Tmem160 Variant Search Result - Rat Genome Database

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17 records found for search term Tmem160

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156204588	CV2252491	single nucleotide variant	NM_017854.2(TMEM160):c.10G>T (p.Gly4Cys)	not specified [RCV004116606]	uncertain significance	19	47048605	47048605	Human		name
155920340	CV2210785	single nucleotide variant	NM_017854.2(TMEM160):c.49C>T (p.Arg17Cys)	not specified [RCV004085878]	uncertain significance	19	47048566	47048566	Human		name
156050316	CV2336586	single nucleotide variant	NM_017854.2(TMEM160):c.35G>T (p.Arg12Leu)	not specified [RCV004196834]	uncertain significance	19	47048580	47048580	Human		name
401749512	CV2703172	single nucleotide variant	NM_017854.2(TMEM160):c.70C>T (p.Pro24Ser)	not specified [RCV004315240]	uncertain significance	19	47048545	47048545	Human		name
407453362	CV3486423	single nucleotide variant	NM_017854.2(TMEM160):c.37C>G (p.Leu13Val)	not specified [RCV004684518]	uncertain significance	19	47048578	47048578	Human		name
598213220	CV3917445	single nucleotide variant	NM_017854.2(TMEM160):c.98C>G (p.Ala33Gly)	not specified [RCV005292275]	uncertain significance	19	47048517	47048517	Human		name
156085007	CV2289770	single nucleotide variant	NM_017854.2(TMEM160):c.112G>A (p.Ala38Thr)	not specified [RCV004150455]	uncertain significance	19	47048503	47048503	Human		name
405794530	CV3336028	single nucleotide variant	NM_017854.2(TMEM160):c.145C>G (p.Pro49Ala)	not specified [RCV004475273]	uncertain significance	19	47048470	47048470	Human		name
597752986	CV3616917	single nucleotide variant	NM_017854.2(TMEM160):c.124G>A (p.Gly42Ser)	not specified [RCV004867278]	uncertain significance	19	47048491	47048491	Human		name
597753000	CV3616920	single nucleotide variant	NM_017854.2(TMEM160):c.215T>C (p.Leu72Pro)	not specified [RCV004867281]	uncertain significance	19	47046679	47046679	Human		name
155962755	CV2285693	single nucleotide variant	NM_017854.2(TMEM160):c.326G>A (p.Cys109Tyr)	not specified [RCV004141541]	uncertain significance	19	47046228	47046228	Human		name
156196173	CV2297312	single nucleotide variant	NM_017854.2(TMEM160):c.371T>C (p.Leu124Pro)	not specified [RCV004152973]	uncertain significance	19	47046183	47046183	Human		name
329354142	CV2447186	single nucleotide variant	NM_017854.2(TMEM160):c.469A>G (p.Met157Val)	not specified [RCV004262489]	uncertain significance	19	47046085	47046085	Human		name
401778938	CV2732998	single nucleotide variant	NM_017854.2(TMEM160):c.452G>A (p.Cys151Tyr)	not specified [RCV004331173]	uncertain significance	19	47046102	47046102	Human		name
401891136	CV2769070	single nucleotide variant	NM_017854.2(TMEM160):c.431C>T (p.Ala144Val)	not specified [RCV004348933]	uncertain significance	19	47046123	47046123	Human		name
405794536	CV3336030	single nucleotide variant	NM_017854.2(TMEM160):c.461G>A (p.Gly154Asp)	not specified [RCV004475275]	uncertain significance	19	47046093	47046093	Human		name
597752995	CV3616919	single nucleotide variant	NM_017854.2(TMEM160):c.352G>A (p.Ala118Thr)	not specified [RCV004867280]	likely benign	19	47046202	47046202	Human		name