ClinVar Miner

Submissions for variant NM_001352514.2(HLCS):c.910C>T (p.Leu304Phe)

gnomAD frequency: 0.00004  dbSNP: rs763508196
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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 RCV001945303 SCV002190266 uncertain significance Holocarboxylase synthetase deficiency 2021-10-14 criteria provided, single submitter clinical testing This sequence change replaces leucine with phenylalanine at codon 157 of the HLCS protein (p.Leu157Phe). The leucine residue is weakly conserved and there is a small physicochemical difference between leucine and phenylalanine. This variant is present in population databases (rs763508196, ExAC 0.01%). This variant has not been reported in the literature in individuals affected with HLCS-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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