Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001379484 | SCV001577293 | likely pathogenic | Combined malonic and methylmalonic acidemia | 2020-07-28 | criteria provided, single submitter | clinical testing | This variant results in a copy number gain of the genomic region encompassing exon(s) 5-10 of the ACSF3 gene. While the exact position of this variant cannot be determined from the data, sub-genic copy number gains are generally in tandem (PMID: 25640679). This variant is predicted to be out-of-frame, and may result in an absent or disrupted protein product. This variant has not been reported in the literature in individuals with ACSF3-related conditions. Loss-of-function variants in ACSF3 are known to be pathogenic (PMID: 21841779, 26827111). 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. |