ClinVar Miner

List of variants in gene BRAF reported as uncertain significance

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Total variants: 120
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HGVS dbSNP
NC_000007.13:g.(?_140434377)_(140534692_?)dup
NC_000007.13:g.(?_140434387)_(140534682_?)dup
NC_000007.14:g.140778013T>G
NM_004333.4(BRAF):c.2128-16_2128-15delCT rs886062015
NM_004333.5(BRAF):c.2128-28dup rs60814637
NM_004333.6(BRAF):c.*3C>T rs746680490
NM_004333.6(BRAF):c.*7T>C rs727502903
NM_004333.6(BRAF):c.-95_-90GCCTCC[3] rs727502907
NM_004333.6(BRAF):c.-9G>T rs1161647286
NM_004333.6(BRAF):c.1001C>T (p.Pro334Leu) rs730880418
NM_004333.6(BRAF):c.1022C>A (p.Pro341Gln) rs863224722
NM_004333.6(BRAF):c.1022C>T (p.Pro341Leu) rs863224722
NM_004333.6(BRAF):c.1024A>G (p.Ile342Val) rs201481342
NM_004333.6(BRAF):c.1027C>T (p.Pro343Ser) rs758935249
NM_004333.6(BRAF):c.1031A>T (p.Gln344Leu) rs758920663
NM_004333.6(BRAF):c.1040G>C (p.Arg347Pro) rs397516884
NM_004333.6(BRAF):c.1055A>G (p.Asp352Gly) rs201882896
NM_004333.6(BRAF):c.1079G>A (p.Arg360Gln) rs730880415
NM_004333.6(BRAF):c.107C>T (p.Ser36Phe) rs886041827
NM_004333.6(BRAF):c.111G>A (p.Ser37=) rs727502906
NM_004333.6(BRAF):c.113C>T (p.Ala38Val) rs886042293
NM_004333.6(BRAF):c.1144T>A (p.Leu382Met)
NM_004333.6(BRAF):c.1157A>G (p.Gln386Arg) rs1554401118
NM_004333.6(BRAF):c.1165C>T (p.Arg389Cys) rs397507472
NM_004333.6(BRAF):c.1166G>A (p.Arg389His) rs577372072
NM_004333.6(BRAF):c.1168G>A (p.Gly390Ser) rs886041424
NM_004333.6(BRAF):c.1178-10A>G rs527835644
NM_004333.6(BRAF):c.1183A>G (p.Thr395Ala) rs397516886
NM_004333.6(BRAF):c.1189G>T (p.Gly397Cys) rs760702929
NM_004333.6(BRAF):c.1190G>A (p.Gly397Asp) rs1554400237
NM_004333.6(BRAF):c.1196C>T (p.Ser399Phe) rs1554400234
NM_004333.6(BRAF):c.1205C>G (p.Pro402Arg)
NM_004333.6(BRAF):c.1206C>T (p.Pro402=) rs201758035
NM_004333.6(BRAF):c.1207C>G (p.Pro403Ala) rs749792302
NM_004333.6(BRAF):c.1237G>A (p.Val413Met) rs377093637
NM_004333.6(BRAF):c.1283C>T (p.Ser428Leu) rs1562957703
NM_004333.6(BRAF):c.1305G>A (p.Arg435=) rs763771673
NM_004333.6(BRAF):c.1317A>G (p.Lys439=)
NM_004333.6(BRAF):c.131C>T (p.Pro44Leu) rs794726917
NM_004333.6(BRAF):c.138+17C>G rs756400234
NM_004333.6(BRAF):c.138+3G>A rs1554430994
NM_004333.6(BRAF):c.1382A>G (p.Gln461Arg) rs1554399925
NM_004333.6(BRAF):c.1391G>A (p.Gly464Glu) rs121913348
NM_004333.6(BRAF):c.1405G>T (p.Gly469Ter) rs121913357
NM_004333.6(BRAF):c.1411G>T (p.Val471Phe) rs121913376
NM_004333.6(BRAF):c.1433-19A>G rs369635503
NM_004333.6(BRAF):c.1455G>T (p.Leu485Phe) rs180177036
NM_004333.6(BRAF):c.1488A>C (p.Gln496His) rs1554399258
NM_004333.6(BRAF):c.1518-9T>G rs758498850
NM_004333.6(BRAF):c.1595G>A (p.Cys532Tyr) rs397507479
NM_004333.6(BRAF):c.1643T>C (p.Phe548Ser) rs1562954580
NM_004333.6(BRAF):c.1661T>C (p.Ile554Thr) rs878854675
NM_004333.6(BRAF):c.1694+2T>C rs1057517930
NM_004333.6(BRAF):c.1756G>A (p.Glu586Lys) rs121913340
NM_004333.6(BRAF):c.1775T>C (p.Ile592Thr) rs55939351
NM_004333.6(BRAF):c.1781A>T (p.Asp594Val) rs121913338
NM_004333.6(BRAF):c.1786G>T (p.Gly596Cys) rs121913361
NM_004333.6(BRAF):c.1796C>T (p.Thr599Ile) rs121913375
NM_004333.6(BRAF):c.1799T>G (p.Val600Gly) rs113488022
NM_004333.6(BRAF):c.1860+3A>G rs886041842
NM_004333.6(BRAF):c.1940A>G (p.Tyr647Cys) rs1562939198
NM_004333.6(BRAF):c.1950G>C (p.Met650Ile) rs879255380
NM_004333.6(BRAF):c.2015G>T (p.Gly672Val) rs1428696172
NM_004333.6(BRAF):c.2026C>T (p.Pro676Ser) rs1554389860
NM_004333.6(BRAF):c.2029G>A (p.Asp677Asn) rs886041260
NM_004333.6(BRAF):c.2064C>T (p.Ala688=) rs1554389847
NM_004333.6(BRAF):c.206G>C (p.Gly69Ala) rs1554412417
NM_004333.6(BRAF):c.2082A>G (p.Ala694=) rs375174370
NM_004333.6(BRAF):c.2101A>G (p.Arg701Gly) rs886041257
NM_004333.6(BRAF):c.2125C>A (p.Gln709Lys) rs1554389828
NM_004333.6(BRAF):c.2128-15dup rs373442098
NM_004333.6(BRAF):c.2128-27_2128-16delinsTCT rs886062016
NM_004333.6(BRAF):c.2128-2_2128del rs1176881402
NM_004333.6(BRAF):c.2128-4del rs886062014
NM_004333.6(BRAF):c.2135C>T (p.Ala712Val)
NM_004333.6(BRAF):c.2264_2265delinsGT (p.Ile755Ser) rs1064795542
NM_004333.6(BRAF):c.2279A>G (p.Tyr760Cys) rs1305119093
NM_004333.6(BRAF):c.240+11G>A rs730880379
NM_004333.6(BRAF):c.254A>G (p.Tyr85Cys) rs1131691387
NM_004333.6(BRAF):c.259A>G (p.Ser87Gly) rs876661018
NM_004333.6(BRAF):c.272C>T (p.Ala91Val) rs886041256
NM_004333.6(BRAF):c.281A>G (p.Gln94Arg) rs1562985576
NM_004333.6(BRAF):c.316G>A (p.Gly106Arg) rs749247588
NM_004333.6(BRAF):c.325T>A (p.Phe109Ile) rs397507460
NM_004333.6(BRAF):c.358G>A (p.Val120Ile) rs766748977
NM_004333.6(BRAF):c.365C>A (p.Ser122Tyr) rs397507462
NM_004333.6(BRAF):c.37G>A (p.Glu13Lys) rs1563042573
NM_004333.6(BRAF):c.398C>T (p.Ser133Leu) rs1057517889
NM_004333.6(BRAF):c.39G>C (p.Glu13Asp)
NM_004333.6(BRAF):c.41C>G (p.Pro14Arg) rs397507455
NM_004333.6(BRAF):c.437G>A (p.Arg146Gln) rs557241012
NM_004333.6(BRAF):c.469G>A (p.Val157Ile) rs1258111302
NM_004333.6(BRAF):c.48G>C (p.Gln16His) rs1563042542
NM_004333.6(BRAF):c.517T>C (p.Cys173Arg) rs749677118
NM_004333.6(BRAF):c.523G>T (p.Val175Phe) rs1554404622
NM_004333.6(BRAF):c.527C>T (p.Thr176Ile) rs780556975
NM_004333.6(BRAF):c.533G>A (p.Arg178Gln) rs746348396
NM_004333.6(BRAF):c.622A>G (p.Ile208Val) rs727504571
NM_004333.6(BRAF):c.64G>A (p.Asp22Asn) rs397507456
NM_004333.6(BRAF):c.653C>G (p.Thr218Ser) rs1554404461
NM_004333.6(BRAF):c.68T>A (p.Met23Lys)
NM_004333.6(BRAF):c.69G>T (p.Met23Ile) rs1064796897
NM_004333.6(BRAF):c.70G>A (p.Glu24Lys) rs730880416
NM_004333.6(BRAF):c.711+4T>C rs1562969586
NM_004333.6(BRAF):c.722C>A (p.Thr241Lys) rs387906660
NM_004333.6(BRAF):c.739T>G (p.Phe247Val) rs397516903
NM_004333.6(BRAF):c.73C>A (p.Pro25Thr) rs730880412
NM_004333.6(BRAF):c.793G>C (p.Gly265Arg) rs397516905
NM_004333.6(BRAF):c.812G>A (p.Arg271His) rs730880413
NM_004333.6(BRAF):c.83_88GCGCCG[1] (p.28_29GA[1]) rs397507458
NM_004333.6(BRAF):c.83_88GCGCCG[2] (p.28_29GA[2]) rs397507458
NM_004333.6(BRAF):c.83_88GCGCCG[4] (p.28_29GA[4]) rs397507458
NM_004333.6(BRAF):c.83_88GCGCCG[5] (p.28_29GA[5]) rs397507458
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.956C>T (p.Ser319Phe) rs886041599
NM_004333.6(BRAF):c.967T>C (p.Ser323Pro) rs730880414
NM_004333.6(BRAF):c.968C>T (p.Ser323Leu) rs397516907
NM_004333.6(BRAF):c.977T>C (p.Ile326Thr) rs368435578
NM_004333.6(BRAF):c.981-14C>A rs200002171

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