Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Counsyl | RCV000666810 | SCV000791166 | uncertain significance | Carnitine palmitoyl transferase 1A deficiency | 2017-05-01 | criteria provided, single submitter | clinical testing | |
Invitae | RCV000666810 | SCV001495634 | likely pathogenic | Carnitine palmitoyl transferase 1A deficiency | 2023-10-19 | criteria provided, single submitter | clinical testing | This sequence change replaces glycine, which is neutral and non-polar, with arginine, which is basic and polar, at codon 465 of the CPT1A protein (p.Gly465Arg). This variant is present in population databases (rs80356784, gnomAD 0.004%). This missense change has been observed in individual(s) with carnitine palmitoyltransferase I (CPT1) deficiency (PMID: 27066452). ClinVar contains an entry for this variant (Variation ID: 551684). 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 CPT1A protein function. Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant may disrupt the consensus splice site. This variant disrupts the p.Gly465 amino acid residue in CPT1A. Other variant(s) that disrupt this residue have been observed in individuals with CPT1A-related conditions (PMID: 15110323, 32781271), which suggests that this may be a clinically significant amino acid residue. 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. |
Natera, |
RCV000666810 | SCV002092952 | uncertain significance | Carnitine palmitoyl transferase 1A deficiency | 2020-12-04 | no assertion criteria provided | clinical testing |