Tmem190 Variant Search Result - Rat Genome Database

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28 records found for search term Tmem190

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
407453535	CV3486490	single nucleotide variant	NM_139172.3(TMEM190):c.41T>A (p.Leu14Gln)	not specified [RCV004684578]	uncertain significance	19	55376894	55376894	Human		name
156087744	CV2337025	single nucleotide variant	NM_139172.3(TMEM190):c.152G>T (p.Ser51Ile)	not specified [RCV004192793]	uncertain significance	19	55377650	55377650	Human		name
156091626	CV2389482	single nucleotide variant	NM_139172.3(TMEM190):c.145A>G (p.Ile49Val)	not specified [RCV004243564]	uncertain significance	19	55377643	55377643	Human		name
401752567	CV2682863	single nucleotide variant	NM_139172.3(TMEM190):c.194G>A (p.Gly65Glu)	not specified [RCV004283663]	uncertain significance	19	55377692	55377692	Human		name
401870015	CV2772594	single nucleotide variant	NM_139172.3(TMEM190):c.212G>A (p.Arg71His)	not specified [RCV004355348]	uncertain significance	19	55377710	55377710	Human		name
405753468	CV3336189	single nucleotide variant	NM_139172.3(TMEM190):c.122A>T (p.Glu41Val)	not specified [RCV004467416]	uncertain significance	19	55377620	55377620	Human		name
407453546	CV3486494	single nucleotide variant	NM_139172.3(TMEM190):c.131G>C (p.Gly44Ala)	not specified [RCV004684582]	uncertain significance	19	55377629	55377629	Human		name
407453551	CV3486496	single nucleotide variant	NM_139172.3(TMEM190):c.260C>T (p.Thr87Met)	not specified [RCV004684584]	uncertain significance	19	55377841	55377841	Human		name
597753703	CV3613619	single nucleotide variant	NM_139172.3(TMEM190):c.187C>T (p.Arg63Cys)	not specified [RCV004867430]	uncertain significance	19	55377685	55377685	Human		name
156122641	CV2241149	single nucleotide variant	NM_139172.3(TMEM190):c.325G>A (p.Val109Met)	not specified [RCV004104176]	likely benign	19	55377994	55377994	Human		name
156170501	CV2247386	single nucleotide variant	NM_139172.3(TMEM190):c.422C>T (p.Thr141Met)	not specified [RCV004108723]	uncertain significance	19	55378091	55378091	Human		name
156344922	CV2294304	single nucleotide variant	NM_139172.3(TMEM190):c.317G>A (p.Arg106His)	not specified [RCV004151432]	uncertain significance	19	55377986	55377986	Human		name
155902180	CV2356407	single nucleotide variant	NM_139172.3(TMEM190):c.325G>C (p.Val109Leu)	not specified [RCV004206208]	likely benign	19	55377994	55377994	Human		name
401730229	CV2680054	single nucleotide variant	NM_139172.3(TMEM190):c.376G>A (p.Val126Ile)	not specified [RCV004286550]	uncertain significance	19	55378045	55378045	Human		name
401749438	CV2712353	single nucleotide variant	NM_139172.3(TMEM190):c.332A>G (p.His111Arg)	not specified [RCV004313836]	uncertain significance	19	55378001	55378001	Human		name
405753463	CV3336190	single nucleotide variant	NM_139172.3(TMEM190):c.316C>T (p.Arg106Cys)	not specified [RCV004467417]	uncertain significance	19	55377985	55377985	Human		name
405753453	CV3336191	single nucleotide variant	NM_139172.3(TMEM190):c.356C>T (p.Pro119Leu)	not specified [RCV004467418]	uncertain significance	19	55378025	55378025	Human		name
405753448	CV3336192	single nucleotide variant	NM_139172.3(TMEM190):c.371A>G (p.Lys124Arg)	not specified [RCV004467419]	likely benign	19	55378040	55378040	Human		name
405753443	CV3336193	single nucleotide variant	NM_139172.3(TMEM190):c.404C>T (p.Thr135Ile)	not specified [RCV004467420]	uncertain significance	19	55378073	55378073	Human		name
405753436	CV3336194	single nucleotide variant	NM_139172.3(TMEM190):c.430G>A (p.Val144Met)	not specified [RCV004467421]	uncertain significance	19	55378099	55378099	Human		name
405753431	CV3336195	single nucleotide variant	NM_139172.3(TMEM190):c.478G>A (p.Glu160Lys)	not specified [RCV004467422]	uncertain significance	19	55378147	55378147	Human		name
405753425	CV3336196	single nucleotide variant	NM_139172.3(TMEM190):c.491C>G (p.Thr164Arg)	not specified [RCV004467423]	uncertain significance	19	55378160	55378160	Human		name
405753418	CV3336197	single nucleotide variant	NM_139172.3(TMEM190):c.500G>A (p.Gly167Asp)	not specified [RCV004467424]	uncertain significance	19	55378169	55378169	Human		name
407453538	CV3486491	single nucleotide variant	NM_139172.3(TMEM190):c.517G>A (p.Glu173Lys)	not specified [RCV004684579]	uncertain significance	19	55378186	55378186	Human		name
407453540	CV3486492	single nucleotide variant	NM_139172.3(TMEM190):c.413C>T (p.Thr138Met)	not specified [RCV004684580]	uncertain significance	19	55378082	55378082	Human		name
407453549	CV3486495	single nucleotide variant	NM_139172.3(TMEM190):c.527A>T (p.Glu176Val)	not specified [RCV004684583]	uncertain significance	19	55378196	55378196	Human		name
597753695	CV3613617	single nucleotide variant	NM_139172.3(TMEM190):c.340G>A (p.Gly114Ser)	not specified [RCV004867428]	uncertain significance	19	55378009	55378009	Human		name
597753699	CV3613618	single nucleotide variant	NM_139172.3(TMEM190):c.481G>C (p.Gly161Arg)	not specified [RCV004867429]	uncertain significance	19	55378150	55378150	Human		name

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