Map2k5 Variant Search Result - Rat Genome Database

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32 records found for search term Map2k5

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15185294	CV744921	single nucleotide variant	NM_145160.3(MAP2K5):c.184+7C>T	not provided [RCV000908486]	benign	15	67550089	67550089	Human		name
15200364	CV778131	single nucleotide variant	NM_145160.3(MAP2K5):c.586-8A>G	not provided [RCV000957308]	benign	15	67646223	67646223	Human		name
405270314	CV3187683	single nucleotide variant	NM_145160.3(MAP2K5):c.1074+1G>A	not provided [RCV003887767]	uncertain significance	15	67727946	67727946	Human		name
8584538	CV119111	single nucleotide variant	NM_145160.2(MAP2K5):c.1075-4271C>T	Lung cancer [RCV000099631]	uncertain significance	15	67743960	67743960	Human		name
405657620	CV3288577	single nucleotide variant	NM_145160.3(MAP2K5):c.20G>T (p.Gly7Val)	not specified [RCV004416173]	uncertain significance	15	67543355	67543355	Human		name
15153402	CV726215	single nucleotide variant	NM_145160.3(MAP2K5):c.849C>T (p.Asp283=)	not provided [RCV000880002]	benign	15	67692480	67692480	Human		name
405657618	CV3288576	single nucleotide variant	NM_145160.3(MAP2K5):c.198T>G (p.Asp66Glu)	not specified [RCV004416172]	uncertain significance	15	67563296	67563296	Human		name
405657623	CV3288578	single nucleotide variant	NM_145160.3(MAP2K5):c.295A>G (p.Ile99Val)	not specified [RCV004416174]	uncertain significance	15	67580796	67580796	Human		name
597626706	CV3699999	single nucleotide variant	NM_145160.3(MAP2K5):c.260C>T (p.Ser87Phe)	not specified [RCV004938736]	uncertain significance	15	67580761	67580761	Human		name
597626709	CV3700000	single nucleotide variant	NM_145160.3(MAP2K5):c.224A>T (p.Asp75Val)	not specified [RCV004938737]	uncertain significance	15	67563322	67563322	Human		name
156278474	CV2297438	single nucleotide variant	NM_145160.3(MAP2K5):c.755A>G (p.Tyr252Cys)	not specified [RCV004153375]	uncertain significance	15	67658571	67658571	Human		name
155968278	CV2312817	single nucleotide variant	NM_145160.3(MAP2K5):c.797C>T (p.Ala266Val)	not specified [RCV004171318]	uncertain significance	15	67658613	67658613	Human		name
155925201	CV2358286	single nucleotide variant	NM_145160.3(MAP2K5):c.373C>T (p.Arg125Trp)	not specified [RCV004212070]	uncertain significance	15	67586855	67586855	Human		name
401720407	CV2673313	single nucleotide variant	NM_145160.3(MAP2K5):c.469G>A (p.Ala157Thr)	not specified [RCV004288300]	uncertain significance	15	67592963	67592963	Human		name
401752486	CV2682836	single nucleotide variant	NM_145160.3(MAP2K5):c.670A>G (p.Ile224Val)	not specified [RCV004281804]	uncertain significance	15	67646403	67646403	Human		name
405657628	CV3288579	single nucleotide variant	NM_145160.3(MAP2K5):c.698T>C (p.Val233Ala)	not specified [RCV004416175]	uncertain significance	15	67646431	67646431	Human		name
407493715	CV3446446	single nucleotide variant	NM_145160.3(MAP2K5):c.340G>A (p.Glu114Lys)	not specified [RCV004642810]	uncertain significance	15	67585907	67585907	Human		name
407493724	CV3446448	single nucleotide variant	NM_145160.3(MAP2K5):c.542A>G (p.Tyr181Cys)	not specified [RCV004642812]	uncertain significance	15	67600746	67600746	Human		name
597626703	CV3699998	single nucleotide variant	NM_145160.3(MAP2K5):c.374G>A (p.Arg125Gln)	not specified [RCV004938735]	uncertain significance	15	67586856	67586856	Human		name
597626715	CV3700001	single nucleotide variant	NM_145160.3(MAP2K5):c.886C>G (p.Gln296Glu)	not specified [RCV004938738]	uncertain significance	15	67692517	67692517	Human		name
597626718	CV3700002	single nucleotide variant	NM_145160.3(MAP2K5):c.759G>C (p.Arg253Ser)	not specified [RCV004938739]	uncertain significance	15	67658575	67658575	Human		name
598166194	CV3988656	single nucleotide variant	NM_145160.3(MAP2K5):c.506G>A (p.Arg169Gln)	not specified [RCV005369304]	uncertain significance	15	67600710	67600710	Human		name
598196867	CV3988657	single nucleotide variant	NM_145160.3(MAP2K5):c.448G>T (p.Ala150Ser)	not specified [RCV005375339]	uncertain significance	15	67592942	67592942	Human		name
156278832	CV2316714	single nucleotide variant	NM_145160.3(MAP2K5):c.1331A>G (p.Gln444Arg)	not specified [RCV004171939]	uncertain significance	15	67806734	67806734	Human		name
401782898	CV2707579	single nucleotide variant	NM_145160.3(MAP2K5):c.1037T>C (p.Phe346Ser)	not specified [RCV004306523]	uncertain significance	15	67703401	67703401	Human		name
405657615	CV3288575	single nucleotide variant	NM_145160.3(MAP2K5):c.1306C>T (p.Arg436Trp)	not specified [RCV004416171]	uncertain significance	15	67806709	67806709	Human		name
407493712	CV3446445	single nucleotide variant	NM_145160.3(MAP2K5):c.1307G>A (p.Arg436Gln)	not specified [RCV004642809]	uncertain significance	15	67806710	67806710	Human		name
407493719	CV3446447	single nucleotide variant	NM_145160.3(MAP2K5):c.1307G>T (p.Arg436Leu)	not specified [RCV004642811]	uncertain significance	15	67806710	67806710	Human		name
407493728	CV3446449	single nucleotide variant	NM_145160.3(MAP2K5):c.1090G>C (p.Gly364Arg)	not specified [RCV004642813]	uncertain significance	15	67748246	67748246	Human		name
597626802	CV3700003	single nucleotide variant	NM_145160.3(MAP2K5):c.1294A>G (p.Met432Val)	not specified [RCV004938740]	uncertain significance	15	67806697	67806697	Human		name
597626805	CV3700004	single nucleotide variant	NM_145160.3(MAP2K5):c.1040T>C (p.Met347Thr)	not specified [RCV004938741]	uncertain significance	15	67703404	67703404	Human		name
598196860	CV3988655	single nucleotide variant	NM_145160.3(MAP2K5):c.1325G>A (p.Arg442Gln)	not specified [RCV005375338]	uncertain significance	15	67806728	67806728	Human		name

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