"Laboratory of Translational Genomics, National Cancer Institute"[subm - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 132971	NM_033360.4(KRAS):c.219G>A (p.Arg73=)	KRAS	Single nucleotide variant (synonymous variant)	Sarcoma	Gnot provided
Select item 132970	NM_033360.4(KRAS):c.216G>A (p.Met72Ile)	KRAS (M72I)	Single nucleotide variant (missense variant)	Sarcoma	Gnot provided
Select item 132969	NM_033360.4(KRAS):c.176C>T (p.Ala59Val)	KRAS (A59V)	Single nucleotide variant (missense variant)	Familial cancer of breast	Gnot provided
Select item 12589	NM_004985.5(KRAS):c.40G>A (p.Val14Ile)	KRAS (V14I)	Single nucleotide variant (missense variant)	Noonan syndrome	GPathogenic FDA Recognized database
Select item 12584	NM_004985.5(KRAS):c.34G>A (p.Gly12Ser)	KRAS (G12S)	Single nucleotide variant (missense variant)	not provided +2 more	GPathogenic
Select item 12578	NM_004985.5(KRAS):c.34G>T (p.Gly12Cys)	KRAS (G12C)	Single nucleotide variant (missense variant)	RASopathy	GLikely pathogenic

ClinVar