RGS4[gene] and "single gene"[properties] - ClinVar

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Items: 20

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2407598	NM_001102445.3(RGS4):c.44G>A (p.Gly15Glu)	RGS4 (G15E)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2338099	NM_001102445.3(RGS4):c.61G>T (p.Ala21Ser)	RGS4 (A21S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2395459	NM_001102445.3(RGS4):c.89C>T (p.Ala30Val)	RGS4 (A30V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2350784	NM_001102445.3(RGS4):c.124G>T (p.Gly42Cys)	RGS4 (G42C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3314127	NM_001102445.3(RGS4):c.127C>A (p.Arg43Ser)	RGS4 (R43S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3314125	NM_001102445.3(RGS4):c.128G>T (p.Arg43Leu)	RGS4 (R43L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2220400	NM_001102445.3(RGS4):c.155C>A (p.Thr52Lys)	RGS4 (T52K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2459444	NM_005613.6(RGS4):c.-62G>T	RGS4 (R77L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3153910	NM_005613.6(RGS4):c.-47C>T	RGS4 (S82F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2303420	NM_005613.6(RGS4):c.89C>T (p.Ser30Phe)	RGS4 (S127F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3314126	NM_005613.6(RGS4):c.220G>A (p.Ala74Thr)	RGS4 (A56T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2353579	NM_005613.6(RGS4):c.232G>A (p.Ala78Thr)	RGS4 (A175T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2558084	NM_005613.6(RGS4):c.338A>G (p.Lys113Arg)	RGS4 (K113R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3153911	NM_005613.6(RGS4):c.395G>A (p.Cys132Tyr)	RGS4 (C114Y +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2246155	NM_005613.6(RGS4):c.400A>T (p.Arg134Trp)	RGS4 (R116W +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3153913	NM_005613.6(RGS4):c.451G>A (p.Glu151Lys)	RGS4 (E133K +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3314124	NM_005613.6(RGS4):c.497G>A (p.Arg166His)	RGS4 (R263H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2309855	NM_005613.6(RGS4):c.523C>A (p.Leu175Ile)	RGS4 (L175I +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3153914	NM_005613.6(RGS4):c.539C>G (p.Pro180Arg)	RGS4 (P180R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2589105	NM_005613.6(RGS4):c.539C>T (p.Pro180Leu)	RGS4 (P162L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 20