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Variants search result for Homo sapiens
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28 records found for search term Kctd12
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401881438CV2759415single nucleotide variantNM_138444.4(KCTD12):c.22C>G (p.Arg8Gly)not specified [RCV004338415]uncertain significance137688612776886127Humanname
15169366CV713972single nucleotide variantNM_138444.4(KCTD12):c.261C>T (p.Phe87=)not provided [RCV000971797]benign137688588876885888Humanname
15152029CV713973single nucleotide variantNM_138444.4(KCTD12):c.204G>A (p.Gln68=)not provided [RCV000968267]benign137688594576885945Humanname
405812320CV3265151single nucleotide variantNM_138444.4(KCTD12):c.73T>A (p.Ser25Thr)not specified [RCV004408891]uncertain significance137688607676886076Humanname
407516746CV3445230single nucleotide variantNM_138444.4(KCTD12):c.64T>A (p.Ser22Thr)not specified [RCV004628298]uncertain significance137688608576886085Humanname
597796657CV3694892single nucleotide variantNM_138444.4(KCTD12):c.74C>T (p.Ser25Phe)not specified [RCV004935539]uncertain significance137688607576886075Humanname
401881435CV2759414single nucleotide variantNM_138444.4(KCTD12):c.227G>A (p.Ser76Asn)not specified [RCV004338414]uncertain significance137688592276885922Humanname
407516725CV3445225single nucleotide variantNM_138444.4(KCTD12):c.188T>C (p.Met63Thr)not specified [RCV004628293]uncertain significance137688596176885961Humanname
407516729CV3445226single nucleotide variantNM_138444.4(KCTD12):c.196C>G (p.Gln66Glu)not specified [RCV004628294]uncertain significance137688595376885953Humanname
407516734CV3445227single nucleotide variantNM_138444.4(KCTD12):c.185G>T (p.Arg62Leu)not specified [RCV004628295]uncertain significance137688596476885964Humanname
407516742CV3445229single nucleotide variantNM_138444.4(KCTD12):c.157G>A (p.Val53Met)not specified [RCV004628297]uncertain significance137688599276885992Humanname
156236742CV2193503single nucleotide variantNM_138444.4(KCTD12):c.457G>A (p.Gly153Ser)not specified [RCV004072984]uncertain significance137688569276885692Humanname
156258482CV2322150single nucleotide variantNM_138444.4(KCTD12):c.596A>T (p.Gln199Leu)not specified [RCV004175934]uncertain significance137688555376885553Humanname
156151459CV2369171single nucleotide variantNM_138444.4(KCTD12):c.669C>A (p.Asp223Glu)not specified [RCV004208095]uncertain significance137688548076885480Humanname
329374078CV2452827single nucleotide variantNM_138444.4(KCTD12):c.873G>A (p.Met291Ile)not specified [RCV004275358]uncertain significance137688527676885276Humanname
401729015CV2729964single nucleotide variantNM_138444.4(KCTD12):c.859T>G (p.Ser287Ala)not specified [RCV004332956]uncertain significance137688529076885290Humanname
405812314CV3265148single nucleotide variantNM_138444.4(KCTD12):c.606C>G (p.Asp202Glu)not specified [RCV004408888]uncertain significance137688554376885543Humanname
405812316CV3265149single nucleotide variantNM_138444.4(KCTD12):c.636C>G (p.Ile212Met)not specified [RCV004408889]uncertain significance137688551376885513Humanname
405812318CV3265150single nucleotide variantNM_138444.4(KCTD12):c.681C>G (p.Asp227Glu)not specified [RCV004408890]uncertain significance137688546876885468Humanname
405812322CV3265152single nucleotide variantNM_138444.4(KCTD12):c.782G>T (p.Arg261Leu)not specified [RCV004408892]uncertain significance137688536776885367Humanname
407516739CV3445228single nucleotide variantNM_138444.4(KCTD12):c.556C>G (p.Pro186Ala)not specified [RCV004628296]uncertain significance137688559376885593Humanname
597796660CV3694893single nucleotide variantNM_138444.4(KCTD12):c.571G>T (p.Ala191Ser)not specified [RCV004935540]uncertain significance137688557876885578Humanname
597796663CV3694894single nucleotide variantNM_138444.4(KCTD12):c.361G>A (p.Glu121Lys)not specified [RCV004935541]uncertain significance137688578876885788Humanname
597796666CV3694896single nucleotide variantNM_138444.4(KCTD12):c.410C>T (p.Pro137Leu)not specified [RCV004935542]uncertain significance137688573976885739Humanname
597796669CV3694897single nucleotide variantNM_138444.4(KCTD12):c.607G>A (p.Gly203Ser)not specified [RCV004935543]uncertain significance137688554276885542Humanname
597796672CV3694898single nucleotide variantNM_138444.4(KCTD12):c.447G>C (p.Glu149Asp)not specified [RCV004935544]uncertain significance137688570276885702Humanname
597796675CV3694899single nucleotide variantNM_138444.4(KCTD12):c.932A>G (p.Asp311Gly)not specified [RCV004935545]uncertain significance137688521776885217Humanname
598213243CV3976394single nucleotide variantNM_138444.4(KCTD12):c.425C>G (p.Ser142Trp)not specified [RCV005358960]uncertain significance137688572476885724Humanname