"Mayo Clinic Laboratories, Mayo Clinic"[submitter] AND "BRAF"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 252627	NM_004333.6(BRAF):c.1950G>C (p.Met650Ile)	BRAF (M650I +7 more)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 13974	NM_004333.6(BRAF):c.1406G>A (p.Gly469Glu)	BRAF (G469E +7 more)	Single nucleotide variant (missense variant)	RASopathy	GPathogenic FDA Recognized database
Select item 1163474	NM_004333.6(BRAF):c.1402T>C (p.Phe468Leu)	BRAF (F380L +7 more)	Single nucleotide variant (missense variant)	not provided	GLikely pathogenic
Select item 1163475	NM_004333.6(BRAF):c.786A>G (p.Gln262=)	BRAF	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 13965	NM_004333.6(BRAF):c.736G>C (p.Ala246Pro)	BRAF (A246P +4 more)	Single nucleotide variant (missense variant)	Cardio-facio-cutaneous syndrome	GPathogenic FDA Recognized database
Select item 505121	NM_004333.6(BRAF):c.316G>A (p.Gly106Arg)	BRAF (G106R +2 more)	Single nucleotide variant (missense variant +1 more)	not provided +4 more	GUncertain significance
Select item 1047782	NM_004333.6(BRAF):c.112G>C (p.Ala38Pro)	BRAF (A38P)	Single nucleotide variant (missense variant)	not provided +9 more	GUncertain significance
Select item 2683000	NM_004333.6(BRAF):c.74C>T (p.Pro25Leu)	BRAF (P25L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

ClinVar