Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001872259 | SCV002119679 | pathogenic | Pyruvate dehydrogenase E3 deficiency | 2022-07-26 | criteria provided, single submitter | clinical testing | This sequence change creates a premature translational stop signal (p.Gln262Asnfs*13) in the DLD gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in DLD are known to be pathogenic (PMID: 8968745, 9934985). For these reasons, this variant has been classified as Pathogenic. ClinVar contains an entry for this variant (Variation ID: 1359450). This variant has not been reported in the literature in individuals affected with DLD-related conditions. This variant is present in population databases (no rsID available, gnomAD 0.0009%). |