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11 records found for search term Atp6v1f
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156062675CV2263228single nucleotide variantNM_004231.4(ATP6V1F):c.159-244C>Tnot specified [RCV004131451]uncertain significance7128865133128865133Humanname
156232215CV2245145single nucleotide variantNM_004231.4(ATP6V1F):c.19C>T (p.Leu7Phe)not specified [RCV004106930]uncertain significance7128862923128862923Humanname
401880580CV2780257single nucleotide variantNM_004231.4(ATP6V1F):c.26C>G (p.Ala9Gly)not specified [RCV004355890]uncertain significance7128862930128862930Humanname
597674487CV3620835single nucleotide variantNM_004231.4(ATP6V1F):c.89A>G (p.Lys30Arg)not specified [RCV004882872]uncertain significance7128862993128862993Humanname
156150804CV2197797single nucleotide variantNM_004231.4(ATP6V1F):c.211G>A (p.Ala71Thr)not specified [RCV004077038]uncertain significance7128865429128865429Humanname
156357439CV2318299single nucleotide variantNM_004231.4(ATP6V1F):c.259G>C (p.Ala87Pro)not specified [RCV004179470]uncertain significance7128865477128865477Humanname
329359611CV2461571single nucleotide variantNM_004231.4(ATP6V1F):c.208A>G (p.Ile70Val)not specified [RCV004269754]uncertain significance7128865426128865426Humanname
407528466CV3486977single nucleotide variantNM_004231.4(ATP6V1F):c.161A>T (p.Gln54Leu)not specified [RCV004680397]uncertain significance7128865379128865379Humanname
405667349CV3297708single nucleotide variantNM_004231.4(ATP6V1F):c.344C>T (p.Ala115Val)not specified [RCV004418786]uncertain significance7128865562128865562Humanname
407528448CV3486966single nucleotide variantNM_004231.4(ATP6V1F):c.319C>T (p.Arg107Cys)not specified [RCV004680387]uncertain significance7128865537128865537Humanname
597674393CV3620824single nucleotide variantNM_004231.4(ATP6V1F):c.350A>G (p.Asp117Gly)not specified [RCV004882863]uncertain significance7128865568128865568Humanname