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

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3151653	NM_000966.6(RARG):c.511G>C (p.Val171Leu)	RARG (V50L +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2543727	NM_000966.6(RARG):c.511G>A (p.Val171Met)	RARG (V50M +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2214248	NM_000966.6(RARG):c.495C>G (p.Asn165Lys)	RARG (N154K +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151652	NM_000966.6(RARG):c.383G>A (p.Arg128His)	RARG (R128H +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151654	NM_000966.6(RARG):c.82G>A (p.Ala28Thr)	RARG (A28T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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