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Variants search result for Homo sapiens
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48 records found for search term Ffar3
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
155970781CV2262276single nucleotide variantNM_005304.5(FFAR3):c.4G>A (p.Asp2Asn)not specified [RCV004128479]uncertain significance193535889435358894Humanname
401881343CV2759380single nucleotide variantNM_005304.5(FFAR3):c.34G>C (p.Gly12Arg)not specified [RCV004338384]uncertain significance193535892435358924Humanname
401863847CV2773489single nucleotide variantNM_005304.5(FFAR3):c.40C>T (p.His14Tyr)not specified [RCV004354119]uncertain significance193535893035358930Humanname
401928685CV2808515single nucleotide variantNM_005304.5(FFAR3):c.960G>A (p.Ala320=)not provided [RCV003406935]likely benign193535985035359850Humanname
15191429CV706410single nucleotide variantNM_005304.5(FFAR3):c.603C>T (p.Ser201=)not provided [RCV000954773]likely benign193535949335359493Humanname
15167467CV706411single nucleotide variantNM_005304.5(FFAR3):c.768G>A (p.Ala256=)not provided [RCV000949063]likely benign193535965835359658Humanname
156049806CV2319333single nucleotide variantNM_005304.5(FFAR3):c.237G>A (p.Met79Ile)not specified [RCV004180158]uncertain significance193535912735359127Humanname
156167541CV2320022single nucleotide variantNM_005304.5(FFAR3):c.175G>A (p.Ala59Thr)not specified [RCV004167887]uncertain significance193535906535359065Humanname
156158273CV2398015single nucleotide variantNM_005304.5(FFAR3):c.251C>T (p.Pro84Leu)not specified [RCV004241614]uncertain significance193535914135359141Humanname
401731845CV2712181single nucleotide variantNM_005304.5(FFAR3):c.235A>G (p.Met79Val)not specified [RCV004311900]uncertain significance193535912535359125Humanname
405758899CV3253464single nucleotide variantNM_005304.5(FFAR3):c.173C>A (p.Thr58Asn)not specified [RCV004393898]uncertain significance193535906335359063Humanname
405758903CV3253465single nucleotide variantNM_005304.5(FFAR3):c.214A>G (p.Met72Val)not specified [RCV004393899]uncertain significance193535910435359104Humanname
405758908CV3253466single nucleotide variantNM_005304.5(FFAR3):c.220G>A (p.Glu74Lys)not specified [RCV004393900]uncertain significance193535911035359110Humanname
407501175CV3439059single nucleotide variantNM_005304.5(FFAR3):c.215T>C (p.Met72Thr)not specified [RCV004623201]uncertain significance193535910535359105Humanname
597751145CV3672529single nucleotide variantNM_005304.5(FFAR3):c.125A>G (p.Lys42Arg)not specified [RCV004923672]uncertain significance193535901535359015Humanname
597751150CV3672530single nucleotide variantNM_005304.5(FFAR3):c.254T>A (p.Phe85Tyr)not specified [RCV004923673]uncertain significance193535914435359144Humanname
598240991CV3959351single nucleotide variantNM_005304.5(FFAR3):c.145G>A (p.Ala49Thr)not specified [RCV005344270]uncertain significance193535903535359035Humanname
598241010CV3959354single nucleotide variantNM_005304.5(FFAR3):c.181G>A (p.Asp61Asn)not specified [RCV005344273]uncertain significance193535907135359071Humanname
15162815CV706409single nucleotide variantNM_005304.5(FFAR3):c.134G>A (p.Arg45His)not provided [RCV000947934]benign193535902435359024Humanname
155967912CV2216924single nucleotide variantNM_005304.5(FFAR3):c.857A>T (p.Asp286Val)not specified [RCV004083335]uncertain significance193535974735359747Humanname
155901971CV2237873single nucleotide variantNM_005304.5(FFAR3):c.706G>T (p.Val236Phe)not specified [RCV004109102]uncertain significance193535959635359596Humanname
156292562CV2246679single nucleotide variantNM_005304.5(FFAR3):c.787C>T (p.Leu263Phe)not specified [RCV004110410]uncertain significance193535967735359677Humanname
156206268CV2249941single nucleotide variantNM_005304.5(FFAR3):c.896G>C (p.Gly299Ala)not specified [RCV004122913]uncertain significance193535978635359786Humanname
156279428CV2338313single nucleotide variantNM_005304.5(FFAR3):c.454G>A (p.Val152Ile)not specified [RCV004186367]likely benign193535934435359344Humanname
156280042CV2338358single nucleotide variantNM_005304.5(FFAR3):c.347G>A (p.Ser116Asn)not specified [RCV004186409]uncertain significance193535923735359237Humanname
156117762CV2349498single nucleotide variantNM_005304.5(FFAR3):c.307G>A (p.Ala103Thr)not specified [RCV004201465]uncertain significance193535919735359197Humanname
155929057CV2356637single nucleotide variantNM_005304.5(FFAR3):c.445G>A (p.Val149Met)not specified [RCV004201999]uncertain significance193535933535359335Humanname
401747492CV2696714single nucleotide variantNM_005304.5(FFAR3):c.496A>C (p.Asn166His)not specified [RCV004290690]uncertain significance193535938635359386Humanname
401775890CV2724257single nucleotide variantNM_005304.5(FFAR3):c.764C>T (p.Pro255Leu)not specified [RCV004328138]uncertain significance193535965435359654Humanname
401882782CV2788589single nucleotide variantNM_005304.5(FFAR3):c.697A>T (p.Asn233Tyr)not specified [RCV004361086]uncertain significance193535958735359587Humanname
405758914CV3253467single nucleotide variantNM_005304.5(FFAR3):c.337C>T (p.Arg113Cys)not specified [RCV004393901]uncertain significance193535922735359227Humanname
405758920CV3253468single nucleotide variantNM_005304.5(FFAR3):c.539T>A (p.Ile180Asn)not specified [RCV004393902]uncertain significance193535942935359429Humanname
405758926CV3253469single nucleotide variantNM_005304.5(FFAR3):c.550G>A (p.Val184Met)not specified [RCV004393903]uncertain significance193535944035359440Humanname
405758934CV3253470single nucleotide variantNM_005304.5(FFAR3):c.643G>T (p.Gly215Cys)not specified [RCV004393904]uncertain significance193535953335359533Humanname
405758939CV3253471single nucleotide variantNM_005304.5(FFAR3):c.769T>C (p.Trp257Arg)not specified [RCV004393905]uncertain significance193535965935359659Humanname
405758945CV3253472single nucleotide variantNM_005304.5(FFAR3):c.785C>T (p.Thr262Met)not specified [RCV004393906]likely benign193535967535359675Humanname
405758950CV3253473single nucleotide variantNM_005304.5(FFAR3):c.895G>A (p.Gly299Ser)not specified [RCV004393907]uncertain significance193535978535359785Humanname
405758956CV3253474single nucleotide variantNM_005304.5(FFAR3):c.919A>C (p.Met307Leu)not specified [RCV004393908]uncertain significance193535980935359809Humanname
407501181CV3439060single nucleotide variantNM_005304.5(FFAR3):c.521G>A (p.Arg174Gln)not specified [RCV004623202]likely benign193535941135359411Humanname
407501185CV3439061single nucleotide variantNM_005304.5(FFAR3):c.774G>C (p.Arg258Ser)not specified [RCV004623203]uncertain significance193535966435359664Humanname
597751129CV3672526single nucleotide variantNM_005304.5(FFAR3):c.615C>A (p.Ser205Arg)not specified [RCV004923669]uncertain significance193535950535359505Humanname
597751140CV3672528single nucleotide variantNM_005304.5(FFAR3):c.554G>C (p.Arg185Pro)not specified [RCV004923671]uncertain significance193535944435359444Humanname
598240984CV3959349single nucleotide variantNM_005304.5(FFAR3):c.727G>A (p.Val243Met)not specified [RCV005344269]likely benign193535961735359617Humanname
598271976CV3959350single nucleotide variantNM_005304.5(FFAR3):c.554G>A (p.Arg185Gln)not specified [RCV005327861]uncertain significance193535944435359444Humanname
598240996CV3959352single nucleotide variantNM_005304.5(FFAR3):c.739G>A (p.Val247Met)not specified [RCV005344271]uncertain significance193535962935359629Humanname
15175068CV706408single nucleotide variantNM_005304.5(FFAR3):c.919A>G (p.Met307Val)not provided [RCV000950488]benign193535980935359809Humanname
597751134CV3672527single nucleotide variantNM_005304.5(FFAR3):c.1001G>A (p.Gly334Asp)not specified [RCV004923670]uncertain significance193535989135359891Humanname
598241004CV3959353single nucleotide variantNM_005304.5(FFAR3):c.1012G>T (p.Gly338Cys)not specified [RCV005344272]uncertain significance193535990235359902Humanname