"Ambry Genetics"[submitter] AND "GPRC5B"[gene] - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2603803	NM_016235.3(GPRC5B):c.1193C>T (p.Thr398Ile)	GPRC5B (T529I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2228843	NM_016235.3(GPRC5B):c.1100C>T (p.Pro367Leu)	GPRC5B (P367L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2311155	NM_016235.3(GPRC5B):c.983G>A (p.Arg328Gln)	GPRC5B (R328Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2389347	NM_016235.3(GPRC5B):c.932C>T (p.Ser311Leu)	GPRC5B (S311L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2313491	NM_016235.3(GPRC5B):c.919T>A (p.Tyr307Asn)	GPRC5B (Y438N +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2344554	NM_016235.3(GPRC5B):c.850G>A (p.Val284Ile)	GPRC5B (V284I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2380750	NM_016235.3(GPRC5B):c.787C>A (p.Gln263Lys)	GPRC5B (Q394K +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2348605	NM_016235.3(GPRC5B):c.670G>A (p.Gly224Ser)	GPRC5B (G224S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2612632	NM_016235.3(GPRC5B):c.661A>C (p.Thr221Pro)	GPRC5B (T352P +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2386207	NM_016235.3(GPRC5B):c.455G>A (p.Arg152Gln)	GPRC5B (R283Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2383914	NM_016235.3(GPRC5B):c.442C>T (p.Arg148Trp)	GPRC5B (R279W +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2605681	NM_016235.3(GPRC5B):c.208A>T (p.Thr70Ser)	GPRC5B (T201S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2229276	NM_016235.3(GPRC5B):c.38A>G (p.Gln13Arg)	GPRC5B (Q13R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance