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Variants search result for Homo sapiens
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27 records found for search term Kcng3
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8630357CV85512single nucleotide variantNM_133329.5(KCNG3):c.666-1G>AMalignant melanoma [RCV000065595]not provided24244458042444580Humanname
329371311CV2458073single nucleotide variantNM_133329.6(KCNG3):c.169G>C (p.Glu57Gln)not specified [RCV004271902]uncertain significance24249333342493333Humanname
405806435CV3268558single nucleotide variantNM_133329.6(KCNG3):c.172C>T (p.Arg58Cys)not specified [RCV004406072]uncertain significance24249333042493330Humanname
407467966CV3444986single nucleotide variantNM_133329.6(KCNG3):c.156C>G (p.Asp52Glu)not specified [RCV004636090]uncertain significance24249334642493346Humanname
597787774CV3687392single nucleotide variantNM_133329.6(KCNG3):c.193C>T (p.Arg65Trp)not specified [RCV004932583]uncertain significance24249330942493309Humanname
598212858CV3980249single nucleotide variantNM_133329.6(KCNG3):c.173G>T (p.Arg58Leu)not specified [RCV005358890]uncertain significance24249332942493329Humanname
156384697CV2231161single nucleotide variantNM_133329.6(KCNG3):c.697A>G (p.Thr233Ala)not specified [RCV004094369]uncertain significance24244454842444548Humanname
156223238CV2232935single nucleotide variantNM_133329.6(KCNG3):c.632G>A (p.Arg211Lys)not specified [RCV004103316]uncertain significance24249287042492870Humanname
156293751CV2233574single nucleotide variantNM_133329.6(KCNG3):c.362C>T (p.Ser121Phe)not specified [RCV004100049]uncertain significance24249314042493140Humanname
156171390CV2400676single nucleotide variantNM_133329.6(KCNG3):c.437A>C (p.Glu146Ala)not specified [RCV004242352]uncertain significance24249306542493065Humanname
405806437CV3268559single nucleotide variantNM_133329.6(KCNG3):c.417G>C (p.Glu139Asp)not specified [RCV004406073]uncertain significance24249308542493085Humanname
405806441CV3268561single nucleotide variantNM_133329.6(KCNG3):c.445C>T (p.Pro149Ser)not specified [RCV004406075]uncertain significance24249305742493057Humanname
405806443CV3268562single nucleotide variantNM_133329.6(KCNG3):c.483C>G (p.Phe161Leu)not specified [RCV004406076]uncertain significance24249301942493019Humanname
405806445CV3268563single nucleotide variantNM_133329.6(KCNG3):c.752A>G (p.Lys251Arg)not specified [RCV004406077]uncertain significance24244449342444493Humanname
407467964CV3444985single nucleotide variantNM_133329.6(KCNG3):c.626G>A (p.Arg209Gln)not specified [RCV004636089]uncertain significance24249287642492876Humanname
407467970CV3444988single nucleotide variantNM_133329.6(KCNG3):c.427G>T (p.Gly143Cys)not specified [RCV004636092]uncertain significance24249307542493075Humanname
407467972CV3444989single nucleotide variantNM_133329.6(KCNG3):c.395C>G (p.Pro132Arg)not specified [RCV004636093]uncertain significance24249310742493107Humanname
597787761CV3687389single nucleotide variantNM_133329.6(KCNG3):c.524G>C (p.Ser175Thr)not specified [RCV004932580]uncertain significance24249297842492978Humanname
597787769CV3687391single nucleotide variantNM_133329.6(KCNG3):c.407G>A (p.Gly136Asp)not specified [RCV004932582]uncertain significance24249309542493095Humanname
597787778CV3687393single nucleotide variantNM_133329.6(KCNG3):c.436G>A (p.Glu146Lys)not specified [RCV004932584]uncertain significance24249306642493066Humanname
597787878CV3687394single nucleotide variantNM_133329.6(KCNG3):c.523A>G (p.Ser175Gly)not specified [RCV004932585]uncertain significance24249297942492979Humanname
597787882CV3687395single nucleotide variantNM_133329.6(KCNG3):c.424C>T (p.Pro142Ser)not specified [RCV004932586]uncertain significance24249307842493078Humanname
598259550CV3980245single nucleotide variantNM_133329.6(KCNG3):c.664G>C (p.Gly222Arg)not specified [RCV005347450]uncertain significance24249283842492838Humanname
598234940CV3980246single nucleotide variantNM_133329.6(KCNG3):c.407G>T (p.Gly136Val)not specified [RCV005363585]uncertain significance24249309542493095Humanname
401750286CV2696005single nucleotide variantNM_133329.6(KCNG3):c.1111A>G (p.Met371Val)not specified [RCV004308264]uncertain significance24244413442444134Humanname
597787767CV3687390single nucleotide variantNM_133329.6(KCNG3):c.1022C>T (p.Ser341Phe)not specified [RCV004932581]uncertain significance24244422342444223Humanname
598212852CV3980247single nucleotide variantNM_133329.6(KCNG3):c.1174G>A (p.Val392Ile)not specified [RCV005358889]uncertain significance24244407142444071Humanname