ClinVar (all) for Orgtrack (Select 507812) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 983225	NM_000245.4(MET):c.3028G>A (p.Asp1010Asn)	MET (D1010N +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 160364	NM_005343.4(HRAS):c.182A>G (p.Gln61Arg)	LRRC56, HRAS (Q61R)	Single nucleotide variant (missense variant +1 more)	Noonan syndrome and Noonan-related syndrome +1 more	GLikely pathogenic