ClinVar Miner

List of variants in gene BRAF reported as likely benign

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Total variants: 88
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HGVS dbSNP
NC_000007.14:g.140924603G>A
NC_000007.14:g.140924615C>T
NM_004333.5(BRAF):c.-295G>A
NM_004333.5(BRAF):c.2128-6_2128-5dup rs373442098
NM_004333.6(BRAF):c.*111C>T rs539860876
NM_004333.6(BRAF):c.*387G>A rs114105685
NM_004333.6(BRAF):c.*7T>C rs727502903
NM_004333.6(BRAF):c.-19C>T rs71645935
NM_004333.6(BRAF):c.-24dup rs1395865715
NM_004333.6(BRAF):c.-5A>G rs71645936
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.1068A>G (p.Gln356=) rs143335467
NM_004333.6(BRAF):c.1084C>A (p.Arg362=) rs397516885
NM_004333.6(BRAF):c.111G>A (p.Ser37=) rs727502906
NM_004333.6(BRAF):c.1141-12A>G rs375704079
NM_004333.6(BRAF):c.1150A>G (p.Arg384Gly) rs545495379
NM_004333.6(BRAF):c.1178-104C>G
NM_004333.6(BRAF):c.1203C>T (p.Thr401=) rs370130654
NM_004333.6(BRAF):c.1207C>G (p.Pro403Ala) rs749792302
NM_004333.6(BRAF):c.1209T>C (p.Pro403=) rs397516887
NM_004333.6(BRAF):c.1227A>G (p.Ser409=) rs145035762
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.1332G>A (p.Arg444=) rs56101602
NM_004333.6(BRAF):c.1347T>C (p.Asp449=) rs397516889
NM_004333.6(BRAF):c.1383A>G (p.Gln461=) rs56216404
NM_004333.6(BRAF):c.1433-19A>G rs369635503
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.1632T>C (p.Ile544=) rs149702741
NM_004333.6(BRAF):c.1694+13C>T
NM_004333.6(BRAF):c.1694+14G>A rs184144181
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.193T>C (p.Leu65=) rs866875749
NM_004333.6(BRAF):c.1956A>C (p.Gly652=) rs1554392528
NM_004333.6(BRAF):c.1960T>C (p.Leu654=) rs727502905
NM_004333.6(BRAF):c.1993-18dup rs759069424
NM_004333.6(BRAF):c.2019C>T (p.Tyr673=) rs759664527
NM_004333.6(BRAF):c.2127+3A>G rs371976102
NM_004333.6(BRAF):c.2127+7A>G rs371857758
NM_004333.6(BRAF):c.2128-10T>C rs397516898
NM_004333.6(BRAF):c.2128-4G>T rs956143558
NM_004333.6(BRAF):c.2128-5del rs373442098
NM_004333.6(BRAF):c.2128-6T>A rs397516900
NM_004333.6(BRAF):c.2136C>T (p.Ala712=) rs377165711
NM_004333.6(BRAF):c.2142T>C (p.Ile714=) rs1554388024
NM_004333.6(BRAF):c.2196C>G (p.Ser732=) rs142592480
NM_004333.6(BRAF):c.2224G>A (p.Asp742Asn) rs1057520665
NM_004333.6(BRAF):c.2229T>C (p.Phe743=) rs397516901
NM_004333.6(BRAF):c.2235A>G (p.Leu745=) rs56046546
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.279A>G (p.Gln93=) rs150050723
NM_004333.6(BRAF):c.36G>A (p.Ala12=) rs397507454
NM_004333.6(BRAF):c.375T>G (p.Ser125=) rs201507202
NM_004333.6(BRAF):c.439A>G (p.Ser147Gly) rs397507464
NM_004333.6(BRAF):c.483G>C (p.Leu161=) rs61730029
NM_004333.6(BRAF):c.504+17A>G rs201797624
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.708C>T (p.Asn236=) rs138333692
NM_004333.6(BRAF):c.711+15A>G rs1554404457
NM_004333.6(BRAF):c.714A>T (p.Val238=) rs397516902
NM_004333.6(BRAF):c.723G>A (p.Thr241=) rs369182143
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.73C>T (p.Pro25Ser) rs730880412
NM_004333.6(BRAF):c.76G>A (p.Glu26Lys) rs397507457
NM_004333.6(BRAF):c.78G>T (p.Glu26Asp) rs371877084
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.918C>G (p.Ser306=) rs794727865
NM_004333.6(BRAF):c.92C>G (p.Ala31Gly) rs397516906
NM_004333.6(BRAF):c.976A>G (p.Ile326Val) rs775040765
NM_004333.6(BRAF):c.981-14C>A rs200002171
NM_004333.6(BRAF):c.995C>T (p.Thr332Ile) rs1008080053

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