CN029449[trait identifier] AND "Institute for Genomic Statistics and B - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 376289	NM_004333.6(BRAF):c.1798G>C (p.Val600Leu)	BRAF (V600L +7 more)	Single nucleotide variant (missense variant)	Cardiofaciocutaneous syndrome 1	GPathogenic/Likely pathogenic
Select item 280033	NM_004333.6(BRAF):c.1796C>G (p.Thr599Arg)	BRAF (T599R +7 more)	Single nucleotide variant (missense variant)	RASopathy	GPathogenic FDA Recognized database
Select item 40387	NM_004333.6(BRAF):c.1787G>T (p.Gly596Val)	BRAF (G596V +7 more)	Single nucleotide variant (missense variant)	RASopathy	GPathogenic FDA Recognized database
Select item 13974	NM_004333.6(BRAF):c.1406G>A (p.Gly469Glu)	BRAF (G469E +7 more)	Single nucleotide variant (missense variant)	Cardio-facio-cutaneous syndrome	GPathogenic FDA Recognized database
Select item 13973	NM_004333.6(BRAF):c.770A>G (p.Gln257Arg)	BRAF (Q257R +4 more)	Single nucleotide variant (missense variant)	Cardio-facio-cutaneous syndrome	GPathogenic FDA Recognized database
Select item 163768	NM_004985.5(KRAS):c.108A>G (p.Ile36Met)	KRAS (I36M)	Single nucleotide variant (missense variant)	KRAS-related condition +6 more	GPathogenic/Likely pathogenic

ClinVar