A145T (p.Ala145Thr) variant of ATP6V0A4 (Q9HBG4)
A145T (p.Ala145Thr) in ATP6V0A4 (Q9HBG4) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.20 / 1. The record also includes population frequency data and structural context.
A145T (p.Ala145Thr) variant details
- p.Ala145Thr
- ExAC rs767434417
- gnomAD rs767434417
- Missense
- Variant Prioritization Score for Impact Estimate 0.2
- REVEL 0.11
- ESM-1b 0.00
- AlphaMissense 0.07
- MetaLR 0.28
- MetaSVM -0.88
- CADD 12.70
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available