ClinVar Miner

Submissions for variant NM_000136.3(FANCC):c.828A>G (p.Ile276Met) (rs587779908)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000115360 SCV000149269 uncertain significance not provided 2018-04-20 criteria provided, single submitter clinical testing This variant is denoted FANCC c.828A>G at the cDNA level, p.Ile276Met (I276M) at the protein level, and results in the change of an Isoleucine to a Methionine (ATA>ATG). This variant has not, to our knowledge, been published in the literature as pathogenic or benign. FANCC Ile276Met was not observed in large population cohorts (Lek 2016). This variant is located in the GRP94 and Hsp70 binding domains (Gordon 2000). In silico analysis, which includes protein predictors and evolutionary conservation, supports that this variant does not alter protein structure/function. Based on currently available evidence, it is unclear whether FANCC Ile276Met is a pathogenic or benign variant. We consider it to be a variant of uncertain significance.

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