ClinVar Miner

Submissions for variant NM_000277.3(PAH):c.1259G>C (p.Arg420Thr)

dbSNP: rs767075719
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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 RCV002024160 SCV002315742 likely pathogenic Phenylketonuria 2021-11-04 criteria provided, single submitter clinical testing This variant is not present in population databases (gnomAD no frequency). This variant has not been reported in the literature in individuals affected with PAH-related conditions. Advanced modeling of protein sequence and biophysical properties (such as structural, functional, and spatial information, amino acid conservation, physicochemical variation, residue mobility, and thermodynamic stability) performed at Invitae indicates that this missense variant is expected to disrupt PAH protein function. This variant disrupts the p.Arg420 amino acid residue in PAH. Other variant(s) that disrupt this residue have been determined to be pathogenic (PMID: 27121329; Invitae). This suggests that this residue is clinically significant, and that variants that disrupt this residue are likely to be disease-causing. In summary, the currently available evidence indicates that the variant is pathogenic, but additional data are needed to prove that conclusively. Therefore, this variant has been classified as Likely Pathogenic. This sequence change replaces arginine, which is basic and polar, with threonine, which is neutral and polar, at codon 420 of the PAH protein (p.Arg420Thr).

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