ClinVar Miner

Submissions for variant NM_145261.4(DNAJC19):c.344A>G (p.Lys115Arg)

gnomAD frequency: 0.00001  dbSNP: rs1253268997
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001338724 SCV001532410 uncertain significance 3-methylglutaconic aciduria type 5 2022-10-03 criteria provided, single submitter clinical testing 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 arginine amino acid residue is found in multiple mammalian species, which suggests that this missense change does not adversely affect protein function. ClinVar contains an entry for this variant (Variation ID: 1035808). This variant has not been reported in the literature in individuals affected with DNAJC19-related conditions. This variant is present in population databases (no rsID available, gnomAD 0.006%). This sequence change replaces lysine, which is basic and polar, with arginine, which is basic and polar, at codon 115 of the DNAJC19 protein (p.Lys115Arg). 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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