ClinVar Miner

Submissions for variant NM_144997.7(FLCN):c.1086C>T (p.Arg362=)

dbSNP: rs2046951541
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001314450 SCV001504984 uncertain significance Birt-Hogg-Dube syndrome 2020-01-23 criteria provided, single submitter clinical testing In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant may create or strengthen a splice site, but this prediction has not been confirmed by published transcriptional studies. This variant has not been reported in the literature in individuals with FLCN-related conditions. This variant is not present in population databases (ExAC no frequency). This sequence change affects codon 362 of the FLCN mRNA. It is a 'silent' change, meaning that it does not change the encoded amino acid sequence of the FLCN protein.

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