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Variants search result for Homo sapiens
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37 records found for search term Znf250
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
155904888CV2298888single nucleotide variantNM_001109689.4(ZNF250):c.43-6T>Gnot specified [RCV004156428]uncertain significance8144890065144890065Humanname
8632912CV88127single nucleotide variantNM_001109689.3(ZNF250):c.42+57C>TMalignant melanoma [RCV000068219]not provided8144890251144890251Humanname
156145807CV2292558single nucleotide variantNM_001109689.4(ZNF250):c.11C>G (p.Ala4Gly)not specified [RCV004150329]uncertain significance8144890339144890339Humanname
156158717CV2398060single nucleotide variantNM_001109689.4(ZNF250):c.278A>G (p.Tyr93Cys)not specified [RCV004241650]uncertain significance8144889586144889586Humanname
401886866CV2767943single nucleotide variantNM_001109689.4(ZNF250):c.262G>A (p.Gly88Ser)not specified [RCV004348194]uncertain significance8144889602144889602Humanname
597742913CV3628230single nucleotide variantNM_001109689.4(ZNF250):c.212G>A (p.Arg71Gln)not specified [RCV004891070]uncertain significance8144889652144889652Humanname
155947771CV2245777single nucleotide variantNM_001109689.4(ZNF250):c.307A>G (p.Thr103Ala)not specified [RCV004111637]uncertain significance8144886879144886879Humanname
156111208CV2353315single nucleotide variantNM_001109689.4(ZNF250):c.565A>T (p.Ser189Cys)not specified [RCV004205784]uncertain significance8144882618144882618Humanname
156003523CV2357467single nucleotide variantNM_001109689.4(ZNF250):c.508C>G (p.Arg170Gly)not specified [RCV004202755]uncertain significance8144882675144882675Humanname
156256533CV2369155single nucleotide variantNM_001109689.4(ZNF250):c.835G>A (p.Glu279Lys)not specified [RCV004208080]uncertain significance8144882348144882348Humanname
156137924CV2374179single nucleotide variantNM_001109689.4(ZNF250):c.509G>A (p.Arg170His)not specified [RCV004229327]uncertain significance8144882674144882674Humanname
329356206CV2430633single nucleotide variantNM_001109689.4(ZNF250):c.404C>T (p.Ser135Leu)not specified [RCV004253825]uncertain significance8144882779144882779Humanname
329377230CV2442634single nucleotide variantNM_001109689.4(ZNF250):c.785G>T (p.Ser262Ile)not specified [RCV004264988]uncertain significance8144882398144882398Humanname
401898776CV2782683single nucleotide variantNM_001109689.4(ZNF250):c.459T>A (p.Asn153Lys)not specified [RCV004359696]uncertain significance8144882724144882724Humanname
405712233CV3350440single nucleotide variantNM_001109689.4(ZNF250):c.389C>T (p.Pro130Leu)not specified [RCV004494014]likely benign8144882794144882794Humanname
405712238CV3350441single nucleotide variantNM_001109689.4(ZNF250):c.856G>A (p.Ala286Thr)not specified [RCV004494015]uncertain significance8144882327144882327Humanname
407463465CV3488701single nucleotide variantNM_001109689.4(ZNF250):c.545C>T (p.Thr182Ile)not specified [RCV004688264]uncertain significance8144882638144882638Humanname
597742892CV3628226single nucleotide variantNM_001109689.4(ZNF250):c.519G>C (p.Gln173His)not specified [RCV004891066]uncertain significance8144882664144882664Humanname
597742902CV3628228single nucleotide variantNM_001109689.4(ZNF250):c.965G>A (p.Arg322Gln)not specified [RCV004891068]uncertain significance8144882218144882218Humanname
597742908CV3628229single nucleotide variantNM_001109689.4(ZNF250):c.304A>G (p.Thr102Ala)not specified [RCV004891069]uncertain significance8144886882144886882Humanname
597743457CV3628231single nucleotide variantNM_001109689.4(ZNF250):c.539C>A (p.Pro180Gln)not specified [RCV004891071]uncertain significance8144882644144882644Humanname
598271144CV3930897single nucleotide variantNM_001109689.4(ZNF250):c.587G>A (p.Cys196Tyr)not specified [RCV005302881]uncertain significance8144882596144882596Humanname
598160650CV3930898single nucleotide variantNM_001109689.4(ZNF250):c.481T>G (p.Cys161Gly)not specified [RCV005306859]uncertain significance8144882702144882702Humanname
156334849CV2214827single nucleotide variantNM_001109689.4(ZNF250):c.1240G>A (p.Glu414Lys)not specified [RCV004090621]uncertain significance8144881943144881943Humanname
156388240CV2231740single nucleotide variantNM_001109689.4(ZNF250):c.1471G>A (p.Val491Met)not specified [RCV004098559]uncertain significance8144881712144881712Humanname
156269281CV2240104single nucleotide variantNM_001109689.4(ZNF250):c.1429A>G (p.Thr477Ala)not specified [RCV004110875]likely benign8144881754144881754Humanname
401745502CV2729032single nucleotide variantNM_001109689.4(ZNF250):c.1024A>G (p.Thr342Ala)not specified [RCV004331701]likely benign8144882159144882159Humanname
401892822CV2791816single nucleotide variantNM_001109689.4(ZNF250):c.1116C>G (p.Ser372Arg)not specified [RCV004359267]uncertain significance8144882067144882067Humanname
405712208CV3350437single nucleotide variantNM_001109689.4(ZNF250):c.1096G>A (p.Glu366Lys)not specified [RCV004494011]uncertain significance8144882087144882087Humanname
405712221CV3350439single nucleotide variantNM_001109689.4(ZNF250):c.1264G>A (p.Glu422Lys)not specified [RCV004494013]uncertain significance8144881919144881919Humanname
407463457CV3488699single nucleotide variantNM_001109689.4(ZNF250):c.1107G>C (p.Lys369Asn)not specified [RCV004688262]uncertain significance8144882076144882076Humanname
407463461CV3488700single nucleotide variantNM_001109689.4(ZNF250):c.1597G>A (p.Gly533Arg)not specified [RCV004688263]uncertain significance8144881586144881586Humanname
597742886CV3628225single nucleotide variantNM_001109689.4(ZNF250):c.1282G>A (p.Val428Ile)not specified [RCV004891065]uncertain significance8144881901144881901Humanname
597742897CV3628227single nucleotide variantNM_001109689.4(ZNF250):c.1378T>C (p.Ser460Pro)not specified [RCV004891067]uncertain significance8144881805144881805Humanname
597742924CV3628232single nucleotide variantNM_001109689.4(ZNF250):c.1180G>C (p.Glu394Gln)not specified [RCV004891072]uncertain significance8144882003144882003Humanname
598160655CV3930899single nucleotide variantNM_001109689.4(ZNF250):c.1205G>A (p.Arg402His)not specified [RCV005306860]uncertain significance8144881978144881978Humanname
8632911CV88126single nucleotide variantNM_001109689.3(ZNF250):c.1316T>A (p.Val439Asp)Malignant melanoma [RCV000068218]not provided8144881867144881867Humanname