ClinVar Miner

Submissions for variant NM_144997.7(FLCN):c.1176G>C (p.Arg392=)

dbSNP: rs2046948026
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001202618 SCV001373737 pathogenic Birt-Hogg-Dube syndrome 2023-08-10 criteria provided, single submitter clinical testing For these reasons, this variant has been classified as Pathogenic. Variants that disrupt the consensus splice site are a relatively common cause of aberrant splicing (PMID: 17576681, 9536098). Studies have shown that this variant results in activation of a cryptic splice site and introduces a premature termination codon (Invitae). The resulting mRNA is expected to undergo nonsense-mediated decay. ClinVar contains an entry for this variant (Variation ID: 934263). This variant has been observed in individual(s) with clinical features of Birt-Hogg-Dubé syndrome (Invitae). This variant is not present in population databases (gnomAD no frequency). This sequence change affects codon 392 of the FLCN mRNA. It is a 'silent' change, meaning that it does not change the encoded amino acid sequence of the FLCN protein. RNA analysis indicates that this variant induces altered splicing and may result in an absent or disrupted protein product.

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