Tspyl5 Variant Search Result - Rat Genome Database

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40 records found for search term Tspyl5

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156235559	CV2224052	single nucleotide variant	NM_033512.3(TSPYL5):c.67G>C (p.Ala23Pro)	not specified [RCV004095926]	uncertain significance	8	97277778	97277778	Human		name
401909256	CV2821186	single nucleotide variant	NM_033512.3(TSPYL5):c.819A>G (p.Val273=)	not provided [RCV003423954]	likely benign	8	97277026	97277026	Human		name
405799101	CV3340977	single nucleotide variant	NM_033512.3(TSPYL5):c.32C>T (p.Ser11Phe)	not specified [RCV004476722]	uncertain significance	8	97277813	97277813	Human		name
156181366	CV2201807	single nucleotide variant	NM_033512.3(TSPYL5):c.220G>A (p.Gly74Arg)	not specified [RCV004082242]	uncertain significance	8	97277625	97277625	Human		name
329394777	CV2461480	single nucleotide variant	NM_033512.3(TSPYL5):c.214C>T (p.Arg72Trp)	not specified [RCV004269411]	uncertain significance	8	97277631	97277631	Human		name
597788517	CV3618133	single nucleotide variant	NM_033512.3(TSPYL5):c.140A>C (p.Asp47Ala)	not specified [RCV004875880]	uncertain significance	8	97277705	97277705	Human		name
156028554	CV2238239	single nucleotide variant	NM_033512.3(TSPYL5):c.409C>G (p.Arg137Gly)	not specified [RCV004113328]	uncertain significance	8	97277436	97277436	Human		name
156176731	CV2258119	single nucleotide variant	NM_033512.3(TSPYL5):c.436G>C (p.Gly146Arg)	not specified [RCV004121510]	uncertain significance	8	97277409	97277409	Human		name
156116956	CV2283051	single nucleotide variant	NM_033512.3(TSPYL5):c.741T>G (p.Asn247Lys)	not specified [RCV004143668]	uncertain significance	8	97277104	97277104	Human		name
156242700	CV2283210	single nucleotide variant	NM_033512.3(TSPYL5):c.593C>T (p.Thr198Met)	not specified [RCV004145887]	uncertain significance	8	97277252	97277252	Human		name
156146264	CV2311076	single nucleotide variant	NM_033512.3(TSPYL5):c.449C>G (p.Pro150Arg)	not specified [RCV004164077]	uncertain significance	8	97277396	97277396	Human		name
156273443	CV2334021	single nucleotide variant	NM_033512.3(TSPYL5):c.505A>G (p.Lys169Glu)	not specified [RCV004183547]	uncertain significance	8	97277340	97277340	Human		name
329389829	CV2441363	single nucleotide variant	NM_033512.3(TSPYL5):c.977C>T (p.Thr326Ile)	not specified [RCV004257170]	uncertain significance	8	97276868	97276868	Human		name
405799104	CV3340978	single nucleotide variant	NM_033512.3(TSPYL5):c.440A>G (p.Lys147Arg)	not specified [RCV004476723]	uncertain significance	8	97277405	97277405	Human		name
405799107	CV3340979	single nucleotide variant	NM_033512.3(TSPYL5):c.602G>A (p.Ser201Asn)	not specified [RCV004476724]	uncertain significance	8	97277243	97277243	Human		name
405799110	CV3340980	single nucleotide variant	NM_033512.3(TSPYL5):c.686A>G (p.Lys229Arg)	not specified [RCV004476725]	uncertain significance	8	97277159	97277159	Human		name
405799113	CV3340981	single nucleotide variant	NM_033512.3(TSPYL5):c.760C>A (p.Gln254Lys)	not specified [RCV004476726]	uncertain significance	8	97277085	97277085	Human		name
407528658	CV3487083	single nucleotide variant	NM_033512.3(TSPYL5):c.517G>T (p.Ala173Ser)	not specified [RCV004680492]	uncertain significance	8	97277328	97277328	Human		name
407528660	CV3487084	single nucleotide variant	NM_033512.3(TSPYL5):c.814G>C (p.Glu272Gln)	not specified [RCV004680493]	uncertain significance	8	97277031	97277031	Human		name
407528662	CV3487085	single nucleotide variant	NM_033512.3(TSPYL5):c.575G>T (p.Gly192Val)	not specified [RCV004680494]	uncertain significance	8	97277270	97277270	Human		name
597788511	CV3618132	single nucleotide variant	NM_033512.3(TSPYL5):c.836G>A (p.Ser279Asn)	not specified [RCV004875879]	uncertain significance	8	97277009	97277009	Human		name
597788521	CV3618134	single nucleotide variant	NM_033512.3(TSPYL5):c.661A>G (p.Arg221Gly)	not specified [RCV004875881]	uncertain significance	8	97277184	97277184	Human		name
597788529	CV3618137	single nucleotide variant	NM_033512.3(TSPYL5):c.317C>T (p.Pro106Leu)	not specified [RCV004875883]	uncertain significance	8	97277528	97277528	Human		name
597788533	CV3618138	single nucleotide variant	NM_033512.3(TSPYL5):c.473G>T (p.Arg158Met)	not specified [RCV004875884]	uncertain significance	8	97277372	97277372	Human		name
597788537	CV3618139	single nucleotide variant	NM_033512.3(TSPYL5):c.568G>C (p.Asp190His)	not specified [RCV004875885]	uncertain significance	8	97277277	97277277	Human		name
598216900	CV3924977	single nucleotide variant	NM_033512.3(TSPYL5):c.824G>A (p.Ser275Asn)	not specified [RCV005292946]	uncertain significance	8	97277021	97277021	Human		name
598216906	CV3924978	single nucleotide variant	NM_033512.3(TSPYL5):c.725A>G (p.Asn242Ser)	not specified [RCV005292947]	uncertain significance	8	97277120	97277120	Human		name
598216920	CV3924980	single nucleotide variant	NM_033512.3(TSPYL5):c.746C>G (p.Pro249Arg)	not specified [RCV005292949]	uncertain significance	8	97277099	97277099	Human		name
598238547	CV3924981	single nucleotide variant	NM_033512.3(TSPYL5):c.301G>T (p.Ala101Ser)	not specified [RCV005296434]	uncertain significance	8	97277544	97277544	Human		name
598216927	CV3924982	single nucleotide variant	NM_033512.3(TSPYL5):c.412G>A (p.Val138Ile)	not specified [RCV005292950]	uncertain significance	8	97277433	97277433	Human		name
598238551	CV3924983	single nucleotide variant	NM_033512.3(TSPYL5):c.953C>T (p.Ser318Phe)	not specified [RCV005296435]	uncertain significance	8	97276892	97276892	Human		name
598216934	CV3924984	single nucleotide variant	NM_033512.3(TSPYL5):c.431C>T (p.Pro144Leu)	not specified [RCV005292951]	uncertain significance	8	97277414	97277414	Human		name
15130747	CV711668	single nucleotide variant	NM_033512.3(TSPYL5):c.407C>T (p.Pro136Leu)	not provided [RCV000964486]	likely benign	8	97277438	97277438	Human		name
156255019	CV2280938	single nucleotide variant	NM_033512.3(TSPYL5):c.1237G>A (p.Val413Met)	not specified [RCV004145178]	uncertain significance	8	97276608	97276608	Human		name
155991395	CV2355432	single nucleotide variant	NM_033512.3(TSPYL5):c.1042C>T (p.Arg348Cys)	not specified [RCV004205286]	uncertain significance	8	97276803	97276803	Human		name
401782750	CV2715960	single nucleotide variant	NM_033512.3(TSPYL5):c.1162C>T (p.Arg388Cys)	not specified [RCV004329355]	uncertain significance	8	97276683	97276683	Human		name
405799098	CV3340976	single nucleotide variant	NM_033512.3(TSPYL5):c.1156G>A (p.Gly386Arg)	not specified [RCV004476721]	uncertain significance	8	97276689	97276689	Human		name
407528656	CV3487082	single nucleotide variant	NM_033512.3(TSPYL5):c.1020C>A (p.Ser340Arg)	not specified [RCV004680491]	uncertain significance	8	97276825	97276825	Human		name
597788525	CV3618135	single nucleotide variant	NM_033512.3(TSPYL5):c.1085C>T (p.Ser362Phe)	not specified [RCV004875882]	uncertain significance	8	97276760	97276760	Human		name
598238556	CV3924985	single nucleotide variant	NM_033512.3(TSPYL5):c.1069C>T (p.His357Tyr)	not specified [RCV005296436]	uncertain significance	8	97276776	97276776	Human		name

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