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25 records found for search term Pga5
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8627082CV82226single nucleotide variantNM_014224.3(PGA5):c.762C>T (p.Ile254=)Malignant melanoma [RCV000062305]not provided116124852461248524Humanname
156268239CV2198887single nucleotide variantNM_014224.5(PGA5):c.799G>A (p.Ala267Thr)not specified [RCV004077922]uncertain significance116124969461249694Humanname
156249941CV2199605single nucleotide variantNM_014224.5(PGA5):c.754T>C (p.Trp252Arg)not specified [RCV004072352]uncertain significance116124851661248516Humanname
156243151CV2210851single nucleotide variantNM_014224.5(PGA5):c.884G>A (p.Ser295Asn)not specified [RCV004085938]uncertain significance116124977961249779Humanname
156400768CV2217152single nucleotide variantNM_014224.5(PGA5):c.815G>T (p.Cys272Phe)not specified [RCV004085822]uncertain significance116124971061249710Humanname
156235164CV2224022single nucleotide variantNM_014224.5(PGA5):c.856C>G (p.Pro286Ala)not specified [RCV004095898]uncertain significance116124975161249751Humanname
329351724CV2459327single nucleotide variantNM_014224.5(PGA5):c.958A>G (p.Ile320Val)not specified [RCV004274742]uncertain significance116124995561249955Humanname
401741972CV2676865single nucleotide variantNM_014224.5(PGA5):c.658G>A (p.Asp220Asn)not specified [RCV004291030]likely benign116124842061248420Humanname
401770130CV2719050single nucleotide variantNM_014224.5(PGA5):c.766G>A (p.Val256Met)not specified [RCV004322629]uncertain significance116124852861248528Humanname
401928931CV2816665single nucleotide variantNM_014224.5(PGA5):c.664A>C (p.Lys222Gln)not provided [RCV003390065]likely benign116124842661248426Humanname
405746570CV3368583single nucleotide variantNM_014224.5(PGA5):c.745G>A (p.Glu249Lys)not specified [RCV004498481]uncertain significance116124850761248507Humanname
405746587CV3368585single nucleotide variantNM_014224.5(PGA5):c.916G>A (p.Asp306Asn)not specified [RCV004498483]uncertain significance116124981161249811Humanname
407464240CV3466854single nucleotide variantNM_014224.5(PGA5):c.742G>A (p.Val248Ile)not specified [RCV004659899]uncertain significance116124850461248504Humanname
407528929CV3466855single nucleotide variantNM_014224.5(PGA5):c.671G>T (p.Gly224Val)not specified [RCV004655779]uncertain significance116124843361248433Humanname
597725054CV3575861single nucleotide variantNM_014224.5(PGA5):c.835G>A (p.Gly279Ser)not specified [RCV004842256]uncertain significance116124973061249730Humanname
597725064CV3575863single nucleotide variantNM_014224.5(PGA5):c.853G>A (p.Gly285Ser)not specified [RCV004842257]uncertain significance116124974861249748Humanname
597725072CV3575866single nucleotide variantNM_014224.5(PGA5):c.958A>C (p.Ile320Leu)not specified [RCV004842258]uncertain significance116124995561249955Humanname
598262235CV3999765single nucleotide variantNM_014224.5(PGA5):c.695T>C (p.Ile232Thr)not specified [RCV005387048]uncertain significance116124845761248457Humanname
401882838CV2775121single nucleotide variantNM_014224.5(PGA5):c.1015C>A (p.Gln339Lys)not specified [RCV004346481]uncertain significance116125001261250012Humanname
401857705CV2777723single nucleotide variantNM_014224.5(PGA5):c.1136A>C (p.Asn379Thr)not specified [RCV004345558]uncertain significance116125125061251250Humanname
597766707CV3575862single nucleotide variantNM_014224.5(PGA5):c.1126G>A (p.Asp376Asn)not specified [RCV004850321]uncertain significance116125124061251240Humanname
597766712CV3575864single nucleotide variantNM_014224.5(PGA5):c.1069T>C (p.Ser357Pro)not specified [RCV004850322]uncertain significance116125118361251183Humanname
597766717CV3575865single nucleotide variantNM_014224.5(PGA5):c.1012C>A (p.Leu338Met)not specified [RCV004850323]uncertain significance116125000961250009Humanname
598262240CV3999766single nucleotide variantNM_014224.5(PGA5):c.1148G>C (p.Gly383Ala)not specified [RCV005387049]uncertain significance116125126261251262Humanname
598262245CV3999767single nucleotide variantNM_014224.5(PGA5):c.1126G>C (p.Asp376His)not specified [RCV005387050]uncertain significance116125124061251240Humanname