ClinVar Miner

Submissions for variant NM_006118.3(HAX1):c.11T>C (p.Phe4Ser)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000807437 SCV000947490 uncertain significance Severe congenital neutropenia 3, autosomal recessive 2018-07-19 criteria provided, single submitter clinical testing This sequence change replaces phenylalanine with serine at codon 4 of the HAX1 protein (p.Phe4Ser). The phenylalanine residue is moderately conserved and there is a large physicochemical difference between phenylalanine and serine. This variant is present in population databases (rs780614125, ExAC 0.01%). This variant has not been reported in the literature in individuals with HAX1-related disease. Algorithms developed to predict the effect of missense changes on protein structure and function are either unavailable or do not agree on the potential impact of this missense change (SIFT: "Deleterious"; PolyPhen-2: "Benign"; Align-GVGD: "Class C0"). 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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