ClinVar Miner

Submissions for variant NM_199242.3(UNC13D):c.2074G>A (p.Gly692Ser)

dbSNP: rs2143875873
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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 RCV001870297 SCV002127310 uncertain significance Familial hemophagocytic lymphohistiocytosis 3 2021-05-28 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 output the following: SIFT: "Not Available"; PolyPhen-2: "Benign"; Align-GVGD: "Not Available". The serine amino acid residue is found in multiple mammalian species, suggesting that this missense change does not adversely affect protein function. 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 UNC13D-related conditions. This variant is not present in population databases (ExAC no frequency). This sequence change replaces glycine with serine at codon 692 of the UNC13D protein (p.Gly692Ser). The glycine residue is weakly conserved and there is a small physicochemical difference between glycine and serine.

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