Nsmce4a Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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32 records found for search term Nsmce4a

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401903772	CV2809680	single nucleotide variant	NM_017615.3(NSMCE4A):c.940-8C>T	not provided [RCV003394535]	likely benign	10	121960414	121960414	Human		name
155994254	CV2379521	single nucleotide variant	NM_017615.3(NSMCE4A):c.22C>T (p.Arg8Cys)	not specified [RCV004217231]	uncertain significance	10	121975144	121975144	Human		name
156194782	CV2297149	single nucleotide variant	NM_017615.3(NSMCE4A):c.43C>G (p.Arg15Gly)	not specified [RCV004151045]	uncertain significance	10	121975123	121975123	Human		name
401772836	CV2719775	single nucleotide variant	NM_017615.3(NSMCE4A):c.54C>A (p.Asp18Glu)	not specified [RCV004329205]	uncertain significance	10	121975112	121975112	Human		name
405710653	CV3359452	single nucleotide variant	NM_017615.3(NSMCE4A):c.47G>A (p.Gly16Asp)	not specified [RCV004493800]	uncertain significance	10	121975119	121975119	Human		name
156245172	CV2313326	single nucleotide variant	NM_017615.3(NSMCE4A):c.130C>T (p.Arg44Trp)	not specified [RCV004163358]	uncertain significance	10	121975036	121975036	Human		name
156070707	CV2354218	single nucleotide variant	NM_017615.3(NSMCE4A):c.206A>C (p.Asp69Ala)	not specified [RCV004206643]	uncertain significance	10	121974960	121974960	Human		name
329378178	CV2457183	single nucleotide variant	NM_017615.3(NSMCE4A):c.158C>G (p.Pro53Arg)	not specified [RCV004265267]	uncertain significance	10	121975008	121975008	Human		name
405710640	CV3359450	single nucleotide variant	NM_017615.3(NSMCE4A):c.148C>T (p.Pro50Ser)	not specified [RCV004493798]	uncertain significance	10	121975018	121975018	Human		name
407517106	CV3462080	single nucleotide variant	NM_017615.3(NSMCE4A):c.203T>C (p.Met68Thr)	not specified [RCV004650523]	uncertain significance	10	121974963	121974963	Human		name
597707702	CV3577073	single nucleotide variant	NM_017615.3(NSMCE4A):c.194A>G (p.Asp65Gly)	not specified [RCV004840481]	uncertain significance	10	121974972	121974972	Human		name
156256158	CV2325842	single nucleotide variant	NM_017615.3(NSMCE4A):c.901A>C (p.Thr301Pro)	not specified [RCV004173719]	uncertain significance	10	121961461	121961461	Human		name
155909060	CV2387507	single nucleotide variant	NM_017615.3(NSMCE4A):c.934A>T (p.Ile312Leu)	not specified [RCV004240362]	uncertain significance	10	121961428	121961428	Human		name
329372666	CV2451597	single nucleotide variant	NM_017615.3(NSMCE4A):c.851C>T (p.Thr284Ile)	not specified [RCV004274528]	uncertain significance	10	121961511	121961511	Human		name
401782950	CV2707627	single nucleotide variant	NM_017615.3(NSMCE4A):c.974G>A (p.Arg325Gln)	not specified [RCV004306567]	uncertain significance	10	121960372	121960372	Human		name
401778161	CV2718530	single nucleotide variant	NM_017615.3(NSMCE4A):c.470C>A (p.Ser157Tyr)	not specified [RCV004318335]	uncertain significance	10	121970970	121970970	Human		name
401779698	CV2731968	single nucleotide variant	NM_017615.3(NSMCE4A):c.898C>T (p.Arg300Cys)	not specified [RCV004333204]	uncertain significance	10	121961464	121961464	Human		name
401859984	CV2768431	single nucleotide variant	NM_017615.3(NSMCE4A):c.517G>A (p.Val173Ile)	not specified [RCV004344322]	uncertain significance	10	121967791	121967791	Human		name
405710645	CV3359451	single nucleotide variant	NM_017615.3(NSMCE4A):c.299G>T (p.Arg100Leu)	not specified [RCV004493799]	uncertain significance	10	121974075	121974075	Human		name
405710659	CV3359453	single nucleotide variant	NM_017615.3(NSMCE4A):c.848A>T (p.Asp283Val)	not specified [RCV004493801]	uncertain significance	10	121961514	121961514	Human		name
407477035	CV3462078	single nucleotide variant	NM_017615.3(NSMCE4A):c.524C>T (p.Pro175Leu)	not specified [RCV004638750]	uncertain significance	10	121967784	121967784	Human		name
407517103	CV3462079	single nucleotide variant	NM_017615.3(NSMCE4A):c.664A>G (p.Ile222Val)	not specified [RCV004650522]	uncertain significance	10	121965375	121965375	Human		name
597707679	CV3577068	single nucleotide variant	NM_017615.3(NSMCE4A):c.646C>T (p.His216Tyr)	not specified [RCV004840478]	uncertain significance	10	121967662	121967662	Human		name
597643257	CV3577069	single nucleotide variant	NM_017615.3(NSMCE4A):c.539A>C (p.Glu180Ala)	not specified [RCV004832578]	uncertain significance	10	121967769	121967769	Human		name
597643263	CV3577070	single nucleotide variant	NM_017615.3(NSMCE4A):c.512T>C (p.Met171Thr)	not specified [RCV004832579]	uncertain significance	10	121967796	121967796	Human		name
597707687	CV3577071	single nucleotide variant	NM_017615.3(NSMCE4A):c.637C>T (p.His213Tyr)	not specified [RCV004840479]	uncertain significance	10	121967671	121967671	Human		name
597707696	CV3577072	single nucleotide variant	NM_017615.3(NSMCE4A):c.464T>C (p.Leu155Pro)	not specified [RCV004840480]	uncertain significance	10	121970976	121970976	Human		name
598221000	CV3994761	single nucleotide variant	NM_017615.3(NSMCE4A):c.728A>G (p.Gln243Arg)	not specified [RCV005379591]	uncertain significance	10	121965311	121965311	Human		name
598264954	CV3994762	single nucleotide variant	NM_017615.3(NSMCE4A):c.515G>A (p.Gly172Asp)	not specified [RCV005387860]	uncertain significance	10	121967793	121967793	Human		name
598221009	CV3994763	single nucleotide variant	NM_017615.3(NSMCE4A):c.502C>T (p.Leu168Phe)	not specified [RCV005379592]	uncertain significance	10	121967806	121967806	Human		name
405710634	CV3359449	single nucleotide variant	NM_017615.3(NSMCE4A):c.1028A>G (p.His343Arg)	not specified [RCV004493797]	uncertain significance	10	121959556	121959556	Human		name
598264958	CV3994764	single nucleotide variant	NM_017615.3(NSMCE4A):c.1105A>G (p.Ile369Val)	not specified [RCV005387861]	uncertain significance	10	121959389	121959389	Human		name

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