ClinVar Miner

Variants in gene BRAF with conflicting interpretations "uncertain significance" and "likely benign"

Submission 1 (uncertain significance) minimum review status: Submission 1 (uncertain significance) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 7
Download table as spreadsheet
NM_001374258.1(BRAF):c.111G>A (p.Ser37=) rs727502906
NM_001374258.1(BRAF):c.1553-19A>G rs369635503
NM_001374258.1(BRAF):c.622A>G (p.Ile208Val) rs727504571
NM_001374258.1(BRAF):c.83GCGCCG[4] (p.28GA[4]) rs397507458
NM_001374258.1(BRAF):c.92C>G (p.Ala31Gly) rs397516906
NM_004333.6(BRAF):c.1207C>G (p.Pro403Ala) rs749792302
NM_004333.6(BRAF):c.918C>G (p.Ser306=) rs794727865

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.