Rgs8 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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14 records found for search term Rgs8

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156319896	CV2200622	single nucleotide variant	NM_001102450.3(RGS8):c.-164G>A	not specified [RCV004078959]	uncertain significance	1	182671717	182671717	Human		name
329391934	CV2463789	single nucleotide variant	NM_001102450.3(RGS8):c.-123A>G	not specified [RCV004279618]	uncertain significance	1	182671676	182671676	Human		name
156308235	CV2332267	single nucleotide variant	NM_001102450.3(RGS8):c.30C>A (p.Asn10Lys)	not specified [RCV004182437]	uncertain significance	1	182666970	182666970	Human		name
407474372	CV3472855	single nucleotide variant	NM_001102450.3(RGS8):c.62C>G (p.Ser21Cys)	not specified [RCV004662983]	uncertain significance	1	182666938	182666938	Human		name
155972333	CV2271519	single nucleotide variant	NM_001102450.3(RGS8):c.252A>T (p.Glu84Asp)	not specified [RCV004128610]	uncertain significance	1	182648245	182648245	Human		name
405716161	CV3309288	single nucleotide variant	NM_001102450.3(RGS8):c.147A>T (p.Glu49Asp)	not specified [RCV004449227]	uncertain significance	1	182666015	182666015	Human		name
407454067	CV3416456	single nucleotide variant	NM_001102450.3(RGS8):c.284C>T (p.Thr95Ile)	not provided [RCV004597714]	benign	1	182648213	182648213	Human		name
598189432	CV3902617	single nucleotide variant	NM_001102450.3(RGS8):c.118C>T (p.Arg40Cys)	not specified [RCV005266711]	uncertain significance	1	182666882	182666882	Human		name
598189446	CV3902619	single nucleotide variant	NM_001102450.3(RGS8):c.276C>A (p.Phe92Leu)	not specified [RCV005266713]	uncertain significance	1	182648221	182648221	Human		name
156144892	CV2196745	single nucleotide variant	NM_001102450.3(RGS8):c.298A>G (p.Lys100Glu)	not specified [RCV004069766]	uncertain significance	1	182648199	182648199	Human		name
155919737	CV2279469	single nucleotide variant	NM_001102450.3(RGS8):c.501G>C (p.Met167Ile)	not specified [RCV004141996]	uncertain significance	1	182646777	182646777	Human		name
156201984	CV2313186	single nucleotide variant	NM_001102450.3(RGS8):c.356G>A (p.Arg119Gln)	not specified [RCV004161445]	uncertain significance	1	182648141	182648141	Human		name
405716167	CV3309289	single nucleotide variant	NM_001102450.3(RGS8):c.402C>A (p.Asn134Lys)	not specified [RCV004449228]	uncertain significance	1	182646876	182646876	Human		name
597775933	CV3586418	single nucleotide variant	NM_001102450.3(RGS8):c.484T>C (p.Phe162Leu)	not specified [RCV004852386]	uncertain significance	1	182646794	182646794	Human		name