ClinVar Miner

Submissions for variant NM_000136.3(FANCC):c.1399C>G (p.Leu467Val) (rs1554828405)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000519297 SCV000617899 uncertain significance not provided 2017-03-01 criteria provided, single submitter clinical testing This variant is denoted FANCC c.1399C>G at the cDNA level, p.Leu467Val (L467V) at the protein level, and results in the change of a Leucine to a Valine (CTG>GTG). This variant has not, to our knowledge, been published in the literature as pathogenic or benign. FANCC Leu467Val was not observed in the Exome Aggregation Consortium (ExAC) data set, suggesting it is not a common benign variant. Since Leucine and Valine share similar properties, this is considered a conservative amino acid substitution. FANCC Leu467Val occurs at a position where amino acids with properties similar to Leucine are tolerated across species and is not located in a known functional domain. In silico analyses are inconsistent regarding the effect this variant may have on protein structure and function. Based on currently available evidence, it is unclear whether FANCC Leu467Val is a pathogenic or benign variant. We consider it to be a variant of uncertain significance.

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