ClinVar Miner

Submissions for variant NM_022725.4(FANCF):c.817G>C (p.Val273Leu)

dbSNP: rs1858619819
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001937395 SCV002133443 uncertain significance Fanconi anemia 2021-08-13 criteria provided, single submitter clinical testing This sequence change replaces valine with leucine at codon 273 of the FANCF protein (p.Val273Leu). The valine residue is weakly conserved and there is a small physicochemical difference between valine and leucine. This variant is not present in population databases (ExAC no frequency). This variant has not been reported in the literature in individuals affected with FANCF-related conditions. Algorithms developed to predict the effect of missense changes on protein structure and function (SIFT, PolyPhen-2, Align-GVGD) all suggest that this variant is likely to be tolerated. 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.

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