ClinVar Miner

List of variants in gene BRAF reported as uncertain significance for not provided

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Gene type:
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Total variants: 98
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HGVS dbSNP gnomAD frequency
NM_004333.6(BRAF):c.1433-19A>G rs369635503 0.00114
NM_004333.6(BRAF):c.915G>A (p.Ala305=) rs145675911 0.00004
NM_004333.6(BRAF):c.240+11G>A rs730880379 0.00003
NM_004333.6(BRAF):c.977T>C (p.Ile326Thr) rs368435578 0.00003
NM_004333.6(BRAF):c.1165C>T (p.Arg389Cys) rs397507472 0.00002
NM_004333.6(BRAF):c.138+17C>G rs756400234 0.00002
NM_004333.6(BRAF):c.1518-9T>G rs758498850 0.00002
NM_004333.6(BRAF):c.61G>C (p.Gly21Arg) rs587778113 0.00002
NM_004333.6(BRAF):c.-9G>T rs1161647286 0.00001
NM_004333.6(BRAF):c.107C>T (p.Ser36Phe) rs886041827 0.00001
NM_004333.6(BRAF):c.113C>T (p.Ala38Val) rs886042293 0.00001
NM_004333.6(BRAF):c.1168G>A (p.Gly390Ser) rs886041424 0.00001
NM_004333.6(BRAF):c.1305G>A (p.Arg435=) rs763771673 0.00001
NM_004333.6(BRAF):c.1673G>A (p.Arg558Gln) rs1278812236 0.00001
NM_004333.6(BRAF):c.2015G>T (p.Gly672Val) rs1428696172 0.00001
NM_004333.6(BRAF):c.2029G>A (p.Asp677Asn) rs886041260 0.00001
NM_004333.6(BRAF):c.2156G>A (p.Arg719His) rs368528867 0.00001
NM_004333.6(BRAF):c.254A>G (p.Tyr85Cys) rs1131691387 0.00001
NM_004333.6(BRAF):c.365C>A (p.Ser122Tyr) rs397507462 0.00001
NM_004333.6(BRAF):c.41C>G (p.Pro14Arg) rs397507455 0.00001
NM_004333.6(BRAF):c.712G>A (p.Val238Ile) rs373935661 0.00001
NM_004333.6(BRAF):c.111G>A (p.Ser37=) rs727502906
NM_004333.6(BRAF):c.112G>T (p.Ala38Ser)
NM_004333.6(BRAF):c.1141G>A (p.Asp381Asn) rs2129031601
NM_004333.6(BRAF):c.1189G>T (p.Gly397Cys) rs760702929
NM_004333.6(BRAF):c.1205C>A (p.Pro402His) rs199927105
NM_004333.6(BRAF):c.1207C>G (p.Pro403Ala) rs749792302
NM_004333.6(BRAF):c.1209del (p.Ala404fs)
NM_004333.6(BRAF):c.1258C>T (p.Pro420Ser)
NM_004333.6(BRAF):c.1283C>T (p.Ser428Leu) rs1562957703
NM_004333.6(BRAF):c.1317A>G (p.Lys439=) rs569455230
NM_004333.6(BRAF):c.131C>T (p.Pro44Leu) rs794726917
NM_004333.6(BRAF):c.1444G>C (p.Val482Leu) rs765715150
NM_004333.6(BRAF):c.159G>A (p.Met53Ile) rs2129073763
NM_004333.6(BRAF):c.1694+2T>C rs1057517930
NM_004333.6(BRAF):c.1695-1G>T rs2128999725
NM_004333.6(BRAF):c.1723A>G (p.Arg575Gly)
NM_004333.6(BRAF):c.1726G>T (p.Asp576Tyr) rs1057517915
NM_004333.6(BRAF):c.1742A>C (p.Asn581Thr) rs121913370
NM_004333.6(BRAF):c.1750C>T (p.Leu584Phe) rs1586015221
NM_004333.6(BRAF):c.1775T>C (p.Ile592Thr) rs55939351
NM_004333.6(BRAF):c.1789C>T (p.Leu597=) rs121913369
NM_004333.6(BRAF):c.1790T>C (p.Leu597Pro) rs121913366
NM_004333.6(BRAF):c.1794_1796dup (p.Thr599dup) rs727502902
NM_004333.6(BRAF):c.1798G>A (p.Val600Met) rs121913378
NM_004333.6(BRAF):c.1798_1799delinsAA (p.Val600Lys) rs121913227
NM_004333.6(BRAF):c.1799T>A (p.Val600Glu) rs113488022
NM_004333.6(BRAF):c.1799T>G (p.Val600Gly) rs113488022
NM_004333.6(BRAF):c.1799_1801del (p.Val600_Lys601delinsGlu) rs397516897
NM_004333.6(BRAF):c.1807C>T (p.Arg603Ter) rs104886015
NM_004333.6(BRAF):c.1860+3A>G rs886041842
NM_004333.6(BRAF):c.1891A>T (p.Asn631Tyr)
NM_004333.6(BRAF):c.1897T>C (p.Tyr633His) rs746010267
NM_004333.6(BRAF):c.1933G>C (p.Val645Leu)
NM_004333.6(BRAF):c.1939T>C (p.Tyr647His) rs1797600635
NM_004333.6(BRAF):c.1940A>G (p.Tyr647Cys) rs1562939198
NM_004333.6(BRAF):c.1976T>C (p.Ile659Thr) rs2128994327
NM_004333.6(BRAF):c.1990C>G (p.Gln664Glu) rs754481830
NM_004333.6(BRAF):c.1992+3A>G rs1797595959
NM_004333.6(BRAF):c.1995A>G (p.Ile665Met) rs2130901050
NM_004333.6(BRAF):c.2026C>T (p.Pro676Ser) rs1554389860
NM_004333.6(BRAF):c.2044C>T (p.Arg682Trp)
NM_004333.6(BRAF):c.206G>C (p.Gly69Ala) rs1554412417
NM_004333.6(BRAF):c.2101A>G (p.Arg701Gly) rs886041257
NM_004333.6(BRAF):c.2128-2_2128del rs1176881402
NM_004333.6(BRAF):c.2134G>A (p.Ala712Thr) rs1481562268
NM_004333.6(BRAF):c.2135C>T (p.Ala712Val) rs727502904
NM_004333.6(BRAF):c.2264_2265delinsGT (p.Ile755Ser) rs1064795542
NM_004333.6(BRAF):c.2290C>T (p.Pro764Ser)
NM_004333.6(BRAF):c.2291C>T (p.Pro764Leu) rs139420557
NM_004333.6(BRAF):c.260G>A (p.Ser87Asn) rs1033856250
NM_004333.6(BRAF):c.272C>T (p.Ala91Val) rs886041256
NM_004333.6(BRAF):c.27_32dup (p.Gly11_Ala12insGlyGly)
NM_004333.6(BRAF):c.325T>A (p.Phe109Ile) rs397507460
NM_004333.6(BRAF):c.37G>A (p.Glu13Lys) rs1563042573
NM_004333.6(BRAF):c.413T>C (p.Phe138Ser) rs1339350570
NM_004333.6(BRAF):c.48G>C (p.Gln16His) rs1563042542
NM_004333.6(BRAF):c.497G>A (p.Arg166Lys) rs2129061937
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.69G>T (p.Met23Ile) rs1064796897
NM_004333.6(BRAF):c.70G>A (p.Glu24Lys) rs730880416
NM_004333.6(BRAF):c.73C>A (p.Pro25Thr) rs730880412
NM_004333.6(BRAF):c.74C>T (p.Pro25Leu)
NM_004333.6(BRAF):c.779G>A (p.Arg260His) rs1586213318
NM_004333.6(BRAF):c.786A>G (p.Gln262=) rs2129044317
NM_004333.6(BRAF):c.812G>A (p.Arg271His) rs730880413
NM_004333.6(BRAF):c.83GCGCCG[1] (p.28GA[1]) rs397507458
NM_004333.6(BRAF):c.83GCGCCG[2] (p.28GA[2]) rs397507458
NM_004333.6(BRAF):c.83GCGCCG[4] (p.28GA[4]) rs397507458
NM_004333.6(BRAF):c.83GCGCCG[5] (p.28GA[5]) rs397507458
NM_004333.6(BRAF):c.913G>A (p.Ala305Thr) rs964235659
NM_004333.6(BRAF):c.918C>G (p.Ser306=) rs794727865
NM_004333.6(BRAF):c.943G>A (p.Gly315Arg)
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.973T>G (p.Ser325Ala)
NM_004333.6(BRAF):c.98C>T (p.Ala33Val) rs2129153230

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