A267S (p.Ala267Ser) variant of PCCB (P05166)
A267S (p.Ala267Ser) in PCCB (P05166) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Propionic acidemia. The available variant effect predictions contribute to a CATVariant prioritization score of 0.72 / 1. The record also includes population frequency data, published literature, and structural context.
A267S (p.Ala267Ser) variant details
- p.Ala267Ser
- rs770733810
- ClinGen CA2631874
- ClinVar RCV002611735
- ExAC rs770733810
- Uncertain significance
- Propionic acidemia
- Missense
- Variant Prioritization Score for Impact Estimate 0.719
- REVEL 0.77
- ESM-1b 1.00
- AlphaMissense 0.19
- CADD 24.30
- PolyPhen-2 0.24
- SIFT 0.02
- ClinVar: Uncertain significance (Propionic acidemia)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Most common in the Latino/Admixed American population (allele frequency 6.5e-05)
- Structural context available
- Cited in: Propionic Acidemia. (PMID 22593918)