Me3 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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44 records found for search term Me3

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8653310	CV129885	single nucleotide variant	NM_001014811.1(ME3):c.467+11151A>T	Lung cancer [RCV000110372]	uncertain significance	11	86545402	86545402	Human		name
8653311	CV129886	single nucleotide variant	NM_001014811.1(ME3):c.183+21877G>T	Lung cancer [RCV000110373]	uncertain significance	11	86649885	86649885	Human		name
155925688	CV2258596	single nucleotide variant	NM_001161586.3(ME3):c.86C>A (p.Ala29Glu)	not specified [RCV004116070]	uncertain significance	11	86671859	86671859	Human		name
401897205	CV2789901	single nucleotide variant	NM_001161586.3(ME3):c.61G>A (p.Ala21Thr)	not specified [RCV004362283]	uncertain significance	11	86671884	86671884	Human		name
405680917	CV3285305	single nucleotide variant	NM_001161586.3(ME3):c.28C>T (p.Arg10Trp)	not specified [RCV004421624]	uncertain significance	11	86671917	86671917	Human		name
407474071	CV3453515	single nucleotide variant	NM_001161586.3(ME3):c.468T>C (p.Arg156=)	not specified [RCV004638048]	likely benign	11	86508867	86508867	Human		name
15109827	CV724783	single nucleotide variant	NM_001161586.3(ME3):c.682C>T (p.Leu228=)	not provided [RCV000893943]	benign	11	86497986	86497986	Human		name
405680906	CV3285303	single nucleotide variant	NM_001161586.3(ME3):c.112C>T (p.Pro38Ser)	not specified [RCV004421622]	uncertain significance	11	86671833	86671833	Human		name
598239984	CV3988800	single nucleotide variant	NM_001161586.3(ME3):c.167A>T (p.Asn56Ile)	not specified [RCV005364527]	uncertain significance	11	86671778	86671778	Human		name
156372874	CV2204633	single nucleotide variant	NM_001161586.3(ME3):c.962G>A (p.Arg321Gln)	not specified [RCV004081738]	uncertain significance	11	86450356	86450356	Human		name
155920609	CV2240388	single nucleotide variant	NM_001161586.3(ME3):c.351C>A (p.Asn117Lys)	not specified [RCV004117290]	uncertain significance	11	86556669	86556669	Human		name
156033765	CV2256517	single nucleotide variant	NM_001161586.3(ME3):c.497G>A (p.Gly166Asp)	not specified [RCV004118720]	uncertain significance	11	86508838	86508838	Human		name
156159069	CV2262543	single nucleotide variant	NM_001161586.3(ME3):c.533A>G (p.Asp178Gly)	not specified [RCV004130754]	uncertain significance	11	86508802	86508802	Human		name
156263204	CV2368615	single nucleotide variant	NM_001161586.3(ME3):c.513G>A (p.Met171Ile)	not specified [RCV004221394]	uncertain significance	11	86508822	86508822	Human		name
329392465	CV2439003	single nucleotide variant	NM_001161586.3(ME3):c.851A>G (p.Asn284Ser)	not specified [RCV004264510]	uncertain significance	11	86465159	86465159	Human		name
401741268	CV2680582	single nucleotide variant	NM_001161586.3(ME3):c.866G>A (p.Arg289His)	not specified [RCV004291209]	uncertain significance	11	86465144	86465144	Human		name
401725056	CV2697259	single nucleotide variant	NM_001161586.3(ME3):c.659C>T (p.Pro220Leu)	not specified [RCV004304024]	uncertain significance	11	86498009	86498009	Human		name
405680919	CV3285306	single nucleotide variant	NM_001161586.3(ME3):c.746A>C (p.Gln249Pro)	not specified [RCV004421625]	uncertain significance	11	86487400	86487400	Human		name
407474056	CV3453511	single nucleotide variant	NM_001161586.3(ME3):c.751G>A (p.Val251Met)	not specified [RCV004638044]	uncertain significance	11	86487395	86487395	Human		name
407474060	CV3453512	single nucleotide variant	NM_001161586.3(ME3):c.724C>G (p.Leu242Val)	not specified [RCV004638045]	uncertain significance	11	86487422	86487422	Human		name
407474064	CV3453513	single nucleotide variant	NM_001161586.3(ME3):c.518A>G (p.Asn173Ser)	not specified [RCV004638046]	uncertain significance	11	86508817	86508817	Human		name
597659239	CV3553279	single nucleotide variant	NM_001161586.3(ME3):c.322A>G (p.Ile108Val)	not specified [RCV004828172]	uncertain significance	11	86556698	86556698	Human		name
597634325	CV3553280	single nucleotide variant	NM_001161586.3(ME3):c.452C>G (p.Thr151Ser)	not specified [RCV004824135]	uncertain significance	11	86556568	86556568	Human		name
597659263	CV3553284	single nucleotide variant	NM_001161586.3(ME3):c.515T>G (p.Leu172Arg)	not specified [RCV004828176]	uncertain significance	11	86508820	86508820	Human		name
598211992	CV3988797	single nucleotide variant	NM_001161586.3(ME3):c.373C>G (p.Leu125Val)	not specified [RCV005378103]	uncertain significance	11	86556647	86556647	Human		name
598212000	CV3988802	single nucleotide variant	NM_001161586.3(ME3):c.359T>C (p.Leu120Pro)	not specified [RCV005378104]	uncertain significance	11	86556661	86556661	Human		name
156401081	CV2213860	single nucleotide variant	NM_001161586.3(ME3):c.1057G>C (p.Glu353Gln)	not specified [RCV004089911]	uncertain significance	11	86449963	86449963	Human		name
156275362	CV2290589	single nucleotide variant	NM_001161586.3(ME3):c.1265C>T (p.Thr422Met)	not specified [RCV004149132]	uncertain significance	11	86447180	86447180	Human		name
156294795	CV2302989	single nucleotide variant	NM_001161586.3(ME3):c.1352C>T (p.Thr451Met)	not specified [RCV004156785]	uncertain significance	11	86447093	86447093	Human		name
156255854	CV2325797	single nucleotide variant	NM_001161586.3(ME3):c.1463A>C (p.Asn488Thr)	not specified [RCV004173682]	uncertain significance	11	86446405	86446405	Human		name
156271233	CV2333826	single nucleotide variant	NM_001161586.3(ME3):c.1625G>A (p.Arg542Gln)	not specified [RCV004181325]	uncertain significance	11	86442849	86442849	Human		name
155915972	CV2336059	single nucleotide variant	NM_001161586.3(ME3):c.1660G>A (p.Asp554Asn)	not specified [RCV004603315]	uncertain significance	11	86441434	86441434	Human		name
401775441	CV2692375	single nucleotide variant	NM_001161586.3(ME3):c.1557A>T (p.Gln519His)	not specified [RCV004310353]	uncertain significance	11	86442917	86442917	Human		name
401773417	CV2698205	single nucleotide variant	NM_001161586.3(ME3):c.1211G>T (p.Arg404Met)	not specified [RCV004304771]	uncertain significance	11	86448176	86448176	Human		name
401857213	CV2760018	single nucleotide variant	NM_001161586.3(ME3):c.1300G>A (p.Glu434Lys)	not specified [RCV004345430]	uncertain significance	11	86447145	86447145	Human		name
401870130	CV2792285	single nucleotide variant	NM_001161586.3(ME3):c.1015G>A (p.Glu339Lys)	not specified [RCV004361472]	uncertain significance	11	86450303	86450303	Human		name
405680896	CV3285301	single nucleotide variant	NM_001161586.3(ME3):c.1042C>T (p.Leu348Phe)	not specified [RCV004421620]	uncertain significance	11	86449978	86449978	Human		name
405680901	CV3285302	single nucleotide variant	NM_001161586.3(ME3):c.1073C>T (p.Pro358Leu)	not specified [RCV004421621]	uncertain significance	11	86449947	86449947	Human		name
407474067	CV3453514	single nucleotide variant	NM_001161586.3(ME3):c.1159G>A (p.Glu387Lys)	not specified [RCV004638047]	uncertain significance	11	86448228	86448228	Human		name
597659257	CV3553283	single nucleotide variant	NM_001161586.3(ME3):c.1235T>C (p.Ile412Thr)	not specified [RCV004828175]	uncertain significance	11	86448152	86448152	Human		name
597659268	CV3553285	single nucleotide variant	NM_001161586.3(ME3):c.1057G>A (p.Glu353Lys)	not specified [RCV004828177]	uncertain significance	11	86449963	86449963	Human		name
597659274	CV3553286	single nucleotide variant	NM_001161586.3(ME3):c.1066G>A (p.Gly356Ser)	not specified [RCV004828178]	uncertain significance	11	86449954	86449954	Human		name
598239971	CV3988798	single nucleotide variant	NM_001161586.3(ME3):c.1555C>A (p.Gln519Lys)	not specified [RCV005364525]	uncertain significance	11	86442919	86442919	Human		name
598239977	CV3988799	single nucleotide variant	NM_001161586.3(ME3):c.1419T>G (p.Ser473Arg)	not specified [RCV005364526]	uncertain significance	11	86446449	86446449	Human		name

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