ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 53
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_004333.6(BRAF):c.64G>A (p.Asp22Asn) rs397507456 0.00025
NM_004333.6(BRAF):c.968C>T (p.Ser323Leu) rs397516907 0.00012
NM_004333.6(BRAF):c.505-12A>G rs377433501 0.00006
NM_004333.6(BRAF):c.52C>G (p.Leu18Val) rs1222192591 0.00006
NM_004333.6(BRAF):c.1992+8T>C rs753545284 0.00005
NM_004333.6(BRAF):c.*7T>C rs727502903 0.00002
NM_004333.6(BRAF):c.1166G>A (p.Arg389His) rs577372072 0.00001
NM_004333.6(BRAF):c.1178-10A>G rs527835644 0.00001
NM_004333.6(BRAF):c.1237G>A (p.Val413Met) rs377093637 0.00001
NM_004333.6(BRAF):c.1369A>T (p.Ile457Phe) rs1008100536 0.00001
NM_004333.6(BRAF):c.1673G>A (p.Arg558Gln) rs1278812236 0.00001
NM_004333.6(BRAF):c.1690A>G (p.Met564Val) rs745783052 0.00001
NM_004333.6(BRAF):c.2029G>A (p.Asp677Asn) rs886041260 0.00001
NM_004333.6(BRAF):c.316G>A (p.Gly106Arg) rs749247588 0.00001
NM_004333.6(BRAF):c.437G>A (p.Arg146Gln) rs557241012 0.00001
NM_004333.6(BRAF):c.612G>C (p.Glu204Asp) rs1202874043 0.00001
NM_004333.6(BRAF):c.82G>A (p.Gly28Ser) rs1437317949 0.00001
NM_001378469.1(BRAF):c.1178-61A>G rs397516886
NM_004333.6(BRAF):c.1151G>A (p.Arg384Lys)
NM_004333.6(BRAF):c.1189G>A (p.Gly397Ser)
NM_004333.6(BRAF):c.1205C>G (p.Pro402Arg) rs199927105
NM_004333.6(BRAF):c.121C>T (p.Pro41Ser)
NM_004333.6(BRAF):c.1253A>G (p.Lys418Arg)
NM_004333.6(BRAF):c.1256C>T (p.Ser419Phe) rs2129026318
NM_004333.6(BRAF):c.1327_1388dup (p.Gly464fs) rs1800883856
NM_004333.6(BRAF):c.139-16T>C rs1809013029
NM_004333.6(BRAF):c.1405G>T (p.Gly469Ter) rs121913357
NM_004333.6(BRAF):c.1441G>A (p.Ala481Thr)
NM_004333.6(BRAF):c.1488A>C (p.Gln496His) rs1554399258
NM_004333.6(BRAF):c.1518-7T>G rs199745091
NM_004333.6(BRAF):c.159G>A (p.Met53Ile) rs2129073763
NM_004333.6(BRAF):c.1756G>A (p.Glu586Lys) rs121913340
NM_004333.6(BRAF):c.1786G>T (p.Gly596Cys) rs121913361
NM_004333.6(BRAF):c.1861-5A>G rs2128994669
NM_004333.6(BRAF):c.1889A>G (p.Lys630Arg) rs1797604920
NM_004333.6(BRAF):c.1950G>C (p.Met650Ile) rs879255380
NM_004333.6(BRAF):c.2045G>A (p.Arg682Gln) rs1796764011
NM_004333.6(BRAF):c.20G>A (p.Gly7Asp)
NM_004333.6(BRAF):c.2128-16_2128-6del rs749903414
NM_004333.6(BRAF):c.281A>G (p.Gln94Arg) rs1562985576
NM_004333.6(BRAF):c.331G>T (p.Val111Phe) rs1807139980
NM_004333.6(BRAF):c.398C>T (p.Ser133Leu) rs1057517889
NM_004333.6(BRAF):c.39G>C (p.Glu13Asp) rs868441785
NM_004333.6(BRAF):c.469G>A (p.Val157Ile) rs1258111302
NM_004333.6(BRAF):c.527C>T (p.Thr176Ile) rs780556975
NM_004333.6(BRAF):c.608+19G>A rs200908826
NM_004333.6(BRAF):c.653C>G (p.Thr218Ser) rs1554404461
NM_004333.6(BRAF):c.708C>A (p.Asn236Lys) rs138333692
NM_004333.6(BRAF):c.711+4T>C rs1562969586
NM_004333.6(BRAF):c.739T>G (p.Phe247Val) rs397516903
NM_004333.6(BRAF):c.826G>C (p.Val276Leu) rs1057518105
NM_004333.6(BRAF):c.858T>G (p.Leu286=) rs758553809
NM_004333.6(BRAF):c.980+13T>C rs1802961360

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.