DCAF11
SNP - dbSNP
dbSNPTypeAllelesHetSe(het)Fxn-classGene NameAssemblyChr-posSequenceEntrez Gene
rs743273snpA/G00intron-variant, upstream-variant-2KBDCAF11, NRLGRCh38.p714:24116629GGTCATGTCCACAGC[A/G]TATTGGTCTTGCTCT80344
rs762093snpC/G0.4860670.0822953intron-variantDCAF11GRCh38.p714:24122709AGTTAAGGAAATGCA[C/G]TGGCTTTGAAGATTT80344
rs1134334snpA/G0.4983690.0285077utr-variant-3-prime, nc-transcript-variantDCAF11GRCh38.p714:24124905aaaaactagccggat[A/G]tggtggcgggtgcct80344
rs1134340snpC/T0.492630.0602539utr-variant-3-prime, nc-transcript-variantDCAF11GRCh38.p714:24125004tgcagtgagccaaga[C/T]catgccattacactc80344
rs2277479snpA/G0.1520010.229992intron-variantDCAF11GRCh38.p714:24118295TCCCATGATAAAGGG[A/G]AGACTCCACAGGTAC80344
rs2277480snpA/G0.4783540.101757intron-variantDCAF11GRCh38.p714:24118306AGGGAAGACTCCACA[A/G]GTACACTGAGTGGGA80344
rs2277481snpA/G0.485460.0840147intron-variantDCAF11GRCh38.p714:24118336AGATGTCTAATCTAG[A/G]AAAGTTACAAGGAAA80344
rs2277482snpC/T0.4519820.14732intron-variantDCAF11GRCh38.p714:24118586TGGGACCTGAGGTTT[C/T]CATGTGCCTGTCCCC80344
rs2277483snpA/G0.4985030.0273153intron-variantDCAF11GRCh38.p714:24122683TTTGTGGTGCCTTCC[A/G]TATCTTACTAAAATC80344
rs3207709snpA/G00utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KBDCAF11, NRLGRCh38.p714:24115581ACAGGACCTAAGAAT[A/G]CTGTGACCAGAAGAT80344
rs3742499snpC/T0.1421550.225543intron-variantDCAF11GRCh38.p714:24117624ATATGGCTGAAGTGG[C/T]CCTCTATTTCTGCTA80344
rs3811175snpA/T0.1279440.218179upstream-variant-2KB, intron-variantDCAF11, NRLGRCh38.p714:24114255AGCCAGGGATTGTCT[A/T]AAAAAATTGTCAGAC80344
rs3825583snpA/T0.2577320.24988upstream-variant-2KB, intron-variantDCAF11, NRLGRCh38.p714:24114637CTGGCAGTTCCCACT[A/T]ACTCCTCCCCAGCAA80344
rs3825584snpA/G0.4533430.145435missense, nc-transcript-variantDCAF11GRCh38.p714:24118430GATATGGCCGTTTCC[A/G]TAAATTCAAGAGCAT80344
rs6573565snpA/G0.48620.0819127downstream-variant-500BDCAF11GRCh38.p714:24125524ttttaTGTTATCGAA[A/G]TAATGTAAAATGTTT80344
rs7141186snpA/G0.01092860.0731087utr-variant-3-prime, nc-transcript-variantDCAF11GRCh38.p714:24124035TGGGAACCTGGCTCA[A/G]TGTCTGTCTCTCTCT80344
rs7359087snpA/G1.6473e-050.00286988synonymous-codon, intron-variant, nc-transcript-variantDCAF11GRCh38.p714:24116938AGTGAGGTTGGTGCA[A/G]GGAGGAGGTGCAGCA80344
rs8008888snpA/G0.3184150.240457intron-variant, upstream-variant-2KBDCAF11, NRLGRCh38.p714:24116053GCTTGAAAAAAAAAA[A/G]GGGGGGGTCCTAGTG80344
rs8009511snpA/G0.4983690.0285077utr-variant-3-prime, nc-transcript-variantDCAF11GRCh38.p714:24124771agtaggccgggcacg[A/G]tggttcacacctgta80344
rs8012480snpA/T0.04449080.142359downstream-variant-500BDCAF11GRCh38.p714:24125437ATTCAAATTGTTAGT[A/T]TCCTTATAGCTTCAT80344
rs10134506snpC/G0.1615960.233848intron-variantDCAF11GRCh38.p714:24120609aaTGGAAGACAATCT[C/G]ATTAAGGCTAGAATA80344
rs10138006snpC/T0.0467750.145601upstream-variant-2KB, intron-variantDCAF11, NRLGRCh38.p714:24113959TCAACCCACACGTCC[C/T]CACCCAGCCAGGGCG80344
rs10146643snpA/C0.4973590.0362457intron-variantDCAF11GRCh38.p714:24120261TAAAAAAAAAAACAA[A/C]AAAAAAAAACTAAGG80344
rs11428836in-del-/G00upstream-variant-2KB, intron-variantDCAF11, NRLGRCh38.p714:24113293ATGACACGTTAGTGG[-/G]TGCAGCGCACCAGCA80344
rs11549425snpC/T0.05019050.150254utr-variant-3-prime, nc-transcript-variantDCAF11GRCh38.p714:24123777GTGCTGAGGAAACAC[C/T]CTTACCCATGCCCCT80344
rs11848386snpA/C0.03913870.134304intron-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variantDCAF11, NRLGRCh38.p714:24115054AGGAGGGGTGTTAGG[A/C]CAAATTCTATTTTCA80344
rs12435994snpA/C0.4984590.0277128intron-variantDCAF11GRCh38.p714:24120252CTATTTATTTAAAAA[A/C]AAAAACAAAAAAAAA80344
rs12435995snpA/C0.4984590.0277128intron-variantDCAF11GRCh38.p714:24120255TTTATTTAAAAAAAA[A/C]AACAAAAAAAAAAAA80344
rs17101347snpG/T0.03837150.133092utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variantDCAF11, NRLGRCh38.p714:24114903CTCGCGCCGCTGCGG[G/T]TCCTGCGACCGCTCC80344
rs17101367snpC/T0.3856890.209972synonymous-codon, nc-transcript-variantDCAF11GRCh38.p714:24118458CATCAAGGCCCGCGA[C/T]GTAGGCTGGAGCGTC80344
rs17101392snpC/G0.1185840.212673utr-variant-3-prime, nc-transcript-variantDCAF11GRCh38.p714:24124205ATTTGTTCACTGAGC[C/G]TTGCAATAGGTGCTC80344
rs34097612in-del-/Adownstream-variant-500BDCAF11GRCh38.p714:24125353CTGCCAAGTGATAAA[-/A]GTTACCTAAGGTGCT80344
rs34426457snpA/G0.0003139950.0125259synonymous-codon, nc-transcript-variantDCAF11GRCh38.p714:24122987CTTCACAATGTGGCC[A/G]CTTAGAAGGTCGTAC80344
rs34701145in-del-/Cintron-variantDCAF11GRCh38.p714:24122041ATGGTGGCACAGGCC[-/C]TGTAGTCCCAGCTAC80344
rs35069044in-del-/Cframeshift-variant, nc-transcript-variantDCAF11GRCh38.p714:24121386GAAGCTGAAGCTCCC[-/C]AGGGGACAGCTCCTT80344
rs35577926in-del-/TG0.4983690.0285077downstream-variant-500BDCAF11GRCh38.p714:24125566ATACCTAGGAGATAT[-/TG]TGAGTTCATTTCCAG80344
rs35596427in-del-/Cintron-variantDCAF11GRCh38.p714:24118587GGACCTGAGGTTTCC[-/C]ATGTGCCTGTCCCCT80344
rs55668591snpA/Gintron-variantDCAF11GRCh38.p714:24122513AAAAAAAAAGAAAAA[A/G]AAAAAAAAAACCAGA80344
rs55963929in-del-/Aintron-variantDCAF11GRCh38.p714:24122158GTGAGAAACTGTCTC[-/A]AAAAAAAAAAAAAAA80344
rs56271764snpA/Cintron-variantDCAF11GRCh38.p714:24120258ATTTAAAAAAAAAAA[A/C]AAAAAAAAAAAACTA80344
rs60825374snpA/Cintron-variantDCAF11GRCh38.p714:24120257TATTTAAAAAAAAAA[A/C]CAAAAAAAAAAAACT80344
rs61744791snpA/C/G/T0.01393910.0823128missense, nc-transcript-variantDCAF11GRCh38.p714:24117358GGGCTTAGGCGGGCC[A/C/G/T]CCCAGAAGCACAGCT80344
rs73603087snpA/C/G0.01097190.0732508intron-variantDCAF11GRCh38.p714:24121304TTGCTCAGGACTGGT[A/C/G]GTACGAAACAATCCC80344
rs74040010snpA/G0.07888430.182262intron-variant, upstream-variant-2KBDCAF11, NRLGRCh38.p714:24116696TGGGAGGTCAACTTA[A/G]TAGGTCACGTCCACA80344
rs74040011snpA/G0.007955320.062565intron-variant, upstream-variant-2KBDCAF11, NRLGRCh38.p714:24116842AGTGGTCTAAGAGCT[A/G]GATAGCCATTGACTC80344
rs74040012snpC/T0.007162660.059414intron-variantDCAF11GRCh38.p714:24119073GATGTGCCTTACAAC[C/T]GTTGTCAGATTTTAT80344
rs74665383snpC/G0.50intron-variantDCAF11GRCh38.p714:24120534TACACTCCAGCCTGG[C/G]TGACAGAGCAAGACT80344
rs75570711snpA/C0.50intron-variantDCAF11GRCh38.p714:24122491GCGAGACTCCATCTC[A/C]AAAAAAAAAAAAAAA80344
rs75719972snpA/G0.01652780.0893908intron-variant, upstream-variant-2KBDCAF11, NRLGRCh38.p714:24115924AGCTCCATACCCAGT[A/G]AGAGTGGTTCTTACC80344
rs76180205snpA/T00upstream-variant-2KB, intron-variantDCAF11, NRLGRCh38.p714:24113390TAATAAAAAAAAAAA[A/T]TGATTCCGTCACATT80344
rs76629917snpC/G0.003985640.0444627upstream-variant-2KB, intron-variantDCAF11, NRLGRCh38.p714:24113631TACTAATAATTTCAA[C/G]ACCGTTAACACTAGA80344
rs77478594snpC/T0.003985640.0444627intron-variantDCAF11GRCh38.p714:24121058GGAGGACCTCCCCCT[C/T]AGCCCTCTTTGCCAG80344
rs77582680snpA/C00intron-variantDCAF11GRCh38.p714:24122160GAGAAACTGTCTCAA[A/C]AAAAAAAAAAAAAAG80344
rs77652957snpA/C0.50intron-variantDCAF11GRCh38.p714:24122490AGCGAGACTCCATCT[A/C]AAAAAAAAAAAAAAA80344
rs77883085snpA/G/T0.01427360.0832652intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KBDCAF11, NRLGRCh38.p714:24115405AAGGTTTGTGTTCCC[A/G/T]ACGCCTTGGTAGTTG80344
rs77935488snpG/T0.001197370.0244387intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KBDCAF11, NRLGRCh38.p714:24115510GGAGACCCTGGTATT[G/T]CTAGAGCACGCTTTG80344
rs78107024snpA/G0.003924690.0441242intron-variantDCAF11GRCh38.p714:24119930CTGTACAGCCAGGCC[A/G]CTAAGGTTCTAGTTG80344
rs78265727snpC/T0.01584690.0875917utr-variant-3-prime, nc-transcript-variantDCAF11GRCh38.p714:24124428TCACACTCAGAACCT[C/T]ATACCCCAGAGCAAA80344
rs78469280snpA/C/G0.005552460.0523972missense, nc-transcript-variantDCAF11GRCh38.p714:24118471GACGTAGGCTGGAGC[A/C/G]TCTTGGATGTGGCCT80344
rs78584440snpA/C0.01416580.0829593utr-variant-3-prime, nc-transcript-variantDCAF11GRCh38.p714:24123320AGTAGATCCAACCTC[A/C]AGCCCCATATAGGGT80344
rs79254253snpC/T0.03837150.133092upstream-variant-2KB, intron-variantDCAF11, NRLGRCh38.p714:24113787CCTCACTGGGAGAGG[C/T]CCCAGGAGGGCCCAA80344
rs111289851snpC/T0.50downstream-variant-500BDCAF11GRCh38.p714:24125377AGGTGCTACCCATCT[C/T]ACCCAGAACCTGTGT80344
rs111512015snpC/T0.001197370.0244387intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KBDCAF11, NRLGRCh38.p714:24115359GCGCACTACGGTTCA[C/T]TCTTGCTTTCTTTGC80344
rs111567488snpC/T0.006369360.0560724upstream-variant-2KB, intron-variantDCAF11, NRLGRCh38.p714:24113674ACATTCAGGACCCTT[C/T]TAAGCGCAGAGGCCA80344
rs111766644snpA/C/G0.008565640.0648803stop-gained, nc-transcript-variantDCAF11GRCh38.p714:24123204GCGTCTGTGGCAGTA[A/C/G]CGCCAGGCTGAGTAC80344
rs112317051snpA/G0.04829460.147699upstream-variant-2KB, intron-variantDCAF11, NRLGRCh38.p714:24113167TCTCACTCATAGGTG[A/G]GAATTGAACAATGAG80344
rs112340123snpA/G0.003189780.0398085intron-variantDCAF11GRCh38.p714:24121946TTGGGAGGCCAATGA[A/G]GGCAGATCACTTGAG80344
rs112450292snpG/T0.50intron-variantDCAF11GRCh38.p714:24119678TATAAGACCTAGAAA[G/T]AGGTCTTATATCCTG80344
rs112454085snpC/G/T1.64762e-050.00287016intron-variantDCAF11GRCh38.p714:24117060GTAAGAGGAAAAGCC[C/G/T]CTAATGTTGGAAGAC80344
rs112788511snpA/G0.50intron-variantDCAF11GRCh38.p714:24117054CACCTGGTAAGAGGA[A/G]AAGCCCCTAATGTTG80344
rs113086867snpC/T0.0003992810.0141238intron-variantDCAF11GRCh38.p714:24122444GCAGTGAGCCAAGAT[C/T]GCGCCACGGCACTCT80344
rs113214905in-del-/G0.50upstream-variant-2KB, intron-variantDCAF11, NRLGRCh38.p714:24114042CATAAACCCGCAGGA[-/G]GGGGCAGGAGGGGGC80344
rs113382865snpC/T0.003587790.0422022intron-variant, upstream-variant-2KBDCAF11, NRLGRCh38.p714:24116539GAATATTGTCTTCTG[C/T]GGTGGACTTCTCAGG80344
rs113395814snpA/G3.6186e-050.00425343utr-variant-3-prime, nc-transcript-variantDCAF11GRCh38.p714:24123348GGTGAACCTCTTGAT[A/G]AGCTCTCTGCCTCCT80344
rs113445360snpC/G3.29473e-050.00405864intron-variantDCAF11GRCh38.p714:24119534ATCATGGCTCCAGGA[C/G]CCTCCTTTATCCCTT80344
rs113595618snpC/T0.50intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KBDCAF11, NRLGRCh38.p714:24115356GTAGCGCACTACGGT[C/T]CACTCTTGCTTTCTT80344
rs113861802snpC/G9.93435e-050.00704712intron-variantDCAF11GRCh38.p714:24117760CTTGGTGAAGAGACT[C/G]TAAGGGCCAGATAGG80344
rs113984103snpC/T0.50utr-variant-3-prime, nc-transcript-variantDCAF11GRCh38.p714:24125079AGCCAGATGTGGTGA[C/T]GCATGCCTGTAGTCC80344
rs117078522snpC/T0.006369360.0560724intron-variant, upstream-variant-2KBDCAF11, NRLGRCh38.p714:24115952ACCTAGGGAGGGTCA[C/T]CAAGAGGACCTGCTC80344
rs117087796snpA/G0.009538730.0683987intron-variant, upstream-variant-2KBDCAF11, NRLGRCh38.p714:24116504AGACTACAGTTGCAC[A/G]CACCACCGCACCCAG80344
rs118146993snpA/G0.005972470.0543191upstream-variant-2KB, intron-variantDCAF11, NRLGRCh38.p714:24114041AAACCCGCAGGAGGG[A/G]GCAGGAGGGGGCAGG80344
rs137897532snpC/T0.0003992810.0141238utr-variant-3-prime, nc-transcript-variantDCAF11GRCh38.p714:24124360GAGGTAGCCCCTGAA[C/T]GCAGAGCCTAAGAGA80344
rs137913082snpC/G0.0007984030.0199641intron-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variantDCAF11, NRLGRCh38.p714:24115199GTGAAGCGCTTTCTT[C/G]CGAGAGGGATTTCGA80344
rs138016331snpA/G0.009538730.0683987intron-variantDCAF11GRCh38.p714:24118605GTGCCTGTCCCCTCT[A/G]AGCCAGGATCCCTCA80344
rs138347528snpC/T0.0009557230.0218391synonymous-codon, nc-transcript-variantDCAF11GRCh38.p714:24121417GATGACCTACCGGGG[C/T]CACGGAGTGCTGCAC80344
rs138449987snpC/T4.94173e-050.00497053 DCAF1114 allele_origin=T(somatic)/C(germline)14:24119602GACCGAGAACAGAAC[C/T]GGCGCACCCTTCAGG80344
rs138549012snpG/T0.00239330.0345097intron-variantDCAF11GRCh38.p714:24119338TTCTCCCAAGGTCAG[G/T]ATTTACAAGTTGCTT80344
rs138577883snpC/T0.0007984030.0199641utr-variant-3-prime, nc-transcript-variantDCAF11GRCh38.p714:24124763ATACAAAAAGTAGGC[C/T]GGGCACGGTGGTTCA80344
rs138662169snpA/C0.0003992810.0141238upstream-variant-2KB, intron-variantDCAF11, NRLGRCh38.p714:24113960CAACCCACACGTCCC[A/C]ACCCAGCCAGGGCGA80344
rs139297459snpC/G0.0008727930.0208754synonymous-codon, nc-transcript-variantDCAF11GRCh38.p714:24119577CAATGATGGCTGCCT[C/G]TATGTCTTTGACCGA80344
rs139504177snpA/C/G0.0008449580.0205372missense, nc-transcript-variantDCAF11GRCh38.p714:24117380AGCACAGCTTTCCTC[A/C/G]AATGTTGCACCAGGT80344
rs139790081snpC/T0.04449080.142359intron-variantDCAF11GRCh38.p714:24120338GAGGCGGGCAGATCA[C/T]GAGGTCAGGAGATCG80344
rs139933200snpA/G0.003587790.0422022intron-variantDCAF11GRCh38.p714:24117577GTGTCCATTTCTATA[A/G]CAAGAGCAATATCTT80344
rs139960788snpA/G0.0001483590.00861149missense, nc-transcript-variantDCAF11GRCh38.p714:24123036GCCTGTGTGCGTGAC[A/G]TCAGTTGGCACCCCT80344
rs140074757snpA/G3.61246e-050.00424982missense, nc-transcript-variantDCAF11GRCh38.p714:24123257CTGAGGAATGTGCCA[A/G]CGCCCCTGCCCCAGT80344
rs140077163snpA/G0.01387990.0821421intron-variantDCAF11GRCh38.p714:24120122GAAAAATGGAAGACC[A/G]GTCAGGTACAGCGGC80344
rs140199178snpA/G0.0007984030.0199641utr-variant-3-prime, nc-transcript-variantDCAF11GRCh38.p714:24123967TTAAGGAAGTAGGTT[A/G]AAGTAGGACTCCTTC80344
rs140411068snpC/G0.0005121550.0159942intron-variantDCAF11GRCh38.p714:24118344AATCTAGAAAAGTTA[C/G]AAGGAAACTGTCCCA80344
rs140555404snpC/T6.64132e-050.00576213intron-variantDCAF11GRCh38.p714:24120821TGATGCTTCACTATC[C/T]ACCTTTGGATTCATA80344
rs140993634snpA/T0.003587790.0422022intron-variantDCAF11GRCh38.p714:24122738CTGTAGCCCCTATGA[A/T]ATTTAGCTAAGGGCC80344
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