"Ambry Genetics"[submitter] AND "RGS8"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2290963	NM_001102450.3(RGS8):c.501G>C (p.Met167Ile)	RGS8 (M185I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2316501	NM_001102450.3(RGS8):c.356G>A (p.Arg119Gln)	RGS8 (R119Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2206810	NM_001102450.3(RGS8):c.298A>G (p.Lys100Glu)	RGS8 (K118E +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2275216	NM_001102450.3(RGS8):c.252A>T (p.Glu84Asp)	RGS8 (E102D +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2347794	NM_001102450.3(RGS8):c.30C>A (p.Asn10Lys)	RGS8 (N10K +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2488539	NM_001102450.3(RGS8):c.-123A>G	RGS8 (M21V)	Single nucleotide variant (5 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2208528	NM_001102450.3(RGS8):c.-164G>A	RGS8 (R7Q)	Single nucleotide variant (5 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance

ClinVar