Cmtm4 Variant Search Result - Rat Genome Database

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18 records found for search term Cmtm4

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
155915749	CV2239552	single nucleotide variant	NM_181521.3(CMTM4):c.*4764C>A	not specified [RCV004114550]	uncertain significance	16	66617294	66617294	Human		name
156281817	CV2348806	single nucleotide variant	NM_181521.3(CMTM4):c.212G>C (p.Cys71Ser)	not specified [RCV004203252]	uncertain significance	16	66636556	66636556	Human		name
401865912	CV2786196	single nucleotide variant	NM_181521.3(CMTM4):c.182A>G (p.Gln61Arg)	not specified [RCV004359993]	uncertain significance	16	66696344	66696344	Human		name
405662981	CV3305124	single nucleotide variant	NM_181521.3(CMTM4):c.164G>T (p.Gly55Val)	not specified [RCV004439646]	uncertain significance	16	66696362	66696362	Human		name
407469720	CV3429440	single nucleotide variant	NM_181521.3(CMTM4):c.122C>T (p.Ala41Val)	not specified [RCV004615272]	uncertain significance	16	66696404	66696404	Human		name
598256747	CV3941065	single nucleotide variant	NM_181521.3(CMTM4):c.201T>G (p.Ile67Met)	not specified [RCV005324267]	uncertain significance	16	66636567	66636567	Human		name
156167413	CV2279806	single nucleotide variant	NM_181521.3(CMTM4):c.434A>G (p.His145Arg)	not specified [RCV004144413]	uncertain significance	16	66623432	66623432	Human		name
156287842	CV2288435	single nucleotide variant	NM_181521.3(CMTM4):c.546G>C (p.Gln182His)	not specified [RCV004151983]	uncertain significance	16	66622139	66622139	Human		name
155927813	CV2365990	single nucleotide variant	NM_181521.3(CMTM4):c.598C>T (p.Arg200Cys)	not specified [RCV004207593]	uncertain significance	16	66622087	66622087	Human		name
156083319	CV2381871	single nucleotide variant	NM_181521.3(CMTM4):c.479C>T (p.Ala160Val)	not specified [RCV004225815]	uncertain significance	16	66622206	66622206	Human		name
405662986	CV3305125	single nucleotide variant	NM_181521.3(CMTM4):c.298G>A (p.Val100Ile)	not specified [RCV004439647]	uncertain significance	16	66636470	66636470	Human		name
405662991	CV3305126	single nucleotide variant	NM_181521.3(CMTM4):c.539G>A (p.Arg180His)	not specified [RCV004439648]	uncertain significance	16	66622146	66622146	Human		name
405662994	CV3305127	single nucleotide variant	NM_181521.3(CMTM4):c.554A>G (p.Asn185Ser)	not specified [RCV004439649]	uncertain significance	16	66622131	66622131	Human		name
407469717	CV3429439	single nucleotide variant	NM_181521.3(CMTM4):c.506T>A (p.Phe169Tyr)	not specified [RCV004615271]	uncertain significance	16	66622179	66622179	Human		name
597798557	CV3653653	single nucleotide variant	NM_181521.3(CMTM4):c.415G>T (p.Val139Leu)	not specified [RCV004904749]	uncertain significance	16	66623451	66623451	Human		name
597798559	CV3653654	single nucleotide variant	NM_181521.3(CMTM4):c.571C>T (p.Arg191Cys)	not specified [RCV004904750]	uncertain significance	16	66622114	66622114	Human		name
597798561	CV3653655	single nucleotide variant	NM_181521.3(CMTM4):c.330C>A (p.His110Gln)	not specified [RCV004904751]	uncertain significance	16	66636438	66636438	Human		name
598256752	CV3941066	single nucleotide variant	NM_181521.3(CMTM4):c.613C>T (p.Arg205Cys)	not specified [RCV005324268]	uncertain significance	16	66622072	66622072	Human		name