Rgs4 Variant Search Result - Rat Genome Database

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27 records found for search term Rgs4

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
329370615	CV2435592	single nucleotide variant	NM_005613.6(RGS4):c.-62G>T	not specified [RCV004254844]	uncertain significance	1	163069423	163069423	Human		name
405716032	CV3309268	single nucleotide variant	NM_005613.6(RGS4):c.-47C>T	not specified [RCV004449207]	uncertain significance	1	163069438	163069438	Human		name
156169669	CV2296659	single nucleotide variant	NM_005613.6(RGS4):c.89C>T (p.Ser30Phe)	not specified [RCV004154712]	uncertain significance	1	163072439	163072439	Human		name
597788159	CV3586404	single nucleotide variant	NM_005613.6(RGS4):c.28G>T (p.Ala10Ser)	not specified [RCV004855425]	uncertain significance	1	163069512	163069512	Human		name
155920263	CV2343320	single nucleotide variant	NM_005613.6(RGS4):c.232G>A (p.Ala78Thr)	not specified [RCV004194937]	uncertain significance	1	163073476	163073476	Human		name
407474329	CV3472844	single nucleotide variant	NM_005613.6(RGS4):c.220G>A (p.Ala74Thr)	not specified [RCV004662972]	uncertain significance	1	163073464	163073464	Human		name
597788155	CV3586403	single nucleotide variant	NM_005613.6(RGS4):c.170A>G (p.Lys57Arg)	not specified [RCV004855424]	uncertain significance	1	163072825	163072825	Human		name
155969746	CV2244649	single nucleotide variant	NM_005613.6(RGS4):c.400A>T (p.Arg134Trp)	not specified [RCV004102362]	uncertain significance	1	163074342	163074342	Human		name
155941791	CV2300929	single nucleotide variant	NM_005613.6(RGS4):c.523C>A (p.Leu175Ile)	not specified [RCV004158116]	uncertain significance	1	163074465	163074465	Human		name
401752033	CV2723095	single nucleotide variant	NM_005613.6(RGS4):c.338A>G (p.Lys113Arg)	not specified [RCV004327570]	uncertain significance	1	163073582	163073582	Human		name
401876736	CV2754461	single nucleotide variant	NM_005613.6(RGS4):c.539C>T (p.Pro180Leu)	not specified [RCV004336673]	uncertain significance	1	163074481	163074481	Human		name
405716036	CV3309269	single nucleotide variant	NM_005613.6(RGS4):c.395G>A (p.Cys132Tyr)	not specified [RCV004449208]	uncertain significance	1	163074337	163074337	Human		name
405716051	CV3309271	single nucleotide variant	NM_005613.6(RGS4):c.451G>A (p.Glu151Lys)	not specified [RCV004449210]	uncertain significance	1	163074393	163074393	Human		name
405716056	CV3309272	single nucleotide variant	NM_005613.6(RGS4):c.539C>G (p.Pro180Arg)	not specified [RCV004449211]	uncertain significance	1	163074481	163074481	Human		name
407508133	CV3472842	single nucleotide variant	NM_005613.6(RGS4):c.497G>A (p.Arg166His)	not specified [RCV004671944]	uncertain significance	1	163074439	163074439	Human		name
597788150	CV3586401	single nucleotide variant	NM_005613.6(RGS4):c.548G>A (p.Cys183Tyr)	not specified [RCV004855423]	uncertain significance	1	163074490	163074490	Human		name
597775897	CV3586402	single nucleotide variant	NM_005613.6(RGS4):c.561G>C (p.Lys187Asn)	not specified [RCV004852377]	uncertain significance	1	163074503	163074503	Human		name
598189319	CV3902602	single nucleotide variant	NM_005613.6(RGS4):c.407A>C (p.Glu136Ala)	not specified [RCV005266696]	uncertain significance	1	163074349	163074349	Human		name
598189327	CV3902603	single nucleotide variant	NM_005613.6(RGS4):c.589T>G (p.Cys197Gly)	not specified [RCV005266697]	uncertain significance	1	163074531	163074531	Human		name
598189336	CV3902604	single nucleotide variant	NM_005613.6(RGS4):c.574A>G (p.Lys192Glu)	not specified [RCV005266698]	uncertain significance	1	163074516	163074516	Human		name
156395339	CV2329142	single nucleotide variant	NM_001102445.3(RGS4):c.61G>T (p.Ala21Ser)	not specified [RCV004173901]	uncertain significance	1	163069254	163069254	Human		name
156048640	CV2382691	single nucleotide variant	NM_001102445.3(RGS4):c.89C>T (p.Ala30Val)	not specified [RCV004233004]	uncertain significance	1	163069282	163069282	Human		name
155996415	CV2398538	single nucleotide variant	NM_001102445.3(RGS4):c.44G>A (p.Gly15Glu)	not specified [RCV004237857]	likely benign	1	163068978	163068978	Human		name
156329031	CV2213749	single nucleotide variant	NM_001102445.3(RGS4):c.155C>A (p.Thr52Lys)	not specified [RCV004089818]	uncertain significance	1	163069348	163069348	Human		name
155916348	CV2336134	single nucleotide variant	NM_001102445.3(RGS4):c.124G>T (p.Gly42Cys)	not specified [RCV004189727]	uncertain significance	1	163069317	163069317	Human		name
407450676	CV3472843	single nucleotide variant	NM_001102445.3(RGS4):c.128G>T (p.Arg43Leu)	not specified [RCV004662971]	uncertain significance	1	163069321	163069321	Human		name
407450678	CV3472845	single nucleotide variant	NM_001102445.3(RGS4):c.127C>A (p.Arg43Ser)	not specified [RCV004662973]	uncertain significance	1	163069320	163069320	Human		name

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