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

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2394591	NM_016732.3(RALY):c.55A>G (p.Ile19Val)	RALY (I19V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151336	NM_016732.3(RALY):c.191A>G (p.Asn64Ser)	RALY (N64S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3312648	NM_016732.3(RALY):c.463G>A (p.Val155Ile)	RALY (V139I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2286762	NM_016732.3(RALY):c.470G>A (p.Arg157His)	RALY (R141H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3312649	NM_016732.3(RALY):c.535A>G (p.Lys179Glu)	RALY (K179E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151337	NM_016732.3(RALY):c.575C>T (p.Thr192Met)	LOC126863016, RALY (T192M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2357183	NM_016732.3(RALY):c.620G>A (p.Arg207His)	LOC126863016, RALY (R191H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2204500	NM_016732.3(RALY):c.665A>G (p.Lys222Arg)	LOC126863016, RALY (K222R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3312647	NM_016732.3(RALY):c.706G>C (p.Gly236Arg)	LOC126863016, RALY (G236R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2386743	NM_016732.3(RALY):c.739G>A (p.Gly247Ser)	LOC126863016, RALY (G247S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151338	NM_016732.3(RALY):c.820C>T (p.Arg274Trp)	LOC126863016, RALY (R258W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance