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39 records found for search term Sh3yl1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405729740CV3318206single nucleotide variantNM_015677.4(SH3YL1):c.5A>G (p.Asn2Ser)not specified [RCV004450848]uncertain significance2253112253112Humanname
155901572CV2345831single nucleotide variantNM_015677.4(SH3YL1):c.228A>C (p.Lys76Asn)not specified [RCV004198877]uncertain significance2247601247601Humanname
329379509CV2443439single nucleotide variantNM_015677.4(SH3YL1):c.104T>A (p.Ile35Asn)not specified [RCV004262279]uncertain significance2253013253013Humanname
401872185CV2754294single nucleotide variantNM_015677.4(SH3YL1):c.209C>T (p.Ala70Val)not specified [RCV004334472]uncertain significance2249748249748Humanname
405729678CV3318198single nucleotide variantNM_015677.4(SH3YL1):c.118G>A (p.Val40Ile)not specified [RCV004450840]uncertain significance2249839249839Humanname
407469349CV3480400single nucleotide variantNM_015677.4(SH3YL1):c.211C>T (p.Arg71Cys)not specified [RCV004661447]uncertain significance2249746249746Humanname
597697501CV3602367single nucleotide variantNM_015677.4(SH3YL1):c.212G>A (p.Arg71His)not specified [RCV004859523]uncertain significance2249745249745Humanname
598240978CV3917926single nucleotide variantNM_015677.4(SH3YL1):c.103A>T (p.Ile35Phe)not specified [RCV005276268]uncertain significance2253014253014Humanname
156132594CV2195891single nucleotide variantNM_015677.4(SH3YL1):c.869C>T (p.Ala290Val)not specified [RCV004072155]uncertain significance2218971218971Humanname
156315717CV2250812single nucleotide variantNM_015677.4(SH3YL1):c.938T>C (p.Ile313Thr)not specified [RCV004129672]uncertain significance2218902218902Humanname
156020814CV2264396single nucleotide variantNM_015677.4(SH3YL1):c.601G>A (p.Glu201Lys)not specified [RCV004138297]uncertain significance2231124231124Humanname
156250594CV2273306single nucleotide variantNM_015677.4(SH3YL1):c.589C>A (p.Pro197Thr)not specified [RCV004132098]uncertain significance2231136231136Humanname
156283685CV2334699single nucleotide variantNM_015677.4(SH3YL1):c.452C>T (p.Thr151Met)not specified [RCV004188681]uncertain significance2233182233182Humanname
156280360CV2348442single nucleotide variantNM_015677.4(SH3YL1):c.610T>C (p.Tyr204His)not specified [RCV004193632]uncertain significance2231115231115Humanname
156345893CV2356412single nucleotide variantNM_015677.4(SH3YL1):c.659G>A (p.Arg220Gln)not specified [RCV004206213]uncertain significance2231066231066Humanname
155962511CV2388249single nucleotide variantNM_015677.4(SH3YL1):c.598G>A (p.Ala200Thr)not specified [RCV004234707]uncertain significance2231127231127Humanname
329386592CV2456116single nucleotide variantNM_015677.4(SH3YL1):c.858A>G (p.Ile286Met)not specified [RCV004273007]uncertain significance2218982218982Humanname
329353377CV2469022single nucleotide variantNM_015677.4(SH3YL1):c.325C>T (p.Arg109Cys)not specified [RCV004274272]uncertain significance2234239234239Humanname
401722451CV2703372single nucleotide variantNM_015677.4(SH3YL1):c.586C>T (p.Arg196Trp)not specified [RCV004315717]uncertain significance2231139231139Humanname
401718412CV2708265single nucleotide variantNM_015677.4(SH3YL1):c.451A>C (p.Thr151Pro)not specified [RCV004311607]uncertain significance2233183233183Humanname
401750963CV2715824single nucleotide variantNM_015677.4(SH3YL1):c.952T>C (p.Ser318Pro)not specified [RCV004328946]uncertain significance2218888218888Humanname
401876959CV2793297single nucleotide variantNM_015677.4(SH3YL1):c.405G>T (p.Arg135Ser)not specified [RCV004362118]uncertain significance2233229233229Humanname
405729682CV3318199single nucleotide variantNM_015677.4(SH3YL1):c.367G>A (p.Gly123Arg)not specified [RCV004450841]uncertain significance2234197234197Humanname
405729694CV3318200single nucleotide variantNM_015677.4(SH3YL1):c.419A>C (p.Asn140Thr)not specified [RCV004450842]uncertain significance2233215233215Humanname
405729712CV3318202single nucleotide variantNM_015677.4(SH3YL1):c.421G>T (p.Val141Leu)not specified [RCV004450844]uncertain significance2233213233213Humanname
405729718CV3318203single nucleotide variantNM_015677.4(SH3YL1):c.564C>A (p.Asp188Glu)not specified [RCV004450845]uncertain significance2231161231161Humanname
405729725CV3318204single nucleotide variantNM_015677.4(SH3YL1):c.581C>T (p.Thr194Ile)not specified [RCV004450846]likely benign2231144231144Humanname
405729733CV3318205single nucleotide variantNM_015677.4(SH3YL1):c.587G>A (p.Arg196Gln)not specified [RCV004450847]uncertain significance2231138231138Humanname
405729755CV3318208single nucleotide variantNM_015677.4(SH3YL1):c.736C>T (p.Pro246Ser)not specified [RCV004450850]uncertain significance2230011230011Humanname
405729762CV3318209single nucleotide variantNM_015677.4(SH3YL1):c.856A>G (p.Ile286Val)not specified [RCV004450851]uncertain significance2218984218984Humanname
407469352CV3480401single nucleotide variantNM_015677.4(SH3YL1):c.764T>A (p.Leu255Gln)not specified [RCV004661448]uncertain significance2229983229983Humanname
407469355CV3480402single nucleotide variantNM_015677.4(SH3YL1):c.434G>A (p.Ser145Asn)not specified [RCV004661449]uncertain significance2233200233200Humanname
597697510CV3602368single nucleotide variantNM_015677.4(SH3YL1):c.554G>A (p.Arg185Gln)not specified [RCV004859524]uncertain significance2231171231171Humanname
597697520CV3602369single nucleotide variantNM_015677.4(SH3YL1):c.703G>C (p.Ala235Pro)not specified [RCV004859525]uncertain significance2230044230044Humanname
598240957CV3917922single nucleotide variantNM_015677.4(SH3YL1):c.326G>A (p.Arg109His)not specified [RCV005276265]uncertain significance2234238234238Humanname
598240965CV3917923single nucleotide variantNM_015677.4(SH3YL1):c.985G>A (p.Gly329Ser)not specified [RCV005276266]uncertain significance2218855218855Humanname
598240972CV3917924single nucleotide variantNM_015677.4(SH3YL1):c.970G>A (p.Glu324Lys)not specified [RCV005276267]uncertain significance2218870218870Humanname
598199099CV3917925single nucleotide variantNM_015677.4(SH3YL1):c.501C>G (p.Ser167Arg)not specified [RCV005268346]uncertain significance2233133233133Humanname
407493093CV3480403single nucleotide variantNM_015677.4(SH3YL1):c.1021A>G (p.Met341Val)not specified [RCV004667292]uncertain significance2218819218819Humanname