ClinVar Miner

Submissions for variant NM_004333.6(BRAF):c.-9G>T

gnomAD frequency: 0.00001  dbSNP: rs1161647286
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000599114 SCV000710552 uncertain significance not provided 2018-02-13 criteria provided, single submitter clinical testing The c.-9 G>T variant of uncertain significance in the BRAF gene has not been published as pathogenic or benign to our knowledge. This variant is not observed in large population cohorts (Lek et al., 2016). The c.-9 G>T variant occurs in the 5'UTR of the BRAF transcript at a position that is conserved across species. However, no other regulatory variants are reported in the Human Gene Mutation Database in association with BRAF-related disorders (Stenson et al., 2014),Therefore, based on the currently available information, it is unclear whether this variant is pathogenic or rare benign. This result cannot be interpreted for diagnosis or used for family member screening at this time.

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