R186G (p.Arg186Gly) variant of MMAB (Q96EY8)
R186G (p.Arg186Gly) in MMAB (Q96EY8) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Methylmalonic aciduria, cblB type. The available variant effect predictions contribute to a CATVariant prioritization score of 0.92 / 1. The record also includes published literature and structural context.
R186G (p.Arg186Gly) variant details
- p.Arg186Gly
- rs28941784
- ClinGen CA386636913
- ClinVar RCV003132658
- Uncertain significance
- Methylmalonic aciduria, cblB type
- Missense
- Variant Prioritization Score for Impact Estimate 0.919
- ESM-1b 1.00
- AlphaMissense 0.64
- MetaLR 0.99
- MetaSVM 1.02
- PolyPhen-2 1.00
- SIFT 0.00
- ClinVar: Uncertain significance (Methylmalonic aciduria, cblB type)
- EBI: Variant of uncertain significance (in MACB)
- UniProt: Uncertain significance (in MACB)
- Structural context available
- Cited in: Isolated Methylmalonic Acidemia. (PMID 20301409)