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Variants search result for Homo sapiens
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12 records found for search term Atp6v1d
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
155978708CV2318141single nucleotide variantNM_015994.4(ATP6V1D):c.89G>A (p.Arg30Gln)not specified [RCV004177552]uncertain significance146735299367352993Humanname
405667313CV3297701single nucleotide variantNM_015994.4(ATP6V1D):c.65G>A (p.Arg22His)not specified [RCV004418779]uncertain significance146735301767353017Humanname
405667318CV3297702single nucleotide variantNM_015994.4(ATP6V1D):c.89G>T (p.Arg30Leu)not specified [RCV004418780]uncertain significance146735299367352993Humanname
401877469CV2790181single nucleotide variantNM_015994.4(ATP6V1D):c.169T>A (p.Leu57Met)not specified [RCV004364105]uncertain significance146735068167350681Humanname
598199542CV3920707single nucleotide variantNM_015994.4(ATP6V1D):c.178G>A (p.Glu60Lys)not specified [RCV005289864]uncertain significance146735067267350672Humanname
155919508CV2360282single nucleotide variantNM_015994.4(ATP6V1D):c.599A>T (p.Tyr200Phe)not specified [RCV004208623]uncertain significance146734044367340443Humanname
401762771CV2720068single nucleotide variantNM_015994.4(ATP6V1D):c.425T>C (p.Val142Ala)not specified [RCV004323640]uncertain significance146734579967345799Humanname
405667289CV3297696single nucleotide variantNM_015994.4(ATP6V1D):c.446C>T (p.Ala149Val)not specified [RCV004418774]uncertain significance146734577867345778Humanname
405667292CV3297697single nucleotide variantNM_015994.4(ATP6V1D):c.484A>G (p.Ile162Val)not specified [RCV004418775]uncertain significance146734341167343411Humanname
405667297CV3297698single nucleotide variantNM_015994.4(ATP6V1D):c.490A>G (p.Ile164Val)not specified [RCV004418776]uncertain significance146734340567343405Humanname
405667303CV3297699single nucleotide variantNM_015994.4(ATP6V1D):c.587G>A (p.Arg196Gln)not specified [RCV004418777]uncertain significance146734045567340455Humanname
405667309CV3297700single nucleotide variantNM_015994.4(ATP6V1D):c.613A>C (p.Ile205Leu)not specified [RCV004418778]uncertain significance146733875267338752Humanname