SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs925817 | snp | A/T | 0.48 | 0.0979796 | intron-variant | DCAF5 | GRCh38.p7 | 14:69097585 | aaaaaaaaaaaaaaa[A/T]aaTAATAATAATAAT | 8816 |
rs963175 | snp | A/T | 0 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69120367 | acttgtaataatccc[A/T]acactttgagaggcc | 8816 |
rs1018315 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69127829 | caaagtctTAAAAAC[A/T]AAACATCATAAGTAA | 8816 |
rs1105625 | snp | A/G | 0.388398 | 0.208197 | intron-variant | DCAF5 | GRCh38.p7 | 14:69082287 | TTTTATTGGGAGGCA[A/G]TGAAATTTCTCTTAC | 8816 |
rs1127817 | snp | C/T | 3.29739e-05 | 0.00406028 | missense | DCAF5 | GRCh38.p7 | 14:69055137 | CGTCTGTCTGCTCTG[C/T]GGCGCTACCAAGACA | 8816 |
rs1128941 | snp | A/T | 0 | 0 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69050951 | AACTCTTCTCTTGTG[A/T]ATATGCAAATAAACA | 8816 |
rs1147478 | snp | A/G | 0.232359 | 0.249377 | intron-variant | DCAF5 | GRCh38.p7 | 14:69148262 | AATATGCGTACTACT[A/G]TAACCTCATTGATGT | 8816 |
rs1147479 | snp | C/T | 0.228547 | 0.249078 | intron-variant | DCAF5 | GRCh38.p7 | 14:69142781 | AAAGACACCTATTTG[C/T]TGACTGAAATTCAGT | 8816 |
rs1147480 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69138883 | gctgggattacaggt[A/G]tgagccactgtgcct | 8816 |
rs1147481 | snp | C/G | 0.437542 | 0.165312 | intron-variant | DCAF5 | GRCh38.p7 | 14:69131052 | ATTGTCCTTGTGTCC[C/G]TAAAGTATCATCCAT | 8816 |
rs1275332 | snp | A/C | 0.00396038 | 0.0443227 | intron-variant | DCAF5 | GRCh38.p7 | 14:69079016 | tacaggcgggcacca[A/C]caTTTCCTGTTACGT | 8816 |
rs1275405 | snp | A/G | 0.233818 | 0.249476 | intron-variant | DCAF5 | GRCh38.p7 | 14:69125492 | ACAACCATTCAGAAA[A/G]GGAAACCCAAATACC | 8816 |
rs1275406 | snp | A/G | 0.307671 | 0.243257 | intron-variant | DCAF5 | GRCh38.p7 | 14:69126022 | actttcctatatacc[A/G]gcaatgaataagtgg | 8816 |
rs1275407 | snp | A/G | 0.437118 | 0.165792 | intron-variant | DCAF5 | GRCh38.p7 | 14:69126735 | tggaacaaaacagag[A/G]ggccaaaaacagacc | 8816 |
rs1275408 | snp | A/G | 0.234982 | 0.249549 | intron-variant | DCAF5 | GRCh38.p7 | 14:69127465 | gacaacaaaaagatc[A/G]ctaattgccagggta | 8816 |
rs1275409 | snp | A/T | 0.233818 | 0.249476 | intron-variant | DCAF5 | GRCh38.p7 | 14:69127480 | actaattgccagggt[A/T]tggaggcaggggttg | 8816 |
rs1275410 | snp | C/T | 0.233818 | 0.249476 | intron-variant | DCAF5 | GRCh38.p7 | 14:69127814 | gaaacttctctaaaa[C/T]aaagtctTAAAAACA | 8816 |
rs1275411 | snp | C/T | 0.262101 | 0.249707 | intron-variant | DCAF5 | GRCh38.p7 | 14:69128196 | ttttttcttcttctt[C/T]ttttttttttttgag | 8816 |
rs1275412 | snp | C/T | 0.234401 | 0.249513 | intron-variant | DCAF5 | GRCh38.p7 | 14:69128234 | ctctgtcacccaggc[C/T]ggagtgcagtggcat | 8816 |
rs1275413 | snp | A/G | 0.387642 | 0.208697 | intron-variant | DCAF5 | GRCh38.p7 | 14:69128378 | ttttttagagacagg[A/G]tttcaccatgttgcc | 8816 |
rs1275414 | snp | A/G | 0.403684 | 0.197183 | intron-variant | DCAF5 | GRCh38.p7 | 14:69140079 | gagactagcctgggc[A/G]acgtagagaaatctc | 8816 |
rs1275415 | snp | C/T | 0.43655 | 0.16643 | intron-variant | DCAF5 | GRCh38.p7 | 14:69144993 | GGTTACTTAATGCAG[C/T]ATTTCACAAGCTTCA | 8816 |
rs1275416 | snp | A/T | 0.382666 | 0.211895 | intron-variant | DCAF5 | GRCh38.p7 | 14:69145524 | AAAATAAAAAAAAAA[A/T]TTTTAATTTCCCATA | 8816 |
rs1275417 | snp | C/T | 0.347032 | 0.230401 | intron-variant | DCAF5 | GRCh38.p7 | 14:69150998 | AAGAGTACCCCCAAA[C/T]TCCCTCACTCGGTAG | 8816 |
rs1275418 | snp | C/G | 0.232651 | 0.249397 | intron-variant | DCAF5 | GRCh38.p7 | 14:69151219 | GATCAGGTTTCTTCA[C/G]AGGATGATCTAGGGC | 8816 |
rs1275419 | snp | A/C | 0.302686 | 0.244385 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69152456 | GCCGTCAAACTTTGT[A/C]GAGCGGTAACCTCGC | 8816 |
rs1275420 | snp | A/G | 0.288386 | 0.247035 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69154203 | CCTTTTCGATGTATT[A/G]TAGTACTTTTCCTGG | 8816 |
rs1296559 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69098833 | tgatctcggctcact[A/G]caagctccgcctcct | 8816 |
rs1299952 | snp | A/C | 0 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69119780 | GTGAATTGATTTGTC[A/C]ATGATCATTTAGTGT | 8816 |
rs1626122 | snp | A/T | 0.346368 | 0.23068 | intron-variant | DCAF5 | GRCh38.p7 | 14:69100472 | GATTGAATTTCAGAG[A/T]CCTTTGAAAATTTTT | 8816 |
rs1629783 | snp | C/G | 0.29789 | 0.24537 | intron-variant | DCAF5 | GRCh38.p7 | 14:69101439 | TAATAAGGGGAAGAT[C/G]TGCCAAGAGAGGACA | 8816 |
rs1710988 | snp | G/T | 0.288906 | 0.246954 | intron-variant | DCAF5 | GRCh38.p7 | 14:69113051 | CTGAAATAAGCTGAT[G/T]AGAGGGCTGGCTGGC | 8816 |
rs1710989 | snp | A/C | 0.403684 | 0.197183 | intron-variant | DCAF5 | GRCh38.p7 | 14:69114519 | ATGCATATGCATAGT[A/C]GTATATACATTACAT | 8816 |
rs1710990 | snp | A/G | 0.365024 | 0.221967 | intron-variant | DCAF5 | GRCh38.p7 | 14:69108337 | CTTGGTAACTATGAC[A/G]TGAACACGTAAAGAA | 8816 |
rs1710991 | snp | C/T | 0.046775 | 0.145601 | intron-variant | DCAF5 | GRCh38.p7 | 14:69108344 | ACTATGACATGAACA[C/T]GTAAAGAAAAATCAA | 8816 |
rs1710993 | snp | C/T | 0.180702 | 0.240204 | intron-variant | DCAF5 | GRCh38.p7 | 14:69119862 | TAGGTCATAGAAATG[C/T]TAAAGATTTTATTGC | 8816 |
rs1814965 | snp | A/C/G | 0 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69143713 | AAATTATTAGTCGCC[A/C/G]CTGCCATTATAATAT | 8816 |
rs1829506 | snp | A/C | 0 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69126007 | atacaaaagtccatc[A/C]ctttcctatatacca | 8816 |
rs1892297 | snp | A/G | 0.435837 | 0.167226 | | | GRCh38.p7 | 14:69121880 | TTGTGGCACACTCTG[A/G]TTTTTTTTTATTCTA | 8816 |
rs1914004 | snp | A/G | 0.4941 | 0.0539917 | intron-variant | DCAF5 | GRCh38.p7 | 14:69059219 | CCTCCCGAGTAACTG[A/G]GAGCACAGGCAGGCA | 8816 |
rs2001355 | snp | C/T | 0.403684 | 0.197183 | intron-variant | DCAF5 | GRCh38.p7 | 14:69094476 | TAAGCATTCTAGGAG[C/T]GAGATTCCTTTGTAC | 8816 |
rs2001998 | snp | G/T | 0.494358 | 0.0528145 | intron-variant | DCAF5 | GRCh38.p7 | 14:69092801 | GCAACAATTAGAAAA[G/T]GAAAATGACTTGTTT | 8816 |
rs2014607 | snp | A/C | 0.223819 | 0.248625 | intron-variant | DCAF5 | GRCh38.p7 | 14:69122941 | GGAAAAAACAATAAC[A/C]ACCAACTTAGACCCA | 8816 |
rs2056153 | snp | A/G | 0.492918 | 0.0590819 | intron-variant | DCAF5 | GRCh38.p7 | 14:69108282 | GTATGTAACAGAGAG[A/G]TCTAGCAAGGAAGTT | 8816 |
rs2176255 | snp | A/G | 0.040671 | 0.13668 | intron-variant | DCAF5 | GRCh38.p7 | 14:69149124 | TATGTTAGTTAAAGT[A/G]TAGGTTGGGTGCTGA | 8816 |
rs2331919 | snp | A/T | 0.492918 | 0.0590819 | intron-variant | DCAF5 | GRCh38.p7 | 14:69106378 | tttttaaatttttat[A/T]tatttttagtgatag | 8816 |
rs2331920 | snp | C/G | 0.498206 | 0.0298983 | intron-variant | DCAF5 | GRCh38.p7 | 14:69133554 | TAGGCAGGGAAGAGG[C/G]GGGGGTACAGGCAGG | 8816 |
rs2859857 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69143578 | GACATTGCTGTTTGT[A/T]aaaaaaaaaaaaaaa | 8816 |
rs2859858 | snp | A/G | 0 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69143343 | tttatggtggagcta[A/G]atttcCAGGTTGGGT | 8816 |
rs2859859 | snp | C/G | 0 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69143335 | ggagctagatttcCA[C/G]GTTGGGTCTGAATGT | 8816 |
rs2877524 | snp | C/T | 0.0948562 | 0.196037 | intron-variant | DCAF5 | GRCh38.p7 | 14:69113098 | AAATGACTCTCCTCC[C/T]ATACCTTCAGGCTAC | 8816 |
rs2877525 | snp | A/G | 0 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69125522 | CAAACATATTATAGA[A/G]GATCTCAAATTCTAT | 8816 |
rs3044673 | in-del | -/AAATTAAA | 0 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69107071 | AATTAAATAATTAAA[-/AAATTAAA]TAAGAAAGTCCATTT | 8816 |
rs3044674 | in-del | -/AC | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69112627 | cacacacacacacac[-/AC]AAATAACACAcaagt | 8816 |
rs3044676 | in-del | -/CC | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69113708 | GTGGTCTCTTCCCCC[-/CC]AAACCAACTTGTACT | 8816 |
rs3223006 | microsatellite | (CA)19/20/22/23/24/25/26/27 | 0.765978 | 0.14163 | intron-variant | DCAF5 | GRCh38.p7 | 14:69099299 | gggactctgtctcaa[(CA)19/20/22/23/24/25/26/27]aaCTNACAAAGCNAA | 8816 |
rs3742898 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | DCAF5 | GRCh38.p7 | 14:69057874 | TCAGCAGTAAGGGGA[A/G]CAGGTAGGAACCCCA | 8816 |
rs3742904 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69116232 | TCTCCTGGCTTGAGA[C/G]ACACTATATATCTTA | 8816 |
rs3742905 | snp | C/G | 0.040671 | 0.13668 | intron-variant | DCAF5 | GRCh38.p7 | 14:69117929 | AGTCACAGGAGGGTG[C/G]AGAAGGACTGGCAAA | 8816 |
rs3832973 | in-del | -/C | 0.479502 | 0.0991411 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69053644 | GGGTTATTTTTTTTT[-/C]CCCTTTCTTAACACA | 8816 |
rs3861671 | snp | A/G | 0 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69077746 | GTTGTGTGTATGTTG[A/G]ACTTACACTTTTTGG | 8816 |
rs3914590 | snp | A/T | 0 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69066008 | GGGTATGTGGTATTT[A/T]ATTTATGGGTACCCA | 8816 |
rs4143922 | snp | C/T | 0.0539704 | 0.155153 | intron-variant | DCAF5 | GRCh38.p7 | 14:69094983 | AATTTCTTTTTTCTC[C/T]GCCTTGTTTTCTCTC | 8816 |
rs4335717 | snp | A/T | 0.5 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69107064 | aaataaaTAATTAAA[A/T]AATTAAATAAGAAAG | 8816 |
rs4899280 | snp | C/T | 0.486 | 0.0824865 | intron-variant | DCAF5 | GRCh38.p7 | 14:69059590 | GGCCTTTCAGGATAA[C/T]GTAAGTGCAGGGTGA | 8816 |
rs4902690 | snp | G/T | 0 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69076991 | AGCTCCAAACTGCTT[G/T]ATCTCAAAAAGGACA | 8816 |
rs4902691 | snp | A/G | 0.0539704 | 0.155153 | intron-variant | DCAF5 | GRCh38.p7 | 14:69129652 | AGTGAAGAATATTTA[A/G]GATCATTTCAGACCA | 8816 |
rs4902693 | snp | A/C | 0.188631 | 0.242351 | intron-variant | DCAF5 | GRCh38.p7 | 14:69150698 | CAAGACTAGCCTGGG[A/C]AACATAGGGAGACTC | 8816 |
rs5809416 | in-del | -/TGTG | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69081753 | GACCTTTATAGAAAA[-/TGTG]TGTGTGTGTGTATGT | 8816 |
rs5809417 | in-del | -/ATTA | 0.182933 | 0.240836 | intron-variant | DCAF5 | GRCh38.p7 | 14:69082465 | TGTAGAAAAAATTCT[-/ATTA]ATTAAGGAATATTCC | 8816 |
rs6573866 | snp | A/T | 0 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69070902 | TCCCGGGTTCAAGCG[A/T]TTCTTCTGCCACAGC | 8816 |
rs6573867 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69074546 | TAAAAATATTTCTTC[C/G]TAATTTCTTTGACGT | 8816 |
rs6573868 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | DCAF5 | GRCh38.p7 | 14:69083610 | TGCTCAAAATGGAGA[C/T]GTGTCTCAAGAAGCA | 8816 |
rs6573869 | snp | A/C | 0.492484 | 0.0608394 | intron-variant | DCAF5 | GRCh38.p7 | 14:69100560 | TTTCTAGATACAAAA[A/C]AAGTTTCCCTTGGTT | 8816 |
rs6573870 | snp | C/T | 0.180702 | 0.240204 | intron-variant | DCAF5 | GRCh38.p7 | 14:69110503 | tcaaactcctgacct[C/T]gtgatccaactgcct | 8816 |
rs7141235 | snp | A/G | 0.143622 | 0.226238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69122532 | ACCATCAATAGGCAC[A/G]TGTTCTCTAGGCCAT | 8816 |
rs7141919 | snp | C/T | 0.180702 | 0.240204 | intron-variant | DCAF5 | GRCh38.p7 | 14:69109137 | ATGAGGTCAGGAGAT[C/T]GAGACCATCCTGGCT | 8816 |
rs7143028 | snp | C/G | 0.0456336 | 0.143994 | intron-variant | DCAF5 | GRCh38.p7 | 14:69067093 | ACTATGTTTATTGTT[C/G]ATTGTTTCCCCTGCT | 8816 |
rs7144307 | snp | C/T | 0.498693 | 0.0255257 | intron-variant | DCAF5 | GRCh38.p7 | 14:69067120 | tgctagaacataagc[C/T]ccatgacagcagggc | 8816 |
rs7145784 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF5 | GRCh38.p7 | 14:69071092 | catgagccactgcac[C/T]cggccCCTTCCTTTA | 8816 |
rs7149707 | snp | A/T | 0.5 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69107051 | tgtctcaaaaaataa[A/T]taaataattaaataa | 8816 |
rs7149982 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69067913 | gtgctgggattacag[A/T]cctgagccactgcac | 8816 |
rs7158145 | snp | C/G | 0.288906 | 0.246954 | intron-variant | DCAF5 | GRCh38.p7 | 14:69115181 | TTCATAGTGCAAAGG[C/G]ACATCAGGGGTCCTG | 8816 |
rs7158165 | snp | A/C | 0 | 0 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69051480 | GTGTGTCTTATGGGG[A/C]CTATCACCCGGTAAG | 8816 |
rs7160629 | snp | G/T | 0.492337 | 0.0614248 | intron-variant | DCAF5 | GRCh38.p7 | 14:69082168 | CATATAATACACCTT[G/T]GATCATACCATTTAT | 8816 |
rs7161255 | snp | C/G | 0.150667 | 0.229419 | intron-variant | DCAF5 | GRCh38.p7 | 14:69108400 | GTGTATGTGTTTTGG[C/G]GGGTGGTGCAAAGGG | 8816 |
rs7400859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69140274 | tctgtctaaaaaaaa[A/G]agagagagagagaga | 8816 |
rs7494642 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69061190 | agagaccacgtccca[C/T]tatgttgcccaggct | 8816 |
rs8003335 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69069786 | agcagcagttagttt[A/T]aaaaaaaaagtttgt | 8816 |
rs8003428 | snp | C/G | 0.150333 | 0.229274 | intron-variant | DCAF5 | GRCh38.p7 | 14:69078976 | caagcaattttcatg[C/G]ctcagcctccccagc | 8816 |
rs8003483 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69099942 | ttaaaaaaaaaaGTT[C/T]CTGATATTTGCAGAA | 8816 |
rs8005658 | snp | C/G | 0.492966 | 0.0588865 | intron-variant | DCAF5 | GRCh38.p7 | 14:69140286 | AAAAAGAGAGAGAGA[C/G]AGAGAAGACAGAGAA | 8816 |
rs8007254 | snp | C/G | 0.150333 | 0.229274 | intron-variant | DCAF5 | GRCh38.p7 | 14:69076183 | cccttgtgcattgct[C/G]gtgggaatgactaac | 8816 |
rs8008184 | snp | A/C | 0.492918 | 0.0590819 | intron-variant | DCAF5 | GRCh38.p7 | 14:69101135 | ACCACACAATCAAGC[A/C]GCCGAAATAGAAGCA | 8816 |
rs8008735 | snp | A/C | 0.207559 | 0.246371 | intron-variant | DCAF5 | GRCh38.p7 | 14:69137527 | ATTAACAACATAATA[A/C]AGCTTTCTTGTCTCT | 8816 |
rs8008829 | snp | A/T | 0.208169 | 0.246476 | intron-variant | DCAF5 | GRCh38.p7 | 14:69119880 | tttctatgacctaac[A/T]ttttaacctacagaa | 8816 |
rs8011193 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69067685 | gagtctcaccaggct[A/G]gagtgcagtggcgtg | 8816 |
rs8015433 | snp | A/C | 0 | 0 | intron-variant, utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69089660 | AAATACCTTCTGTGG[A/C]TCTGCCTATGACAAT | 8816 |
rs8016668 | snp | C/G | 0.0248432 | 0.108648 | intron-variant | DCAF5 | GRCh38.p7 | 14:69126523 | caatgcaatcccact[C/G]aaattctcagcaaat | 8816 |
rs8018654 | snp | A/G | 0 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69095325 | ACATGTTAACAGTGA[A/G]TTCAAATAAAAATAT | 8816 |
rs8019119 | snp | A/T | 0 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69095619 | GTAAAAAGAACATTT[A/T]AAAAAGTACTTAGCC | 8816 |
rs8020025 | snp | C/T | 0.282369 | 0.247896 | intron-variant | DCAF5 | GRCh38.p7 | 14:69102621 | acacacacacacaca[C/T]attagcctagaccta | 8816 |
rs8021509 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69099494 | GGTCCACAGTGATTT[A/G]TCAATGACCATCCAG | 8816 |
rs8021688 | snp | C/T | 0 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69099524 | GGTCTCTACATCTCA[C/T]ATGAAGCCATGACGC | 8816 |
rs8022246 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69099929 | gaataaaataacatt[A/T]aaaaaaaaaGTTTCT | 8816 |
rs8022375 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69099877 | aactgagccactgca[C/T]tgcagcctgggtgac | 8816 |
rs9323521 | snp | A/G | 0.346147 | 0.230772 | intron-variant | DCAF5 | GRCh38.p7 | 14:69086410 | ATAGTGGATATGAAA[A/G]TGCTTTACAAGTTAA | 8816 |
rs9323522 | snp | A/G | 0.498964 | 0.02274 | intron-variant | DCAF5 | GRCh38.p7 | 14:69102025 | ctaccaccatagact[A/G]tataaatattacaca | 8816 |
rs9323524 | snp | C/T | 0.49823 | 0.0296997 | intron-variant | DCAF5 | GRCh38.p7 | 14:69132853 | TGTCGCCGGCACTTA[C/T]TAGCTGTGTGCCTTT | 8816 |
rs10083451 | snp | C/T | 0.493703 | 0.0557558 | intron-variant | DCAF5 | GRCh38.p7 | 14:69112902 | TCAGAGCCTATACTT[C/T]CTACACTAAACCATC | 8816 |
rs10129883 | snp | C/T | 0.125528 | 0.21681 | intron-variant | DCAF5 | GRCh38.p7 | 14:69096380 | AACATGATTCACTGC[C/T]ACATTTCTCTGGCTT | 8816 |
rs10130013 | snp | A/G | 0.499035 | 0.0219437 | intron-variant | DCAF5 | GRCh38.p7 | 14:69096578 | TAATCATTATCTTCC[A/G]GAACAGGAACATGCC | 8816 |
rs10131077 | snp | C/T | 0.498852 | 0.0239341 | intron-variant | DCAF5 | GRCh38.p7 | 14:69146234 | TCCTTTGAACAATAC[C/T]GAGCACAAGGACAAC | 8816 |
rs10134578 | snp | C/T | 0.495634 | 0.0465208 | intron-variant | DCAF5 | GRCh38.p7 | 14:69076467 | agcctttaaaaggaa[C/T]gaaattctgacacat | 8816 |
rs10134594 | snp | A/G | 0.0351356 | 0.127802 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69055345 | CTCGCTGACCCCAGC[A/G]TGCAGTTGGAGGATA | 8816 |
rs10134889 | snp | A/G | 0.132066 | 0.220435 | intron-variant | DCAF5 | GRCh38.p7 | 14:69055692 | ATAAAGAACACCAAG[A/G]CAGAACTTCCCCAGA | 8816 |
rs10135187 | snp | C/T | 0.139903 | 0.224452 | intron-variant | DCAF5 | GRCh38.p7 | 14:69142127 | tagtgagatcctgtc[C/T]ctacaaaaaaaaatt | 8816 |
rs10135643 | snp | A/C | 0.481627 | 0.0940692 | downstream-variant-500B | DCAF5 | GRCh38.p7 | 14:69050689 | AACCTGTTAAGGAGA[A/C]CAAATAAATACCTCC | 8816 |
rs10135971 | snp | A/G | 0.493154 | 0.0581045 | downstream-variant-500B | DCAF5 | GRCh38.p7 | 14:69050777 | AATGACCATTGTCAT[A/G]GATGTGGAACACTGC | 8816 |
rs10138499 | snp | C/T | 0.136506 | 0.222754 | intron-variant | DCAF5 | GRCh38.p7 | 14:69102246 | cctgagcagctggga[C/T]tacaggcacacgtca | 8816 |
rs10139873 | snp | A/G | 0.492484 | 0.0608394 | intron-variant | DCAF5 | GRCh38.p7 | 14:69099376 | ATGAAACCTGATCTC[A/G]AGGGGCAAGCAGCAG | 8816 |
rs10141040 | snp | A/G | 0.498852 | 0.0239341 | intron-variant | DCAF5 | GRCh38.p7 | 14:69145388 | TTATTCACGTTAGCT[A/G]ATTTTTCTAATGTGT | 8816 |
rs10143302 | snp | A/G | 0.494143 | 0.0537956 | intron-variant | DCAF5 | GRCh38.p7 | 14:69070492 | ATGTAAGAAACTGAC[A/G]CTCAGACAAATACTA | 8816 |
rs10143664 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | DCAF5 | GRCh38.p7 | 14:69091961 | ACACATGTTTGCCTA[C/T]GACCTCCTGTCAAGC | 8816 |
rs10143769 | snp | A/G | 0.498813 | 0.0243321 | intron-variant | DCAF5 | GRCh38.p7 | 14:69128710 | GAGGCGGAGGTTGCA[A/G]TGAGCAGAGATCGTG | 8816 |
rs10145145 | snp | A/G | 0.0948562 | 0.196037 | intron-variant | DCAF5 | GRCh38.p7 | 14:69076265 | acatagaactaccac[A/G]tgatgcagcaattac | 8816 |
rs10145565 | snp | A/G | 0.495291 | 0.0482933 | intron-variant | DCAF5 | GRCh38.p7 | 14:69076507 | tggataaaccgtgac[A/G]ttatactaaatgaaa | 8816 |
rs10146339 | snp | C/T | 0.492966 | 0.0588865 | intron-variant | DCAF5 | GRCh38.p7 | 14:69126064 | taaaaTATTTAGGTA[C/T]AAATTTAACAAGATT | 8816 |
rs10147369 | snp | C/T | 0.498794 | 0.0245311 | intron-variant | DCAF5 | GRCh38.p7 | 14:69144008 | TTTTCCACTAATGCA[C/T]TGCCTGTTCTCTGGA | 8816 |
rs10148614 | snp | A/T | 0.492287 | 0.0616198 | intron-variant | DCAF5 | GRCh38.p7 | 14:69068265 | TCTAAGGATACTCAA[A/T]AAGTGAACAAATTGA | 8816 |
rs10149232 | snp | A/C | 0.492871 | 0.0592773 | intron-variant | DCAF5 | GRCh38.p7 | 14:69143135 | CTGCTTACTGGCTCC[A/C]AGTCCACTCCCATCT | 8816 |
rs10150736 | snp | C/T | 0.135825 | 0.222405 | intron-variant | DCAF5 | GRCh38.p7 | 14:69060418 | CTCATTCTAGCCCCA[C/T]GGGGAAATGTGTGCT | 8816 |
rs10151206 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | DCAF5 | GRCh38.p7 | 14:69148673 | gcactccagcctggg[C/T]gacagagcaagactc | 8816 |
rs10498526 | snp | C/G | 0.0948562 | 0.196037 | intron-variant | DCAF5 | GRCh38.p7 | 14:69056506 | AGCTGTCACTGCAAA[C/G]GAGAACGATTAGCTC | 8816 |
rs10498527 | snp | C/T | 0.38821 | 0.208322 | intron-variant | DCAF5 | GRCh38.p7 | 14:69083045 | ACAACTGAACGATTA[C/T]AAACCAGACCATACC | 8816 |
rs10498528 | snp | C/G | 0.0539704 | 0.155153 | intron-variant | DCAF5 | GRCh38.p7 | 14:69096250 | TTCTCTTTTGTTTTC[C/G]TAATGCACTCCTCAG | 8816 |
rs10546836 | in-del | -/TA | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69150447 | CAAGACTAGAGAAAA[-/TA]GAGTTCATTTAAGAT | 8816 |
rs10592463 | in-del | -/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69141352 | TGGGACCTTTTTTTT[-/T]CTTTTTCTTTTATTA | 8816 |
rs10609390 | in-del | -/GTGT | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69081764 | AAAATGTGTGTGTGT[-/GTGT]ATGTGTGTGTTTGTG | 8816 |
rs10637951 | in-del | -/AC | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69112594 | ATGATATATATGTAT[-/AC]ACACACACACACACA | 8816 |
rs11158782 | snp | C/T | 0.492386 | 0.0612297 | intron-variant | DCAF5 | GRCh38.p7 | 14:69083247 | CAATGTAGATGTGTA[C/T]ATTTTTCTGAGATGA | 8816 |
rs11158783 | snp | A/T | 0.355954 | 0.226437 | intron-variant | DCAF5 | GRCh38.p7 | 14:69086621 | GTGCATGGAGTTATT[A/T]AAAAAAAAAAAAAAA | 8816 |
rs11158784 | snp | C/G | 0.365232 | 0.22186 | intron-variant | DCAF5 | GRCh38.p7 | 14:69086688 | AGAGAGTACTTACTA[C/G]TGCATTCCATACCTT | 8816 |
rs11158785 | snp | C/T | 0.346368 | 0.23068 | intron-variant | DCAF5 | GRCh38.p7 | 14:69086703 | CTGCATTCCATACCT[C/T]GGCTATACCCATATA | 8816 |
rs11158786 | snp | A/G | 0.387263 | 0.208947 | intron-variant | DCAF5 | GRCh38.p7 | 14:69086721 | CTATACCCATATAGT[A/G]TCAACCCAGAGAGGT | 8816 |
rs11158787 | snp | C/T | 0.492918 | 0.0590819 | intron-variant, utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69089224 | TTCAACAAATTTTTA[C/T]TGTGTTCTCACTGTG | 8816 |
rs11158788 | snp | A/T | 0.438386 | 0.164349 | intron-variant | DCAF5 | GRCh38.p7 | 14:69105048 | gttatgttttttttt[A/T]aattatctttttatg | 8816 |
rs11158789 | snp | A/C | 0.387832 | 0.208572 | intron-variant | DCAF5 | GRCh38.p7 | 14:69105286 | tgtgtatatccatat[A/C]tgtataatgtatata | 8816 |
rs11158790 | snp | A/G | 0.4944 | 0.0526182 | intron-variant | DCAF5 | GRCh38.p7 | 14:69151255 | TCTACCTAGTCAAAG[A/G]GAAAACGATCTGGGG | 8816 |
rs11396838 | in-del | -/A | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69141168 | AAAAAAAAAAAAAAA[-/A]GTGGCAGCTGAAAGA | 8816 |
rs11442310 | in-del | -/A | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69150729 | ACCTCTACAAAAAAA[-/A]AAAAAAGTTTAAATT | 8816 |
rs11451088 | in-del | -/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69150244 | AGCTAGAGGGAGTAT[-/G]GGGGGGAAGGAAAAG | 8816 |
rs11458918 | in-del | -/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69131760 | AGCACTTTCCAGGCT[-/T]TTTTTTTTTTTTTTA | 8816 |
rs11483352 | in-del | -/T | 0.491885 | 0.0631791 | intron-variant | DCAF5 | GRCh38.p7 | 14:69057348 | GGATTTTTTTTTTTT[-/T]GCATCTTATTTGTAA | 8816 |
rs11620827 | snp | C/G | 0.5 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69109224 | tggcgggcgcctgta[C/G]tcccaactactcaga | 8816 |
rs11621304 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | DCAF5 | GRCh38.p7 | 14:69146010 | CATTTGTGTGACAAG[C/T]TTTACTAGTCAATAA | 8816 |
rs11622889 | snp | A/G | 0.492918 | 0.0590819 | intron-variant | DCAF5 | GRCh38.p7 | 14:69143761 | AAAAACTTGAAAAGC[A/G]GTTATTGGAACCAAA | 8816 |
rs11626985 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | DCAF5 | GRCh38.p7 | 14:69134492 | GAACAGGCACATTTA[C/T]GACCTCCTTAAGAGA | 8816 |
rs11627004 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | DCAF5 | GRCh38.p7 | 14:69134370 | AAGTTTCTTTCAAAT[A/G]CTGTTTATAAGGAAA | 8816 |
rs11627476 | snp | A/G | 0.040671 | 0.13668 | intron-variant | DCAF5 | GRCh38.p7 | 14:69129898 | TCATCTGAGAACCCC[A/G]AGAAAATACAACTAC | 8816 |
rs11628126 | snp | G/T | 0.405255 | 0.195948 | intron-variant | DCAF5 | GRCh38.p7 | 14:69098476 | cccactagatgatta[G/T]cttttacatcttttc | 8816 |
rs11845679 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | DCAF5 | GRCh38.p7 | 14:69067829 | tttagtagagatggg[A/G]tttcgccatgttagc | 8816 |
rs11846184 | snp | A/T | 0.0952156 | 0.196321 | intron-variant | DCAF5 | GRCh38.p7 | 14:69142141 | ctctacaaaaaaaaa[A/T]tttttttaattagct | 8816 |
rs11846520 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | DCAF5 | GRCh38.p7 | 14:69102087 | ttctttctgcaataa[C/T]taaccttagtttact | 8816 |
rs11847564 | snp | C/G | 0.0189856 | 0.0955633 | intron-variant | DCAF5 | GRCh38.p7 | 14:69104455 | aaaacctgagtcaga[C/G]gaatatgctaaatta | 8816 |
rs12147222 | snp | C/G | 0.040671 | 0.13668 | intron-variant | DCAF5 | GRCh38.p7 | 14:69143651 | CCGGGGAGTGCTGCA[C/G]ATCAGCAGGGGATGT | 8816 |
rs12431846 | snp | C/T | 0.492823 | 0.0594727 | intron-variant | DCAF5 | GRCh38.p7 | 14:69058166 | AATTGGTAATCTCTT[C/T]ACACTGGAAAGTTAA | 8816 |
rs12432619 | snp | A/C | 0.00542001 | 0.0517748 | intron-variant | DCAF5 | GRCh38.p7 | 14:69097985 | cagccagaggagatg[A/C]tgaaccatgaatcta | 8816 |
rs12432645 | snp | G/T | 0.455977 | 0.141681 | intron-variant | DCAF5 | GRCh38.p7 | 14:69132766 | CTTAGTCTCCACGTA[G/T]TAAGACATAGGAAAA | 8816 |
rs12434775 | snp | A/G | 0.492775 | 0.059668 | intron-variant | DCAF5 | GRCh38.p7 | 14:69058092 | TTATAAGTACTGACC[A/G]TTCCTATTATCTTGG | 8816 |
rs12435594 | snp | C/G | 0.492966 | 0.0588865 | intron-variant | DCAF5 | GRCh38.p7 | 14:69089149 | CCTGATTTACAGTTA[C/G]AGAAGACTTAGGCCC | 8816 |
rs12435819 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69134547 | TTTGATATACATCCA[C/G]ATGCAAACAGGGTTA | 8816 |
rs12436807 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69102591 | tttgttaaaaacaaa[C/G]acacacacacacaca | 8816 |
rs12437418 | snp | A/T | 0.492435 | 0.0610346 | intron-variant | DCAF5 | GRCh38.p7 | 14:69099594 | CTAATCATGTAAGGA[A/T]CCAACAAGATAATTT | 8816 |
rs12586650 | snp | C/T | 0.458545 | 0.137872 | intron-variant | DCAF5 | GRCh38.p7 | 14:69083023 | CCAGGTCACCTTGTG[C/T]TCCTTTACAACTGAA | 8816 |
rs12589028 | snp | G/T | 0.493703 | 0.0557558 | intron-variant | DCAF5 | GRCh38.p7 | 14:69076025 | tggctagtaagtata[G/T]gaaaagatgctcaac | 8816 |
rs12879923 | snp | G/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69152609 | CCCCTCCCCCTGCAA[G/T]GGTTTTAATTTGACA | 8816 |
rs12883059 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69070804 | tcttttttttttttt[G/T]tttttcttttttgag | 8816 |
rs12883900 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69070791 | TAATTTTTATTtttc[C/T]ttttttttttttgtt | 8816 |
rs12883917 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69070811 | ttttttttgtttttc[C/T]tttttgagacggagt | 8816 |
rs12884333 | snp | G/T | 0 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69063816 | TATGACAGCAAAAGG[G/T]TCCAGACTGCACCCA | 8816 |
rs12888669 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69110376 | ctgggttcaagcctc[A/C]tgcctcagcctccca | 8816 |
rs12891532 | snp | A/G | 0.5 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69098911 | aaaaaaaaaaaaaaa[A/G]aaaagaaaaGAAAAA | 8816 |
rs12894224 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69065561 | CATTTGTTTAAGGTA[A/C]CCAAGACTGTGTACA | 8816 |
rs12894228 | snp | A/C | 0 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69065567 | TTTAAGGTAACCAAG[A/C]CTGTGTACAATCATA | 8816 |
rs12894822 | snp | A/G | 0.456568 | 0.140818 | intron-variant | DCAF5 | GRCh38.p7 | 14:69065674 | TACTGAACAGTTTAC[A/G]TACAATCATTTTTTG | 8816 |
rs12895568 | snp | C/T | 0 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69065552 | TATAGTGGCCATTTG[C/T]TTAAGGTAACCAAGA | 8816 |
rs17106714 | snp | A/G | 0.0667028 | 0.170006 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69051281 | CTATTAAAAATATCT[A/G]TTATGGAAGAAATTG | 8816 |
rs17106717 | snp | A/G | 0.0539704 | 0.155153 | intron-variant | DCAF5 | GRCh38.p7 | 14:69055729 | CTGTAATTTAACTAG[A/G]ACTTGCTAACCAACT | 8816 |
rs17106754 | snp | C/T | 0.0810805 | 0.184299 | intron-variant | DCAF5 | GRCh38.p7 | 14:69118937 | ATTATGGTTCCTTCT[C/T]TTCTAAACTCTTGTT | 8816 |
rs17836065 | snp | C/T | 0.234692 | 0.249531 | intron-variant | DCAF5 | GRCh38.p7 | 14:69059850 | GAAGAGGGTTCAGAT[C/T]CCATGCAAACTAGGG | 8816 |
rs17836099 | snp | A/G | 0.233527 | 0.249457 | intron-variant | DCAF5 | GRCh38.p7 | 14:69121328 | CCAGGCCAAACTAAC[A/G]GATGAGTATGAGAGG | 8816 |
rs28432699 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | DCAF5 | GRCh38.p7 | 14:69130313 | GTCTGGTTAAAATTA[G/T]TGTTTAATAAAATAA | 8816 |
rs28436153 | snp | A/G | 0.211819 | 0.247067 | intron-variant | DCAF5 | GRCh38.p7 | 14:69075239 | GTCACAGCTTATGTT[A/G]GAAATGTTGTCCTCT | 8816 |
rs28527397 | snp | C/G | 0.155987 | 0.23165 | intron-variant | DCAF5 | GRCh38.p7 | 14:69062779 | TCAATGAAACCAAAG[C/G]CACTTAAAACATTTC | 8816 |
rs28613298 | snp | C/T | 0.494358 | 0.0528145 | intron-variant | DCAF5 | GRCh38.p7 | 14:69111279 | AAACAGACAGTTAAC[C/T]GAGAGGTCCCCAAAC | 8816 |
rs28710350 | snp | C/T | 0.0948562 | 0.196037 | intron-variant | DCAF5 | GRCh38.p7 | 14:69064332 | TTTTTTAACATCCTA[C/T]TTCTACCTCTACTCC | 8816 |
rs28799989 | snp | G/T | 0.0948562 | 0.196037 | intron-variant | DCAF5 | GRCh38.p7 | 14:69104793 | ACCCAGGAGGTGGAG[G/T]TTGCAGTGAGCCAAG | 8816 |
rs33936553 | in-del | -/A | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69119705 | GAGAGAGACTGTCTC[-/A]AAAAAAAAAAAAAGT | 8816 |
rs33949479 | in-del | -/AAGTT | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69060947 | AATAAAATAATCACA[-/AAGTT]ATTTTTATTTTTTTC | 8816 |
rs34005299 | in-del | -/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69065115 | TTTTTTTTTTTTTTT[-/T]GAGACGGAGTCTTGC | 8816 |
rs34020632 | in-del | -/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69063071 | TTCCCCCCGATAGCA[-/G]GGGAGAACTAAGGAT | 8816 |
rs34035158 | in-del | -/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69066790 | CATAACATTCAGCCA[-/G]GGGGTTTATTGCCTC | 8816 |
rs34047873 | in-del | -/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69069383 | ACTCAATCAGCCATT[-/C]CCAGGTGGGTAGCAA | 8816 |
rs34081162 | in-del | -/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69150989 | GTCTCTAAAAGAGTA[-/C]CCCCCAAATTCCCTC | 8816 |
rs34095292 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69118757 | TGACCTTCTGTTATC[G/T]AACATGTCTGTGACT | 8816 |
rs34165446 | in-del | -/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69069888 | GCCTCCCAAAGTGCT[-/G]GGGATTACAGGCATG | 8816 |
rs34239696 | in-del | -/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69073032 | ACTTTCTGAAACACT[-/G]GCATAGTGCATTTTA | 8816 |
rs34275720 | in-del | -/CA | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69099252 | GGGACTCTGTCTCAA[-/CA]CACACACACACACAC | 8816 |
rs34278781 | in-del | -/A | 0.181978 | 0.240568 | intron-variant | DCAF5 | GRCh38.p7 | 14:69088989 | TCTGACTTCTTGTGC[-/A]ACACTTAAAAAAAAC | 8816 |
rs34357294 | in-del | -/T | 0.497959 | 0.0318836 | intron-variant | DCAF5 | GRCh38.p7 | 14:69145668 | TATTTTATAAGAATA[-/T]TTTTTTAAACAATGT | 8816 |
rs34412569 | in-del | -/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69057073 | CCACTCTTAGAGGTT[-/G]CTGATTCAGTAAGTC | 8816 |
rs34416347 | in-del | -/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69075271 | CTGCTAAAGATCTGT[-/C]CCCTCAGGGCACAGC | 8816 |
rs34483517 | in-del | -/A | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69141139 | CTCCATCTCAAATTT[-/A]AAAAAAAAAAAAAAA | 8816 |
rs34493073 | in-del | -/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69085496 | GGACTTATCTAACAA[-/G]GAGTATAAATTGAAT | 8816 |
rs34526558 | in-del | -/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69093792 | TTTTAGGATTGGAAT[-/G]GAAAGTAAAGAGGGA | 8816 |
rs34555932 | in-del | -/A | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69086621 | GTGCATGGAGTTATT[-/A]AAAAAAAAAAAAAAA | 8816 |
rs34581291 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69073309 | GAGAAAAGTGAGAAC[A/C]CAGTGAGAAGGTGGC | 8816 |
rs34608088 | in-del | -/A | 0.381113 | 0.21286 | intron-variant | DCAF5 | GRCh38.p7 | 14:69150722 | AGACTCCACCTCTAC[-/A]AAAAAAAAAAAAAGT | 8816 |
rs34627446 | snp | A/C | 0.0185938 | 0.0946107 | intron-variant | DCAF5 | GRCh38.p7 | 14:69149870 | AGGTGTTGACTGCTA[A/C]TGAGAGACAAAGATA | 8816 |
rs34748237 | in-del | -/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69065096 | ATGCAATATGACCTC[-/T]TTTTTTTTTTTTTTT | 8816 |
rs34805141 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69119589 | AACTGGTGGCACACC[C/T]TTGAAGTCCCAGCTA | 8816 |
rs34817641 | in-del | -/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69152314 | TTCCCAGCCCCAAGA[-/C]CCCTTTTCCTTAACG | 8816 |
rs34820385 | in-del | -/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69077536 | TACAGGCAGGCACCA[-/C]CCACACCCAGCTAAT | 8816 |
rs34845708 | in-del | -/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69060481 | CAAAGCCTAAATCAA[-/G]GGAAGTTGGACTAAG | 8816 |
rs34867305 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | DCAF5 | GRCh38.p7 | 14:69132975 | TTAATGAGATAGATC[C/T]GTGTAAAAGACTTGG | 8816 |
rs34867364 | in-del | -/A | 0.498813 | 0.0243321 | intron-variant | DCAF5 | GRCh38.p7 | 14:69122872 | CCTGACTCTTACAGT[-/A]AATAGGATCTAGACA | 8816 |
rs34888089 | in-del | -/TA | 0.00358779 | 0.0422022 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69155247 | TTTACTGTGGCAGTG[-/TA]TATAATACGCATCCT | 8816 |
rs34910599 | in-del | -/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69108397 | ATGTGTATGTGTTTT[-/G]GGGGGGTGGTGCAAA | 8816 |
rs34961102 | in-del | -/A | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69096805 | AAACGCCCTCTACCC[-/A]AAAGCTGGTGAAATA | 8816 |
rs35008190 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | DCAF5 | GRCh38.p7 | 14:69147048 | CAGATAATGTGCTTT[C/T]AGACTAATTTATCTA | 8816 |
rs35075766 | in-del | -/AT | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69105915 | CCCTAATAAACTGTC[-/AT]ATATATATATATATA | 8816 |
rs35090961 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | DCAF5 | GRCh38.p7 | 14:69099375 | CATGAAACCTGATCT[C/T]GAGGGGCAAGCAGCA | 8816 |
rs35094924 | in-del | -/A | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69135841 | GATTTGGAAAACCTG[-/A]AAAACTCAGTGAACC | 8816 |
rs35187638 | in-del | -/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69113235 | TCATCACTGCTCCAA[-/G]GGAGATTATCTGTTT | 8816 |
rs35191369 | in-del | -/C | 0 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69099787 | TCTCTACAAAAAAAA[-/C]AATACAAAAATTAGC | 8816 |
rs35238903 | in-del | -/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69143395 | CCTAACTTCTGTAAG[-/C]CCTCAGTTCCCTCAT | 8816 |
rs35270301 | in-del | -/A | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69105944 | TATATATATATATAT[-/A]ATCTCCTATTGGTTC | 8816 |
rs35292168 | in-del | -/A | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69141668 | GTTACAAAGGATCCC[-/A]AACAATCAACAAGGC | 8816 |
rs35359938 | in-del | -/T/TT | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69136113 | ACTGATGTGTAAAAC[-/T/TT]TTTTTTTTTTTTTTT | 8816 |
rs35379143 | in-del | -/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69133452 | TGCCAGATCTCCCAA[-/T]TTTTGGCCCAGGGAT | 8816 |
rs35444793 | in-del | -/TCT | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69098145 | CACCTCCTAGGACTC[-/TCT]TCTTACCTTATTCAA | 8816 |
rs35458084 | in-del | -/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69082740 | AGTATTTATACTCTT[-/C]CATTCAAGCAAAGGT | 8816 |
rs35479584 | in-del | -/A | | | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69116833 | ATTCCACATGAGCTG[-/A]AAAAATTCACAACCA | 8816 |
rs35501979 | in-del | -/A | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69098727 | CTCTACTAAAAATAC[-/A]AAAAAAAAAAAAAAA | 8816 |
rs35586847 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | DCAF5 | GRCh38.p7 | 14:69072565 | TGCAGTATGCTATGA[C/T]TGTGCCTGTGAATAG | 8816 |
rs35632281 | snp | C/G | 0.233527 | 0.249457 | intron-variant | DCAF5 | GRCh38.p7 | 14:69103745 | TTATCTGTACAATCA[C/G]AAGACTCCCTCATGC | 8816 |
rs35646057 | in-del | -/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69143455 | ACTTACAAAACATTC[-/T]TTTTAAGTGTTACAT | 8816 |
rs35686041 | snp | A/T | 0.289165 | 0.246913 | intron-variant | DCAF5 | GRCh38.p7 | 14:69088144 | CCCACCACTCCTTAA[A/T]GTTTACTCCTAGCCC | 8816 |
rs35686850 | in-del | -/C | | | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69052229 | TGTGTTTATAAATAA[-/C]CCCCCCCACCCCCAG | 8816 |
rs35775535 | in-del | -/TG | 0.0271762 | 0.113356 | intron-variant | DCAF5 | GRCh38.p7 | 14:69131428 | TACAGAGGCACAGTC[-/TG]TGTGACACACAGCCC | 8816 |
rs35812611 | in-del | -/AAAA | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69110902 | AAAAAAAAAAAAAAA[-/AAAA]GTGGTGTCTGCTGTG | 8816 |
rs35853040 | in-del | -/A | 0 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69076117 | AGGATGACTATTACC[-/A]AAAAAAAAAAAAATT | 8816 |
rs35889366 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | DCAF5 | GRCh38.p7 | 14:69056332 | AGGACACATGCCCCA[A/G]GGACAGGTAACTGCA | 8816 |
rs35902816 | in-del | -/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69112638 | CACACAAATAACACA[-/C]CAAGTTATTTCACCT | 8816 |
rs35956752 | in-del | -/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69093824 | GACTTAGAAAACCCT[-/C]CCTAGAATTCCAGAC | 8816 |
rs36021842 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69117802 | TGAAACTAGGATGCA[A/G]GAAAGTGCATAACGC | 8816 |
rs36091340 | in-del | -/A | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69135146 | AAGGTCTGCAAAGTC[-/A]AAATTTTTTTCGCAA | 8816 |
rs36107903 | in-del | -/T | | | downstream-variant-500B | DCAF5 | GRCh38.p7 | 14:69050571 | AAACATCAGAAAATA[-/T]TTTCTTTGGGAGCTG | 8816 |
rs36214589 | in-del | -/AGCAC | 0.109461 | 0.206758 | intron-variant | DCAF5 | GRCh38.p7 | 14:69132723 | AATGTGGGGCAGCAT[-/AGCAC]AGCACAGCATTCAAA | 8816 |
rs45469294 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant, utr-variant-3-prime, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69090885 | AATAAGATTTGTTGT[C/G]CTTGAGAATAAAAAA | 8816 |
rs45611837 | snp | C/T | | | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69051155 | GAAAATAGAGAGAAA[C/T]GATTTTACATATCTG | 8816 |
rs55794839 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69129602 | GAGATTTATTGTTTA[G/T]TTCCACAGAGAGAGA | 8816 |
rs55845230 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69068465 | GCACTTTGGGAGGCC[A/G]AGGCAGGAGGATCAC | 8816 |
rs55876098 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69083996 | CGTGACTGAAATTCA[A/G]CATAAAAGTATCAGA | 8816 |
rs55975366 | snp | C/T | 0.040671 | 0.13668 | intron-variant | DCAF5 | GRCh38.p7 | 14:69069098 | TTTTTTCCAGTTACA[C/T]GGGAGGAAAAAGCAG | 8816 |
rs56097892 | snp | A/G | 0.040671 | 0.13668 | intron-variant | DCAF5 | GRCh38.p7 | 14:69086606 | TGGGCTTAATCAGGC[A/G]TGCATGGAGTTATTA | 8816 |
rs56140622 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69085532 | TGCAAGCACTGAACA[C/T]TGTTACTTCTATCAA | 8816 |
rs56239027 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69084651 | TTAAGAAGAACCAAA[A/G]AAAGAAGCTTATGGC | 8816 |
rs56274826 | snp | C/T | 0.040671 | 0.13668 | intron-variant | DCAF5 | GRCh38.p7 | 14:69102313 | AGGGTTTCACCATGT[C/T]GGCCAGGCTGGTCTC | 8816 |
rs56286977 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | DCAF5 | GRCh38.p7 | 14:69133530 | TGGCACTTCCCAAAT[C/T]GAAACCAGTAGGCAG | 8816 |
rs56313344 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69121905 | CCACAAATAGGAAGG[G/T]TAAGTATTGTTTCAA | 8816 |
rs56328231 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69069232 | GCCTACTTCATCAGC[A/C]TACTGCCAGTGGGGG | 8816 |
rs56772570 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | DCAF5 | GRCh38.p7 | 14:69097148 | AAATCCTAAGCAGAA[A/G]AGGGTTTGAAAAGAA | 8816 |
rs56788993 | snp | G/T | 0.0539704 | 0.155153 | intron-variant | DCAF5 | GRCh38.p7 | 14:69146544 | CAGGCAAGAGCATTT[G/T]TGCTGTATTAAGTAT | 8816 |
rs56864874 | in-del | -/CA | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69102872 | GGTAAACCAGTAACA[-/CA]GCTGTTTATTATCAA | 8816 |
rs56868917 | snp | C/T | 0.040671 | 0.13668 | intron-variant | DCAF5 | GRCh38.p7 | 14:69104818 | GCCAAGATAGCGCCA[C/T]TGCACTCCAGCCTGG | 8816 |
rs56906226 | in-del | -/TT | | | downstream-variant-500B | DCAF5 | GRCh38.p7 | 14:69050497 | TTGCTTTTTTTTTTT[-/TT]AGAAAAAAGTTTGCA | 8816 |
rs56922727 | snp | A/T | 0.0232847 | 0.105357 | intron-variant | DCAF5 | GRCh38.p7 | 14:69078351 | ACCACCTCATACCCA[A/T]CAGAATGGTTACTAT | 8816 |
rs57027271 | in-del | -/A | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69098748 | AAAAAAAAAAAAAAA[-/A]TTAGCCGGGCGTAGT | 8816 |
rs57084924 | snp | C/T | 0.139564 | 0.224285 | intron-variant | DCAF5 | GRCh38.p7 | 14:69123935 | AAACTCCTGACCTCA[C/T]GATCCACCCACCTCG | 8816 |
rs57089112 | in-del | -/A | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69098915 | AAAAAAAAAAAAAAA[-/A]GAAAAGAAAAAAAAG | 8816 |
rs57114744 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69141258 | TGTGAGGAGCTAAGA[A/G]ACTGGGGTTTTGGTT | 8816 |
rs57255147 | snp | C/T | 0.0126979 | 0.078662 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69117245 | ATCAGGCAGTTCAGA[C/T]GAAGGAGAATTTCAC | 8816 |
rs57334729 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69140761 | CTTTTTTTTCCCTTT[C/T]TAATAAAAGGCAAGT | 8816 |
rs57422627 | snp | A/C | 0.0577344 | 0.159793 | intron-variant | DCAF5 | GRCh38.p7 | 14:69125999 | AGGTTAATATACAAA[A/C]GTCCATCACTTTCCT | 8816 |
rs57470426 | in-del | -/T | 0.495095 | 0.0492773 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69053802 | GTATTCACTAAACAA[-/T]TTTTTTTTTTTTGTA | 8816 |
rs57570724 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | DCAF5 | GRCh38.p7 | 14:69056164 | TTTTTAACTAATGGG[A/C]ATTGCTCACTGGAGC | 8816 |
rs57651700 | in-del | -/TT | 0.492435 | 0.0610346 | intron-variant | DCAF5 | GRCh38.p7 | 14:69141344 | CTTTAAACTGGGACC[-/TT]TTTTTTTCTTTTTCT | 8816 |
rs57674546 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | DCAF5 | GRCh38.p7 | 14:69121829 | AGGACATTCATCTGC[A/G]TTATGGCCAGCATAA | 8816 |
rs57723249 | snp | A/G | 0.136166 | 0.22258 | intron-variant | DCAF5 | GRCh38.p7 | 14:69072426 | GAAGAACAGAAAGAA[A/G]AAGAGAAGATTCATG | 8816 |
rs57751859 | in-del | -/CA | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69112595 | ACACACACACACACA[-/CA]AATAACACACAAGTT | 8816 |
rs57794177 | in-del | -/CTT | 0 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69098149 | TCCTAGGACTCTCTT[-/CTT]ACCTTATTCAACTTC | 8816 |
rs58557271 | in-del | -/TT | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69136114 | CTGATGTGTAAAACT[-/TT]TTTTTTTTTTTTTTT | 8816 |
rs58620965 | in-del | -/TTTTTTTTTT | 0.153665 | 0.230694 | intron-variant | DCAF5 | GRCh38.p7 | 14:69067338 | AGCCGATTTCGTATC[-/TTTTTTTTTT]TTTTTTTTTTTTTTG | 8816 |
rs58861324 | in-del | -/GTTAA | 0 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69060948 | ATAAAATAATCACAA[-/GTTAA]TTTTTATTTTTTTCT | 8816 |
rs59108823 | in-del | -/TT | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69143578 | TTTTTTTTTTTTTTT[-/TT]ACAAACAGCAATGTC | 8816 |
rs59209270 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69099029 | AGGCCAAGGTGGGCA[A/G]ATCACGAGGTCAAGA | 8816 |
rs59428528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69087062 | TCAGACTATCCAGTT[C/T]GAGGCAAACATGCTT | 8816 |
rs59865992 | in-del | -/A | 0 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69119719 | CAAAAAAAAAAAAAA[-/A]GTAGGGGGGAAACAA | 8816 |
rs60135694 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | DCAF5 | GRCh38.p7 | 14:69058571 | AGACATGTCTCATAA[C/T]CGGGCAAAGTTCATG | 8816 |
rs60306767 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69143774 | GCAGTTATTGGAACC[A/C]AATTTTCTATAAAGT | 8816 |
rs60380311 | in-del | -/ATATATATATAT/ATATATATATATATATATATATATATAAT | 0 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69105946 | TATATATATATATAT[lengthTooLong]CTCCTATTGGTTCTG | 8816 |
rs60384175 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69141225 | AAGGCTTTTCTACTA[A/G]AGGCATCCCATAGTG | 8816 |
rs60440875 | in-del | -/AG | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69078783 | GTTTAGTGGGCAGAG[-/AG]TTTCAGTTTGAGATG | 8816 |
rs60478675 | in-del | -/AT/ATAT | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69058551 | CATATATATATATAT[-/AT/ATAT]GGCTAGACATGTCTC | 8816 |
rs60643493 | snp | A/T | 0.0232847 | 0.105357 | intron-variant | DCAF5 | GRCh38.p7 | 14:69072800 | GACAGACTTGCTGTG[A/T]TTAACAATGTAATGC | 8816 |
rs60792430 | in-del | -/TT | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69142147 | AAAAAAAAATTTTTT[-/TT]AATTAGCTGGGCACG | 8816 |
rs60838164 | in-del | -/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69060548 | TTTCTTTTTTTTTTT[-/T]GGAGACAGAGTCTCG | 8816 |
rs60913200 | in-del | -/CA/CACA | 0.5 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69099300 | ACACACACACACACA[-/CA/CACA]ACTAACAAAGCAAAA | 8816 |
rs60974651 | in-del | -/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69130048 | TTAAAGAGTACCCTT[-/T]CCCAAAGGGTCCCGA | 8816 |
rs60977022 | in-del | -/AA | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69141167 | AAAAAAAAAAAAAAA[-/AA]GTGGCAGCTGAAAGA | 8816 |
rs61160887 | snp | A/G | 0.135143 | 0.222054 | intron-variant | DCAF5 | GRCh38.p7 | 14:69058427 | GGGAGGCTGAGGCAG[A/G]AGAATTGCTTGAACC | 8816 |
rs61267160 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DCAF5 | GRCh38.p7 | 14:69079450 | GAGAACAGCTAGGGA[C/T]GATTTTTAGGGAGGG | 8816 |
rs61309740 | in-del | -/AAAA | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69072642 | AAAAAAAAAAAAAAA[-/AAAA]CGAGAGAAAAGAAAA | 8816 |
rs61332233 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69100146 | TGGATATATGGATAT[C/T]AATAGGAAGATACAT | 8816 |
rs61645280 | in-del | -/ATTA/TTAA | 0 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69082466 | AAAAAATTCTATTAA[-/ATTA/TTAA]GGAATATTCCATAAA | 8816 |
rs61741172 | snp | A/G | 0.378367 | 0.214527 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69054628 | TTCATCTGCCTCCCC[A/G]GTCACCAAGGAGGTC | 8816 |
rs61980264 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | DCAF5 | GRCh38.p7 | 14:69145595 | GAATTGAGTAGAAAA[G/T]AAATAGAATTTCATA | 8816 |
rs61981630 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69077210 | ACTGTTTTCCTTTTG[C/T]GTGTGTGTATGTGAC | 8816 |
rs61981631 | snp | A/C/T | 0.5 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69082464 | TGTGTAGAAAAAATT[A/C/T]TATTAAGGAATATTC | 8816 |
rs61981632 | snp | A/T | 0.5 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69086622 | TGCATGGAGTTATTA[A/T]AAAAAAAAAAAAAAA | 8816 |
rs61981645 | snp | G/T | 0.5 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69105536 | TGAGTCAGTGGGCAG[G/T]GAGAACATGACCCGC | 8816 |
rs61981646 | snp | C/T | 0.5 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69107291 | ATCTCTGGCCTAAAC[C/T]CCAAAGACCCTGGGT | 8816 |
rs61981647 | snp | C/T | 0.223522 | 0.248594 | intron-variant | DCAF5 | GRCh38.p7 | 14:69107995 | CAAATGCCTCCTTTC[C/T]GTGAAGCAGCTCCTG | 8816 |
rs61981648 | snp | C/G | 0.288906 | 0.246954 | intron-variant | DCAF5 | GRCh38.p7 | 14:69110357 | TCACTGCAACCTCCA[C/G]CTCCTGGGTTCAAGC | 8816 |
rs61981649 | snp | A/G | 0.223522 | 0.248594 | intron-variant | DCAF5 | GRCh38.p7 | 14:69110423 | GGCACACAACACCAC[A/G]CCCCACTAATTTTCC | 8816 |
rs61981650 | snp | G/T | 0.0275645 | 0.114116 | intron-variant | DCAF5 | GRCh38.p7 | 14:69121596 | TCAGGGGAGGACTAA[G/T]GATCTTGGTTTTAGA | 8816 |
rs61981651 | snp | A/T | 0.5 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69145528 | TAAAAAAAAAAATTT[A/T]AATTTCCCATACTAT | 8816 |
rs67769121 | in-del | -/AAA | 0.330947 | 0.236533 | intron-variant | DCAF5 | GRCh38.p7 | 14:69072624 | AAAAAAAAAAAAAAA[-/AAA]CGAGAGAAAAGAAAA | 8816 |
rs67836121 | in-del | -/T | 0.375 | 0.216506 | intron-variant | DCAF5 | GRCh38.p7 | 14:69070803 | TTCTTTTTTTTTTTT[-/T]GTTTTTCTTTTTTGA | 8816 |
rs67864729 | in-del | -/AG | 0.135143 | 0.222054 | intron-variant | DCAF5 | GRCh38.p7 | 14:69062666 | TAAGTTGCTATGGAA[-/AG]AGAGAAGATGAAACA | 8816 |
rs71102626 | in-del | -/GT/TG | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69095551 | CAATTGAGTGGTTTT[-/GT/TG]TGTGTGTGTGTGTGT | 8816 |
rs71102627 | in-del | -/T | 0 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69098728 | ACTACGCCCGGCTAA[-/T]TTTTTTTTTTTTTTT | 8816 |
rs71102628 | in-del | -/T | 0 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69098894 | TTTTCTTTTCTTTTC[-/T]TTTTTTTTTTTTTTT | 8816 |
rs71102630 | in-del | -/TGTG | 0 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69112626 | AACTTGTGTGTTATT[-/TGTG]TGTGTGTGTGTGTGT | 8816 |
rs71102632 | in-del | -/G | 0 | 0 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69152481 | CTGAAAGTGTAGGTC[-/G]GGGAGGGGGGCGAGG | 8816 |
rs71423345 | snp | C/T | 0.5 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69123065 | AAACCATAGCAAGCT[C/T]TACACCTCCACCTCC | 8816 |
rs71423346 | snp | G/T | 0.5 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69135985 | AATTATTCGATATGG[G/T]TTTATATTCTACATT | 8816 |
rs71446368 | in-del | -/G | 0.5 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69068450 | ATGCCTGTAATCCCA[-/G]CACTTTGGGAGGCCG | 8816 |
rs71446369 | in-del | -/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69079082 | ATTCCTGCTACCCTG[-/C]CCCCCATACCACTGC | 8816 |
rs71446371 | in-del | -/ACAC | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69112595 | ATGATATATATGTAT[-/ACAC]ACACACACACACACA | 8816 |
rs71446373 | in-del | -/AA | 0.5 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69148103 | GTTCATTTTCTTCGC[-/AA]AAAAAAAAAAAAAAA | 8816 |
rs71953676 | in-del | -/TTATTTAT | 0.437401 | 0.165472 | intron-variant | DCAF5 | GRCh38.p7 | 14:69077366 | ACCACGACATGTAGC[-/TTATTTAT]TTATTTATTTATTTA | 8816 |
rs72520605 | in-del | -/CTT | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69098148 | CTCCTAGGACTYTCT[-/CTT]TMYCTTATTCAACTT | 8816 |
rs72718273 | snp | A/G | 0.000708093 | 0.0188028 | missense | DCAF5 | GRCh38.p7 | 14:69054957 | AGGTAGAGGCTCGGC[A/G]TTCATTCAGCTCCTC | 8816 |
rs72718275 | snp | C/T | 0.150333 | 0.229274 | intron-variant | DCAF5 | GRCh38.p7 | 14:69056685 | GGCCCCTCAATTCCC[C/T]ATCCTTCATCTAGAC | 8816 |
rs72718277 | snp | C/T | 0.150333 | 0.229274 | intron-variant | DCAF5 | GRCh38.p7 | 14:69062314 | GAGGTCCTACATAAA[C/T]TGTTCTAGTTTCTTC | 8816 |
rs72718279 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | DCAF5 | GRCh38.p7 | 14:69066668 | ACACCTTGCTCAAAA[C/T]TCAGATAAAGATCTT | 8816 |
rs72718283 | snp | G/T | 0.0240643 | 0.107019 | intron-variant | DCAF5 | GRCh38.p7 | 14:69073481 | AGATGGTCGACATCC[G/T]AAATCAGTAAAGAAA | 8816 |
rs72718285 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | DCAF5 | GRCh38.p7 | 14:69073763 | ATTCCAGAGAATAGT[C/T]CTGGGGAGAAGAAGG | 8816 |
rs72718286 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | DCAF5 | GRCh38.p7 | 14:69074034 | CTAGAAGAGGAAAAG[C/T]CCTTTTGTAACTTGT | 8816 |
rs72718289 | snp | G/T | 0.150333 | 0.229274 | intron-variant | DCAF5 | GRCh38.p7 | 14:69077556 | ACCCAGCTAATTTTT[G/T]ATAGTGACAGGGGTC | 8816 |
rs72718291 | snp | C/T | 0.040671 | 0.13668 | intron-variant | DCAF5 | GRCh38.p7 | 14:69079049 | CACGTTTAAAAGAGG[C/T]TATCAACTTCATGTG | 8816 |
rs72718292 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | DCAF5 | GRCh38.p7 | 14:69080331 | CACTGCAGGTCTAGG[C/T]GGGCCATCTTACAAA | 8816 |
rs72718299 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | DCAF5 | GRCh38.p7 | 14:69096622 | TTCTAGAGCCCAGAA[C/T]GCTTCAACTTTTTTG | 8816 |
rs72718302 | snp | A/G | 0.150333 | 0.229274 | intron-variant | DCAF5 | GRCh38.p7 | 14:69097966 | CAGTTTATCCTTAAC[A/G]AAGCAGCCAGAGGAG | 8816 |
rs72720208 | snp | C/T | 0.0704125 | 0.17392 | intron-variant | DCAF5 | GRCh38.p7 | 14:69109312 | TCGCGCCACTCTAGC[C/T]TGGGAGACAGAGCAA | 8816 |
rs72720212 | snp | C/T | 0.040671 | 0.13668 | intron-variant | DCAF5 | GRCh38.p7 | 14:69120224 | TAGTAGCTGGAACTA[C/T]AGGCATGTGTCACTA | 8816 |
rs72720213 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | DCAF5 | GRCh38.p7 | 14:69127304 | ACAGAAACTTTTTCA[A/G]TGATAAAAAGAAACG | 8816 |
rs72720218 | snp | C/G | 0.040671 | 0.13668 | intron-variant | DCAF5 | GRCh38.p7 | 14:69136793 | CACAGGACAGCTCCT[C/G]ATAACAAAGACTTAT | 8816 |
rs73275602 | snp | C/T | 0.0232847 | 0.105357 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69052257 | CAGTGCCTGAATTCA[C/T]CCACATCTTCTGCCT | 8816 |
rs73277004 | snp | C/G | 0.0162398 | 0.0886349 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69052609 | CTAAACCTGTATCTA[C/G]CTCAATAAAACTGAG | 8816 |
rs73277010 | snp | C/G | 0.0252325 | 0.109451 | intron-variant | DCAF5 | GRCh38.p7 | 14:69060783 | CTGATCCACTTGCCT[C/G]GGCCTCCCAGAGTGT | 8816 |
rs73277013 | snp | A/T | 0.0287284 | 0.116357 | intron-variant | DCAF5 | GRCh38.p7 | 14:69067156 | TCTCCACTGTATCCC[A/T]AGTCTCTAGAACTGT | 8816 |
rs73277015 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | DCAF5 | GRCh38.p7 | 14:69067656 | AGCCCAGATATTCTT[C/T]TTTTTTTAAGATGGA | 8816 |
rs73277016 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | DCAF5 | GRCh38.p7 | 14:69068835 | TTCCAGTGTCAAACC[A/G]TAAAGAGGACCATCA | 8816 |
rs73277022 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | DCAF5 | GRCh38.p7 | 14:69080562 | GTCTTTTCTTTTATC[C/T]TGATGATCTAATTTC | 8816 |
rs73277024 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | DCAF5 | GRCh38.p7 | 14:69082988 | AGATTACATCAATTC[C/T]ACTTGTTCCTAAGAA | 8816 |
rs73277032 | snp | G/T | 0.0248432 | 0.108648 | intron-variant | DCAF5 | GRCh38.p7 | 14:69088275 | TTCTAGCCCTGGTTT[G/T]CCTACAAACTTGTAT | 8816 |
rs73278952 | snp | A/C | 0.0232847 | 0.105357 | intron-variant | DCAF5 | GRCh38.p7 | 14:69092255 | GTTGTATCCACTCTA[A/C]CTGGGTAGTCATGGA | 8816 |
rs73278958 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | DCAF5 | GRCh38.p7 | 14:69104881 | AAAAAAGTGAGAGAC[A/G]GGGGTACCTACAAAC | 8816 |
rs73278965 | snp | G/T | 0.0248432 | 0.108648 | intron-variant | DCAF5 | GRCh38.p7 | 14:69108134 | GCCACAGATCATAAG[G/T]ACTTTACAGAGATTC | 8816 |
rs73278972 | snp | C/T | 0.00646749 | 0.056497 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69116546 | GTACCTGTGGGCCAC[C/T]GGCAGGCAGATAATC | 8816 |
rs73278980 | snp | G/T | 0.0209421 | 0.100162 | intron-variant | DCAF5 | GRCh38.p7 | 14:69121168 | AGACAGATAGATTGG[G/T]ATTTAGACTTCATTC | 8816 |
rs73278988 | snp | A/C/T | 0.0194034 | 0.096768 | intron-variant | DCAF5 | GRCh38.p7 | 14:69128790 | ACAACAACAAAAAAA[A/C/T]CAAAAACAGAATATC | 8816 |
rs73278990 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | DCAF5 | GRCh38.p7 | 14:69128814 | GAATATCTGCCAGGC[C/T]CAGTGGCTCATGCCA | 8816 |
rs73278991 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | DCAF5 | GRCh38.p7 | 14:69132429 | TCTCAGAGCGCATCA[C/T]TCTACAAACAGTTTG | 8816 |
rs73278993 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | DCAF5 | GRCh38.p7 | 14:69136601 | CACTTATGAAAACTA[A/G]TATTTTTTCAGTTTG | 8816 |
rs73278996 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | DCAF5 | GRCh38.p7 | 14:69147750 | TAATTAATACTTTGA[A/G]ACATCATAGTTGCTC | 8816 |
rs73278999 | snp | A/T | 0.0162398 | 0.0886349 | intron-variant | DCAF5 | GRCh38.p7 | 14:69149916 | TAAACATGACACTAG[A/T]TTTAAACGTGGGAAA | 8816 |
rs73279000 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | DCAF5 | GRCh38.p7 | 14:69150921 | TAAATAAAGGTGTGT[C/G]AAGCTGGGCAACGTG | 8816 |
rs73280805 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | DCAF5 | GRCh38.p7 | 14:69151397 | CCGAAGGTTACTCGC[A/G]AAGACGGATGCTTTG | 8816 |
rs74059868 | snp | C/G | 0.136166 | 0.22258 | intron-variant | DCAF5 | GRCh38.p7 | 14:69070050 | AGTTTGGTAAGATTA[C/G]GAAATTTTTCCAAAG | 8816 |
rs74059870 | snp | A/G | 0.136166 | 0.22258 | intron-variant | DCAF5 | GRCh38.p7 | 14:69070053 | TTGGTAAGATTAGGA[A/G]ATTTTTCCAAAGCCC | 8816 |
rs74353329 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69125252 | GCCTTAGTAGCATAA[A/C]TCATAAATGTTAAGT | 8816 |
rs74385359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69068817 | GTGAACAGTTGCAGG[A/G]TCTTCCAGTGTCAAA | 8816 |
rs74580154 | snp | C/T | 0.0260105 | 0.111035 | downstream-variant-500B | DCAF5 | GRCh38.p7 | 14:69050487 | GATACGAGTTTTGCT[C/T]TTTTTTTTTTTAGAA | 8816 |
rs74633174 | snp | A/C | 0 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69143583 | TTTTTTTTTTTACAA[A/C]CAGCAATGTCTCAGC | 8816 |
rs74650157 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | DCAF5 | GRCh38.p7 | 14:69146758 | CTCAAAAACTATTTG[C/T]TGCACTAATAAATAG | 8816 |
rs74663571 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69122872 | ACCTGACTCTTACAG[A/T]AATAGGATCTAGACA | 8816 |
rs74704721 | snp | C/T | 0.5 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69074474 | AAAGCTCAGATAGCT[C/T]AAATACAAATTTATG | 8816 |
rs74765133 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | DCAF5 | GRCh38.p7 | 14:69143617 | ACATTGGGCGAGGCA[C/T]TCCTTAATTTGGTAG | 8816 |
rs74858593 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | DCAF5 | GRCh38.p7 | 14:69065823 | GACCATGCTGGTCAA[C/T]AGTAGTATCAAATTG | 8816 |
rs74896498 | snp | A/T | 0.5 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69142148 | AAAAAAAATTTTTTT[A/T]AATTAGCTGGGCACG | 8816 |
rs74978015 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | DCAF5 | GRCh38.p7 | 14:69056706 | TCATCTAGACCAAGA[C/T]TTCGTTTCCCCAAAG | 8816 |
rs74985090 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant | DCAF5 | GRCh38.p7 | 14:69100986 | TTCAGTAAATTTAAT[G/T]TCCAAAATGTTTTCA | 8816 |
rs75033446 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | DCAF5 | GRCh38.p7 | 14:69111122 | TTTTCCAGCCTTTGA[C/T]ATTAAGCCCCTGGGC | 8816 |
rs75038759 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | DCAF5 | GRCh38.p7 | 14:69082722 | TCACTTCAGTCCATA[C/T]ATGAGTATTTATACT | 8816 |
rs75093233 | in-del | -/AACGA | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69072644 | AAAAAAAAAAAAAAA[-/AACGA]GAGAAAAGAAAAAAA | 8816 |
rs75100347 | snp | A/T | 0 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69097589 | TTATTATTATTTTTT[A/T]TTTTTTTTTTTTTTT | 8816 |
rs75183997 | snp | A/G | 0.077417 | 0.180873 | intron-variant | DCAF5 | GRCh38.p7 | 14:69060307 | AAAGGGCAGGGCTCT[A/G]TCCTAGCTTTGCCAC | 8816 |
rs75191880 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | DCAF5 | GRCh38.p7 | 14:69100094 | TGTCCTACCCAATTA[C/T]GCTCAAAAATAGATA | 8816 |
rs75199538 | snp | A/T | 0.0178098 | 0.0926698 | intron-variant | DCAF5 | GRCh38.p7 | 14:69074478 | CTCAGATAGCTTAAA[A/T]ACAAATTTATGGAAA | 8816 |
rs75254982 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | DCAF5 | GRCh38.p7 | 14:69114267 | GCCTGGTTATAAAGA[C/T]AGATTTATAACCAGG | 8816 |
rs75258359 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | DCAF5 | GRCh38.p7 | 14:69133918 | TTTCTCCAAAATCAG[A/G]TGACTAATAGCAGTG | 8816 |
rs75264631 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69128555 | AACAAGACTGCAGGA[A/T]GGGCTGGGATACTCA | 8816 |
rs75434331 | snp | C/G | 0.077417 | 0.180873 | intron-variant | DCAF5 | GRCh38.p7 | 14:69087456 | CAAGACTAGAAGGTA[C/G]GCTTGCTTTAAACAA | 8816 |
rs75473945 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | DCAF5 | GRCh38.p7 | 14:69112756 | GATGGTCAATACTCC[A/G]ATGGCACGTAATGCT | 8816 |
rs75484318 | snp | G/T | 0.0611083 | 0.163768 | intron-variant | DCAF5 | GRCh38.p7 | 14:69105039 | AATATTGTGGTTATG[G/T]TTTTTTTTTAATTAT | 8816 |
rs75556723 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | DCAF5 | GRCh38.p7 | 14:69150129 | GAACAAATAGGAAAA[A/G]CTAGGTGTATCTTAG | 8816 |
rs75596316 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | DCAF5 | GRCh38.p7 | 14:69060396 | ACGAAAAAGTAAAAA[C/T]GATTTCCTCATTCTA | 8816 |
rs75617097 | snp | G/T | 0.5 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69128209 | TTTTTTTTTTTTTTT[G/T]AGAGTCTCACTCTGT | 8816 |
rs75617918 | snp | G/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69111795 | ACCTTGTCAGAACAT[G/T]CAATGTACACTTGTA | 8816 |
rs75683171 | in-del | -/CA | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69095564 | TACACACACACACAC[-/CA]AMAAACCACTCAATT | 8816 |
rs75744046 | snp | A/C | 0.0170251 | 0.090679 | intron-variant | DCAF5 | GRCh38.p7 | 14:69126567 | ATCAGCAAAATGATT[A/C]TAATATTTATAGGAG | 8816 |
rs75857728 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | DCAF5 | GRCh38.p7 | 14:69141812 | CCAACATTATCTCTG[C/T]TATGTGGATCCATTA | 8816 |
rs75877922 | snp | A/C | 0.5 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69148104 | TTCATTTTCTTCGCA[A/C]AAAAAAAAAAAAAAA | 8816 |
rs75971729 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | DCAF5 | GRCh38.p7 | 14:69065022 | AGATCTAAAGACTAA[C/T]TGAAGGCTATCAATG | 8816 |
rs76019739 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | DCAF5 | GRCh38.p7 | 14:69107561 | CAGTGACCTGGTGTC[C/T]TCCAGTGGGCAAAAC | 8816 |
rs76020806 | snp | C/T | 0.0126979 | 0.078662 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69052587 | AAATCTGTTGCTCTT[C/T]TCTCTTCTAAACCTG | 8816 |
rs76035513 | snp | C/G | 0.0770498 | 0.180522 | intron-variant | DCAF5 | GRCh38.p7 | 14:69063108 | AGAAAGAAAAATTTG[C/G]ATCACTTTCATAATA | 8816 |
rs76087782 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | DCAF5 | GRCh38.p7 | 14:69076726 | GCACAGCAATGTGAT[C/T]GTACTTAATGCCACT | 8816 |
rs76097645 | snp | A/C | 0.5 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69075035 | GTGAAACTTTGTCTC[A/C]AAAAAAAAAAAAATC | 8816 |
rs76128674 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | DCAF5 | GRCh38.p7 | 14:69151120 | TAGGTCTATAAAGAA[A/G]AGGTCTTCCCCCATT | 8816 |
rs76230681 | snp | G/T | 0.5 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69060548 | ATTTCTTTTTTTTTT[G/T]GGAGACAGAGTCTCG | 8816 |
rs76276335 | snp | C/T | | | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69053644 | GGGTTATTTTTTTTT[C/T]CCCTTTCTTAACACA | 8816 |
rs76288665 | snp | C/G | 0.0158469 | 0.0875917 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69154754 | CATTATAATCACCAC[C/G]TAAAAATTAGTAGCA | 8816 |
rs76320561 | snp | G/T | 0.5 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69126195 | TTCACTTTTTTTTTT[G/T]TGCCCAGGCTGGAGT | 8816 |
rs76334799 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | DCAF5 | GRCh38.p7 | 14:69086564 | ATTTCAGATAAAGGA[A/G]AACATATGGCATGCC | 8816 |
rs76378143 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | DCAF5 | GRCh38.p7 | 14:69112840 | TTATTCAAGATCACA[C/T]GCCTATTAAGGTGTA | 8816 |
rs76464984 | snp | A/T | 0.0372196 | 0.131242 | intron-variant | DCAF5 | GRCh38.p7 | 14:69146262 | AACTTTTTGATGTAT[A/T]AATAACAATGTCTAA | 8816 |
rs76573951 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | DCAF5 | GRCh38.p7 | 14:69107926 | AAGATGAATAAAACA[C/T]GCACCTGCCCTTAAA | 8816 |
rs76578652 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | DCAF5 | GRCh38.p7 | 14:69062775 | ATTGTCAATGAAACC[A/G]AAGCCACTTAAAACA | 8816 |
rs76640185 | snp | C/G | 0.077417 | 0.180873 | intron-variant | DCAF5 | GRCh38.p7 | 14:69092813 | AAAGGAAAATGACTT[C/G]TTTTCCTTTACAATT | 8816 |
rs76644505 | in-del | -/AA | 0.44252 | 0.159487 | intron-variant | DCAF5 | GRCh38.p7 | 14:69119705 | GAGAGAGACTGTCTC[-/AA]AAAAAAAAAAAAAGT | 8816 |
rs76647108 | snp | A/C | 0.0189856 | 0.0955633 | intron-variant | DCAF5 | GRCh38.p7 | 14:69145043 | TTTTGCCATATCAAC[A/C]TAACACTTTTATTGT | 8816 |
rs76700614 | snp | A/T | 0.077417 | 0.180873 | intron-variant | DCAF5 | GRCh38.p7 | 14:69064129 | AAGGGAAGCTGGGCC[A/T]GTCAAAATGAAAATA | 8816 |
rs76709626 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | DCAF5 | GRCh38.p7 | 14:69113988 | TGGGCTCTGAAAACC[A/G]TAGGTTATCAAAGAA | 8816 |
rs76716478 | snp | A/C | 0.0146672 | 0.084371 | intron-variant | DCAF5 | GRCh38.p7 | 14:69085433 | CTTTGTCCTAAAATG[A/C]TTCTTTTCCTCCCTT | 8816 |
rs76782730 | snp | A/G | | | intron-variant, utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69089756 | GCAATTTTCCCCCCA[A/G]GGGACAATGTCTGGA | 8816 |
rs76828648 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | DCAF5 | GRCh38.p7 | 14:69061155 | AACCACAGGTATACA[C/T]TAATTTTTAAATTTT | 8816 |
rs76839837 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | DCAF5 | GRCh38.p7 | 14:69134177 | AGTTACAGGCAGAGT[A/G]GGATTCAAATCCAAG | 8816 |
rs76893499 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | DCAF5 | GRCh38.p7 | 14:69111965 | TACACCTGTATTAAG[A/G]CATCAAGAAGTGGTG | 8816 |
rs76942805 | snp | C/T | 0.0577344 | 0.159793 | intron-variant | DCAF5 | GRCh38.p7 | 14:69082892 | TCTGTTCCCCTTCAT[C/T]AACATCTACCAGGGA | 8816 |
rs76943819 | snp | A/C | 0 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69071317 | TGTATAGCAAAAAAA[A/C]CAAAGACTGATTAAC | 8816 |
rs76971709 | snp | G/T | 0.5 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69126197 | CACTTTTTTTTTTTT[G/T]CCCAGGCTGGAGTGC | 8816 |
rs76981261 | snp | G/T | 0.5 | 0 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69053813 | ACAATTTTTTTTTTT[G/T]TGTAAGGCTACTTTT | 8816 |
rs76999509 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DCAF5 | GRCh38.p7 | 14:69132204 | TCTACTTTTAACTTT[C/T]TGAGGAATGCCATAC | 8816 |
rs77001676 | snp | A/G | 0 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69130399 | ATCAGAGACAAAGTA[A/G]AATGGCAGTGGCCAG | 8816 |
rs77078467 | snp | A/C | 0.0287284 | 0.116357 | intron-variant | DCAF5 | GRCh38.p7 | 14:69070238 | ATTCAGGGAAAGAGA[A/C]GGGAAAGGCAATATA | 8816 |
rs77104252 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | DCAF5 | GRCh38.p7 | 14:69110058 | ATTTGCACTGCTCTC[A/G]TGAGTGATAAAGTTC | 8816 |
rs77112709 | snp | A/G | 0.0577344 | 0.159793 | intron-variant | DCAF5 | GRCh38.p7 | 14:69096354 | TGAATGAACACATTT[A/G]TTTTCCCCAGAACAT | 8816 |
rs77198677 | snp | A/C | 0.077417 | 0.180873 | intron-variant | DCAF5 | GRCh38.p7 | 14:69144007 | TTTTTCCACTAATGC[A/C]TTGCCTGTTCTCTGG | 8816 |
rs77209359 | snp | A/G | 0.5 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69146281 | AACAATGTCTAATGT[A/G]ACTAATGATCAGCAG | 8816 |
rs77240284 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69105943 | TATATATATATATAT[A/C]TATCTCCTATTGGTT | 8816 |
rs77267298 | snp | G/T | 0.5 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69070802 | TTTCTTTTTTTTTTT[G/T]TGTTTTTCTTTTTTG | 8816 |
rs77327054 | snp | A/G | 0.0759472 | 0.179459 | intron-variant | DCAF5 | GRCh38.p7 | 14:69129366 | CCCTATGCAAAGGCA[A/G]TCTTCAAGTATGCGT | 8816 |
rs77329698 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | DCAF5 | GRCh38.p7 | 14:69080095 | TTTTAAAATATAAGG[C/T]AGCCATTAAGAGCTC | 8816 |
rs77365479 | snp | C/T | 0.112983 | 0.209108 | intron-variant | DCAF5 | GRCh38.p7 | 14:69128432 | TTCAAGTGATCTGCC[C/T]GCCTTGGCCTCCCAA | 8816 |
rs77428265 | snp | A/C | 0.5 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69075034 | AGTGAAACTTTGTCT[A/C]AAAAAAAAAAAAAAT | 8816 |
rs77561112 | snp | G/T | 0.5 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69060949 | ATAAAATAATCACAA[G/T]TTTTATTTTTTTCTC | 8816 |
rs77576841 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | DCAF5 | GRCh38.p7 | 14:69146419 | ACAAATAATGTGTAT[A/C]TATAAATATTCACAT | 8816 |
rs77613362 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69094761 | TGGCTTCAAGTGTAA[A/G]ATGCATGAAAAATCA | 8816 |
rs77775926 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69071852 | GCCAACATTTAAAAA[C/T]TGAGGTATTACATAT | 8816 |
rs77789092 | snp | A/G | 0.5 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69139092 | GGAGGCAGAGGCTGC[A/G]GTAAGCTGTGATCAC | 8816 |
rs77958215 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | DCAF5 | GRCh38.p7 | 14:69076365 | CAGCATTATTCACAA[C/T]AGCCAAAAGGTGGAA | 8816 |
rs78147392 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | DCAF5 | GRCh38.p7 | 14:69068405 | CTGGTAGAATTAAGA[A/G]TTTACTGCAAGGGCC | 8816 |
rs78158892 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | DCAF5 | GRCh38.p7 | 14:69086960 | ATCTTATACTTTCTC[A/C]TTTTGTGTACATCCT | 8816 |
rs78207357 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | DCAF5 | GRCh38.p7 | 14:69100153 | ATGGATATCAATAGG[A/T]AGATACATTAACTAG | 8816 |
rs78366593 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | DCAF5 | GRCh38.p7 | 14:69135938 | AAGACAGATCAATGG[A/G]TTTTAATGTAACAAT | 8816 |
rs78374209 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | DCAF5 | GRCh38.p7 | 14:69097029 | AGGTAAACAGGCAGT[C/T]TCTGATGGCAAGACA | 8816 |
rs78419482 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | DCAF5 | GRCh38.p7 | 14:69059538 | TCAGCACCCTCACTT[C/T]CCAGATGGGAGACAG | 8816 |
rs78567694 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | DCAF5 | GRCh38.p7 | 14:69120516 | TTATATTCATGATAT[A/G]TGTAGTCCTGCCTTC | 8816 |
rs78616683 | snp | C/G | 0.0777841 | 0.181223 | intron-variant | DCAF5 | GRCh38.p7 | 14:69105765 | TTGGGCCTTTGGCAT[C/G]AGACTGAAGCCTCTA | 8816 |
rs78808857 | snp | A/T | 0.00318978 | 0.0398085 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69052252 | ACCCCCAGTGCCTGA[A/T]TTCATCCACATCTTC | 8816 |
rs78843288 | snp | C/T | 0.0759472 | 0.179459 | intron-variant | DCAF5 | GRCh38.p7 | 14:69085640 | TTTCTTGTGATGATA[C/T]AATATTTTAATTTTA | 8816 |
rs78960065 | snp | A/G | 0.147656 | 0.228091 | intron-variant | DCAF5 | GRCh38.p7 | 14:69127276 | GATAAATCAACTGTA[A/G]TACAACCAGACAACA | 8816 |
rs78980530 | snp | A/T | 0.5 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69082461 | TTCTGTGTAGAAAAA[A/T]TTCTATTAAGGAATA | 8816 |
rs79027402 | snp | A/G | 0.5 | 0 | downstream-variant-500B | DCAF5 | GRCh38.p7 | 14:69050499 | GCTTTTTTTTTTTTT[A/G]GAAAAAAGTTTGCAG | 8816 |
rs79163231 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | DCAF5 | GRCh38.p7 | 14:69128087 | TTTCCTTTAAAACTT[C/T]CCAGAAAAAAAAGTA | 8816 |
rs79330714 | snp | A/G | 0.5 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69139095 | GGCAGAGGCTGCAGT[A/G]AGCTGTGATCACACC | 8816 |
rs79370061 | snp | A/C | 0.0352966 | 0.128072 | intron-variant, utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69089319 | AAAAAAGCCAAATAT[A/C]AATCTCTGTATTTTA | 8816 |
rs79376904 | snp | A/G | 0.0741063 | 0.177655 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69153887 | GGGATAAAGAAGTAG[A/G]AAGAAAATTGCCAAA | 8816 |
rs79378462 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | DCAF5 | GRCh38.p7 | 14:69133723 | CTTATCTACCTATTA[C/T]CTCATTTTTCCATGT | 8816 |
rs79628290 | snp | A/C/T | 0.00318978 | 0.0398085 | intron-variant | DCAF5 | GRCh38.p7 | 14:69095862 | TCCTCATTGTTTCCA[A/C/T]GTGAAAGCTCTATAA | 8816 |
rs79639501 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69154054 | CGAGTGGGGAGCACT[A/G]AGGTTGGACAGCTGT | 8816 |
rs79640156 | snp | A/T | 0.0166325 | 0.0896639 | intron-variant | DCAF5 | GRCh38.p7 | 14:69148378 | GAGACTACAATCATC[A/T]AGTATAAGCTAGTCT | 8816 |
rs79673745 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | DCAF5 | GRCh38.p7 | 14:69148819 | GGCAATCTGTTATCC[C/T]CATTTTACAGATGAG | 8816 |
rs79698149 | snp | G/T | 0.5 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69128208 | CTTTTTTTTTTTTTT[G/T]GAGAGTCTCACTCTG | 8816 |
rs79705044 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69147919 | AACTTCGATTCAGGG[A/G]AAATAATATAGCCAC | 8816 |
rs79808914 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | DCAF5 | GRCh38.p7 | 14:69151684 | GCCCTGGGCCCGCGA[C/T]CCCAGGGAGGAGGGG | 8816 |
rs79869396 | snp | A/C | 0.5 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69099787 | GTCTCTACAAAAAAA[A/C]AATACAAAAATTAGC | 8816 |
rs79872336 | snp | A/T | 0.0810805 | 0.184299 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69154402 | AATAATAATTTTTTT[A/T]AAAAAAAAAGATCGG | 8816 |
rs79903076 | snp | A/C | 0.375 | 0.216506 | intron-variant | DCAF5 | GRCh38.p7 | 14:69108122 | TGCAACATGAATGCC[A/C]CAGATCATAAGTACT | 8816 |
rs79924269 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | DCAF5 | GRCh38.p7 | 14:69072093 | GATCTGTAAGACCCA[A/C]AGCCCCATTTCCCTA | 8816 |
rs79996666 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant, utr-variant-3-prime, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69090447 | CTAAGACTCCAACAT[G/T]AGTATAAATTCTGAA | 8816 |
rs80015397 | snp | A/T | 0.5 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69060954 | ATAATCACAATTTTT[A/T]TTTTTTTCTCTGAAA | 8816 |
rs80019208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69068327 | AAGCTTGAAGTTAAA[A/G]TTATCTGCTAAAATG | 8816 |
rs80037431 | snp | C/G | 0.0581099 | 0.160244 | intron-variant | DCAF5 | GRCh38.p7 | 14:69108454 | CAGTGCAGTCAGAAC[C/G]TTATGGAGAGACGGA | 8816 |
rs80095021 | snp | A/T | 0.5 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69131774 | CTTTTTTTTTTTTTT[A/T]AATGATTTTATCTAT | 8816 |
rs80123288 | snp | A/G | 0.0770498 | 0.180522 | intron-variant | DCAF5 | GRCh38.p7 | 14:69120493 | CTTATTCTATCAAAG[A/G]ATATAAATTATATTC | 8816 |
rs80186008 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | DCAF5 | GRCh38.p7 | 14:69092844 | CCCCACAAGTTTATA[C/T]GTAGCTTTAAAATAT | 8816 |
rs80230232 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69115060 | CCAAATCCTGCCTTT[C/T]GTAATACGGATGAGG | 8816 |
rs80255237 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | DCAF5 | GRCh38.p7 | 14:69143484 | ATATGCCTGGCACAT[A/G]AAATGCCCCCAAATA | 8816 |
rs80343864 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | DCAF5 | GRCh38.p7 | 14:69107346 | CATGGACCTCTCTGA[C/T]TAACCACTGCTTCCA | 8816 |
rs111231371 | snp | A/G | 0.5 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69146689 | TTGAAAACATAATTT[A/G]TACCTGATTCATTGT | 8816 |
rs111342101 | snp | A/G | 0.5 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69106520 | ACTGCAGACTCTGCC[A/G]CTACCCCACCTGGCT | 8816 |
rs111354001 | in-del | -/T | 0.5 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69098481 | CACTAGATGATTATC[-/T]TTTACATCTTTTCTT | 8816 |
rs111376782 | snp | A/C | 0.5 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69106680 | CCCAGCCTACTTTTA[A/C]ACATATTTGAAAAAA | 8816 |
rs111387868 | snp | A/G | 0.5 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69097477 | CATTAAACAATAATT[A/G]GCACCTACTATATGC | 8816 |
rs111394045 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69141353 | GGGACCTTTTTTTTT[C/T]TTTTTCTTTTATTAT | 8816 |
rs111421952 | snp | A/G | 0.5 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69144469 | CCCAACTACTCGGGA[A/G]GCTGAGGCAGGAGAA | 8816 |
rs111424756 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | DCAF5 | GRCh38.p7 | 14:69083016 | GAACAATCCAGGTCA[C/T]CTTGTGTTCCTTTAC | 8816 |
rs111550197 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | DCAF5 | GRCh38.p7 | 14:69121393 | ACTAGATGTGTAAAT[G/T]TAAGAAAGGCAGGTT | 8816 |
rs111586347 | snp | G/T | 0.5 | 0 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69051684 | ACTACCAAGTAGCTA[G/T]TTCCCAAGGGAACTT | 8816 |
rs111824529 | snp | A/G | 0.5 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69072852 | CAAACCCTCAATTAC[A/G]GTGAATCCAACAACA | 8816 |
rs111828127 | snp | C/T | 0.5 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69140902 | CGGGCAGATCACCCC[C/T]GCCTAGGGACTGAAC | 8816 |
rs111828849 | snp | A/G | 0.5 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69082074 | CTGACCTTCTGTCAG[A/G]AAGGGAAAAACAATG | 8816 |
rs111865117 | snp | A/G | 0.5 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69126653 | ACATTACCTGACTTC[A/G]GGTTACCACTAATAT | 8816 |
rs111866642 | snp | A/G | 0.5 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69123252 | GTAATCCATTTGCAT[A/G]AAACAAAATTTTTAA | 8816 |
rs111877228 | snp | G/T | 0.5 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69085801 | TCCTAAAACATTCAC[G/T]CTCTAAAAAAGACAT | 8816 |
rs112009200 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69141352 | TGGGACCTTTTTTTT[C/T]CTTTTTCTTTTATTA | 8816 |
rs112025098 | snp | A/G | 0.5 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69137234 | TCAAATAGAGCTGGG[A/G]GACACTAAAAACGGG | 8816 |
rs112135843 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69123334 | GGCACCTACATGAGT[C/G]CTCCAAGGAATGAGC | 8816 |
rs112235688 | snp | G/T | 0.5 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69128663 | GTCCCAGCTACTGGG[G/T]AGGATGAGGCAGGAG | 8816 |
rs112275966 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69072635 | CTTTAAAAAAAAAAA[A/C]AAAAAAAAAACGAGA | 8816 |
rs112319004 | snp | A/G | 0.5 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69084946 | GAGACCTAAATGGGA[A/G]AAGGCATGCCTTGCT | 8816 |
rs112398952 | snp | A/G | 0.000197742 | 0.00994143 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69054145 | CCCCAAGTTCTGCCC[A/G]TTATTGTGAGGGTGA | 8816 |
rs112491070 | snp | A/G | 0.5 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69077138 | TAAGGTGAGGTCAGC[A/G]TTACTTCGTCCTGTC | 8816 |
rs112542913 | snp | C/T | 0.0777841 | 0.181223 | intron-variant | DCAF5 | GRCh38.p7 | 14:69072723 | CCAAATGAGTCAAGA[C/T]ATGCTAAAAATAATC | 8816 |
rs112563406 | snp | A/G | 0.5 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69059232 | TGAGAGCACAGGCAG[A/G]CACCACCATGCCTGG | 8816 |
rs112610997 | snp | G/T | 0.0225045 | 0.103662 | intron-variant | DCAF5 | GRCh38.p7 | 14:69134823 | AGTCTCATAATACAT[G/T]GGTCCAAGTGTAAAT | 8816 |
rs112693118 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant, utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69089469 | CAAAAAGAAGTCTTG[C/T]CTGTCAGAGAGAATA | 8816 |
rs112721837 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DCAF5 | GRCh38.p7 | 14:69060310 | GGGCAGGGCTCTATC[C/T]TAGCTTTGCCACCAA | 8816 |
rs112822376 | snp | A/T | 0.0209421 | 0.100162 | intron-variant | DCAF5 | GRCh38.p7 | 14:69133539 | CCAAATCGAAACCAG[A/T]AGGCAGGGAAGAGGC | 8816 |
rs112905717 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | DCAF5 | GRCh38.p7 | 14:69106821 | GAGATGAGTGGATCA[C/T]TTGAAGTCAGGAGTT | 8816 |
rs113029499 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69141351 | CTGGGACCTTTTTTT[C/T]TCTTTTTCTTTTATT | 8816 |
rs113123004 | snp | A/G | 0.5 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69142332 | GTAACTAAAGTGACA[A/G]ACTACTACTGTCAAG | 8816 |
rs113190407 | in-del | -/CTTT | 0.5 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69062046 | AGCATTTTAAATCAC[-/CTTT]CTTTCTTCTTTTTTT | 8816 |
rs113245283 | snp | G/T | 0.031825 | 0.122064 | intron-variant | DCAF5 | GRCh38.p7 | 14:69086504 | CACAACAAATCAAAG[G/T]CTGGAAACCAACGGT | 8816 |
rs113260043 | snp | A/G | 0 | 0 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69153559 | CGCCCGTACGAGTTC[A/G]GGGAAAATGCGGCTG | 8816 |
rs113354947 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69076199 | GTGGGAATGACTAAC[A/G]AACGGTGCAACTGCT | 8816 |
rs113409058 | snp | C/T | 0.5 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69137608 | GGAATGCACACTACA[C/T]CCAGCCACCCACCAG | 8816 |
rs113502201 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | DCAF5 | GRCh38.p7 | 14:69060693 | CACACCACCACACCC[A/G]ACTAATTTTTGTAGT | 8816 |
rs113507502 | snp | G/T | 0.5 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69103663 | CTATGCTATGGAAAC[G/T]CGCTTGTATAGCTTG | 8816 |
rs113615810 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69153270 | TTCCGCCGGCTGCGG[A/G]GCCCCGAGAACGCGG | 8816 |
rs113617485 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | DCAF5 | GRCh38.p7 | 14:69139049 | CCAGCTACTCCAGAG[A/G]TTGAGGTGGGAGGAT | 8816 |
rs113642560 | snp | C/G | 0.0486741 | 0.148216 | intron-variant | DCAF5 | GRCh38.p7 | 14:69150746 | AAAAAGTTTAAATTA[C/G]CTGGGCATGATAGCA | 8816 |
rs113659323 | snp | A/G | 0.5 | 0 | intron-variant | DCAF5 | GRCh38.p7 | 14:69067531 | TGTACTTTTTGTAGA[A/G]ATGGGGTTTTGCCAT | 8816 |
rs114025914 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | DCAF5 | GRCh38.p7 | 14:69145171 | TAAAGGTGCACGCCA[A/C]CATACCCAGCTAGTT | 8816 |
rs114064174 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | DCAF5 | GRCh38.p7 | 14:69103946 | CAACACAGTTAGTTC[C/G]TTTTCATCACTGAGT | 8816 |
rs114099921 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | DCAF5 | GRCh38.p7 | 14:69127395 | GCCAATCTGAAAAGG[C/T]TACATACTGTATGAC | 8816 |
rs114140525 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | DCAF5 | GRCh38.p7 | 14:69070436 | AGCTTCCAAGATTAT[C/T]AAATCAACACACAAT | 8816 |
rs114152113 | snp | A/C/G | 0.0205629 | 0.0993781 | intron-variant | DCAF5 | GRCh38.p7 | 14:69104515 | GAATATAAGAAATTC[A/C/G]TAAGACAAATAATCC | 8816 |
rs114155736 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69116827 | AACTGAATTCCACAT[A/G]AGCTGAAAAAATTCA | 8816 |
rs114164966 | snp | A/G | 0.0626037 | 0.165477 | intron-variant | DCAF5 | GRCh38.p7 | 14:69066625 | AATCCACTTACTACC[A/G]TAGGGGACCCCAGGA | 8816 |
rs114220246 | snp | A/T | 0.0189856 | 0.0955633 | intron-variant | DCAF5 | GRCh38.p7 | 14:69084544 | GTATGTTGGTGTTGA[A/T]GACGATAAAGCTAAT | 8816 |
rs114249615 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | DCAF5 | GRCh38.p7 | 14:69148016 | AACATATAAAAAGGC[A/G]GAGTAACAATCCAAG | 8816 |
rs114270006 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | DCAF5 | GRCh38.p7 | 14:69079905 | TAAACAGCAGGTTAG[C/T]GCATATAGGGAGTGC | 8816 |
rs114273672 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | DCAF5 | GRCh38.p7 | 14:69109955 | GTATGAGTGTTTCAG[C/T]TGGTCCATACCCTTG | 8816 |
rs114337753 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | DCAF5 | GRCh38.p7 | 14:69141834 | GATCCATTATAAACC[G/T]GTCAATTTCCTCAGA | 8816 |
rs114376158 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | DCAF5 | GRCh38.p7 | 14:69147085 | ACTGATTTCATAAAA[C/T]GTGATATAAACTAGT | 8816 |
rs114412040 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | DCAF5 | GRCh38.p7 | 14:69127194 | GTACATGGATTTATT[C/T]TACAACAGCTTTATT | 8816 |
rs114430088 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | DCAF5 | GRCh38.p7 | 14:69132163 | GTATATAACCAGAAG[C/T]GAAATTGCTGGATCC | 8816 |
rs114474675 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | DCAF5 | GRCh38.p7 | 14:69113197 | GGTTAAGCCAGGAAG[A/G]AGAAGGTGTTCAGGG | 8816 |
rs114478612 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | DCAF5 | GRCh38.p7 | 14:69105910 | ATTTTCCCTAATAAA[C/T]TGTCATATATATATA | 8816 |
rs114491257 | snp | G/T | 0.021333 | 0.101051 | intron-variant | DCAF5 | GRCh38.p7 | 14:69076771 | TAAATGGTTAAAATG[G/T]TAAATCTCATGTTAT | 8816 |
rs114567519 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | DCAF5 | GRCh38.p7 | 14:69142899 | CTGGGCTAACAGACA[A/G]GAGAAACCAACTTGA | 8816 |
rs114573625 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | DCAF5 | GRCh38.p7 | 14:69138834 | CCAACCAGATCACTT[A/T]AACATTTCACAACAT | 8816 |
rs114671216 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | DCAF5 | GRCh38.p7 | 14:69124795 | GTTCTCTATAGTCTC[C/T]ACTCCTATGGTTTTC | 8816 |
rs114704929 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant, utr-variant-3-prime, missense | DCAF5 | GRCh38.p7 | 14:69089988 | GGTCTTCTAAGGTCC[A/G]TGAAGATAGGCTTTG | 8816 |
rs114769447 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | DCAF5 | GRCh38.p7 | 14:69061864 | ATTAGTTTAAAAAAA[C/T]GGTTCCAAGCCAGGT | 8816 |
rs114857623 | snp | C/T | 0.0777841 | 0.181223 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69052607 | TTCTAAACCTGTATC[C/T]ACCTCAATAAAACTG | 8816 |
rs114879930 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69115862 | TCCTTTTGATAAACA[C/G]AAAATGCACTTATTT | 8816 |
rs114882752 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | DCAF5 | GRCh38.p7 | 14:69149737 | CAAACCAGACAAGAC[A/C]CAAGAACAACAAAAT | 8816 |
rs114883300 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | DCAF5 | GRCh38.p7 | 14:69142780 | GAAAGACACCTATTT[C/G]TTGACTGAAATTCAG | 8816 |
rs114883503 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | DCAF5 | GRCh38.p7 | 14:69084234 | CCTATGGGTTGATAA[C/T]GGGTGGCAGTAATAG | 8816 |
rs114885574 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | DCAF5 | GRCh38.p7 | 14:69076899 | CCTTACTGCCAGCTG[A/G]TATCTTTGAGCAGGA | 8816 |
rs114931466 | snp | A/G | 0.0168055 | 0.0901129 | intron-variant | DCAF5 | GRCh38.p7 | 14:69147292 | ACTGTGCCATGTGCA[A/G]TATATGTTAGATGTT | 8816 |
rs115030374 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | DCAF5 | GRCh38.p7 | 14:69135686 | AAAATTCAAGCTTTC[A/G]AGTAAAAATAAAAAT | 8816 |
rs115075589 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | DCAF5 | GRCh38.p7 | 14:69112134 | ATATCAGGTAGACCA[A/G]AATATCTCTGTGGGT | 8816 |
rs115142897 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | DCAF5 | GRCh38.p7 | 14:69079970 | GGTGGTCACAGAAGG[C/T]CTCTTTGATAAAATG | 8816 |
rs115245753 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | DCAF5 | GRCh38.p7 | 14:69081920 | ATAGTAATTGATTAA[C/T]GATTCTCCAGTAAAT | 8816 |
rs115441185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69077146 | GGTCAGCATTACTTC[A/G]TCCTGTCTTTTGCCC | 8816 |
rs115445515 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | DCAF5 | GRCh38.p7 | 14:69124999 | AGTTTCATCAAACAT[A/C]AAATGGTAATCATAA | 8816 |
rs115458082 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | DCAF5 | GRCh38.p7 | 14:69138965 | AGCCTGGGCAACATG[A/G]TAAGACCCCGTCTTT | 8816 |
rs115458220 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | DCAF5 | GRCh38.p7 | 14:69059319 | GGACTCTTCTCCTAG[C/G]CAGGAAGGTGGCAGT | 8816 |
rs115493292 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | DCAF5 | GRCh38.p7 | 14:69101245 | AGCATCAGACTGCAA[C/T]GCATCAGGGCCAGAA | 8816 |
rs115591808 | snp | G/T | 0.0182019 | 0.0936463 | intron-variant | DCAF5 | GRCh38.p7 | 14:69079900 | AAAATTAAACAGCAG[G/T]TTAGCGCATATAGGG | 8816 |
rs115616423 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69094685 | TCTGGTTTGCCGGGA[A/C]GGCAAAGCTTGGAAG | 8816 |
rs115667164 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | DCAF5 | GRCh38.p7 | 14:69083343 | AATAAAGTTATATTC[C/T]GGAACTGAGTAGCTG | 8816 |
rs115672203 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | DCAF5 | GRCh38.p7 | 14:69114643 | ATTTTAAAAACATAC[A/C]AGTAACAGAGATAAT | 8816 |
rs115679903 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | DCAF5 | GRCh38.p7 | 14:69134500 | ACATTTACGACCTCC[A/T]TAAGAGAGGGACTCT | 8816 |
rs115710942 | snp | C/T | 0.00478085 | 0.0486577 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69053589 | CCACAGAGCCTTGCG[C/T]GGCACACTACGCTCA | 8816 |
rs115748098 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | DCAF5 | GRCh38.p7 | 14:69084465 | GACAGACGATGCTCT[C/T]TTCTGCCACCCAAAC | 8816 |
rs115777991 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | DCAF5 | GRCh38.p7 | 14:69095670 | CAAGAGAAACAGGCC[A/C]AGGCTGTTTCCAGGG | 8816 |
rs115816313 | snp | C/T | 0.00461096 | 0.0477935 | intron-variant | DCAF5 | GRCh38.p7 | 14:69075449 | GATAACATTATATAT[C/T]ATAATATAGAATAAA | 8816 |
rs115844748 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | DCAF5 | GRCh38.p7 | 14:69139411 | AGGCTGAGGCAGGAG[C/G]ATCAATTAAGCTTAG | 8816 |
rs115913950 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | DCAF5 | GRCh38.p7 | 14:69131553 | TCTCATTTTATTGTC[A/C]CTTGTGAGGTAAGGA | 8816 |
rs115923797 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF5 | GRCh38.p7 | 14:69067097 | TGTTTATTGTTCATT[A/G]TTTCCCCTGCTAGAA | 8816 |
rs115928859 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | DCAF5 | GRCh38.p7 | 14:69073882 | TTCTCAACGAATCAA[A/G]CTAGGAATTACAGGG | 8816 |
rs115984610 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | DCAF5 | GRCh38.p7 | 14:69149606 | ATAAGTTAATTCTAT[C/T]AAGTAGTATGTGTCA | 8816 |
rs116020143 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | DCAF5 | GRCh38.p7 | 14:69059367 | AGAAGGGGGAGTAGA[A/G]AGAGAAAAGCAGGTC | 8816 |
rs116043632 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant, utr-variant-3-prime, missense, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69090033 | CTGAAGAAAATCACC[G/T]TTCCCTCAGCCTCTG | 8816 |
rs116053741 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | DCAF5 | GRCh38.p7 | 14:69133000 | ACTTGGCCCAGTGCC[C/T]GATACATATTAAGAG | 8816 |
rs116064110 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant, utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69089555 | TCTAAATAGAGAAAA[A/G]TCAAAAGCCATTCAA | 8816 |
rs116087115 | snp | A/C | 0.00914312 | 0.0669923 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69051940 | CTTGGGCTTATAAAA[A/C]CAGCATTTACAATTA | 8816 |
rs116107951 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69057053 | TATAATGTTGATTCC[C/T]CAGTCCCACTCTTAG | 8816 |
rs116142228 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | DCAF5 | GRCh38.p7 | 14:69135491 | TGTGAAAAAGTATCT[A/G]TGAGATAGTTTGCAT | 8816 |
rs116182003 | snp | A/C | 0.000990066 | 0.0222273 | missense | DCAF5 | GRCh38.p7 | 14:69054621 | CTCTCCCTTCATCTG[A/C]CTCCCCGGTCACCAA | 8816 |
rs116213526 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | DCAF5 | GRCh38.p7 | 14:69095695 | CCAGGGAAAGTGATT[A/G]AGCGTATCACTTCTA | 8816 |
rs116214892 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | DCAF5 | GRCh38.p7 | 14:69086474 | GAGATGAAAAAAAAA[A/G]GAGTAGCCTAAAATC | 8816 |
rs116265573 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | DCAF5 | GRCh38.p7 | 14:69057101 | GTCATGAACAGGTAT[C/T]AGGACCATGCATTTT | 8816 |
rs116330067 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69056757 | CTCCCTGTGGGAATT[A/C]TCCTGAGTCCCATTC | 8816 |
rs116335419 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | DCAF5 | GRCh38.p7 | 14:69079734 | GAGTTGATCAAAAGA[C/G]ACCCTGTTCCTGTCC | 8816 |
rs116404625 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | DCAF5 | GRCh38.p7 | 14:69111132 | TTTGACATTAAGCCC[C/T]TGGGCTTTATTTTCC | 8816 |
rs116406048 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | DCAF5 | GRCh38.p7 | 14:69104322 | AAACAGAGAGATAAC[C/T]AGGCATTTTTAATTT | 8816 |
rs116490758 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | DCAF5 | GRCh38.p7 | 14:69107319 | GGTCTGAGTGAACTT[A/G]AGCAAATTCAACATG | 8816 |
rs116575627 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | DCAF5 | GRCh38.p7 | 14:69108800 | AACCAGAAGGCATGC[A/C]CCCGACTAAAGCTAA | 8816 |
rs116614546 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | DCAF5 | GRCh38.p7 | 14:69147910 | AATGCCTTAAACTTC[A/G]ATTCAGGGGAAATAA | 8816 |
rs116630527 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | DCAF5 | GRCh38.p7 | 14:69077958 | CTTTATCTGCAAAAT[C/G]AGAGAACTGGACTGG | 8816 |
rs116663279 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | DCAF5 | GRCh38.p7 | 14:69062963 | ATCTCTAATCCATTT[A/G]CCCTCAGTTTCTATG | 8816 |
rs116735454 | snp | C/T | 0.039522 | 0.134904 | intron-variant | DCAF5 | GRCh38.p7 | 14:69087518 | GGCTAATTGCTTCTG[C/T]TGATACCCAGCCAAC | 8816 |
rs116769655 | snp | C/G/T | 0.0166325 | 0.0896639 | intron-variant | DCAF5 | GRCh38.p7 | 14:69068126 | AAGCCACTTTTACAT[C/G/T]GAGTGCATATGTCTG | 8816 |
rs116770689 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | DCAF5 | GRCh38.p7 | 14:69123443 | AGCCCTATCTAGATG[C/G]CTATAAAAGAAGCTG | 8816 |
rs116771235 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | DCAF5 | GRCh38.p7 | 14:69058955 | GAGATGAGACAAATA[C/T]TTTCCTCTCCATGCA | 8816 |
rs116818766 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | DCAF5 | GRCh38.p7 | 14:69148338 | CCATCCCTCAAAGGA[C/T]TAACACACATAAATA | 8816 |
rs116864930 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | DCAF5 | GRCh38.p7 | 14:69148218 | AGATGCAACCAAAGA[A/C]CTAAAGGGTAAACCC | 8816 |
rs116927875 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | DCAF5 | GRCh38.p7 | 14:69135495 | AAAAAGTATCTATGA[C/G]ATAGTTTGCATTGTG | 8816 |
rs116948447 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | DCAF5 | GRCh38.p7 | 14:69072005 | GGTTGCCAATTGACA[C/T]TGACCCAAAGAGGTT | 8816 |
rs116956410 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | DCAF5 | GRCh38.p7 | 14:69055794 | GGTTATGTATGAAAA[C/T]TGAGGTTTTTAGAAT | 8816 |
rs116974708 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69079786 | ATGGGAAGAGGAAAA[C/T]ATTACAGACATATAT | 8816 |
rs117037080 | snp | A/G | 0.0329836 | 0.124112 | intron-variant, utr-variant-3-prime, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69090668 | TTTACTTCAAAAAGC[A/G]AGGTCTTGCCAGTTT | 8816 |
rs117306721 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | DCAF5 | GRCh38.p7 | 14:69085889 | CATTGCTTGATCTCT[A/G]TAACACAGTGGGCAG | 8816 |
rs117361597 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | DCAF5 | GRCh38.p7 | 14:69138308 | AGAATTCCTCCTCCT[A/G]AGTAATGTTCTTGGA | 8816 |
rs117377609 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69132171 | CCAGAAGTGAAATTG[C/T]TGGATCCATATGGTA | 8816 |
rs117425603 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | DCAF5 | GRCh38.p7 | 14:69122022 | GTGAAGAAAAGCAAA[A/C]AAAAGAGAAGAGAGA | 8816 |
rs117582264 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69155370 | ATCTGGTCACATGCC[A/G]GCCCAAATCTAGGAC | 8816 |
rs117591245 | snp | C/G | 0.0221141 | 0.102801 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69052242 | TAACCCCCCCACCCC[C/G]AGTGCCTGAATTCAT | 8816 |
rs117679351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69058703 | AACATGGCAAAACCC[C/T]GTCTCTACAAAATAC | 8816 |
rs117712363 | snp | C/T | 0.00835141 | 0.0640778 | downstream-variant-500B | DCAF5 | GRCh38.p7 | 14:69050542 | GCAAGGCAGGAAATG[C/T]AATTTGGTATTTGGA | 8816 |
rs117792005 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69050934 | GTGAGAAGTGAATAA[C/T]AGGTTTATTTGCATA | 8816 |
rs117804862 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69154215 | ATTATAGTACTTTTC[C/T]TGGAAGCTATCCTCT | 8816 |
rs117823369 | snp | A/G | 0.039522 | 0.134904 | intron-variant | DCAF5 | GRCh38.p7 | 14:69079944 | GGGGTGTTAGTTTCC[A/G]TTTTACAGAGGGTGG | 8816 |
rs117870589 | snp | A/G | 0.0707826 | 0.174302 | intron-variant | DCAF5 | GRCh38.p7 | 14:69104734 | TAGCAGCGGGCGCCT[A/G]TAATCCCAGCTACTC | 8816 |
rs117948349 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | DCAF5 | GRCh38.p7 | 14:69102397 | CGGGCATGAGCCACC[A/G]CGCCCGACCATTAGT | 8816 |
rs118020680 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | DCAF5 | GRCh38.p7 | 14:69121798 | ACACTTTTCAAACAG[C/G]AGCCATCTGTGGGTC | 8816 |
rs118030788 | snp | C/G | 0.0209421 | 0.100162 | intron-variant | DCAF5 | GRCh38.p7 | 14:69152203 | GGGGGCGGCCCACAG[C/G]GACCCTACCGCCCCA | 8816 |
rs118141293 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69089937 | TGGGAAACCATGGTC[C/T]AGGTGCTTACATGTT | 8816 |
rs118154244 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | DCAF5 | GRCh38.p7 | 14:69078315 | TGATCATTAGGGAAA[G/T]GCAAATCAAAACAAT | 8816 |
rs118185637 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | DCAF5 | GRCh38.p7 | 14:69124212 | TGTATGCATATTTTG[C/T]TTATCCACTAATCCA | 8816 |
rs137863861 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DCAF5 | GRCh38.p7 | 14:69123204 | ATGTCCAAAGATACC[C/T]GTTAAGGGGGAAAAT | 8816 |
rs137898187 | in-del | -/T | 0.0185938 | 0.0946107 | intron-variant | DCAF5 | GRCh38.p7 | 14:69056829 | GCAGAGGACCCCCCA[-/T]TTTCCAAAGAGGCTG | 8816 |
rs137919514 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69091758 | CTGAAACACAGGCAG[A/G]CGGGAATGGATGTCA | 8816 |
rs137944175 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | DCAF5 | GRCh38.p7 | 14:69081602 | GCTCGAGCATAGGAA[A/G]AGATCAACAACTCTC | 8816 |
rs137952177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69118775 | CATGTCTGTGACTCC[A/G]TTTCCTGATCTAGAA | 8816 |
rs137995474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69133301 | GCCTCGCAAATATAA[A/G]AGGCCAGGCAGCAAA | 8816 |
rs138067776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69087914 | AGCACAGAGGTTTCA[A/G]ACTGGTGGATCCAGA | 8816 |
rs138074572 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | DCAF5 | GRCh38.p7 | 14:69140753 | GTTTCAGCCTTTTTT[C/T]TCCCTTTCTAATAAA | 8816 |
rs138099009 | snp | G/T | 0.00398564 | 0.0444627 | downstream-variant-500B | DCAF5 | GRCh38.p7 | 14:69050440 | GGCAAGAATTTTTCA[G/T]TTAACTGTAGCAGGC | 8816 |
rs138177045 | snp | A/G | 0.00181037 | 0.0300318 | missense | DCAF5 | GRCh38.p7 | 14:69054884 | GTGGGCTTGATTGGG[A/G]CACTGGGCTTGTCTT | 8816 |
rs138230127 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF5 | GRCh38.p7 | 14:69056809 | TTCCTGAGAGGTGGT[A/G]TCTCTGCAGAGGACC | 8816 |
rs138249498 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | DCAF5 | GRCh38.p7 | 14:69099685 | TGGTGGTTCATGCCT[C/G]TAATCCCAACACTTT | 8816 |
rs138293272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69121663 | ATATCCAGTGGGAAA[A/G]TCTGCAGCTCAGAAA | 8816 |
rs138336716 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69096047 | TAAGGAATATGGGAT[C/G]TTTTGTATTTCCTAT | 8816 |
rs138338565 | snp | A/G | 0.0103295 | 0.0711199 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69153840 | ATTGTTCCGTCTGGC[A/G]GATTAGAGTGGTACA | 8816 |
rs138343044 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69110061 | TGCACTGCTCTCATG[A/T]GTGATAAAGTTCAGT | 8816 |
rs138360542 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69112005 | ACTAACATCATAAAG[A/G]TTTTGGCTGACTATT | 8816 |
rs138369508 | snp | C/T | 9.88338e-05 | 0.00702902 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69054793 | GCTCCGCTCAGGGGA[C/T]GAGGTTGGGGAGGAG | 8816 |
rs138371026 | in-del | -/TCT/TG | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69098143 | ACCTCCTAGGACTCT[-/TCT/TG]CTTACCTTATTCAAC | 8816 |
rs138375167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69146235 | CCTTTGAACAATACT[A/G]AGCACAAGGACAACT | 8816 |
rs138578301 | snp | C/T | 0.000307953 | 0.0124049 | missense, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69122246 | TTAGTGTTCCCACTG[C/T]TGAAAGCCAGGCAAA | 8816 |
rs138605377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69087188 | AACAAGAGCCAAGTG[C/T]TGTCTTATATGTGCA | 8816 |
rs138635646 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | DCAF5 | GRCh38.p7 | 14:69139750 | GAACCCAGGAGGTGG[C/T]GACTGCAGTGAGTGA | 8816 |
rs138637532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69082088 | GAAAGGGAAAAACAA[C/T]GTGATTGAAAACTTT | 8816 |
rs138662036 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69095300 | GCAATATATTGAAAG[A/C]ACTAGTAAAACATGT | 8816 |
rs138692045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69072979 | TTAACAGATCATGGG[C/T]TCTGTGGCCTCTAAA | 8816 |
rs138717449 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | DCAF5 | GRCh38.p7 | 14:69133872 | CAGCAACACCCTAAC[G/T]AGACAGCTAGAGCCC | 8816 |
rs138782695 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | DCAF5 | GRCh38.p7 | 14:69100173 | ACATTAACTAGACTA[C/T]AGAACTTGGGTCATT | 8816 |
rs138878615 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | DCAF5 | GRCh38.p7 | 14:69066292 | GGCGCACACCACCAC[A/G]CCCAGCTAATTTTTT | 8816 |
rs138908553 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | DCAF5 | GRCh38.p7 | 14:69076100 | ACTATTTCACACCCA[C/T]TAGGATGACTATTAC | 8816 |
rs138920004 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69060719 | GTAGTTTTAGTAGAG[A/T]CAGGGTTTCACCATT | 8816 |
rs138921999 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69116959 | TGACAAAATTAAGAC[G/T]TGGTGAAACACAATG | 8816 |
rs138991642 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69068127 | AGCCACTTTTACATC[A/G/T]AGTGCATATGTCTGT | 8816 |
rs138992681 | snp | C/G/T | 0.0134861 | 0.0810011 | intron-variant | DCAF5 | GRCh38.p7 | 14:69144571 | GACAGAGCGAGACTC[C/G/T]GTTTAAAAAAAAAAG | 8816 |
rs139060552 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | DCAF5 | GRCh38.p7 | 14:69102657 | GGTCAGGCTCATCAA[A/T]ATCACTATCTTCTAC | 8816 |
rs139078174 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69051205 | TATGTACAGAATGCA[A/G]GAAAAAAACATAAGA | 8816 |
rs139087648 | snp | A/G | 0.0528381 | 0.153711 | intron-variant | DCAF5 | GRCh38.p7 | 14:69140973 | ACCCCGTCTTTACTA[A/G]AAGTACAAAAATTAG | 8816 |
rs139087981 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69149161 | ACAACAAGCCCCTCA[G/T]GTAGGTGCCAATATT | 8816 |
rs139127121 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69073739 | TCTCTCTATTCAAAC[G/T]TGAAAAACATTCCAG | 8816 |
rs139172027 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69123994 | TGAATCACTGTGCCC[A/G]GCCAAGTAGTCACTA | 8816 |
rs139254188 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69129204 | ACAGCCCAATCCATG[A/G]GAGATTGGAATCACT | 8816 |
rs139478500 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69078806 | TTTGAGATGAAGAAG[A/T]AGTTCTAGAGATGGA | 8816 |
rs139500055 | snp | A/C/T | 0.000264611 | 0.0114996 | missense | DCAF5 | GRCh38.p7 | 14:69055226 | TTTGTGGTGGTGACC[A/C/T]GCAGGGGCCCCAGGT | 8816 |
rs139507663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69103661 | CACTATGCTATGGAA[A/G]CTCGCTTGTATAGCT | 8816 |
rs139540728 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | DCAF5 | GRCh38.p7 | 14:69113102 | GACTCTCCTCCTATA[C/T]CTTCAGGCTACCAAG | 8816 |
rs139633526 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | DCAF5 | GRCh38.p7 | 14:69108398 | ATGTGTATGTGTTTT[A/G]GGGGGTGGTGCAAAG | 8816 |
rs139722903 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69083668 | CCCCAGAAATCCACC[A/G]TATTAACCAATGGAG | 8816 |
rs139729138 | snp | A/G | 0.00125185 | 0.0249872 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69054232 | CCTCTCCTCACTGTC[A/G]TCAGACTGGGTCCTG | 8816 |
rs139750153 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69155319 | TGAATTCCTGGGAAA[A/G]TTGTCCCATTTACCT | 8816 |
rs139771764 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69062738 | CCTTTAAGCATTGCC[C/T]ACACTCACCCACTGC | 8816 |
rs139792645 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | DCAF5 | GRCh38.p7 | 14:69058285 | GCACTTTGGGAGGCC[A/G]TGGCGGGTAGATCAC | 8816 |
rs139797856 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69148712 | CCACCGCCCAAAAAA[A/C]AAGTAATGTTCACTC | 8816 |
rs139816348 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | DCAF5 | GRCh38.p7 | 14:69142437 | AACCTTTCTTTTTAC[C/T]CATTCAGTGAATGGC | 8816 |
rs139879313 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69097587 | TATTATTATTATTTT[A/T]TTTTTTTTTTTTTTT | 8816 |
rs139932437 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | DCAF5 | GRCh38.p7 | 14:69092385 | ACTTTGGGAGTCTGA[A/G]GCAGGAGGATCACTT | 8816 |
rs139943240 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | DCAF5 | GRCh38.p7 | 14:69078084 | AGCCCAAGTGATTTG[A/G]TAAGTCACTCCACAA | 8816 |
rs139953923 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69090433 | CAGCTAAGTAGGCCC[A/T]AAGACTCCAACATGA | 8816 |
rs139958295 | in-del | -/G | 0.0189856 | 0.0955633 | intron-variant | DCAF5 | GRCh38.p7 | 14:69074103 | AAGTAGGCCCCAACA[-/G]GTTTTGAAAGGCAGA | 8816 |
rs139971753 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | DCAF5 | GRCh38.p7 | 14:69142106 | TCAAGACCAGCCTGG[A/G]CAAAATAGTGAGATC | 8816 |
rs140007912 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69125113 | GAGCTAAGATTCAAA[A/C]GCAAGCAGTAAATAT | 8816 |
rs140051016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69141827 | CTATGTGGATCCATT[A/G]TAAACCTGTCAATTT | 8816 |
rs140051191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69084446 | AAACTTTTGCCAACA[C/T]GTAGACAGACGATGC | 8816 |
rs140087222 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | DCAF5 | GRCh38.p7 | 14:69136979 | ACTAAATGTGTATCA[A/G]AAAGGCTACATGTTC | 8816 |
rs140151718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69058030 | ATTTGGCAATTGAAT[A/G]CCTCAACCAGAATGT | 8816 |
rs140157894 | snp | C/T | 0.00107189 | 0.0231257 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69055300 | GCGAGGCAATGAGGC[C/T]GAAGACTCTGAGTCA | 8816 |
rs140171257 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69107177 | TTGTTTGCAGAGCTC[C/G]CCTCCATTTACCAGG | 8816 |
rs140235474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69097405 | AAATTTTTTTATAGT[A/G]ACCCTTCATAATTTT | 8816 |
rs140282339 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69094109 | TTTGTAGGACTGACT[A/G]GGAGTTGGGGGTTGG | 8816 |
rs140303855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69143634 | CCTTAATTTGGTAGG[C/T]GCCGGGGAGTGCTGC | 8816 |
rs140349238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69140174 | TGGGAAGCTGAGGCA[C/T]GAGAATCTCTTGAAC | 8816 |
rs140375099 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF5 | GRCh38.p7 | 14:69068785 | TCCAAGCCTCTTAGC[A/G]TTTCAAAAAGGCCCA | 8816 |
rs140388397 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69099167 | TGAGGCAAAAGAATC[C/G]CTTGAACCTGGGAGG | 8816 |
rs140432448 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | DCAF5 | GRCh38.p7 | 14:69114403 | TAGATCTGTTAGTGT[G/T]GGTATGAAAAAAGGC | 8816 |
rs140467924 | snp | A/T | 0.0228947 | 0.104514 | intron-variant | DCAF5 | GRCh38.p7 | 14:69119423 | CTTACAGAGAATTTT[A/T]AAAAAATAATGGCAT | 8816 |
rs140509635 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69113517 | TCACAAATTCCTTAA[A/C]ATCTCTCCCTACACT | 8816 |
rs140514208 | snp | C/T | 0.021333 | 0.101051 | intron-variant | DCAF5 | GRCh38.p7 | 14:69074837 | TCAGGAATTTGAGAC[C/T]AGGCTGGCCAACATG | 8816 |
rs140586300 | in-del | -/CT | 0.00199481 | 0.0315187 | intron-variant | DCAF5 | GRCh38.p7 | 14:69067023 | CCACTTCCCGTCTTC[-/CT]CTGTTCTACTTTTTC | 8816 |
rs140605282 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69071738 | AATTTTCCTCATCTA[A/C]GCATTCAAAGTTAGA | 8816 |
rs140716418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69086916 | GATCTCAGTGCTCAG[A/G]TACGCCAGTGCTCAG | 8816 |
rs140766678 | in-del | -/AAGG | 0.0111196 | 0.0737302 | intron-variant | DCAF5 | GRCh38.p7 | 14:69136045 | TTTTGGTACAGTATT[-/AAGG]AAGAATATACAGTTA | 8816 |
rs140836273 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69095205 | CCTGACTTGCTTTCT[A/G]GACACTTATCTTGAT | 8816 |
rs140850060 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69053693 | CTAGACATTCAGACC[C/T]GTTGTTGAATGTTGG | 8816 |
rs140882097 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | DCAF5 | GRCh38.p7 | 14:69144294 | AAAGGGGCACAAGGC[C/T]AGGCGCGGTGGCTCA | 8816 |
rs140917906 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | DCAF5 | GRCh38.p7 | 14:69071061 | CCTCAGCCTCCCAAA[A/G]TGCCGGGATTATAGG | 8816 |
rs140925254 | in-del | -/AT | 0.151001 | 0.229563 | intron-variant | DCAF5 | GRCh38.p7 | 14:69150446 | CCAAGACTAGAGAAA[-/AT]AGAGTTCATTTAAGA | 8816 |
rs140976204 | in-del | -/TGACCCGCA | | | cds-indel | DCAF5 | GRCh38.p7 | 14:69055221 | CTGTGTTTGTGGTGG[-/TGACCCGCA]GGGGCCCCAGGTGGA | 8816 |
rs141027118 | snp | A/C | 0.00792657 | 0.0624536 | intron-variant | DCAF5 | GRCh38.p7 | 14:69075443 | TATATAGATAACATT[A/C]TATATTATAATATAG | 8816 |
rs141049186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69126577 | TGATTCTAATATTTA[C/T]AGGAGAGGCAAAAGG | 8816 |
rs141085287 | in-del | -/AAAT | 0.0260105 | 0.111035 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69154597 | GGGGAAAAGGGCAAA[-/AAAT]AAATAAATTTTTAAA | 8816 |
rs141094613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69081112 | AATGAAACTCACTTC[A/G]CACAGCCTTTTATCT | 8816 |
rs141224557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69120649 | TAGAAAGCAAAAGTA[A/G]CAGTAAAGATATGGC | 8816 |
rs141248749 | snp | C/G | 6.59174e-05 | 0.00574059 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69062429 | GATCATGTAGGTGTG[C/G]GGATTAAATCGGACT | 8816 |
rs141293340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69115162 | GACAGCAAGCCTCCT[A/G]AAGTTCATAGTGCAA | 8816 |
rs141338246 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69103807 | GGCAATCAATAATCT[A/G]TACTTATCTTGAGAA | 8816 |
rs141444828 | snp | A/G | 1.64866e-05 | 0.00287106 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69054583 | GGAAGAAGGGGCTGG[A/G]TTGTCTTTGTGGCTG | 8816 |
rs141465735 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | DCAF5 | GRCh38.p7 | 14:69106214 | GGGGCCCACCACTAC[A/G]CCCGGCTAATTTTGT | 8816 |
rs141468073 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69055069 | TGTGTCTAGTTCCAC[C/T]TCACAGACATTCTCC | 8816 |
rs141472313 | snp | A/G | 0.077417 | 0.180873 | intron-variant | DCAF5 | GRCh38.p7 | 14:69151706 | TGGGGGCGCTCGCCG[A/G]CGTCGTCCCCTCCTC | 8816 |
rs141665497 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | DCAF5 | GRCh38.p7 | 14:69087194 | AGCCAAGTGCTGTCT[C/T]ATATGTGCATGCCAG | 8816 |
rs141697915 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69077077 | ATAGCAACGAGAGAG[C/T]AATTTTGAGAGTTCA | 8816 |
rs141756128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69080404 | GACCAAACAGTGCCA[A/G]TGGCACTGTTTCACT | 8816 |
rs141763102 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | DCAF5 | GRCh38.p7 | 14:69082314 | AAAAGCATACAAATA[C/T]GCATACCCATAAGAT | 8816 |
rs141798652 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69134802 | GACCAGCAGAAGCCA[C/T]GATGCAGTCTCATAA | 8816 |
rs141805011 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | DCAF5 | GRCh38.p7 | 14:69083299 | TCAAAAAGGTCCAGG[A/G]TTCAAAAAGAGTTAT | 8816 |
rs141849205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69131353 | GAGTGTACTGTGTAA[A/G]ACCAAACCTCCTTTT | 8816 |
rs141851016 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | DCAF5 | GRCh38.p7 | 14:69076349 | ATACCCATTTTCATA[C/G]CAGCATTATTCACAA | 8816 |
rs141851502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69135997 | TGGTTTTATATTCTA[C/T]ATTGCAACTAATCTT | 8816 |
rs141866946 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69153939 | GAAGCACGAGGTACT[C/T]CTCTCCGTTCCAGAT | 8816 |
rs141874345 | in-del | -/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69102108 | TAGTTTACTATAACT[-/T]TTTTTTTTTTTTTTT | 8816 |
rs141889339 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69060187 | ATGCAAGGGACTGGG[A/C]CATTTCAATGACTGC | 8816 |
rs141889893 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69127509 | TGAATATATGGAGCA[G/T]AGAAGATTTTTAGGG | 8816 |
rs141894389 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | DCAF5 | GRCh38.p7 | 14:69128721 | TGCAGTGAGCAGAGA[A/T]CGTGCCACAGCACTC | 8816 |
rs142007200 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | DCAF5 | GRCh38.p7 | 14:69067690 | TCACCAGGCTGGAGT[A/G]CAGTGGCGTGATCTC | 8816 |
rs142025502 | snp | A/G | 0.00195915 | 0.0312368 | intron-variant | DCAF5 | GRCh38.p7 | 14:69118304 | AGAGAGCAAGACAGA[A/G]GCACACACATACACA | 8816 |
rs142048025 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69093867 | CCTGGTATCCCTGCA[A/G]GCCCCAAGTAGTAAT | 8816 |
rs142069568 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | DCAF5 | GRCh38.p7 | 14:69058334 | GACCAGCCTGGCCAA[C/T]GTGGTAAAACCCTGT | 8816 |
rs142090069 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | DCAF5 | GRCh38.p7 | 14:69108050 | AAATACTGGCCTACC[A/G]GGAGACAAGACATAG | 8816 |
rs142115865 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69066816 | GCCTCAGGCCTTTGA[A/T]GAGCCAGAATACTAT | 8816 |
rs142169806 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | DCAF5 | GRCh38.p7 | 14:69059191 | CTGGGCCCAAGTGAT[A/C]GTCCCACCTCAGCCT | 8816 |
rs142170434 | in-del | -/TG | 0.0111196 | 0.0737302 | intron-variant | DCAF5 | GRCh38.p7 | 14:69079292 | GAAGGAAGAAAACTC[-/TG]TCCCAGAGTTAAGGC | 8816 |
rs142197218 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | DCAF5 | GRCh38.p7 | 14:69113991 | GCTCTGAAAACCGTA[A/G]GTTATCAAAGAAACT | 8816 |
rs142263137 | snp | A/C | 0.000535743 | 0.016358 | intron-variant | DCAF5 | GRCh38.p7 | 14:69055654 | ACAAGGAGTAACTGG[A/C]AAGTATTCTTTCACT | 8816 |
rs142285972 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69107556 | GAAACCAGTGACCTG[A/G]TGTCCTCCAGTGGGC | 8816 |
rs142371006 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | DCAF5 | GRCh38.p7 | 14:69079722 | GAAGGGAAGGCAGAG[C/T]TGATCAAAAGAGACC | 8816 |
rs142376576 | in-del | -/AC | 0.0103295 | 0.0711199 | intron-variant | DCAF5 | GRCh38.p7 | 14:69102869 | ACAGGTAAACCAGTA[-/AC]ACAGCTGTTTATTAT | 8816 |
rs142415676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69096416 | ACAGATGAATTCAGT[A/G]TACTTTTTGAATCTC | 8816 |
rs142500337 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | DCAF5 | GRCh38.p7 | 14:69138523 | ATGTACTGGCAGAGT[A/G]AGCCACTTAGGAGTT | 8816 |
rs142538470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69063510 | TGTTCATTTATCTAC[C/T]CAAGGGATCCCCTCT | 8816 |
rs142559952 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69110760 | GCATGAGCCTGTGGT[C/T]TCAGCTACTTGGGAA | 8816 |
rs142579821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69128522 | TATGTTTAATGTTCA[C/T]GATAGAAAAAGAAAA | 8816 |
rs142624300 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69086327 | GGAGCCACTGCACTC[C/T]GGCCTGGGTGATAGA | 8816 |
rs142646646 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | DCAF5 | GRCh38.p7 | 14:69070856 | AGGCTGGAGTGCAGC[A/G]GTGCAATCTCGGCTC | 8816 |
rs142704212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69076698 | GTTCTGAAGGTAGAT[A/G]GTGGTGATGGCTGCA | 8816 |
rs142729354 | snp | A/C | 0.143622 | 0.226238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69072636 | TTTAAAAAAAAAAAA[A/C]AAAAAAAAACGAGAG | 8816 |
rs142735523 | snp | C/G | 0.0189856 | 0.0955633 | intron-variant | DCAF5 | GRCh38.p7 | 14:69120276 | AATTTTTTTTGTAGA[C/G]ATCTAACATGTTGGG | 8816 |
rs142751184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69073216 | AACTTAGGGGTACTA[C/T]CCCTGGAGAACATCT | 8816 |
rs142883023 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69110067 | GCTCTCATGAGTGAT[A/C]AAGTTCAGTACTTTT | 8816 |
rs142890884 | snp | A/G | 1.6537e-05 | 0.00287545 | missense | DCAF5 | GRCh38.p7 | 14:69054023 | GGGGTCTCACAGGCC[A/G]TTTCAGACCCGCAAC | 8816 |
rs142929985 | snp | C/T | 0.00874735 | 0.0655527 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69052286 | CTTCATAGGCAGCCT[C/T]CCCTTGGCTCCAGTT | 8816 |
rs142936096 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69141879 | TGACTCCTACATAAT[A/C]CCAGCCCTTTGGAAT | 8816 |
rs142975149 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | DCAF5 | GRCh38.p7 | 14:69106899 | ACAAAAAAATTAACC[A/G]GGCATGGTGGCACAT | 8816 |
rs143008359 | in-del | -/AT | 0.489142 | 0.0728777 | intron-variant | DCAF5 | GRCh38.p7 | 14:69058537 | AAAGAAAAAAAATAC[-/AT]CATATATATATATAT | 8816 |
rs143020145 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | DCAF5 | GRCh38.p7 | 14:69144817 | GAAAAGAGAGAAACA[A/G]CACCTGCCTGGGAGC | 8816 |
rs143061112 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | DCAF5 | GRCh38.p7 | 14:69141236 | ACTAGAGGCATCCCA[C/T]AGTGAATGTGAGGAG | 8816 |
rs143069736 | snp | A/G | 1.64773e-05 | 0.00287026 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69055519 | CAGCACAAGGCTGAT[A/G]TACTCTTCATGGGTA | 8816 |
rs143080357 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69081916 | TTCCATAGTAATTGA[C/T]TAATGATTCTCCAGT | 8816 |
rs143141789 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | DCAF5 | GRCh38.p7 | 14:69149139 | TACTTTAACTAACAT[A/G]GTTCTCACAACAAGC | 8816 |
rs143230122 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69142494 | ACAGAAGCAGAGTGA[C/T]GTTGTGGTGACAGAA | 8816 |
rs143374922 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69071999 | TCTGGGGGTTGCCAA[C/T]TGACATTGACCCAAA | 8816 |
rs143432477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69123205 | TGTCCAAAGATACCC[A/G]TTAAGGGGGAAAATG | 8816 |
rs143433106 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69078109 | CCACAAACATGCTCA[A/C]GACAAGGAAACTCAT | 8816 |
rs143473281 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | DCAF5 | GRCh38.p7 | 14:69118791 | TTTCCTGATCTAGAA[C/T]GGAGATGACAATAGT | 8816 |
rs143520455 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | DCAF5 | GRCh38.p7 | 14:69074190 | GCACTACTATAGACA[C/T]GTTTTGTGTAATATA | 8816 |
rs143538693 | snp | C/G | 0.00560459 | 0.0526392 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69055462 | GGGGTCTTCCTGGAC[C/G]GACTGGTTGGCGTAG | 8816 |
rs143542140 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF5 | GRCh38.p7 | 14:69144100 | GACAATTAATGCAAA[A/G]CCTTCAAATCTCCTT | 8816 |
rs143602483 | in-del | -/ACACACACACAC/ACACACACACACACACACAC | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69102591 | TTGTTAAAAACAAAG[lengthTooLong]ACACACACACACACA | 8816 |
rs143606121 | in-del | -/T | 0.211516 | 0.24702 | intron-variant | DCAF5 | GRCh38.p7 | 14:69060537 | CCAATATTATATTTC[-/T]CTTTTTTTTTTTGGA | 8816 |
rs143615049 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | DCAF5 | GRCh38.p7 | 14:69071230 | TGATCTCCTCAGCCC[A/G]CTAGGAAGTCCTATT | 8816 |
rs143615117 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | DCAF5 | GRCh38.p7 | 14:69125237 | TTGAAGGGATTGTCC[A/G]CCTTAGTAGCATAAC | 8816 |
rs143645404 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69060041 | GAGTGCACACTCAAG[A/C]AGGAATTCCTCTTGT | 8816 |
rs143654100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69121103 | CATTCTTAAAATGAC[A/G]AATAGTTTGGTGGGC | 8816 |
rs143675762 | in-del | -/GTTAA | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69060944 | TGAAATAAAATAATC[-/GTTAA]ACAATTTTTATTTTT | 8816 |
rs143692626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69109636 | ATCCATGTCAATGTG[C/T]ATATTTATAGTTTGT | 8816 |
rs143724119 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, upstream-variant-2KB, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69116413 | TCCTTCCTTTGAATT[A/G]GCTGTGGCCAACAAC | 8816 |
rs143759459 | snp | A/T | 0.00199481 | 0.0315187 | downstream-variant-500B | DCAF5 | GRCh38.p7 | 14:69050758 | CCCAATACCTAAAAG[A/T]GACAATGACCATTGT | 8816 |
rs143800716 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69117526 | CTAAGGCTGGTACTA[G/T]AGGAAGGGGCCTTTT | 8816 |
rs143848228 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69099825 | AGTGGCACATGCCTG[C/T]AGTCCCAGCTACTCA | 8816 |
rs143850623 | snp | C/T | 0.000150415 | 0.00867092 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69053890 | CTCTGAGGAGGAATT[C/T]TCTGAATCTGTATCT | 8816 |
rs143868385 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69107649 | CTGGCTCTCTGCCAC[A/G]TAACTAATTGACGGT | 8816 |
rs143900162 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69058079 | AAACTTCTGAACATT[A/G]TAAGTACTGACCGTT | 8816 |
rs143913072 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | DCAF5 | GRCh38.p7 | 14:69096208 | TTTATTTTATGTGAG[C/T]TGGAAGGGAGATGAA | 8816 |
rs143936824 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69053516 | ATGAGACAATAAGCG[C/T]ACACGTGCCATTGTG | 8816 |
rs143997492 | snp | C/T | 3.29451e-05 | 0.00405851 | missense | DCAF5 | GRCh38.p7 | 14:69054923 | GTCTTCTGTCGGCGC[C/T]GCATGGCATTCCGCT | 8816 |
rs144002006 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69103087 | CATGTGGGTCCATTA[C/T]TGACTGAAACATCAT | 8816 |
rs144021491 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | DCAF5 | GRCh38.p7 | 14:69097556 | TCTAAATTGATTTCA[G/T]CACCCACTGGATTAT | 8816 |
rs144112920 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69073865 | TTAAACCCAAAGATT[A/G]CTTCTCAACGAATCA | 8816 |
rs144148659 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69088934 | GAAAGTCAGAGCCTA[A/T]AAATCACCTTTGAGA | 8816 |
rs144184761 | snp | A/G | 0.000115694 | 0.00760484 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69055231 | GGTGGTGACCCGCAG[A/G]GGCCCCAGGTGGAAG | 8816 |
rs144212669 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69078807 | TTGAGATGAAGAAGA[A/T]GTTCTAGAGATGGAT | 8816 |
rs144249744 | snp | C/G | 0.0189856 | 0.0955633 | intron-variant | DCAF5 | GRCh38.p7 | 14:69074844 | TTTGAGACCAGGCTG[C/G]CCAACATGGTGAAAC | 8816 |
rs144331484 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69057709 | AACACAGGATTAAGA[C/G]GCAGGAGTCTTGAGT | 8816 |
rs144335451 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69147286 | TGGTGTACTGTGCCA[C/T]GTGCAGTATATGTTA | 8816 |
rs144433314 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | DCAF5 | GRCh38.p7 | 14:69064985 | AATCTTTCTGACTTG[A/G]AACACAATTAAAGTA | 8816 |
rs144436627 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69063139 | AGCAGGGTCCAAGTA[C/T]TGAAAATCAGAATTA | 8816 |
rs144456141 | snp | C/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69113040 | TTTTTTTTTCTGCCA[C/G]CCAGCCCTCTAATCA | 8816 |
rs144483093 | snp | G/T | 0.000181215 | 0.00951706 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69054541 | GTTCCTCTGGGCCAT[G/T]GCTATGTTTAGACAG | 8816 |
rs144494429 | in-del | -/C | 0.00799586 | 0.0627216 | intron-variant | DCAF5 | GRCh38.p7 | 14:69055662 | TAACTGGAAAGTATT[-/C]TTTCACTGGTGGTGA | 8816 |
rs144549078 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69097177 | AAAAATCATGATTTA[C/G]TACTTTCTAAAAAGA | 8816 |
rs144556740 | snp | C/T | 0.00122838 | 0.0247524 | synonymous-codon, upstream-variant-2KB, intron-variant, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69152838 | GTGGCCGAGGAGGTC[C/T]TTCTTGTAGAGGTTT | 8816 |
rs144563888 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | DCAF5 | GRCh38.p7 | 14:69119678 | TACGATCGCACTCCA[G/T]CCTGGGCAACAGAGA | 8816 |
rs144567584 | in-del | -/T | 0.0193772 | 0.0965046 | intron-variant | DCAF5 | GRCh38.p7 | 14:69105039 | AATATTGTGGTTATG[-/T]TTTTTTTTTAATTAT | 8816 |
rs144616606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69135252 | CACTGGTGCCTTGGC[A/G]CTAGGGCAGTGACGG | 8816 |
rs144675264 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | DCAF5 | GRCh38.p7 | 14:69139582 | ACTTTGGGAGGCTGA[A/G]GCAGGTGAATCACTT | 8816 |
rs144701959 | in-del | -/TTTTC | 0.0869089 | 0.189476 | intron-variant | DCAF5 | GRCh38.p7 | 14:69141355 | GACCTTTTTTTTTCT[-/TTTTC]TTTTATTATTATACT | 8816 |
rs144733424 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69051854 | ACACACTGAGTGATC[A/G]TATTTTTTTTGTATA | 8816 |
rs144764491 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69136684 | GGGAAAATCACCCTT[A/C/G]ACAATATGTGACATT | 8816 |
rs144765488 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | DCAF5 | GRCh38.p7 | 14:69133658 | TACAGGCATTACTTC[C/T]GCTGACACCCTGTTT | 8816 |
rs144780043 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69101682 | GTTGTGTAAACATTA[C/T]AGAGAGTATTCACAC | 8816 |
rs144801049 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | DCAF5 | GRCh38.p7 | 14:69130373 | ATTCCACTTACATGA[G/T]GAATAGTCAAATCAG | 8816 |
rs144976862 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | DCAF5 | GRCh38.p7 | 14:69150480 | CAGGGGAGCGTCCTG[A/C]CCAAGGATAAAAGTA | 8816 |
rs145033296 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69065647 | AGGTTTGATATTATT[C/G]AATATAGCTGCTACT | 8816 |
rs145082258 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69116769 | GACACAAAACAGAAA[C/T]GGCCACTAAAAATGG | 8816 |
rs145094673 | snp | C/G | 1.64914e-05 | 0.00287149 | missense | DCAF5 | GRCh38.p7 | 14:69054599 | TTGTCTTTGTGGCTG[C/G]TTCCTGCTCTCCCTT | 8816 |
rs145170788 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69113329 | AAACCTGATAAGGAA[A/C]CACAACAGGTTTAAA | 8816 |
rs145194481 | snp | C/T | 0.166506 | 0.235645 | intron-variant | DCAF5 | GRCh38.p7 | 14:69065253 | AGGCATCCACCACCA[C/T]GCCCAGCTAATTTTT | 8816 |
rs145198076 | snp | A/G | 3.29603e-05 | 0.00405944 | missense | DCAF5 | GRCh38.p7 | 14:69054180 | GACGAGGGTGTAAGC[A/G]TCCATTGTTGTGGTT | 8816 |
rs145211898 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | DCAF5 | GRCh38.p7 | 14:69108434 | AGAGACGCAAGCTAA[G/T]GAGCCAGTGCAGTCA | 8816 |
rs145255372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69129853 | GCCTTCTAAGCCTGG[C/T]TTCCTCACAAACAAT | 8816 |
rs145319007 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69095566 | ACACACACACACACA[A/C]AAACCACTCAATTGG | 8816 |
rs145417782 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69137839 | TTTTATTACAGTATA[A/G]TATTATAATTGTTCT | 8816 |
rs145431489 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | DCAF5 | GRCh38.p7 | 14:69087617 | AAAGAAACAAACTAT[G/T]TATTTGTAGCCAAAA | 8816 |
rs145485360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69091016 | ACTTCAGAACTTCTA[C/T]GGTTAAGACAGAAAG | 8816 |
rs145517654 | snp | C/T | 0.00478211 | 0.048664 | missense | DCAF5 | GRCh38.p7 | 14:69054920 | GTTGTCTTCTGTCGG[C/T]GCCGCATGGCATTCC | 8816 |
rs145563995 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69103800 | AACTCCTGGCAATCA[A/G]TAATCTGTACTTATC | 8816 |
rs145579704 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69084981 | TTGCACCCAGAAGAA[C/T]TGGGTTTTCTTCACT | 8816 |
rs145620983 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | DCAF5 | GRCh38.p7 | 14:69137256 | AAAAACGGGTTCTTA[A/G]GCCCTCAAAACCAGT | 8816 |
rs145678347 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69109560 | GAGCATCATGCAAAT[A/G]GAATCACAGAGATTC | 8816 |
rs145705724 | snp | A/G | 0.000428965 | 0.0146389 | missense | DCAF5 | GRCh38.p7 | 14:69054464 | CCTGGGCCATTGCTG[A/G]GAGTTCTAGGAGTCT | 8816 |
rs145712347 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | DCAF5 | GRCh38.p7 | 14:69132161 | GGGTATATAACCAGA[A/C]GTGAAATTGCTGGAT | 8816 |
rs145739815 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69071769 | ACTCAAGGGATGCAT[A/C]CAGCCCACAGATATC | 8816 |
rs145767871 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69084159 | TTCTCTCACCTACTA[C/G]AGAACTAGCCATGCA | 8816 |
rs145774601 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | DCAF5 | GRCh38.p7 | 14:69066999 | CATGCTGGGACACTG[C/T]CCTCAATACCACTTC | 8816 |
rs145797975 | in-del | -/TTTT | 0.0166325 | 0.0896639 | intron-variant | DCAF5 | GRCh38.p7 | 14:69120047 | TTCTTTCTTTCTTTC[-/TTTT]GAGACAGGATCTTGC | 8816 |
rs145811173 | snp | C/T | 8.24504e-05 | 0.00642016 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69055384 | ACTGAGGTCACTGTC[C/T]GAGTCAGAGCTCCAG | 8816 |
rs145841457 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | DCAF5 | GRCh38.p7 | 14:69123889 | ATTTTTAGTAGAGAA[A/G]GGGTTTCACTATGTT | 8816 |
rs145873662 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | DCAF5 | GRCh38.p7 | 14:69092963 | AAGATTCACATTTTT[A/T]AAAAAGTTTCACACA | 8816 |
rs145963764 | in-del | -/TGTC | 0.0539704 | 0.155153 | intron-variant, utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69089467 | GCCAAAAAGAAGTCT[-/TGTC]TGTCAGAGAGAATAA | 8816 |
rs145981954 | in-del | -/AAGTT | 0.309894 | 0.242719 | intron-variant | DCAF5 | GRCh38.p7 | 14:69060946 | AAATAAAATAATCAC[-/AAGTT]AATTTTTATTTTTTT | 8816 |
rs146010244 | snp | A/C | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69103708 | GCATAGCTTCATGTA[A/C]CAATCACTGCAATTA | 8816 |
rs146026140 | in-del | -/A | 0.077417 | 0.180873 | intron-variant | DCAF5 | GRCh38.p7 | 14:69133049 | TTATTATGCTATTTG[-/A]AACTCAAACAACAGC | 8816 |
rs146034177 | snp | A/G | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69124198 | ATCGTATATATATTT[A/G]TATGCATATTTTGTT | 8816 |
rs146070190 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | DCAF5 | GRCh38.p7 | 14:69059208 | TCCCACCTCAGCCTC[C/T]CGAGTAACTGAGAGC | 8816 |
rs146263681 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69082603 | CTTTATTTGGCAAAC[C/T]ATTTTGGAAACCTGA | 8816 |
rs146275857 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | DCAF5 | GRCh38.p7 | 14:69078743 | GGTTGCCAGGGCCTA[C/G]TGGCAGGGGAAATGG | 8816 |
rs146338270 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | DCAF5 | GRCh38.p7 | 14:69105188 | AAAAAATTTGTTCAC[A/G]AATGTTAATGATAGT | 8816 |
rs146372955 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69155261 | TGTATAATACGCATC[A/C]TCCTCTGCCCTCTTA | 8816 |
rs146384219 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | DCAF5 | GRCh38.p7 | 14:69061669 | TAGTTTTATCCATGC[C/T]ATATTAGGATGGCAA | 8816 |
rs146394843 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DCAF5 | GRCh38.p7 | 14:69058216 | TGAAAAACCAACTTC[C/T]TGTTACATGTTAAAT | 8816 |
rs146420924 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69053577 | AAAGATTTACTTCCA[C/G]AGAGCCTTGCGCGGC | 8816 |
rs146553663 | snp | A/C/T | 0.00110532 | 0.0234854 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69055279 | ATCTACTGTGGGAGG[A/C/T]GGGGAGCGAGGCAAT | 8816 |
rs146557811 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | DCAF5 | GRCh38.p7 | 14:69114846 | TGCACGGTAAGAAAC[A/T]GGTGGAAGAGAATGG | 8816 |
rs146646042 | snp | A/G/T | 3.29701e-05 | 0.00406005 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69054577 | CTTACTGGAAGAAGG[A/G/T]GCTGGGTTGTCTTTG | 8816 |
rs146663837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69097399 | GCTTTAAAATTTTTT[C/T]ATAGTAACCCTTCAT | 8816 |
rs146674758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69093943 | CTCTCTTGCATACAG[A/G]AAATGAATGACAGGA | 8816 |
rs146675519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69149149 | AACATAGTTCTCACA[A/G]CAAGCCCCTCAGGTA | 8816 |
rs146701436 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | DCAF5 | GRCh38.p7 | 14:69143412 | CTCAGTTCCCTCATA[G/T]GTAATATAAGGATAA | 8816 |
rs146785798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69074640 | AACATGACCAGGGAG[A/G]ACAAAGGAAAGAAAG | 8816 |
rs146795719 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69071324 | CAAAAAAAACAAAGA[C/T]TGATTAACAGTCTTC | 8816 |
rs146796612 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69125346 | GAGTAAACTGAAGGA[A/C]CAGAACAGGACTGCC | 8816 |
rs146821642 | snp | A/C/G | 0.00318978 | 0.0398085 | intron-variant | DCAF5 | GRCh38.p7 | 14:69121154 | AGGGAGGTCAGGCCA[A/C/G]ACAGATAGATTGGGA | 8816 |
rs146894684 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | DCAF5 | GRCh38.p7 | 14:69126866 | CACATGCATAAAAAT[C/G]AATTTAGATACAGAC | 8816 |
rs146905241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69122460 | TTTCCAAAACTGCAC[C/T]TCCCCAACTCCATAA | 8816 |
rs146909727 | in-del | -/T | 0.00358779 | 0.0422022 | intron-variant | DCAF5 | GRCh38.p7 | 14:69112545 | TCTAAAAATAAAAAC[-/T]TAAAAAAAAGAAAAA | 8816 |
rs146918277 | snp | C/T | 3.30852e-05 | 0.00406712 | missense | DCAF5 | GRCh38.p7 | 14:69075408 | CAGAGCCCGAAAGGA[C/T]ATACTGTTGGAACAA | 8816 |
rs147000676 | snp | C/G | 0.0225045 | 0.103662 | intron-variant | DCAF5 | GRCh38.p7 | 14:69104640 | GTGGGTGGATCACTT[C/G]AGGCCAGGAATTCAA | 8816 |
rs147055741 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | DCAF5 | GRCh38.p7 | 14:69144947 | TCCTTCCATTTCTCC[A/G]ATCCCATGCAGAAAA | 8816 |
rs147104505 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | DCAF5 | GRCh38.p7 | 14:69080502 | TAACCAGAAAACTGA[A/G]CTTCACCTCAAGTAG | 8816 |
rs147135454 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | DCAF5 | GRCh38.p7 | 14:69072689 | GATCTGTAAGAATAG[C/T]GGCAGAAGGGTTGAA | 8816 |
rs147158579 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | DCAF5 | GRCh38.p7 | 14:69068639 | GGAGACAGAAGTTGC[A/G]GTGAGCCGAGATCAT | 8816 |
rs147168788 | snp | C/T | 0.000780634 | 0.019741 | intron-variant | DCAF5 | GRCh38.p7 | 14:69119281 | GCAAGGTGGTCCCTG[C/T]CCACATTACAATTTA | 8816 |
rs147191861 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | DCAF5 | GRCh38.p7 | 14:69113337 | TAAGGAACCACAACA[A/G]GTTTAAAACCTAGGG | 8816 |
rs147218072 | in-del | -/AG | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69056978 | TCATAATCTTACCCT[-/AG]AGAGTTTCAAGGGAT | 8816 |
rs147240943 | snp | A/T | 0.000399281 | 0.0141238 | downstream-variant-500B | DCAF5 | GRCh38.p7 | 14:69050764 | ACCTAAAAGTGACAA[A/T]GACCATTGTCATGGA | 8816 |
rs147274707 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | DCAF5 | GRCh38.p7 | 14:69096282 | CCCAAGACTGAAACC[C/T]CCAGAGGGAACCAGA | 8816 |
rs147278299 | in-del | -/G | 0.0138799 | 0.0821421 | intron-variant | DCAF5 | GRCh38.p7 | 14:69133551 | AGTAGGCAGGGAAGA[-/G]GGCGGGGGTACAGGC | 8816 |
rs147296820 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69091558 | TCCAGGCACTCACTG[G/T]TTCCCCTTAATTGTT | 8816 |
rs147355775 | snp | C/T | 0.000181185 | 0.00951628 | missense | DCAF5 | GRCh38.p7 | 14:69054879 | TGTTGGTGGGCTTGA[C/T]TGGGGCACTGGGCTT | 8816 |
rs147380207 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69073618 | AGTCATGCCACTCCA[C/T]TCCAGCCTGGGCAAG | 8816 |
rs147437843 | snp | A/G | 6.61223e-05 | 0.0057495 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69054034 | GGCCATTTCAGACCC[A/G]CAACAATCTTTGTGT | 8816 |
rs147453379 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | DCAF5 | GRCh38.p7 | 14:69095978 | AAGCAAGGTCCTTTC[C/T]ATGGGAGAAAGTCTC | 8816 |
rs147476792 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant, utr-variant-3-prime, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69090070 | GGAAATAAAGCCTAG[A/T]AAACTATTAATATCA | 8816 |
rs147509629 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69136904 | GTTTTAAAATATTAA[G/T]CTTAATATTACAAAA | 8816 |
rs147590456 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | DCAF5 | GRCh38.p7 | 14:69063676 | GAGGGAAAATGACTA[C/T]AACAATGTCCCTTCC | 8816 |
rs147613793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69058938 | GTGAAGAGACAAGAC[A/G]AGAGATGAGACAAAT | 8816 |
rs147624019 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69108897 | AAATTTCTAGGTCCA[C/T]CTGACTCTTCTCGTT | 8816 |
rs147689319 | in-del | -/AAAGA | 0.0189856 | 0.0955633 | intron-variant | DCAF5 | GRCh38.p7 | 14:69088337 | GTTTACTCATCTGTG[-/AAAGA]AAAGGTTTGTATAAA | 8816 |
rs147726930 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | DCAF5 | GRCh38.p7 | 14:69085314 | TGGCTACCAGAAAAC[C/T]AAGAAAGTTGAGAAG | 8816 |
rs147750089 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69081088 | TAAGAAAAAATAAAA[A/T]ACAAAAAAAATGAAA | 8816 |
rs147822185 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | DCAF5 | GRCh38.p7 | 14:69068952 | GCCAATGCTGTCAGT[A/C]CAGCTCAAAGAGCTC | 8816 |
rs147830887 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | DCAF5 | GRCh38.p7 | 14:69065021 | CAGATCTAAAGACTA[A/G]TTGAAGGCTATCAAT | 8816 |
rs147853669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69059394 | GGTCTCAGGCTGGAC[C/T]AGAATGTGGTGGCTA | 8816 |
rs147856787 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | DCAF5 | GRCh38.p7 | 14:69151128 | TAAAGAAGAGGTCTT[A/C]CCCCATTTTTGCTCT | 8816 |
rs147939691 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69130638 | CTTATATATGTACAA[G/T]GCAGCCTAAATAAAT | 8816 |
rs147957521 | in-del | -/AG | | | intron-variant, utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69089872 | TATAATGCATAGGAC[-/AG]AGCTCCACACAACAA | 8816 |
rs147962535 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | DCAF5 | GRCh38.p7 | 14:69127259 | CCTTCAGTATGTAAA[C/T]GGATAAATCAACTGT | 8816 |
rs148013454 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | DCAF5 | GRCh38.p7 | 14:69077011 | CAAAAAGGACACTGT[A/G]CCAGATCTACTCTAA | 8816 |
rs148024025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69128503 | ATAATAAAGAGTTTT[A/G]GATTATGTTTAATGT | 8816 |
rs148043116 | snp | A/G | 0.00235393 | 0.034226 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69055474 | GACCGACTGGTTGGC[A/G]TAGTCATGCGACAGG | 8816 |
rs148068526 | in-del | -/AATTAAAA | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69107064 | AATAAATAATTAAAT[-/AATTAAAA]AATTAAATAAGAAAG | 8816 |
rs148077607 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | DCAF5 | GRCh38.p7 | 14:69135504 | CTATGAGATAGTTTG[A/C]ATTGTGAGCTGAACT | 8816 |
rs148096555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69060100 | TGAGAAACAGAATGA[C/T]GTCAACAGGCCCGGA | 8816 |
rs148152715 | in-del | -/ACACAC | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69099252 | TGGGACTCTGTCTCA[-/ACACAC]ACACACACACACACA | 8816 |
rs148160584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69117815 | CAGGAAAGTGCATAA[C/T]GCCCCCATTCTCTGT | 8816 |
rs148204424 | snp | C/T | 1.65449e-05 | 0.00287614 | missense | DCAF5 | GRCh38.p7 | 14:69053942 | TTGAGGCCACTGTGG[C/T]CATGAACAGCCCTGC | 8816 |
rs148214859 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | DCAF5 | GRCh38.p7 | 14:69123914 | TATGTTGGCCAGGCT[C/G]GTCTCAAACTCCTGA | 8816 |
rs148255814 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | DCAF5 | GRCh38.p7 | 14:69098980 | CTAACAGGCCTGGCG[C/T]AGTGGCTCACACCTG | 8816 |
rs148308767 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | DCAF5 | GRCh38.p7 | 14:69105240 | ATGGGACAATCCAAA[C/T]GGCTATCATTAGATG | 8816 |
rs148381594 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69072546 | CCAGGAGCTCAAGGC[G/T]GTATGCAGTATGCTA | 8816 |
rs148415182 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69063508 | AGTGTTCATTTATCT[A/C]CTCAAGGGATCCCCT | 8816 |
rs148468652 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69069757 | CAGGATTACAGGTAC[A/G]AGCCATTGTGCCTAG | 8816 |
rs148477791 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | DCAF5 | GRCh38.p7 | 14:69119929 | AGAGTAACTGTAAGC[A/G]TAAGAGTACATCTGT | 8816 |
rs148531174 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | DCAF5 | GRCh38.p7 | 14:69125815 | AATAAAAGCAAGTTT[C/T]GAAAGGATATGAAAG | 8816 |
rs148548700 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69051898 | AATTCCAATTTAATA[C/T]ATTTTGGAAAAGCAA | 8816 |
rs148571608 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | DCAF5 | GRCh38.p7 | 14:69101989 | ATGAATGAATGTGAA[C/G]GCCTAGGACATTACT | 8816 |
rs148624294 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | DCAF5 | GRCh38.p7 | 14:69107739 | AACATTTGGATTCAT[A/G]TCATTATACTCAGGG | 8816 |
rs148685247 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | DCAF5 | GRCh38.p7 | 14:69074091 | GAGTTATGCCAAAAG[G/T]AGGCCCCAACAGGTT | 8816 |
rs148692154 | in-del | -/AC | 0.489376 | 0.0721049 | intron-variant | DCAF5 | GRCh38.p7 | 14:69095550 | TTTGTTTTTTTAAGT[-/AC]TACACACACACACAC | 8816 |
rs148707082 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | DCAF5 | GRCh38.p7 | 14:69089741 | GGTTCTCAACCAGGG[A/G]CAATTTTCCCCCCAG | 8816 |
rs148739197 | snp | A/C/G | 0.0123036 | 0.0774623 | intron-variant | DCAF5 | GRCh38.p7 | 14:69079477 | AGGGCGTCTTGCCTC[A/C/G]CTGCCATCTAGTAAG | 8816 |
rs148760990 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69096296 | CTCCAGAGGGAACCA[A/G]AACTGTCGGACAACC | 8816 |
rs148762629 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69129969 | CTAAAATCACTAATT[A/C]ATCAAAAAATGTACT | 8816 |
rs148770884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69147639 | ATCAATATGGTCAGA[A/G]ACCCATTTGAACTAG | 8816 |
rs148816950 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | DCAF5 | GRCh38.p7 | 14:69138302 | TTGCAAAGAATTCCT[A/C]CTCCTGAGTAATGTT | 8816 |
rs148830844 | in-del | -/CTT | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69098147 | CCTCCTAGGACTCTC[-/CTT]TTACCTTATTCAACT | 8816 |
rs148867811 | snp | C/T | 0.00156377 | 0.0279185 | missense | DCAF5 | GRCh38.p7 | 14:69054935 | CGCCGCATGGCATTC[C/T]GCTGCCAGGTAGAGG | 8816 |
rs148931173 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69109596 | TATTTGAATTCTTTT[A/C]TTCAATATTATGACC | 8816 |
rs148942004 | snp | G/T | 1.64738e-05 | 0.00286995 | missense | DCAF5 | GRCh38.p7 | 14:69054534 | GGTCCTGGTTCCTCT[G/T]GGCCATTGCTATGTT | 8816 |
rs148984035 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69117033 | GCCAGTCTGTAATCA[A/G]CTTCACCTAGAAACC | 8816 |
rs148996794 | in-del | -/A | 0.0807149 | 0.183963 | intron-variant | DCAF5 | GRCh38.p7 | 14:69094787 | ATCATCTAGGACTTT[-/A]AAAAAATGTAGATTC | 8816 |
rs149025533 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | DCAF5 | GRCh38.p7 | 14:69093450 | TAAAGAAGTTTTAAT[C/G/T]GCATTGTACCAAGTG | 8816 |
rs149139885 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | DCAF5 | GRCh38.p7 | 14:69065374 | TGCTGGGATTACAGG[C/T]GTGAGCCACCACACC | 8816 |
rs149193908 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | DCAF5 | GRCh38.p7 | 14:69071911 | AGCCATGTTGAAGAG[C/T]AGGGCTGAAAACAGG | 8816 |
rs149216836 | snp | A/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69121930 | TTTCAAATATGTGTG[A/T]GTGTCTGTGTGTGTT | 8816 |
rs149306770 | snp | C/T | 0.000560926 | 0.0167376 | missense, utr-variant-5-prime | DCAF5 | GRCh38.p7 | 14:69122295 | CTCCTTTCAGCTGTA[C/T]GGGCTTGACCCTGGA | 8816 |
rs149331561 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69095729 | CAACATAGGGAATTG[A/G]AAAAGCTTCCAAGAT | 8816 |
rs149336032 | in-del | -/T | 0.126219 | 0.217206 | intron-variant | DCAF5 | GRCh38.p7 | 14:69110440 | CCACTAATTTTCCTA[-/T]TTTTTTTTTAGTAGA | 8816 |
rs149386277 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | DCAF5 | GRCh38.p7 | 14:69101657 | ACGAAATGTGTTGTT[A/T]GGCAATTTTGTTGTG | 8816 |
rs149409214 | snp | A/C/T | 0.0134861 | 0.0810011 | upstream-variant-2KB | DCAF5 | GRCh38.p7 | 14:69154394 | GGGAAAATAATAATA[A/C/T]TTTTTTTTAAAAAAA | 8816 |
rs149461007 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | DCAF5 | GRCh38.p7 | 14:69068388 | TTTCATTCTTGACCC[A/C]ACTGGTAGAATTAAG | 8816 |
rs149481805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69081720 | CTCACTGACCCAAAT[A/G]TCCTCTGTCAATCCA | 8816 |
rs149524986 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | DCAF5 | GRCh38.p7 | 14:69124053 | TACTCTAGGAACCTC[A/G]TATAAGTCAAATCAC | 8816 |
rs149535268 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69088793 | AAATATAAAGCCCAA[A/T]ATAAGGAAAAGGCAG | 8816 |
rs149545299 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | DCAF5 | GRCh38.p7 | 14:69140845 | GCGGAGGCCAGGAGC[A/G]GTAGCTCACACCTGT | 8816 |
rs149598185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69146253 | CACAAGGACAACTTT[C/T]TGATGTATTAATAAC | 8816 |
rs149649190 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | DCAF5 | GRCh38.p7 | 14:69062906 | GCTGGACCAAGGACA[C/T]GCAGAACCAGAAGCA | 8816 |
rs149680696 | snp | A/T | 8.25226e-05 | 0.00642296 | missense | DCAF5 | GRCh38.p7 | 14:69054435 | CTGCCCAAGCATGGC[A/T]GCTGTGCTCATGGCC | 8816 |
rs149703707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | DCAF5 | GRCh38.p7 | 14:69103774 | GCAACTTGTCCTCTA[C/T]TCTCATCTCTAACTC | 8816 |
rs149713519 | snp | C/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69061962 | AAGTTTGAATCCAGC[C/T]TGGGCAACACAGCAA | 8816 |
rs149725333 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | DCAF5 | GRCh38.p7 | 14:69119669 | GCAGTGAGCTACGAT[C/T]GCACTCCAGCCTGGG | 8816 |
rs149801553 | snp | C/T | 1.65141e-05 | 0.00287346 | synonymous-codon | DCAF5 | GRCh38.p7 | 14:69054322 | AGGCGGCTCCTCAGC[C/T]CGACTGCTCAGGGCC | 8816 |
rs149840500 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | DCAF5 | GRCh38.p7 | 14:69092926 | ATGTTCTGGTTCACC[G/T]AATATTCTTCTGCAG | 8816 |
rs149915055 | snp | A/T | 0.0345262 | 0.126772 | intron-variant | DCAF5 | GRCh38.p7 | 14:69058802 | CACCTAAGCCTGGGG[A/T]GGTTGAGGCTGCAGT | 8816 |
rs149917315 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | DCAF5 | GRCh38.p7 | 14:69149189 | ATTCCAACTGTATAC[C/T]TCAGAAAACACATTC | 8816 |
rs149935366 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | DCAF5 | GRCh38.p7 | 14:69073771 | GAATAGTCCTGGGGA[A/G]AAGAAGGATTATCCA | 8816 |
rs149977991 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | DCAF5 | GRCh38.p7 | 14:69114473 | AGTGAGTATTACTAC[A/G]TGCTTCCTTCTGTCT | 8816 |
rs149998923 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | DCAF5 | GRCh38.p7 | 14:69129382 | TCTTCAAGTATGCGT[C/T]GGCAGAAAAACAACC | 8816 |
rs150033987 | in-del | -/T | | | intron-variant | DCAF5 | GRCh38.p7 | 14:69110229 | ATGTATGTATTATGC[-/T]TTTTTTTTTCTGATC | 8816 |
rs150105123 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | DCAF5 | GRCh38.p7 | 14:69087086 | CATGCTTGCTAGACT[A/G]AAAGACTTGCTTACC | 8816 |