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40 records found for search term S1pr3
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
155930745CV2224794single nucleotide variantNM_005226.4(S1PR3):c.-226G>Anot specified [RCV004092610]uncertain significance98899161788991617Humanname
156385397CV2227908single nucleotide variantNM_005226.4(S1PR3):c.-148+289A>Gnot specified [RCV004096168]uncertain significance98899198488991984Humanname
156082839CV2244433single nucleotide variantNM_005226.4(S1PR3):c.-148+196C>Tnot specified [RCV004100402]uncertain significance98899189188991891Humanname
407514185CV3473358single nucleotide variantNM_005226.4(S1PR3):c.23G>A (p.Arg8His)not specified [RCV004674422]uncertain significance98900122389001223Humanname
156188473CV2395443single nucleotide variantNM_005226.4(S1PR3):c.38G>C (p.Arg13Pro)not specified [RCV004241314]likely benign98900123889001238Humanname
598207717CV3910252single nucleotide variantNM_005226.4(S1PR3):c.32C>T (p.Pro11Leu)not specified [RCV005270087]uncertain significance98900123289001232Humanname
8633430CV88645single nucleotide variantNM_005226.3(S1PR3):c.474C>T (p.Ile158=)Malignant melanoma [RCV000068738]not provided98900167489001674Humanname
329391695CV2453047single nucleotide variantNM_005226.4(S1PR3):c.141G>C (p.Leu47Phe)not specified [RCV004277661]uncertain significance98900134189001341Humanname
8626747CV81891single nucleotide variantNM_005226.3(S1PR3):c.179T>C (p.Val60Ala)Malignant melanoma [RCV000061970]not provided98900137989001379Humanname
155959817CV2252616single nucleotide variantNM_005226.4(S1PR3):c.587A>T (p.Tyr196Phe)not specified [RCV004118492]uncertain significance98900178789001787Humanname
156293384CV2293052single nucleotide variantNM_005226.4(S1PR3):c.919C>T (p.Arg307Trp)not specified [RCV004148804]uncertain significance98900211989002119Humanname
156292190CV2321190single nucleotide variantNM_005226.4(S1PR3):c.997G>T (p.Asp333Tyr)not specified [RCV004175312]uncertain significance98900219789002197Humanname
155924069CV2351991single nucleotide variantNM_005226.4(S1PR3):c.439G>A (p.Asp147Asn)not specified [RCV004191092]uncertain significance98900163989001639Humanname
156221517CV2394456single nucleotide variantNM_005226.4(S1PR3):c.931C>G (p.Arg311Gly)not specified [RCV004240823]uncertain significance98900213189002131Humanname
329381822CV2424231single nucleotide variantNM_005226.4(S1PR3):c.704C>T (p.Ser235Leu)not specified [RCV004250353]uncertain significance98900190489001904Humanname
329400091CV2440557single nucleotide variantNM_005226.4(S1PR3):c.480G>T (p.Met160Ile)not specified [RCV004256471]uncertain significance98900168089001680Humanname
401726165CV2699133single nucleotide variantNM_005226.4(S1PR3):c.590T>C (p.Ile197Thr)not specified [RCV004303636]uncertain significance98900179089001790Humanname
401721664CV2710093single nucleotide variantNM_005226.4(S1PR3):c.874G>A (p.Ala292Thr)not specified [RCV004315151]uncertain significance98900207489002074Humanname
401729817CV2731756single nucleotide variantNM_005226.4(S1PR3):c.962G>C (p.Arg321Pro)not specified [RCV004332245]uncertain significance98900216289002162Humanname
401893154CV2755042single nucleotide variantNM_005226.4(S1PR3):c.961C>T (p.Arg321Trp)not specified [RCV004335198]uncertain significance98900216189002161Humanname
401874747CV2756034single nucleotide variantNM_005226.4(S1PR3):c.896C>T (p.Thr299Met)not specified [RCV004338160]uncertain significance98900209689002096Humanname
405702474CV3310190single nucleotide variantNM_005226.4(S1PR3):c.446A>G (p.Asn149Ser)not specified [RCV004447268]uncertain significance98900164689001646Humanname
405702467CV3310191single nucleotide variantNM_005226.4(S1PR3):c.692A>G (p.Asn231Ser)not specified [RCV004447269]likely benign98900189289001892Humanname
407468949CV3473359single nucleotide variantNM_005226.4(S1PR3):c.964G>A (p.Gly322Arg)not specified [RCV004661307]uncertain significance98900216489002164Humanname
407468951CV3473360single nucleotide variantNM_005226.4(S1PR3):c.457C>T (p.Arg153Cys)not specified [RCV004661308]uncertain significance98900165789001657Humanname
407468954CV3473361single nucleotide variantNM_005226.4(S1PR3):c.806G>A (p.Cys269Tyr)not specified [RCV004661309]uncertain significance98900200689002006Humanname
407514152CV3473362single nucleotide variantNM_005226.4(S1PR3):c.709C>T (p.Arg237Trp)not specified [RCV004674423]uncertain significance98900190989001909Humanname
407468957CV3473363single nucleotide variantNM_005226.4(S1PR3):c.538C>T (p.His180Tyr)not specified [RCV004661310]uncertain significance98900173889001738Humanname
597734798CV3597913single nucleotide variantNM_005226.4(S1PR3):c.989C>T (p.Pro330Leu)not specified [RCV004863548]uncertain significance98900218989002189Humanname
597734803CV3597915single nucleotide variantNM_005226.4(S1PR3):c.407G>A (p.Arg136Gln)not specified [RCV004863549]uncertain significance98900160789001607Humanname
598207705CV3910250single nucleotide variantNM_005226.4(S1PR3):c.679C>T (p.Arg227Cys)not specified [RCV005270085]uncertain significance98900187989001879Humanname
598207712CV3910251single nucleotide variantNM_005226.4(S1PR3):c.760G>A (p.Ala254Thr)not specified [RCV005270086]uncertain significance98900196089001960Humanname
598207729CV3910254single nucleotide variantNM_005226.4(S1PR3):c.652A>G (p.Ile218Val)not specified [RCV005270089]uncertain significance98900185289001852Humanname
155926060CV2230552single nucleotide variantNM_005226.4(S1PR3):c.1046C>A (p.Pro349Gln)not specified [RCV004097522]uncertain significance98900224689002246Humanname
156186414CV2292389single nucleotide variantNM_005226.4(S1PR3):c.1098C>A (p.Asp366Glu)not specified [RCV004150193]uncertain significance98900229889002298Humanname
156035538CV2338926single nucleotide variantNM_005226.4(S1PR3):c.1085C>T (p.Ser362Phe)not specified [RCV004184518]uncertain significance98900228589002285Humanname
156307155CV2369613single nucleotide variantNM_005226.4(S1PR3):c.1093A>G (p.Met365Val)not specified [RCV004215025]uncertain significance98900229389002293Humanname
401726800CV2674549single nucleotide variantNM_005226.4(S1PR3):c.1093A>C (p.Met365Leu)not specified [RCV004291427]uncertain significance98900229389002293Humanname
405702480CV3310189single nucleotide variantNM_005226.4(S1PR3):c.1079C>T (p.Pro360Leu)not specified [RCV004447267]uncertain significance98900227989002279Humanname
598207723CV3910253single nucleotide variantNM_005226.4(S1PR3):c.1097A>G (p.Asp366Gly)not specified [RCV005270088]uncertain significance98900229789002297Humanname