ClinVar Miner

Submissions for variant NM_000631.5(NCF4):c.758+69C>T

dbSNP: rs1940180265
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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 RCV001058252 SCV001222809 uncertain significance Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 3 2019-12-30 criteria provided, single submitter clinical testing 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. 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, but these predictions have not been confirmed by published functional studies and their clinical significance is uncertain. This variant has not been reported in the literature in individuals with NCF4-related conditions. This variant is not present in population databases (ExAC no frequency). This sequence change replaces serine with leucine at codon 276 of the NCF4 protein (p.Ser276Leu). The serine residue is weakly conserved and there is a large physicochemical difference between serine and leucine.

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