Q218R (p.Gln218Arg) variant of MMUT (P22033)
Q218R (p.Gln218Arg) in MMUT (P22033) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as pathogenic in the context of Methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency. The available variant effect predictions contribute to a CATVariant prioritization score of 0.84 / 1. The record also includes published literature and structural context.
Q218R (p.Gln218Arg) variant details
- p.Gln218Arg
- rs869320653
- ClinGen CA358798
- ClinVar RCV000210845
- Ensembl rs869320653
- Pathogenic
- Methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency
- Missense
- Variant Prioritization Score for Impact Estimate 0.839
- MutPred 0.84
- ClinVar: Pathogenic (Methylmalonic aciduria due to methylmalonyl-CoA mutase deficienc)
- EBI: Pathogenic (in MAMM)
- UniProt: Pathogenic (in MAMM)
- Structural context available
- Cited in: Isolated Methylmalonic Acidemia. (PMID 20301409)