List of variants in gene BRAF reported as likely pathogenic for B-cell neoplasm

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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: 25

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HGVS	dbSNP	gnomAD frequency
NM_004333.6(BRAF):c.1391G>A (p.Gly464Glu)	rs121913348
NM_004333.6(BRAF):c.1397G>A (p.Gly466Glu)	rs121913351
NM_004333.6(BRAF):c.1397G>C (p.Gly466Ala)	rs121913351
NM_004333.6(BRAF):c.1397G>T (p.Gly466Val)	rs121913351
NM_004333.6(BRAF):c.1405G>C (p.Gly469Arg)	rs121913357
NM_004333.6(BRAF):c.1406G>A (p.Gly469Glu)	rs121913355
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.1574T>G (p.Leu525Arg)	rs869025340
NM_004333.6(BRAF):c.1741A>C (p.Asn581His)	rs180177040
NM_004333.6(BRAF):c.1742A>C (p.Asn581Thr)	rs121913370
NM_004333.6(BRAF):c.1742A>G (p.Asn581Ser)	rs121913370
NM_004333.6(BRAF):c.1780G>A (p.Asp594Asn)	rs397516896
NM_004333.6(BRAF):c.1780G>C (p.Asp594His)	rs397516896
NM_004333.6(BRAF):c.1781A>G (p.Asp594Gly)	rs121913338
NM_004333.6(BRAF):c.1786G>A (p.Gly596Ser)	rs121913361
NM_004333.6(BRAF):c.1786G>C (p.Gly596Arg)	rs121913361
NM_004333.6(BRAF):c.1787G>A (p.Gly596Asp)	rs397507483
NM_004333.6(BRAF):c.1787G>T (p.Gly596Val)	rs397507483
NM_004333.6(BRAF):c.1790T>A (p.Leu597Gln)	rs121913366
NM_004333.6(BRAF):c.1790T>G (p.Leu597Arg)	rs121913366
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.1802A>C (p.Lys601Thr)	rs397507484
NM_004333.6(BRAF):c.1803A>C (p.Lys601Asn)	rs121913365

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