ClinVar Miner

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

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Total variants: 56
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HGVS dbSNP
NM_004333.6(BRAF):c.-9G>T rs1161647286
NM_004333.6(BRAF):c.1001C>T (p.Pro334Leu) rs730880418
NM_004333.6(BRAF):c.1022C>T (p.Pro341Leu) rs863224722
NM_004333.6(BRAF):c.1027C>T (p.Pro343Ser) rs758935249
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.1165C>T (p.Arg389Cys) rs397507472
NM_004333.6(BRAF):c.1168G>A (p.Gly390Ser) rs886041424
NM_004333.6(BRAF):c.1189G>T (p.Gly397Cys) rs760702929
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.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.1433-19A>G rs369635503
NM_004333.6(BRAF):c.1518-9T>G rs758498850
NM_004333.6(BRAF):c.1694+2T>C rs1057517930
NM_004333.6(BRAF):c.1775T>C (p.Ile592Thr) rs55939351
NM_004333.6(BRAF):c.1860+3A>G rs886041842
NM_004333.6(BRAF):c.1940A>G (p.Tyr647Cys) rs1562939198
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.2101A>G (p.Arg701Gly) rs886041257
NM_004333.6(BRAF):c.2128-2_2128del rs1176881402
NM_004333.6(BRAF):c.2135C>T (p.Ala712Val)
NM_004333.6(BRAF):c.2264_2265delinsGT (p.Ile755Ser) rs1064795542
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.325T>A (p.Phe109Ile) rs397507460
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.41C>G (p.Pro14Arg) rs397507455
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.622A>G (p.Ile208Val) rs727504571
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.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.918C>G (p.Ser306=) rs794727865
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.977T>C (p.Ile326Thr) rs368435578

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