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
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HGVS dbSNP
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

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