"3billion"[submitter] AND "KRAS"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 12586	NM_004985.5(KRAS):c.178G>C (p.Gly60Arg)	KRAS (G60R)	Single nucleotide variant (missense variant)	Cardio-facio-cutaneous syndrome	GPathogenic FDA Recognized database
Select item 40454	NM_004985.5(KRAS):c.101C>T (p.Pro34Leu)	KRAS (P34L)	Single nucleotide variant (missense variant)	Noonan syndrome	GPathogenic FDA Recognized database
Select item 1333392	NM_004985.5(KRAS):c.76A>C (p.Asn26His)	KRAS (N26H)	Single nucleotide variant (missense variant)	Noonan syndrome 3	GUncertain significance
Select item 40452	NM_004985.5(KRAS):c.65A>G (p.Gln22Arg)	KRAS (Q22R)	Single nucleotide variant (missense variant)	Noonan syndrome	GPathogenic FDA Recognized database
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 45123	NM_004985.5(KRAS):c.37G>T (p.Gly13Cys)	KRAS (G13C)	Single nucleotide variant (missense variant)	Autoimmune lymphoproliferative syndrome type 4 +3 more	GPathogenic/Likely pathogenic
Select item 12582	NM_004985.5(KRAS):c.35G>A (p.Gly12Asp)	KRAS (G12D)	Single nucleotide variant (missense variant)	RASopathy +6 more	GPathogenic/Likely pathogenic OOncogenic

ClinVar