ClinVar Miner

List of variants in gene BRAF reported as likely benign by GeneDx

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Gene type:
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Total variants: 39
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HGVS dbSNP
NM_004333.5(BRAF):c.-295G>A
NM_004333.6(BRAF):c.-24dup rs1395865715
NM_004333.6(BRAF):c.1023A>G (p.Pro341=) rs56092510
NM_004333.6(BRAF):c.1024A>G (p.Ile342Val) rs201481342
NM_004333.6(BRAF):c.111G>A (p.Ser37=) rs727502906
NM_004333.6(BRAF):c.1141-12A>G rs375704079
NM_004333.6(BRAF):c.1178-104C>G
NM_004333.6(BRAF):c.1236C>T (p.Asn412=) rs397516888
NM_004333.6(BRAF):c.1314+12T>C rs765090629
NM_004333.6(BRAF):c.1314+17T>C rs1057524397
NM_004333.6(BRAF):c.1433-7C>G rs1057522055
NM_004333.6(BRAF):c.1517+185G>A
NM_004333.6(BRAF):c.1518-5T>C rs940384157
NM_004333.6(BRAF):c.1518-7T>C rs199745091
NM_004333.6(BRAF):c.1694+13C>T
NM_004333.6(BRAF):c.1694+8C>T rs1057520453
NM_004333.6(BRAF):c.1742-10T>G rs730880411
NM_004333.6(BRAF):c.1860+16A>G rs368859030
NM_004333.6(BRAF):c.1956A>C (p.Gly652=) rs1554392528
NM_004333.6(BRAF):c.1993-18dup rs759069424
NM_004333.6(BRAF):c.2224G>A (p.Asp742Asn) rs1057520665
NM_004333.6(BRAF):c.240+6C>T rs1320075163
NM_004333.6(BRAF):c.240+72A>G
NM_004333.6(BRAF):c.241-8T>A rs963659807
NM_004333.6(BRAF):c.439A>G (p.Ser147Gly) rs397507464
NM_004333.6(BRAF):c.504+19C>T rs780617193
NM_004333.6(BRAF):c.567T>C (p.Gly189=) rs1057523903
NM_004333.6(BRAF):c.622A>G (p.Ile208Val) rs727504571
NM_004333.6(BRAF):c.675A>G (p.Glu225=) rs755993280
NM_004333.6(BRAF):c.711+15A>G rs1554404457
NM_004333.6(BRAF):c.72G>C (p.Glu24Asp) rs587778114
NM_004333.6(BRAF):c.73C>T (p.Pro25Ser) rs730880412
NM_004333.6(BRAF):c.76G>A (p.Glu26Lys) rs397507457
NM_004333.6(BRAF):c.83_88GCGCCG[2] (p.28_29GA[2]) rs397507458
NM_004333.6(BRAF):c.855A>G (p.Gln285=) rs376575252
NM_004333.6(BRAF):c.861T>C (p.Asp287=)
NM_004333.6(BRAF):c.876C>T (p.Ser292=) rs1554403310
NM_004333.6(BRAF):c.92C>G (p.Ala31Gly) rs397516906
NM_004333.6(BRAF):c.981-14C>A rs200002171

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