Usp46 Variant Search Result - Rat Genome Database

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15 records found for search term Usp46

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15165797	CV698547	single nucleotide variant	NM_022832.4(USP46):c.165C>T (p.Phe55=)	not provided [RCV000948679]	benign	4	52628116	52628116	Human		name
597799059	CV3623177	single nucleotide variant	NM_022832.4(USP46):c.35T>C (p.Met12Thr)	not specified [RCV004879512]	uncertain significance	4	52659116	52659116	Human		name
15196462	CV698546	single nucleotide variant	NM_022832.4(USP46):c.963C>T (p.His321=)	not provided [RCV000956197]	benign	4	52598664	52598664	Human		name
156078717	CV2300847	single nucleotide variant	NM_022832.4(USP46):c.178C>T (p.Arg60Trp)	not specified [RCV004158053]	uncertain significance	4	52628103	52628103	Human		name
156063991	CV2352882	single nucleotide variant	NM_022832.4(USP46):c.233C>T (p.Thr78Met)	not specified [RCV004200929]	uncertain significance	4	52628048	52628048	Human		name
156401844	CV2371012	single nucleotide variant	NM_022832.4(USP46):c.242C>T (p.Ala81Val)	not specified [RCV004220779]	uncertain significance	4	52628039	52628039	Human		name
156339821	CV2268014	single nucleotide variant	NM_022832.4(USP46):c.907G>A (p.Val303Ile)	not specified [RCV004136570]	uncertain significance	4	52601870	52601870	Human		name
329372001	CV2454943	single nucleotide variant	NM_022832.4(USP46):c.798A>C (p.Arg266Ser)	not specified [RCV004272223]	uncertain significance	4	52601979	52601979	Human		name
329380922	CV2464395	single nucleotide variant	NM_022832.4(USP46):c.797G>A (p.Arg266Lys)	not specified [RCV004276330]	uncertain significance	4	52601980	52601980	Human		name
407528950	CV3487682	single nucleotide variant	NM_022832.4(USP46):c.473C>T (p.Ala158Val)	not specified [RCV004680647]	uncertain significance	4	52626106	52626106	Human		name
597799057	CV3623175	single nucleotide variant	NM_022832.4(USP46):c.524C>T (p.Thr175Met)	not specified [RCV004879511]	uncertain significance	4	52626055	52626055	Human		name
597799061	CV3623178	single nucleotide variant	NM_022832.4(USP46):c.851A>G (p.Asn284Ser)	not specified [RCV004879513]	uncertain significance	4	52601926	52601926	Human		name
597799063	CV3623179	single nucleotide variant	NM_022832.4(USP46):c.461T>C (p.Met154Thr)	not specified [RCV004879514]	uncertain significance	4	52626118	52626118	Human		name
598238826	CV3932921	single nucleotide variant	NM_022832.4(USP46):c.781A>C (p.Met261Leu)	not specified [RCV005296481]	uncertain significance	4	52601996	52601996	Human		name
8579955	CV114357	single nucleotide variant	NM_001134223.1(USP46):c.560A>T (p.Asp187Val)	Lung cancer [RCV000094880]	uncertain significance	4	52610598	52610598	Human		name