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22 records found for search term Sh3gl3
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8627713CV82857single nucleotide variantNM_003027.4(SH3GL3):c.45+43258G>AMalignant melanoma [RCV000062937]not provided158349083683490836Humanname
8635602CV90824single nucleotide variantNM_003027.4(SH3GL3):c.246G>A (p.Lys82=)Malignant melanoma [RCV000070922]not provided158356858783568587Humanname
401881542CV2783871single nucleotide variantNM_003027.5(SH3GL3):c.89A>G (p.Asp30Gly)not specified [RCV004360767]uncertain significance158355929683559296Humanname
405708958CV3318019single nucleotide variantNM_003027.5(SH3GL3):c.91G>A (p.Asp31Asn)not specified [RCV004448183]uncertain significance158355929883559298Humanname
156119380CV2354055single nucleotide variantNM_003027.5(SH3GL3):c.241G>T (p.Val81Leu)not specified [RCV004204481]uncertain significance158356858283568582Humanname
401877801CV2786797single nucleotide variantNM_003027.5(SH3GL3):c.119T>C (p.Ile40Thr)not specified [RCV004365964]uncertain significance158356513883565138Humanname
156073732CV2230009single nucleotide variantNM_003027.5(SH3GL3):c.791C>G (p.Ser264Cys)not specified [RCV004105814]uncertain significance158358872483588724Humanname
155999912CV2296252single nucleotide variantNM_003027.5(SH3GL3):c.557C>T (p.Ala186Val)not specified [RCV004154159]uncertain significance158357667483576674Humanname
156265363CV2372193single nucleotide variantNM_003027.5(SH3GL3):c.764A>G (p.Tyr255Cys)not specified [RCV004216973]uncertain significance158358869783588697Humanname
156137620CV2375790single nucleotide variantNM_003027.5(SH3GL3):c.410A>T (p.Gln137Leu)not specified [RCV004224375]uncertain significance158357264383572643Humanname
401748931CV2694535single nucleotide variantNM_003027.5(SH3GL3):c.667T>A (p.Leu223Ile)not specified [RCV004298666]uncertain significance158358702583587025Humanname
401767602CV2729783single nucleotide variantNM_003027.5(SH3GL3):c.844A>G (p.Asn282Asp)not specified [RCV004332799]uncertain significance158361808783618087Humanname
405708949CV3318018single nucleotide variantNM_003027.5(SH3GL3):c.314G>A (p.Gly105Glu)not specified [RCV004448182]uncertain significance158356865583568655Humanname
405708962CV3318020single nucleotide variantNM_003027.5(SH3GL3):c.978G>T (p.Met326Ile)not specified [RCV004448184]uncertain significance158361822183618221Humanname
597696485CV3606115single nucleotide variantNM_003027.5(SH3GL3):c.535C>T (p.Pro179Ser)not specified [RCV004859409]uncertain significance158357665283576652Humanname
597696495CV3606116single nucleotide variantNM_003027.5(SH3GL3):c.310C>G (p.Leu104Val)not specified [RCV004859410]uncertain significance158356865183568651Humanname
597696504CV3606117single nucleotide variantNM_003027.5(SH3GL3):c.841T>C (p.Ser281Pro)not specified [RCV004859411]uncertain significance158361808483618084Humanname
597696511CV3606118single nucleotide variantNM_003027.5(SH3GL3):c.458A>T (p.Glu153Val)not specified [RCV004859412]uncertain significance158357269183572691Humanname
597696527CV3606120single nucleotide variantNM_003027.5(SH3GL3):c.863C>A (p.Pro288His)not specified [RCV004859414]uncertain significance158361810683618106Humanname
597696537CV3606121single nucleotide variantNM_003027.5(SH3GL3):c.599G>T (p.Ser200Ile)not specified [RCV004859415]uncertain significance158357671683576716Humanname
21074661CV797207single nucleotide variantNM_003027.5(SH3GL3):c.974G>A (p.Gly325Glu)not provided [RCV000995408]uncertain significance158361821783618217Humanname
155972923CV2224474single nucleotide variantNM_003027.5(SH3GL3):c.1027G>T (p.Val343Leu)not specified [RCV004098069]uncertain significance158361827083618270Humanname