ClinVar Miner

List of variants in gene BRAF reported as likely benign for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 23
Download table as spreadsheet
HGVS dbSNP
NM_004333.4(BRAF):c.1141-12A>G rs375704079
NM_004333.4(BRAF):c.1314+17T>C rs1057524397
NM_004333.4(BRAF):c.1433-7C>G rs1057522055
NM_004333.4(BRAF):c.1694+8C>T rs1057520453
NM_004333.4(BRAF):c.1860+16A>G rs368859030
NM_004333.4(BRAF):c.567T>C (p.Gly189=) rs1057523903
NM_004333.4(BRAF):c.876C>T (p.Ser292=) rs1554403310
NM_004333.4(BRAF):c.981-14C>A rs200002171
NM_004333.5(BRAF):c.-24dup
NM_004333.5(BRAF):c.-295G>A
NM_004333.5(BRAF):c.1024A>G (p.Ile342Val) rs201481342
NM_004333.5(BRAF):c.111G>A (p.Ser37=) rs727502906
NM_004333.5(BRAF):c.1178-104C>G
NM_004333.5(BRAF):c.1236C>T (p.Asn412=) rs397516888
NM_004333.5(BRAF):c.1517+185G>A
NM_004333.5(BRAF):c.1694+13C>T
NM_004333.5(BRAF):c.1742-10T>G rs730880411
NM_004333.5(BRAF):c.240+72A>G
NM_004333.5(BRAF):c.622A>G (p.Ile208Val) rs727504571
NM_004333.5(BRAF):c.72G>C (p.Glu24Asp) rs587778114
NM_004333.5(BRAF):c.78G>T (p.Glu26Asp) rs371877084
NM_004333.5(BRAF):c.861T>C (p.Asp287=)
NM_004333.5(BRAF):c.95_100del (p.Gly32_Ala33del) rs397507458

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.