Tmem61 Variant Search Result - Rat Genome Database

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29 records found for search term Tmem61

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8629600	CV84747	single nucleotide variant	NM_182532.2(TMEM61):c.264C>T (p.Ser88=)	Malignant melanoma [RCV000064829]	not provided	1	54986345	54986345	Human		name
156133335	CV2195946	single nucleotide variant	NM_182532.3(TMEM61):c.70G>A (p.Gly24Ser)	not specified [RCV004072202]	uncertain significance	1	54986151	54986151	Human		name
156368424	CV2267003	single nucleotide variant	NM_182532.3(TMEM61):c.46C>T (p.Leu16Phe)	not specified [RCV004131646]	uncertain significance	1	54986127	54986127	Human		name
401887295	CV2771867	single nucleotide variant	NM_182532.3(TMEM61):c.98T>A (p.Leu33His)	not specified [RCV004344583]	uncertain significance	1	54986179	54986179	Human		name
597800570	CV3610597	single nucleotide variant	NM_182532.3(TMEM61):c.91G>A (p.Gly31Arg)	not specified [RCV004880279]	uncertain significance	1	54986172	54986172	Human		name
155997794	CV2288665	single nucleotide variant	NM_182532.3(TMEM61):c.106G>A (p.Ala36Thr)	not specified [RCV004152172]	uncertain significance	1	54986187	54986187	Human		name
156101974	CV2291438	single nucleotide variant	NM_182532.3(TMEM61):c.101G>C (p.Cys34Ser)	not specified [RCV004155767]	uncertain significance	1	54986182	54986182	Human		name
329390592	CV2437106	single nucleotide variant	NM_182532.3(TMEM61):c.161C>G (p.Thr54Arg)	not specified [RCV004262913]	uncertain significance	1	54986242	54986242	Human		name
329354627	CV2444577	single nucleotide variant	NM_182532.3(TMEM61):c.166T>C (p.Tyr56His)	not specified [RCV004256800]	likely benign	1	54986247	54986247	Human		name
401721118	CV2702274	single nucleotide variant	NM_182532.3(TMEM61):c.157C>G (p.Pro53Ala)	not specified [RCV004314606]	uncertain significance	1	54986238	54986238	Human		name
405771614	CV3346617	single nucleotide variant	NM_182532.3(TMEM61):c.124G>A (p.Asp42Asn)	not specified [RCV004470388]	uncertain significance	1	54986205	54986205	Human		name
405771619	CV3346618	single nucleotide variant	NM_182532.3(TMEM61):c.260G>T (p.Trp87Leu)	not specified [RCV004470389]	uncertain significance	1	54986341	54986341	Human		name
407526836	CV3482786	single nucleotide variant	NM_182532.3(TMEM61):c.133G>A (p.Ala45Thr)	not specified [RCV004679781]	likely benign	1	54986214	54986214	Human		name
597800572	CV3610598	single nucleotide variant	NM_182532.3(TMEM61):c.181G>T (p.Gly61Cys)	not specified [RCV004880280]	uncertain significance	1	54986262	54986262	Human		name
8629601	CV84748	single nucleotide variant	NM_182532.2(TMEM61):c.280C>T (p.Pro94Ser)	Malignant melanoma [RCV000064830]	not provided	1	54986361	54986361	Human		name
156283954	CV2231103	single nucleotide variant	NM_182532.3(TMEM61):c.406G>A (p.Val136Met)	not specified [RCV004094324]	likely benign	1	54991876	54991876	Human		name
155974476	CV2235707	single nucleotide variant	NM_182532.3(TMEM61):c.455C>T (p.Thr152Met)	not specified [RCV004111845]	likely benign	1	54991925	54991925	Human		name
156232431	CV2273709	single nucleotide variant	NM_182532.3(TMEM61):c.602G>A (p.Gly201Asp)	not specified [RCV004132361]	uncertain significance	1	54992072	54992072	Human		name
156115206	CV2349273	single nucleotide variant	NM_182532.3(TMEM61):c.528C>A (p.Ser176Arg)	not specified [RCV004199220]	uncertain significance	1	54991998	54991998	Human		name
156210170	CV2370204	single nucleotide variant	NM_182532.3(TMEM61):c.299A>G (p.Asp100Gly)	not specified [RCV004211082]	uncertain significance	1	54986380	54986380	Human		name
156045443	CV2381715	single nucleotide variant	NM_182532.3(TMEM61):c.620G>A (p.Arg207Gln)	not specified [RCV004232175]	uncertain significance	1	54992090	54992090	Human		name
405771625	CV3346619	single nucleotide variant	NM_182532.3(TMEM61):c.301C>T (p.Pro101Ser)	not specified [RCV004470390]	uncertain significance	1	54986382	54986382	Human		name
405771630	CV3346620	single nucleotide variant	NM_182532.3(TMEM61):c.374A>T (p.Lys125Ile)	not specified [RCV004470391]	uncertain significance	1	54991844	54991844	Human		name
405771636	CV3346621	single nucleotide variant	NM_182532.3(TMEM61):c.380T>G (p.Val127Gly)	not specified [RCV004470392]	uncertain significance	1	54991850	54991850	Human		name
405771642	CV3346622	single nucleotide variant	NM_182532.3(TMEM61):c.389C>A (p.Pro130His)	not specified [RCV004470393]	uncertain significance	1	54991859	54991859	Human		name
405771648	CV3346623	single nucleotide variant	NM_182532.3(TMEM61):c.424G>A (p.Glu142Lys)	not specified [RCV004470394]	uncertain significance	1	54991894	54991894	Human		name
405771654	CV3346624	single nucleotide variant	NM_182532.3(TMEM61):c.559G>A (p.Val187Ile)	not specified [RCV004470395]	likely benign	1	54992029	54992029	Human		name
597800574	CV3610599	single nucleotide variant	NM_182532.3(TMEM61):c.394T>G (p.Tyr132Asp)	not specified [RCV004880281]	uncertain significance	1	54991864	54991864	Human		name
598252606	CV3913974	single nucleotide variant	NM_182532.3(TMEM61):c.443C>A (p.Pro148His)	not specified [RCV005278113]	uncertain significance	1	54991913	54991913	Human		name

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