001t0002g0091 a0001c0001t0002g0176 others(8): Show |
11 | HG01081.hp1 HG01496.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.214+2019G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69150746 | |||||||
| chr14:69150921 | C | G | 4 | a0001c0001t0005g0172 a0001c0001t0005g0173 a0001c0001t0005g0174 others(1): Show |
4 | HG02145.hp1 HG02559.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.214+1844G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69150921 | |||||||
| chr14:69150998 | C | T | 173 | a0001c0001t0001g0081 a0001c0001t0001g0166 a0001c0001t0002g0011 others(170): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.214+1767G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69150998 | |||||||
| chr14:69151120 | G | A | 1 | a0001c0001t0003g0089 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.214+1645C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69151120 | |||||||
| chr14:69151151 | T | G | 1 | a0001c0001t0001g0145 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.214+1614A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69151151 | |||||||
| chr14:69151219 | G | C | 28 | a0001c0001t0001g0166 a0001c0001t0006g0003 a0001c0001t0006g0168 others(25): Show |
30 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.214+1546C>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69151219 | |||||||
| chr14:69151255 | A | G | 68 | a0001c0001t0001g0081 a0001c0001t0002g0029 a0001c0001t0002g0035 others(65): Show |
68 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.214+1510T>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69151255 | |||||||
| chr14:69151397 | G | A | 4 | a0001c0001t0005g0172 a0001c0001t0005g0173 a0001c0001t0005g0174 others(1): Show |
4 | HG02145.hp1 HG02559.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.214+1368C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69151397 | |||||||
| chr14:69151673 | T | G | 3 | a0001c0001t0002g0176 a0001c0001t0002g0177 a0001c0001t0002g0178 |
3 | HG02451.hp2 HG02622.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.214+1092A>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69151673 | |||||||
| chr14:69151684 | C | T | 16 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(13): Show |
16 | HG01361.hp1 HG02056.hp1 HG02083.hp1 others(13): Show |
intron_variant | MODIFIER | c.214+1081G>A | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69151684 | |||||||
| chr14:69151706 | G | A | 14 | a0001c0001t0004g0008 a0001c0001t0004g0009 a0001c0001t0004g0010 others(11): Show |
14 | HG01069.hp2 HG01175.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.214+1059C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69151706 | |||||||
| chr14:69152203 | C | G | 3 | a0001c0001t0004g0008 a0001c0001t0004g0009 a0001c0001t0004g0010 |
3 | HG01069.hp2 HG01192.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.214+562G>C | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69152203 | |||||||
| chr14:69152390 | A | C | 1 | a0001c0001t0002g0007 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.214+375T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69152390 | |||||||
| chr14:69152456 | A | C | 192 | a0001c0001t0001g0001 a0001c0001t0001g0081 a0001c0001t0001g0129 others(189): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.214+309T>G | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69152456 | |||||||
| chr14:69152696 | G | A | 1 | a0001c0001t0002g0235 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.214+69C>T | DCAF5 | ENSG00000139990.18 | transcript | ENST00000341516.10 | protein_coding | 1/8 | chr14 | 69152696 |