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Variants search result for Homo sapiens
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19 records found for search term Sfn
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156197879CV2357748single nucleotide variantNM_006142.5(SFN):c.94A>G (p.Lys32Glu)not specified [RCV004205042]uncertain significance12686330626863306Humanname
401880258CV2766179single nucleotide variantNM_006142.5(SFN):c.58G>A (p.Glu20Lys)not specified [RCV004340622]uncertain significance12686327026863270Humanname
405763787CV3321481single nucleotide variantNM_006142.5(SFN):c.91G>C (p.Glu31Gln)not specified [RCV004455773]uncertain significance12686330326863303Humanname
156330223CV2210574single nucleotide variantNM_006142.5(SFN):c.245G>A (p.Arg82His)not specified [RCV004083729]uncertain significance12686345726863457Humanname
597673345CV3595582single nucleotide variantNM_006142.5(SFN):c.233G>T (p.Gly78Val)not specified [RCV004856546]uncertain significance12686344526863445Humanname
597673319CV3595585single nucleotide variantNM_006142.5(SFN):c.226G>C (p.Glu76Gln)not specified [RCV004856549]uncertain significance12686343826863438Humanname
598198424CV3921118single nucleotide variantNM_006142.5(SFN):c.177G>T (p.Trp59Cys)not specified [RCV005268247]uncertain significance12686338926863389Humanname
156183915CV2222443single nucleotide variantNM_006142.5(SFN):c.482A>G (p.Glu161Gly)not specified [RCV004099297]uncertain significance12686369426863694Humanname
156001761CV2257891single nucleotide variantNM_006142.5(SFN):c.740A>G (p.Gln247Arg)not specified [RCV004129717]uncertain significance12686395226863952Humanname
156277031CV2276938single nucleotide variantNM_006142.5(SFN):c.715G>C (p.Gly239Arg)not specified [RCV004140272]uncertain significance12686392726863927Humanname
156274198CV2344204single nucleotide variantNM_006142.5(SFN):c.328G>A (p.Glu110Lys)not specified [RCV004197844]uncertain significance12686354026863540Humanname
329390598CV2437110single nucleotide variantNM_006142.5(SFN):c.536T>A (p.Phe179Tyr)not specified [RCV004262917]uncertain significance12686374826863748Humanname
401732467CV2675091single nucleotide variantNM_006142.5(SFN):c.512G>T (p.Gly171Val)not specified [RCV004289872]uncertain significance12686372426863724Humanname
405763769CV3321478single nucleotide variantNM_006142.5(SFN):c.350G>A (p.Arg117Gln)not specified [RCV004455770]uncertain significance12686356226863562Humanname
405763775CV3321479single nucleotide variantNM_006142.5(SFN):c.677A>G (p.Asn226Ser)not specified [RCV004455771]uncertain significance12686388926863889Humanname
405763780CV3321480single nucleotide variantNM_006142.5(SFN):c.707G>A (p.Gly236Glu)not specified [RCV004455772]uncertain significance12686391926863919Humanname
407489864CV3484010single nucleotide variantNM_006142.5(SFN):c.311A>T (p.Asp104Val)not specified [RCV004666176]uncertain significance12686352326863523Humanname
597673336CV3595583single nucleotide variantNM_006142.5(SFN):c.488C>T (p.Pro163Leu)not specified [RCV004856547]uncertain significance12686370026863700Humanname
597673327CV3595584single nucleotide variantNM_006142.5(SFN):c.598G>C (p.Glu200Gln)not specified [RCV004856548]uncertain significance12686381026863810Humanname