ClinVar Miner

List of variants in gene BRAF reported as likely benign for not provided

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Total variants: 44
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HGVS dbSNP
NM_001374258.1(BRAF):c.102G>C (p.Ala34=) rs1372257667
NM_001374258.1(BRAF):c.105C>G (p.Ala35=) rs1320140960
NM_001374258.1(BRAF):c.1084C>A (p.Arg362=) rs397516885
NM_001374258.1(BRAF):c.111G>A (p.Ser37=) rs727502906
NM_001374258.1(BRAF):c.1398G>A (p.Arg466=) rs1586146368
NM_001374258.1(BRAF):c.1637+9G>C rs956390000
NM_001374258.1(BRAF):c.1752T>C (p.Ile584=) rs149702741
NM_001374258.1(BRAF):c.21C>A (p.Gly7=) rs1196182256
NM_001374258.1(BRAF):c.2248-27_2248-7del rs754390169
NM_001374258.1(BRAF):c.357C>T (p.Thr119=) rs552456345
NM_001374258.1(BRAF):c.363A>G (p.Thr121=) rs1586339911
NM_001374258.1(BRAF):c.411T>G (p.Val137=) rs1586339662
NM_001374258.1(BRAF):c.483G>C (p.Leu161=) rs61730029
NM_001374258.1(BRAF):c.622A>G (p.Ile208Val) rs727504571
NM_001374258.1(BRAF):c.687T>C (p.Asn229=) rs1586237175
NM_001374258.1(BRAF):c.738A>G (p.Ala246=) rs1586213511
NM_001374258.1(BRAF):c.78G>T (p.Glu26Asp) rs371877084
NM_001374258.1(BRAF):c.822A>G (p.Thr274=) rs779713260
NM_001374258.1(BRAF):c.862T>C (p.Leu288=) rs773839216
NM_001374258.1(BRAF):c.957C>T (p.Ser319=) rs754029526
NM_004333.5(BRAF):c.-295G>A rs71645931
NM_004333.6(BRAF):c.-24dup rs1395865715
NM_004333.6(BRAF):c.1024A>G (p.Ile342Val) rs201481342
NM_004333.6(BRAF):c.1141-12A>G rs375704079
NM_004333.6(BRAF):c.1178-104C>G rs71645967
NM_004333.6(BRAF):c.1236C>T (p.Asn412=) rs397516888
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 rs117044637
NM_004333.6(BRAF):c.1694+13C>T rs368578780
NM_004333.6(BRAF):c.1694+8C>T rs1057520453
NM_004333.6(BRAF):c.1742-10T>C rs730880411
NM_004333.6(BRAF):c.1742-10T>G rs730880411
NM_004333.6(BRAF):c.1860+16A>G rs368859030
NM_004333.6(BRAF):c.2082A>G (p.Ala694=) rs375174370
NM_004333.6(BRAF):c.2196C>G (p.Ser732=) rs142592480
NM_004333.6(BRAF):c.240+72A>G rs71645941
NM_004333.6(BRAF):c.567T>C (p.Gly189=) rs1057523903
NM_004333.6(BRAF):c.72G>A (p.Glu24=) rs587778114
NM_004333.6(BRAF):c.72G>C (p.Glu24Asp) rs587778114
NM_004333.6(BRAF):c.83_88GCGCCG[2] (p.28_29GA[2]) rs397507458
NM_004333.6(BRAF):c.861T>C (p.Asp287=) rs761326211
NM_004333.6(BRAF):c.876C>T (p.Ser292=) rs1554403310
NM_004333.6(BRAF):c.981-14C>A rs200002171

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