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Variants search result for Homo sapiens
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44 records found for search term Slc46a3
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8582743CV117299single nucleotide variantNM_001135919.1(SLC46A3):c.1060+226C>GLung cancer [RCV000097820]uncertain significance132871245428712454Humanname
8582742CV117298single nucleotide variantNM_001135919.1(SLC46A3):c.1145-2078G>TLung cancer [RCV000097819]uncertain significance132870617728706177Humanname
155904726CV2298852single nucleotide variantNM_181785.4(SLC46A3):c.23C>T (p.Pro8Leu)not specified [RCV004156399]uncertain significance132871797628717976Humanname
156363711CV2330017single nucleotide variantNM_181785.4(SLC46A3):c.22C>G (p.Pro8Ala)not specified [RCV004185510]uncertain significance132871797728717977Humanname
155954112CV2303256single nucleotide variantNM_181785.4(SLC46A3):c.62G>A (p.Gly21Asp)not specified [RCV004157004]uncertain significance132871793728717937Humanname
405711211CV3329425single nucleotide variantNM_181785.4(SLC46A3):c.40G>A (p.Ala14Thr)not specified [RCV004461814]uncertain significance132871795928717959Humanname
156386588CV2225138single nucleotide variantNM_181785.4(SLC46A3):c.158A>G (p.Asn53Ser)not specified [RCV004094947]uncertain significance132871784128717841Humanname
155982947CV2344257single nucleotide variantNM_181785.4(SLC46A3):c.244A>C (p.Ile82Leu)not specified [RCV004195026]uncertain significance132871349628713496Humanname
405711191CV3329422single nucleotide variantNM_181785.4(SLC46A3):c.220C>A (p.Leu74Met)not specified [RCV004461811]uncertain significance132871352028713520Humanname
405711198CV3329423single nucleotide variantNM_181785.4(SLC46A3):c.250G>A (p.Gly84Ser)not specified [RCV004461812]uncertain significance132871349028713490Humanname
405711205CV3329424single nucleotide variantNM_181785.4(SLC46A3):c.280A>G (p.Ile94Val)not specified [RCV004461813]uncertain significance132871346028713460Humanname
407515057CV3484738single nucleotide variantNM_181785.4(SLC46A3):c.165C>A (p.Ser55Arg)not specified [RCV004674791]uncertain significance132871783428717834Humanname
598237396CV3911285single nucleotide variantNM_181785.4(SLC46A3):c.243A>C (p.Leu81Phe)not specified [RCV005275647]uncertain significance132871349728713497Humanname
156327011CV2217188single nucleotide variantNM_181785.4(SLC46A3):c.731G>A (p.Arg244Gln)EBV-positive nodal T- and NK-cell lymphoma [RCV004560067]|not specified [RCV004087643]likely benign|uncertain significance132871300928713009Humanname
155925638CV2230477single nucleotide variantNM_181785.4(SLC46A3):c.341C>A (p.Thr114Asn)not specified [RCV004097453]uncertain significance132871339928713399Humanname
155974020CV2269905single nucleotide variantNM_181785.4(SLC46A3):c.416C>A (p.Ala139Glu)not specified [RCV004127125]uncertain significance132871332428713324Humanname
156015430CV2269906single nucleotide variantNM_181785.4(SLC46A3):c.421T>G (p.Cys141Gly)not specified [RCV004127126]uncertain significance132871331928713319Humanname
156263163CV2282551single nucleotide variantNM_181785.4(SLC46A3):c.535G>A (p.Val179Ile)not specified [RCV004135123]uncertain significance132871320528713205Humanname
155928380CV2363270single nucleotide variantNM_181785.4(SLC46A3):c.535G>C (p.Val179Leu)not specified [RCV004213826]uncertain significance132871320528713205Humanname
156402379CV2363927single nucleotide variantNM_181785.4(SLC46A3):c.427A>G (p.Asn143Asp)not specified [RCV004218897]uncertain significance132871331328713313Humanname
405711217CV3329426single nucleotide variantNM_181785.4(SLC46A3):c.506T>C (p.Ile169Thr)not specified [RCV004461815]uncertain significance132871323428713234Humanname
405711222CV3329427single nucleotide variantNM_181785.4(SLC46A3):c.811T>G (p.Phe271Val)not specified [RCV004461816]uncertain significance132871292928712929Humanname
405711230CV3329428single nucleotide variantNM_181785.4(SLC46A3):c.931A>G (p.Ser311Gly)not specified [RCV004461817]uncertain significance132871280928712809Humanname
407515052CV3484737single nucleotide variantNM_181785.4(SLC46A3):c.672G>C (p.Glu224Asp)not specified [RCV004674790]uncertain significance132871306828713068Humanname
407515060CV3484739single nucleotide variantNM_181785.4(SLC46A3):c.470A>G (p.Asp157Gly)not specified [RCV004674792]uncertain significance132871327028713270Humanname
597766550CV3596741single nucleotide variantNM_181785.4(SLC46A3):c.467T>C (p.Val156Ala)not specified [RCV004870640]uncertain significance132871327328713273Humanname
597723728CV3596743single nucleotide variantNM_181785.4(SLC46A3):c.449C>T (p.Ala150Val)not specified [RCV004862260]uncertain significance132871329128713291Humanname
598244895CV3911280single nucleotide variantNM_181785.4(SLC46A3):c.307C>G (p.Pro103Ala)not specified [RCV005276916]uncertain significance132871343328713433Humanname
598244902CV3911281single nucleotide variantNM_181785.4(SLC46A3):c.785T>C (p.Leu262Ser)not specified [RCV005276917]uncertain significance132871295528712955Humanname
598244920CV3911283single nucleotide variantNM_181785.4(SLC46A3):c.452G>A (p.Cys151Tyr)not specified [RCV005276919]uncertain significance132871328828713288Humanname
598237391CV3911284single nucleotide variantNM_181785.4(SLC46A3):c.896A>G (p.Tyr299Cys)not specified [RCV005275646]uncertain significance132871284428712844Humanname
598244928CV3911286single nucleotide variantNM_181785.4(SLC46A3):c.722T>G (p.Leu241Arg)not specified [RCV005276920]uncertain significance132871301828713018Humanname
9686842CV171535single nucleotide variantNM_181785.4(SLC46A3):c.1189G>A (p.Val397Ile)Prostate cancer [RCV000149060]uncertain significance132870405528704055Human2name
156231459CV2199663single nucleotide variantNM_181785.4(SLC46A3):c.1129C>T (p.Arg377Cys)not specified [RCV004072400]uncertain significance132871077528710775Humanname
155928824CV2346837single nucleotide variantNM_181785.4(SLC46A3):c.1106G>A (p.Arg369Gln)not specified [RCV004199837]uncertain significance132871079828710798Humanname
155908280CV2387271single nucleotide variantNM_181785.4(SLC46A3):c.1300T>C (p.Cys434Arg)not specified [RCV004238363]uncertain significance132870394428703944Humanname
329399156CV2436289single nucleotide variantNM_181785.4(SLC46A3):c.1028C>T (p.Ala343Val)not specified [RCV004251695]uncertain significance132871271228712712Humanname
329378925CV2443220single nucleotide variantNM_181785.4(SLC46A3):c.1195G>A (p.Ala399Thr)not specified [RCV004260032]uncertain significance132870404928704049Humanname
405711184CV3329421single nucleotide variantNM_181785.4(SLC46A3):c.1036A>G (p.Ser346Gly)not specified [RCV004461810]uncertain significance132871270428712704Humanname
597723717CV3596740single nucleotide variantNM_181785.4(SLC46A3):c.1143A>T (p.Gln381His)not specified [RCV004862259]uncertain significance132871076128710761Humanname
597766556CV3596742single nucleotide variantNM_181785.4(SLC46A3):c.1288G>C (p.Ala430Pro)not specified [RCV004870641]uncertain significance132870395628703956Humanname
597766561CV3596744single nucleotide variantNM_181785.4(SLC46A3):c.1244C>T (p.Pro415Leu)not specified [RCV004870642]uncertain significance132870400028704000Humanname
598244910CV3911282single nucleotide variantNM_181785.4(SLC46A3):c.1037G>C (p.Ser346Thr)not specified [RCV005276918]uncertain significance132871270328712703Humanname
8627435CV82579single nucleotide variantNM_001135919.1(SLC46A3):c.899G>A (p.Gly300Glu)Malignant melanoma [RCV000062658]not provided132871284128712841Humanname