ClinVar Miner

List of variants in gene BRAF reported as likely pathogenic for Cutaneous melanoma

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Total variants: 30
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HGVS dbSNP
NM_004333.6(BRAF):c.1330C>T (p.Arg444Trp) rs121913371
NM_004333.6(BRAF):c.1390G>A (p.Gly464Arg) rs121913349
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.1405G>A (p.Gly469Arg) rs121913357
NM_004333.6(BRAF):c.1405G>C (p.Gly469Arg) rs121913357
NM_004333.6(BRAF):c.1405_1406delinsTC (p.Gly469Ser) rs1057519720
NM_004333.6(BRAF):c.1406G>A (p.Gly469Glu) rs121913355
NM_004333.6(BRAF):c.1411G>T (p.Val471Phe) rs121913376
NM_004333.6(BRAF):c.1742A>G (p.Asn581Ser) rs121913370
NM_004333.6(BRAF):c.1756G>A (p.Glu586Lys) rs121913340
NM_004333.6(BRAF):c.1774A>G (p.Ile592Val) rs121913363
NM_004333.6(BRAF):c.1781A>C (p.Asp594Ala) rs121913338
NM_004333.6(BRAF):c.1783T>C (p.Phe595Leu) rs794729219
NM_004333.6(BRAF):c.1784T>C (p.Phe595Ser) rs121913225
NM_004333.6(BRAF):c.1785T>A (p.Phe595Leu) rs121913341
NM_004333.6(BRAF):c.1785T>G (p.Phe595Leu) rs121913341
NM_004333.6(BRAF):c.1786G>C (p.Gly596Arg) rs121913361
NM_004333.6(BRAF):c.1796C>T (p.Thr599Ile) rs121913375
NM_004333.6(BRAF):c.1798G>C (p.Val600Leu) rs121913378
NM_004333.6(BRAF):c.1798G>T (p.Val600Leu) rs121913378
NM_004333.6(BRAF):c.1799T>C (p.Val600Ala) rs113488022
NM_004333.6(BRAF):c.1799_1800delinsAA (p.Val600Glu) rs121913377
NM_004333.6(BRAF):c.1801A>G (p.Lys601Glu) rs121913364
NM_004333.6(BRAF):c.1801_1803del (p.Lys601del) rs121913226
NM_004333.6(BRAF):c.1802A>G (p.Lys601Arg) rs397507484
NM_004333.6(BRAF):c.1803A>C (p.Lys601Asn) rs121913365
NM_004333.6(BRAF):c.1803A>T (p.Lys601Asn) rs121913365
NM_004333.6(BRAF):c.1813_1814delinsTT (p.Ser605Phe) rs121913372
NM_004333.6(BRAF):c.1814G>A (p.Ser605Asn) rs121913373

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