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Variants search result for Homo sapiens
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29 records found for search term Kctd13
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405291605CV3205906single nucleotide variantNM_178863.5(KCTD13):c.-4C>TKCTD13-related disorder [RCV003964020]likely benign162992603729926037Humanname , trait , alternate_id
156277229CV2230679single nucleotide variantNM_178863.5(KCTD13):c.75G>C (p.Glu25Asp)not specified [RCV004097627]uncertain significance162992595929925959Humanname
329368143CV2424198single nucleotide variantNM_178863.5(KCTD13):c.73G>C (p.Glu25Gln)not specified [RCV004250325]uncertain significance162992596129925961Humanname
329378254CV2446909single nucleotide variantNM_178863.5(KCTD13):c.49G>A (p.Glu17Lys)not specified [RCV004257755]uncertain significance162992598529925985Humanname
405286980CV3193099single nucleotide variantNM_178863.5(KCTD13):c.378G>A (p.Val126=)KCTD13-related disorder [RCV003981753]likely benign162992322629923226Humanname , trait , alternate_id
405275465CV3196347single nucleotide variantNM_178863.5(KCTD13):c.681C>T (p.Tyr227=)KCTD13-related disorder [RCV003974196]likely benign162991105029911050Humanname , trait , alternate_id
408367707CV3513286single nucleotide variantNM_178863.5(KCTD13):c.64T>G (p.Ser22Ala)KCTD13-related disorder [RCV004759161]|not specified [RCV005363349]uncertain significance162992597029925970Human1name , trait , alternate_id
597796681CV3694901single nucleotide variantNM_178863.5(KCTD13):c.52G>A (p.Ala18Thr)not specified [RCV004935547]uncertain significance162992598229925982Humanname
156197057CV2400697single nucleotide variantNM_178863.5(KCTD13):c.205A>C (p.Met69Leu)not specified [RCV004242370]uncertain significance162992582929925829Humanname
329387306CV2436374single nucleotide variantNM_178863.5(KCTD13):c.268G>A (p.Gly90Ser)not specified [RCV004251769]uncertain significance162992333629923336Humanname
329361455CV2447140single nucleotide variantNM_178863.5(KCTD13):c.289C>T (p.Leu97Phe)not specified [RCV004260403]uncertain significance162992331529923315Humanname
401883399CV2757908single nucleotide variantNM_178863.5(KCTD13):c.293A>G (p.Asn98Ser)not specified [RCV004337045]uncertain significance162992331129923311Humanname
407516750CV3445231single nucleotide variantNM_178863.5(KCTD13):c.271C>T (p.Arg91Cys)not specified [RCV004628299]uncertain significance162992333329923333Humanname
407516761CV3445234single nucleotide variantNM_178863.5(KCTD13):c.195G>A (p.Met65Ile)not specified [RCV004628302]uncertain significance162992583929925839Humanname
598270258CV3976398single nucleotide variantNM_178863.5(KCTD13):c.193A>G (p.Met65Val)not specified [RCV005350068]uncertain significance162992584129925841Humanname
156200281CV2256067single nucleotide variantNM_178863.5(KCTD13):c.911G>A (p.Arg304His)not specified [RCV004116363]uncertain significance162990695129906951Humanname
156169187CV2276710single nucleotide variantNM_178863.5(KCTD13):c.332C>T (p.Thr111Met)not specified [RCV004146503]uncertain significance162992327229923272Humanname
156255809CV2277535single nucleotide variantNM_178863.5(KCTD13):c.386T>G (p.Leu129Arg)not specified [RCV004145224]uncertain significance162992321829923218Humanname
155969731CV2309104single nucleotide variantNM_178863.5(KCTD13):c.393G>T (p.Glu131Asp)not specified [RCV004171464]uncertain significance162992321129923211Humanname
401885828CV2774560single nucleotide variantNM_178863.5(KCTD13):c.815C>T (p.Pro272Leu)not specified [RCV004350040]uncertain significance162990704729907047Humanname
405812325CV3265153single nucleotide variantNM_178863.5(KCTD13):c.591G>C (p.Glu197Asp)not specified [RCV004408893]uncertain significance162991114029911140Humanname
407516753CV3445232single nucleotide variantNM_178863.5(KCTD13):c.824C>T (p.Pro275Leu)not specified [RCV004628300]uncertain significance162990703829907038Humanname
597796678CV3694900single nucleotide variantNM_178863.5(KCTD13):c.959C>T (p.Pro320Leu)not specified [RCV004935546]uncertain significance162990690329906903Humanname
597796684CV3694902single nucleotide variantNM_178863.5(KCTD13):c.371A>T (p.Tyr124Phe)not specified [RCV004935548]uncertain significance162992323329923233Humanname
597796687CV3694903single nucleotide variantNM_178863.5(KCTD13):c.589G>A (p.Glu197Lys)not specified [RCV004935549]uncertain significance162991114229911142Humanname
597796690CV3694904single nucleotide variantNM_178863.5(KCTD13):c.958C>T (p.Pro320Ser)not specified [RCV004935550]uncertain significance162990690429906904Humanname
598235894CV3976395single nucleotide variantNM_178863.5(KCTD13):c.887A>T (p.Glu296Val)not specified [RCV005363745]uncertain significance162990697529906975Humanname
598235899CV3976397single nucleotide variantNM_178863.5(KCTD13):c.881G>T (p.Arg294Leu)not specified [RCV005363746]uncertain significance162990698129906981Humanname
152981531CV1676856deletionNM_178863.5(KCTD13):c.790del (p.Thr263_Leu264insTer)not specified [RCV002247923]uncertain significance162990707229907072Humanname