KCTD13
SNP - dbSNP
dbSNPTypeAllelesHetSe(het)Fxn-classGene NameAssemblyChr-posSequenceEntrez Gene
rs1129700snpA/G0.4940130.0543839utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B, intron-variantKCTD13, ASPHD1GRCh38.p716:29906713GGCCCTTCTCCACCC[A/G]TCCCAACCCCATTGC253980
rs4076756snpC/T0.1217170.214577intron-variant, utr-variant-3-prime, downstream-variant-500BKCTD13, ASPHD1GRCh38.p716:29919954AAGAAAAAATATTGG[C/T]GATATCTACATTGAC253980
rs4238958snpA/G0.02367460.106192intron-variant, utr-variant-3-prime, nc-transcript-variantKCTD13, ASPHD1GRCh38.p716:29919744TGTGTGTGTGTGTGT[A/G]TTTGCTTGCCAAAAT253980
rs4407079snpC/T0.4700340.11868intron-variant, utr-variant-3-primeKCTD13GRCh38.p716:29920578attcatgttctttac[C/T]agattttctgctttt253980
rs4420550snpC/T0.4943580.0528145upstream-variant-2KB, nc-transcript-variantKCTD13, LOC107984836GRCh38.p716:29927499GCTGTTGGTGCCAGG[C/T]CAGCTCCTAGCAACA253980
rs4424923snpA/G0.4960340.0443518upstream-variant-2KB, intron-variantKCTD13, LOC107984836GRCh38.p716:29927972gcactttgggaggcc[A/G]aggtgggcatatcac253980
rs4548895snpC/T0.4997760.0105807intron-variantKCTD13, ASPHD1GRCh38.p716:29912189AGAGTGGCAGAGAGG[C/T]TGGCGGAGCTTGGAG253980
rs4609871snpA/G0.4948960.0502606intron-variant, utr-variant-3-primeKCTD13GRCh38.p716:29920743GCATGTCCTCATCAA[A/G]ACATGGCATCATCCA253980
rs4788189snpC/T0.4932470.0577133intron-variantKCTD13, ASPHD1GRCh38.p716:29909890gcctgaccaacatgg[C/T]gaagtctctactaaa253980
rs5816505in-del-/A0.4978670.0325897intron-variant, upstream-variant-2KBKCTD13, LOC107984836GRCh38.p716:29925760GTTGGGGGTCTGGGG[-/A]TGGGGGCACGGTAGG253980
rs7184288snpC/G0.4902310.0692021intron-variantKCTD13GRCh38.p716:29923731ctgggcttggtggct[C/G]gtgccagctactcgg253980
rs7197342snpA/G0.02328470.105357intron-variantKCTD13, ASPHD1GRCh38.p716:29917378TAggtcaggtatagc[A/G]gatcacacctgtaat253980
rs7201384snpA/G0.4952130.048687intron-variantKCTD13, ASPHD1GRCh38.p716:29913584gggtggctccggcac[A/G]gggtctcttctgagg253980
rs8047140snpC/T0.4103990.191761intron-variant, nc-transcript-variantKCTD13, ASPHD1GRCh38.p716:29911667AGGACCTGCCTAGAG[C/T]GTCAGGGGTAAGAGG253980
rs8048433snpC/T0.4966810.0405994intron-variant, utr-variant-3-prime, downstream-variant-500BKCTD13, ASPHD1GRCh38.p716:29920272gaggttgcagtgagg[C/T]aagatcgcgccactg253980
rs8050576snpA/G0.4943150.0530107intron-variantKCTD13, ASPHD1GRCh38.p716:29908471ctcactgcaacctcc[A/G]cttcccaagttcaag253980
rs8052502snpC/T0.4703270.118136intron-variantKCTD13, ASPHD1GRCh38.p716:29918407AACGTGAAATACATA[C/T]ATAATATTACCTAAA253980
rs8059619snpC/T0.4699370.118861intron-variantKCTD13, ASPHD1GRCh38.p716:29914124cgtgagccacagcgc[C/T]gggcccctccattgt253980
rs9925913snpC/G00intron-variant, utr-variant-3-primeKCTD13GRCh38.p716:29921479agcctggggtcaaat[C/G]tgagctctgctgctt253980
rs9928945snpA/G0.000865120.0207801intron-variantKCTD13GRCh38.p716:29923403AGATGGCTTTGCTGC[A/G]GGACCTGGAGCTACT253980
rs9936474snpC/T0.4699370.118861intron-variant, utr-variant-3-primeKCTD13GRCh38.p716:29921370CACTGAGGAGTGTGC[C/T]GAGCTGCGTGAGGTG253980
rs10083738snpA/G0.4704240.117954intron-variantKCTD13, ASPHD1GRCh38.p716:29916381agtgtgaaccactgt[A/G]cccagccaatacttt253980
rs11150574snpC/T0.4699370.118861intron-variantKCTD13GRCh38.p716:29923498CTGGGCTCAAGTGAT[C/T]CTCCCATCTCGGCCT253980
rs11150575snpC/G0.4319160.171483intron-variantKCTD13GRCh38.p716:29923745TGGTGCCAGCTACTC[C/G]GGGGGGGGCGAGGCA253980
rs11644809snpA/G0.4977220.0336691intron-variantKCTD13GRCh38.p716:29924184CATCTCAAAAAAAAA[A/G]AAAAGAAAAGAAAAG253980
rs11646118snpC/T0.04563360.143994intron-variantKCTD13, ASPHD1GRCh38.p716:29915150gtcccacctcttcca[C/T]gaaagatgtttgcag253980
rs11647753snpA/G0.4988520.0239341intron-variantKCTD13, ASPHD1GRCh38.p716:29916794tggccctggcccaga[A/G]tctgtcatgaagctg253980
rs11649519snpA/G0.50intron-variantKCTD13, ASPHD1GRCh38.p716:29907524tggcgcagtgactca[A/G]gcctgtaatcccagc253980
rs11865766snpA/Cintron-variant, downstream-variant-500BKCTD13, ASPHD1GRCh38.p716:29918732cacgatctcggctca[A/C]tgcaacctctgcctc253980
rs12232459snpC/T00intron-variantKCTD13, ASPHD1GRCh38.p716:29914357ctcaaagtacagaat[C/T]tcatcatctcagtca253980
rs12444978snpA/T0.4698390.119042intron-variantKCTD13, ASPHD1GRCh38.p716:29913101ACAGAGAATAATAAA[A/T]GTCTACAATTACTGA253980
rs12447999snpG/T0.50intron-variantKCTD13, ASPHD1GRCh38.p716:29908688catgcccggccTTtt[G/T]tttttttttttaatc253980
rs12448030snpA/G0.1265640.217402intron-variantKCTD13GRCh38.p716:29922223AAAAGTTTGAAAAAC[A/G]TGGATATTGTCCAAA253980
rs12596042snpA/T0.4701320.118498intron-variantKCTD13GRCh38.p716:29923433TAAATTAAAAAAAAA[A/T]TTTTGTAGAGATGGA253980
rs12716972snpA/G0.4955210.0471118intron-variant, upstream-variant-2KBKCTD13, LOC107984836GRCh38.p716:29925333GGGAACACAGAGGCA[A/G]ACAAGATCTCCCAGC253980
rs12716973snpA/G0.4713880.116136upstream-variant-2KB, nc-transcript-variantKCTD13, LOC107984836GRCh38.p716:29926331GGCGTGTGGCCTGCG[A/G]GTTCCCCGGGCGGGT253980
rs12932403snpA/G0.446510.154543intron-variantKCTD13GRCh38.p716:29922729GTTTAAAAAAAAAAA[A/G]GAATTAGAAAGCTCC253980
rs12933766snpC/T0.4945260.0520291intron-variant, downstream-variant-500BKCTD13, ASPHD1GRCh38.p716:29910690TGGCAACTATGGACC[C/T]CCTATACAGAAAAAT253980
rs12935265snpA/G0.007162660.059414intron-variant, utr-variant-3-prime, nc-transcript-variantKCTD13, ASPHD1GRCh38.p716:29919707AAAACAGATTATAAA[A/G]CATTTCATACAACAC253980
rs17853574snpA/G00synonymous-codon, nc-transcript-variant, intron-variant, downstream-variant-500BKCTD13, ASPHD1GRCh38.p716:29911065GTAGAAAGACCAGCA[A/G]CAGATCTCGTCCCCC253980
rs34090922in-del-/C0.05923550.161582upstream-variant-2KBKCTD13, LOC107984836GRCh38.p716:29926252CGCAGCCCCGCCCCC[-/C]ATTCAGGGGCGGGGC253980
rs34173971in-del-/Cintron-variant, upstream-variant-2KBKCTD13, LOC107984836GRCh38.p716:29924984CACGCCTTTAATCCC[-/C]AGCACTTTGGGAGGC253980
rs35012369in-del-/Gintron-variant, splice-donor-variantKCTD13, ASPHD1GRCh38.p716:29911660CCCCTGACGCTCTAG[-/G]CAGGTCCTTTCTGCT253980
rs35278775in-del-/Tintron-variantKCTD13, ASPHD1GRCh38.p716:29907414GTTCACTGCTATTTT[-/T]GCAGTGCCTAGAACA253980
rs35345720snpA/T0.04829460.147699intron-variantKCTD13GRCh38.p716:29922282AACAACTTTTGTCTC[A/T]GGGAATACTTACTGG253980
rs35566440in-del-/GAAT0.3044380.244001intron-variantKCTD13, ASPHD1GRCh38.p716:29909050AATGAATGAATGAAT[-/GAAT]CAGTGACCCAGCTTC253980
rs35691158snpC/G0.4444440.157135intron-variantKCTD13, ASPHD1GRCh38.p716:29909173AGGGGGTTTGCATCA[C/G]CAGCGAGGTGTTAGT253980
rs35756092in-del-/Aintron-variantKCTD13, ASPHD1GRCh38.p716:29913121AAAAAAAAAAAAAAA[-/A]TGGCCTCAGTAATTG253980
rs56885319in-del-/CAintron-variant, utr-variant-3-prime, nc-transcript-variantKCTD13, ASPHD1GRCh38.p716:29919759ACACACACACACACA[-/CA]TACTCTCACACAGGA253980
rs57383025snpC/T0.004968910.049596intron-variantKCTD13GRCh38.p716:29923031GGGTGCTGCCTGAGG[C/T]GGCAGGGATGCAGAA253980
rs60476091snpA/Cmissense, nc-transcript-variant, intron-variant, downstream-variant-500BKCTD13, ASPHD1GRCh38.p716:29911006TTCTCCGTAGCATAG[A/C]CAATGGAGGTGCAGC253980
rs62056408snpA/T0.50intron-variantKCTD13, ASPHD1GRCh38.p716:29912898GTTGAGTGAATGAAC[A/T]TCATTGGGTGGGATG253980
rs62056409snpA/G0.50intron-variantKCTD13, ASPHD1GRCh38.p716:29915135GGCTCTCCCTGAGTC[A/G]TCCCACCTCTTCCAT253980
rs62056410snpA/C0.01348610.0810011intron-variantKCTD13, ASPHD1GRCh38.p716:29915644AAGAAAAAAGAAAAT[A/C]TCTGCAAGGTAAGCC253980
rs71276820in-del-/A0.50intron-variantKCTD13, ASPHD1GRCh38.p716:29913122GCAAGACCCTGTCTC[-/A]AAAAAAAAAAAAAAA253980
rs71373213in-del-/G0.50upstream-variant-2KB, nc-transcript-variantKCTD13, LOC107984836GRCh38.p716:29926610GGCCAAAGCGGCCGG[-/G]CGCTGTGGCTCACAC253980
rs71373214in-del-/G0.50upstream-variant-2KB, nc-transcript-variantKCTD13, LOC107984836GRCh38.p716:29926612CAAAGCGGCCGGGCG[-/G]CTGTGGCTCACACCT253980
rs71389436snpC/T0.50intron-variantKCTD13, ASPHD1GRCh38.p716:29914664TCTTTAACTCCTGAC[C/T]TCAGGTGATCCACTT253980
rs72170823in-del-/A/AA/AAAAAAAintron-variantKCTD13GRCh38.p716:29924174GTGAAACTCCATCTC[-/A/AA/AAAAAAA]AAAAAAAAAGAAAAG253980
rs72228738in-del-/TTCAintron-variantKCTD13, ASPHD1GRCh38.p716:29909051TCATTCATTCATTCA[-/TTCA]ATAAATGTTTCCTAG253980
rs72622531snpA/Gintron-variantKCTD13, ASPHD1GRCh38.p716:29914583GGCTTGGTGGTGCGT[A/G]CCTGTAATCCCAGCT253980
rs72798147snpA/G0.002791620.0372561intron-variant, nc-transcript-variantKCTD13, ASPHD1GRCh38.p716:29911737GCCCCCCGTGTGGCC[A/G]TGGCCCTCGCCTTGG253980
rs72798148snpC/T0.169110.236552intron-variantKCTD13, ASPHD1GRCh38.p716:29915231AAGCCGTCTTGTCCT[C/T]TTGCACTGGCTCTGT253980
rs72798151snpC/T0.02834060.115616intron-variantKCTD13GRCh38.p716:29922569ACCCTTATGTCCTGG[C/T]TTCACTTTCCAAGCT253980
rs74017650snpC/G0.02094210.100162intron-variantKCTD13, ASPHD1GRCh38.p716:29916645AAGGCTGGAGGACTG[C/G]TTGAGGTCAGGAGTT253980
rs74214105snpG/T00intron-variantKCTD13, ASPHD1GRCh38.p716:29914551TCAAGTGATTCTTCT[G/T]CCTCAGCCTCCAGAG253980
rs74269399in-del-/TTTGintron-variantKCTD13, ASPHD1GRCh38.p716:29913141TTTTTTTTTTTTTTT[-/TTTG]AGACAGGGTCTTGCT253980
rs74579428snpA/T0.50intron-variantKCTD13, ASPHD1GRCh38.p716:29908701TTTTTTTTTTTTTTA[A/T]TCGTTGTTTGTTTGT253980
rs74859909snpC/T0.05923550.161582upstream-variant-2KB, nc-transcript-variantKCTD13, LOC107984836GRCh38.p716:29927100GAGAAGTGTTTTTAT[C/T]TGACCCGATCTGCAT253980
rs74900223in-del-/AATAintron-variantKCTD13, ASPHD1GRCh38.p716:29910114AAAAAAAAAAAAAAA[-/AATA]GGCTGGGGGCAGTGG253980
rs75225650snpA/G/T0.0003992810.0141238intron-variant, utr-variant-3-prime, downstream-variant-500BKCTD13, ASPHD1GRCh38.p716:29905985CCTCCTCTCTACTGC[A/G/T]GGGGTGGGCGGGGGC253980
rs75365923snpG/T00intron-variantKCTD13, ASPHD1GRCh38.p716:29914450CTTTTTTTTTTTTTT[G/T]TTTGAAATGGAGTCT253980
rs75546749snpC/T0.1262190.217206intron-variantKCTD13, ASPHD1GRCh38.p716:29910015GAGGCAGGAGAATCA[C/T]TTGAATCTGGGAGGC253980
rs75549506snpA/T0.0467750.145601intron-variantKCTD13GRCh38.p716:29922418ATAGAACAGAATAAC[A/T]GGCTTTATGTAAAAC253980
rs75599468snpC/T0.1224110.214991intron-variant, utr-variant-3-primeKCTD13GRCh38.p716:29921377GAGTGTGCTGAGCTG[C/T]GTGAGGTGCAGAGGG253980
rs75621288snpA/C0.02639920.111815intron-variantKCTD13GRCh38.p716:29922146TATCTTTTTATAGAA[A/C]TGTTATTTCAGTTAT253980
rs75651136snpC/G0.01466720.084371utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KBKCTD13, LOC107984836GRCh38.p716:29926119GGCCGGCCCCCAGCC[C/G]TTGGGCCAGACCGCT253980
rs75731600in-del-/TTGintron-variantKCTD13, ASPHD1GRCh38.p716:29914452TTTTTTTTTTTTTTT[-/TTG]AAATGGAGTCTTGCT253980
rs76093043snpA/Gintron-variantKCTD13, ASPHD1GRCh38.p716:29913378AAACACAACAGAGCG[A/G]TCAGAAACAGACCAC253980
rs76603667snpC/T0.02872840.116357intron-variant, utr-variant-3-primeKCTD13GRCh38.p716:29921492ATCTGAGCTCTGCTG[C/T]TTCCCAGCTCTTTCA253980
rs77157526snpG/T00intron-variantKCTD13, ASPHD1GRCh38.p716:29914452TTTTTTTTTTTTTTT[G/T]TGAAATGGAGTCTTG253980
rs78022435snpA/G0.0674460.170804upstream-variant-2KB, nc-transcript-variantKCTD13, LOC107984836GRCh38.p716:29927555CAAAATAATTTCACA[A/G]AAAACATCAGACAAG253980
rs78082053snpA/T00intron-variantKCTD13, ASPHD1GRCh38.p716:29908699TTTTTTTTTTTTTTT[A/T]AATCGTTGTTTGTTT253980
rs78248865snpC/T0.1206740.21395intron-variantKCTD13, ASPHD1GRCh38.p716:29916391ACTGTGCCCAGCCAA[C/T]ACTTTTTAACACTCC253980
rs79019231snpA/G0.003985640.0444627intron-variantKCTD13, ASPHD1GRCh38.p716:29918217TGTGTGTCATTGATA[A/G]GTAACTGCCTTAATA253980
rs79442918snpC/T0.06781740.1712intron-variantKCTD13GRCh38.p716:29922395AGGACATTTTTAACA[C/T]TGTAAAAATAGAACA253980
rs79465885snpA/G0.1227580.215196upstream-variant-2KB, nc-transcript-variantKCTD13, LOC107984836GRCh38.p716:29926299AGTGGCCTCGCTGGG[A/G]GATCCCGTAGAGGTT253980
rs79656893snpC/T00intron-variantKCTD13, ASPHD1GRCh38.p716:29914591ATTAGCGGGGGGTGG[C/T]GGTGCACGCCTGTAA253980
rs79786822snpC/T0.001994810.0315187intron-variant, utr-variant-3-primeKCTD13GRCh38.p716:29921678TAGTTTTAACATTAG[C/T]AAATTTAAAACTACA253980
rs79922206snpA/C/G0.02406430.107019intron-variant, nc-transcript-variantKCTD13, ASPHD1GRCh38.p716:29911296TTTGGTGCTCAACAG[A/C/G]GAGCCTCCTCCACCC253980
rs79931750snpG/T0.01230360.0774623intron-variant, utr-variant-3-primeKCTD13GRCh38.p716:29920793CACTGCTCATTATGA[G/T]GATAAAGTATTATAA253980
rs80273739snpA/G0.01859380.0946107intron-variantKCTD13GRCh38.p716:29922580CTGGCTTCACTTTCC[A/G]AGCTCTGCTCCTCAG253980
rs111532054snpA/G00intron-variantKCTD13, ASPHD1GRCh38.p716:29912502CTGGAGTGCAATGGC[A/G]CCATCTCGGCTCACT253980
rs111999248snpC/T0.007955320.062565intron-variant, utr-variant-3-prime, downstream-variant-500BKCTD13, ASPHD1GRCh38.p716:29906014GCGGAGGATGGGAAC[C/T]GGCTAGTGAGCACTG253980
rs112012242snpA/C00intron-variant, downstream-variant-500BKCTD13, ASPHD1GRCh38.p716:29910880ATCTGGCTCCTGCCT[A/C]CTGGTGGTGGGCTCC253980
rs112698693snpC/T0.1206740.21395intron-variantKCTD13, ASPHD1GRCh38.p716:29914527CACTGAAAACTCTGC[C/T]TCCCAGGTTCAAGTG253980
rs112724897snpA/G0.50intron-variantKCTD13, ASPHD1GRCh38.p716:29907490CTCAGTCATACACTT[A/G]AGAAAATATAAACTA253980
rs113539656snpA/G0.004780850.0486577intron-variant, nc-transcript-variantKCTD13, ASPHD1GRCh38.p716:29911415ACCGGGAGCCAGGCC[A/G]CCTCCCCGGGGGTCC253980
rs113565760snpC/T0.50intron-variant, downstream-variant-500BKCTD13, ASPHD1GRCh38.p716:29918559CACTGCAACCTCTGC[C/T]TCCCAGGTTCATATA253980
rs113767385snpA/C0.50intron-variant, synonymous-codon, nc-transcript-variantKCTD13GRCh38.p716:29923154CTTGGGCAGCTCTCC[A/C]AGGAACATAGGCATG253980
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