"Ambry Genetics"[submitter] AND "LOC117125599"[gene] - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2285030	NM_017805.3(RASIP1):c.2872C>T (p.Pro958Ser)	LOC117125599, RASIP1 (P958S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2367017	NM_017805.3(RASIP1):c.2842G>A (p.Glu948Lys)	LOC117125599, RASIP1 (E948K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2265445	NM_017805.3(RASIP1):c.2840A>G (p.Gln947Arg)	LOC117125599, RASIP1 (Q947R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2265573	NM_017805.3(RASIP1):c.2833G>A (p.Glu945Lys)	LOC117125599, RASIP1 (E945K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2301861	NM_017805.3(RASIP1):c.2813G>A (p.Arg938His)	LOC117125599, RASIP1 (R938H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3312952	NM_017805.3(RASIP1):c.2806A>G (p.Arg936Gly)	LOC117125599, RASIP1 (R936G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2542295	NM_017805.3(RASIP1):c.2793C>A (p.His931Gln)	LOC117125599, RASIP1 (H931Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2403184	NM_017805.3(RASIP1):c.2783A>G (p.Asp928Gly)	LOC117125599, RASIP1 (D928G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151896	NM_017805.3(RASIP1):c.2695G>A (p.Asp899Asn)	LOC117125599, RASIP1 (D899N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance