List of variants in gene BRAF reported as pathogenic for lung disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_004333.6(BRAF):c.1391G>T (p.Gly464Val)	rs121913348
NM_004333.6(BRAF):c.1397G>T (p.Gly466Val)	rs121913351
NM_004333.6(BRAF):c.1405_1406delinsTT (p.Gly469Leu)	rs1057519720
NM_004333.6(BRAF):c.1405_1407del (p.Gly469del)	rs397516890
NM_004333.6(BRAF):c.1406G>C (p.Gly469Ala)	rs121913355
NM_004333.6(BRAF):c.1406G>T (p.Gly469Val)	rs121913355
NM_004333.6(BRAF):c.1415A>G (p.Tyr472Cys)	rs1057519719
NM_004333.6(BRAF):c.1495A>G (p.Lys499Glu)	rs180177037
NM_004333.6(BRAF):c.1781A>G (p.Asp594Gly)	rs121913338
NM_004333.6(BRAF):c.1789C>G (p.Leu597Val)	rs121913369
NM_004333.6(BRAF):c.1790T>G (p.Leu597Arg)	rs121913366
NM_004333.6(BRAF):c.1794_1796dup (p.Thr599dup)	rs727502902
NM_004333.6(BRAF):c.1799T>A (p.Val600Glu)	rs113488022
NM_004333.6(BRAF):c.1801A>G (p.Lys601Glu)	rs121913364
NM_004333.6(BRAF):c.721A>C (p.Thr241Pro)	rs387906661
NM_004333.6(BRAF):c.722C>T (p.Thr241Met)	rs387906660
NM_004333.6(BRAF):c.770A>G (p.Gln257Arg)	rs180177035

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