ClinVar Miner

Submissions for variant NM_144997.7(FLCN):c.106G>C (p.Glu36Gln)

dbSNP: rs1597618071
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV001017196 SCV001178236 uncertain significance Hereditary cancer-predisposing syndrome 2018-06-08 criteria provided, single submitter clinical testing The p.E36Q variant (also known as c.106G>C), located in coding exon 1 of the FLCN gene, results from a G to C substitution at nucleotide position 106. The glutamic acid at codon 36 is replaced by glutamine, an amino acid with highly similar properties. This amino acid position is poorly conserved in available vertebrate species. In addition, this alteration is predicted to be tolerated by in silico analysis. Since supporting evidence is limited at this time, the clinical significance of this alteration remains unclear.

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