Scpep1 Variant Search Result - Rat Genome Database

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45 records found for search term Scpep1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
597692631	CV3598321	single nucleotide variant	NM_021626.3(SCPEP1):c.16C>T (p.Arg6Trp)	not specified [RCV004859029]	uncertain significance	17	56978175	56978175	Human		name
156208366	CV2298118	single nucleotide variant	NM_021626.3(SCPEP1):c.86T>C (p.Ile29Thr)	not specified [RCV004159784]	uncertain significance	17	56981091	56981091	Human		name
8628035	CV83179	single nucleotide variant	NM_021626.2(SCPEP1):c.450C>T (p.Phe150=)	Malignant melanoma [RCV000063259]	not provided	17	56987829	56987829	Human		name
405759314	CV3314003	single nucleotide variant	NM_021626.3(SCPEP1):c.100G>C (p.Glu34Gln)	not specified [RCV004455018]	uncertain significance	17	56981105	56981105	Human		name
405759334	CV3314006	single nucleotide variant	NM_021626.3(SCPEP1):c.233C>T (p.Pro78Leu)	not specified [RCV004455021]	uncertain significance	17	56985385	56985385	Human		name
597692602	CV3598318	single nucleotide variant	NM_021626.3(SCPEP1):c.189G>T (p.Lys63Asn)	not specified [RCV004859026]	uncertain significance	17	56981194	56981194	Human		name
598235446	CV3910560	single nucleotide variant	NM_021626.3(SCPEP1):c.224A>G (p.Gln75Arg)	not specified [RCV005275248]	uncertain significance	17	56981229	56981229	Human		name
156073327	CV2331574	single nucleotide variant	NM_021626.3(SCPEP1):c.545A>T (p.Lys182Met)	not specified [RCV004184215]	uncertain significance	17	56988289	56988289	Human		name
156217434	CV2348141	single nucleotide variant	NM_021626.3(SCPEP1):c.896G>A (p.Arg299His)	not specified [RCV004197816]	uncertain significance	17	56998400	56998400	Human		name
156383690	CV2361643	single nucleotide variant	NM_021626.3(SCPEP1):c.310A>G (p.Thr104Ala)	not specified [RCV004221264]	uncertain significance	17	56985462	56985462	Human		name
156209667	CV2382660	single nucleotide variant	NM_021626.3(SCPEP1):c.581C>T (p.Ala194Val)	not specified [RCV004232977]	uncertain significance	17	56991133	56991133	Human		name
156000998	CV2391838	single nucleotide variant	NM_021626.3(SCPEP1):c.850T>G (p.Ser284Ala)	not specified [RCV004235715]	uncertain significance	17	56997025	56997025	Human		name
401722889	CV2677127	single nucleotide variant	NM_021626.3(SCPEP1):c.557G>A (p.Arg186Gln)	not specified [RCV004295762]	likely benign	17	56991109	56991109	Human		name
401763826	CV2717133	single nucleotide variant	NM_021626.3(SCPEP1):c.323C>A (p.Ala108Asp)	not specified [RCV004324013]	uncertain significance	17	56987702	56987702	Human		name
401878843	CV2754846	single nucleotide variant	NM_021626.3(SCPEP1):c.311C>G (p.Thr104Ser)	not specified [RCV004341321]	uncertain significance	17	56985463	56985463	Human		name
405759341	CV3314007	single nucleotide variant	NM_021626.3(SCPEP1):c.302G>A (p.Arg101Gln)	not specified [RCV004455022]	uncertain significance	17	56985454	56985454	Human		name
405759346	CV3314008	single nucleotide variant	NM_021626.3(SCPEP1):c.304A>G (p.Lys102Glu)	not specified [RCV004455023]	uncertain significance	17	56985456	56985456	Human		name
405759351	CV3314009	single nucleotide variant	NM_021626.3(SCPEP1):c.411G>A (p.Met137Ile)	not specified [RCV004455024]	uncertain significance	17	56987790	56987790	Human		name
405759358	CV3314010	single nucleotide variant	NM_021626.3(SCPEP1):c.413T>A (p.Val138Glu)	not specified [RCV004455025]	uncertain significance	17	56987792	56987792	Human		name
405759364	CV3314011	single nucleotide variant	NM_021626.3(SCPEP1):c.610T>C (p.Ser204Pro)	not specified [RCV004455026]	uncertain significance	17	56991162	56991162	Human		name
405759369	CV3314012	single nucleotide variant	NM_021626.3(SCPEP1):c.667G>A (p.Glu223Lys)	not specified [RCV004455027]	uncertain significance	17	56995516	56995516	Human		name
405759376	CV3314013	single nucleotide variant	NM_021626.3(SCPEP1):c.755T>A (p.Leu252Gln)	not specified [RCV004455028]	uncertain significance	17	56995604	56995604	Human		name
405759381	CV3314014	single nucleotide variant	NM_021626.3(SCPEP1):c.779T>C (p.Ile260Thr)	not specified [RCV004455029]	uncertain significance	17	56995628	56995628	Human		name
405759386	CV3314015	single nucleotide variant	NM_021626.3(SCPEP1):c.917G>A (p.Arg306Gln)	not specified [RCV004455030]	likely benign	17	56998421	56998421	Human		name
407514572	CV3480206	single nucleotide variant	NM_021626.3(SCPEP1):c.398A>G (p.Lys133Arg)	not specified [RCV004674627]	uncertain significance	17	56987777	56987777	Human		name
407461790	CV3480207	single nucleotide variant	NM_021626.3(SCPEP1):c.602C>A (p.Ser201Tyr)	not specified [RCV004658841]	uncertain significance	17	56991154	56991154	Human		name
597692611	CV3598319	single nucleotide variant	NM_021626.3(SCPEP1):c.959A>T (p.Lys320Met)	not specified [RCV004859027]	uncertain significance	17	56998463	56998463	Human		name
598235427	CV3910557	single nucleotide variant	NM_021626.3(SCPEP1):c.548C>T (p.Ala183Val)	not specified [RCV005275245]	uncertain significance	17	56991100	56991100	Human		name
598235433	CV3910558	single nucleotide variant	NM_021626.3(SCPEP1):c.352G>A (p.Val118Met)	not specified [RCV005275246]	uncertain significance	17	56987731	56987731	Human		name
598235440	CV3910559	single nucleotide variant	NM_021626.3(SCPEP1):c.406G>T (p.Ala136Ser)	not specified [RCV005275247]	uncertain significance	17	56987785	56987785	Human		name
156399654	CV2202132	single nucleotide variant	NM_021626.3(SCPEP1):c.1063G>A (p.Glu355Lys)	not specified [RCV004078084]	likely benign	17	57000923	57000923	Human		name
156074102	CV2294731	single nucleotide variant	NM_021626.3(SCPEP1):c.1294A>G (p.Met432Val)	not specified [RCV004161970]	uncertain significance	17	57002179	57002179	Human		name
156244647	CV2347171	single nucleotide variant	NM_021626.3(SCPEP1):c.1120G>A (p.Val374Ile)	not specified [RCV004204645]	uncertain significance	17	57000980	57000980	Human		name
156281192	CV2348520	single nucleotide variant	NM_021626.3(SCPEP1):c.1049T>C (p.Ile350Thr)	not specified [RCV004193704]	uncertain significance	17	57000909	57000909	Human		name
155928001	CV2349916	single nucleotide variant	NM_021626.3(SCPEP1):c.1342G>A (p.Val448Met)	not specified [RCV004206330]	uncertain significance	17	57006218	57006218	Human		name
156136258	CV2357148	single nucleotide variant	NM_021626.3(SCPEP1):c.1117A>T (p.Ile373Phe)	not specified [RCV004206939]	uncertain significance	17	57000977	57000977	Human		name
401767424	CV2729650	single nucleotide variant	NM_021626.3(SCPEP1):c.1151G>A (p.Arg384Gln)	not specified [RCV004331912]	uncertain significance	17	57002036	57002036	Human		name
401899836	CV2758930	single nucleotide variant	NM_021626.3(SCPEP1):c.1172T>G (p.Leu391Arg)	not specified [RCV004340007]	uncertain significance	17	57002057	57002057	Human		name
401894114	CV2770311	single nucleotide variant	NM_021626.3(SCPEP1):c.1351C>A (p.Gln451Lys)	not specified [RCV004356187]	uncertain significance	17	57006227	57006227	Human		name
405759321	CV3314004	single nucleotide variant	NM_021626.3(SCPEP1):c.1087G>A (p.Val363Met)	not specified [RCV004455019]	uncertain significance	17	57000947	57000947	Human		name
405759328	CV3314005	single nucleotide variant	NM_021626.3(SCPEP1):c.1208A>G (p.Tyr403Cys)	not specified [RCV004455020]	uncertain significance	17	57002093	57002093	Human		name
407514575	CV3480208	single nucleotide variant	NM_021626.3(SCPEP1):c.1091C>T (p.Thr364Met)	not specified [RCV004674628]	uncertain significance	17	57000951	57000951	Human		name
597692622	CV3598320	single nucleotide variant	NM_021626.3(SCPEP1):c.1157T>C (p.Leu386Pro)	not specified [RCV004859028]	uncertain significance	17	57002042	57002042	Human		name
597692642	CV3598322	single nucleotide variant	NM_021626.3(SCPEP1):c.1007A>G (p.Asn336Ser)	not specified [RCV004859030]	uncertain significance	17	57000867	57000867	Human		name
597692652	CV3598324	single nucleotide variant	NM_021626.3(SCPEP1):c.1026G>C (p.Glu342Asp)	not specified [RCV004859031]	uncertain significance	17	57000886	57000886	Human		name

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