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 |