ClinVar Miner

Submissions for variant NM_000760.4(CSF3R):c.235T>C (p.Ser79Pro)

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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 RCV002731369 SCV003014931 uncertain significance Autosomal recessive severe congenital neutropenia due to CSF3R deficiency 2022-08-16 criteria provided, single submitter clinical testing This variant has not been reported in the literature in individuals affected with CSF3R-related conditions. This variant is not present in population databases (gnomAD no frequency). This sequence change replaces serine, which is neutral and polar, with proline, which is neutral and non-polar, at codon 79 of the CSF3R protein (p.Ser79Pro). Algorithms developed to predict the effect of missense changes on protein structure and function output the following: SIFT: "Tolerated"; PolyPhen-2: "Benign"; Align-GVGD: "Class C0". The proline amino acid residue is found in multiple mammalian species, which suggests that this missense change does not adversely affect protein function. 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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