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19 records found for search term Rasl12
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401775332CV2710524single nucleotide variantNM_016563.4(RASL12):c.23C>T (p.Pro8Leu)not specified [RCV004319451]uncertain significance156506781365067813Humanname
156184226CV2324568single nucleotide variantNM_016563.4(RASL12):c.56T>A (p.Leu19His)not specified [RCV004179329]uncertain significance156506778065067780Humanname
598185109CV3902256single nucleotide variantNM_016563.4(RASL12):c.41C>T (p.Pro14Leu)not specified [RCV005265859]uncertain significance156506779565067795Humanname
8635534CV90755single nucleotide variantNM_016563.2(RASL12):c.408G>A (p.Leu136=)Malignant melanoma [RCV000070853]not provided156505844465058444Humanname
401752915CV2682979single nucleotide variantNM_016563.4(RASL12):c.245G>A (p.Arg82Lys)not specified [RCV004283768]uncertain significance156505860765058607Humanname
407500917CV3468632single nucleotide variantNM_016563.4(RASL12):c.132G>T (p.Arg44Ser)not specified [RCV004669656]uncertain significance156506524565065245Humanname
597784222CV3589317single nucleotide variantNM_016563.4(RASL12):c.244A>G (p.Arg82Gly)not specified [RCV004854427]uncertain significance156505860865058608Humanname
597707007CV3589318single nucleotide variantNM_016563.4(RASL12):c.178G>A (p.Glu60Lys)not specified [RCV004860564]uncertain significance156505940165059401Humanname
156295488CV2233736single nucleotide variantNM_016563.4(RASL12):c.301G>T (p.Asp101Tyr)not specified [RCV004100181]uncertain significance156505855165058551Humanname
155996229CV2250436single nucleotide variantNM_016563.4(RASL12):c.603G>C (p.Glu201Asp)not specified [RCV004127306]uncertain significance156505509765055097Humanname
155974759CV2318046single nucleotide variantNM_016563.4(RASL12):c.305G>A (p.Ser102Asn)not specified [RCV004177149]uncertain significance156505854765058547Humanname
156069147CV2356983single nucleotide variantNM_016563.4(RASL12):c.679A>G (p.Ile227Val)not specified [RCV004204348]likely benign156505502165055021Humanname
405660184CV3312458single nucleotide variantNM_016563.4(RASL12):c.374G>A (p.Arg125His)not specified [RCV004438778]uncertain significance156505847865058478Humanname
407467027CV3468633single nucleotide variantNM_016563.4(RASL12):c.414G>A (p.Met138Ile)not specified [RCV004660616]uncertain significance156505843865058438Humanname
597784214CV3589313single nucleotide variantNM_016563.4(RASL12):c.598G>A (p.Glu200Lys)not specified [RCV004854425]uncertain significance156505510265055102Humanname
597784218CV3589314single nucleotide variantNM_016563.4(RASL12):c.626C>T (p.Pro209Leu)not specified [RCV004854426]uncertain significance156505507465055074Humanname
597706997CV3589316single nucleotide variantNM_016563.4(RASL12):c.602A>G (p.Glu201Gly)not specified [RCV004860563]uncertain significance156505509865055098Humanname
598185096CV3902254single nucleotide variantNM_016563.4(RASL12):c.620A>C (p.Gln207Pro)not specified [RCV005265857]uncertain significance156505508065055080Humanname
598185102CV3902255single nucleotide variantNM_016563.4(RASL12):c.727G>A (p.Val243Met)not specified [RCV005265858]uncertain significance156505497365054973Humanname