Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000689404 | SCV000817052 | pathogenic | Methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency | 2018-04-24 | criteria provided, single submitter | clinical testing | This sequence change creates a premature translational stop signal (p.Arg629Lysfs*12) in the MUT gene. It is expected to result in an absent or disrupted protein product. This variant is not present in population databases (ExAC no frequency). This variant has been reported in combination with another pathogenic MUT variant in an individual with methylmalonic acidemia (PMID: 16281286). Loss-of-function variants in MUT are known to be pathogenic (PMID: 15781192). For these reasons, this variant has been classified as Pathogenic. |