T98A (p.Thr98Ala) variant of ATP6V0A4 (Q9HBG4)
T98A (p.Thr98Ala) in ATP6V0A4 (Q9HBG4) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.31 / 1. The record also includes population frequency data and structural context.
T98A (p.Thr98Ala) variant details
- p.Thr98Ala
- cosmic curated COSV11486
- Missense
- Variant Prioritization Score for Impact Estimate 0.312
- REVEL 0.19
- ESM-1b 0.00
- AlphaMissense 0.07
- MetaLR 0.25
- MetaSVM -0.69
- CADD 16.80
- Most common in the Non-Finnish European population (allele frequency 2.7e-06)
- Structural context available