A20G (p.Ala20Gly) variant of GALT (P07902)
A20G (p.Ala20Gly) in GALT (P07902) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.40 / 1. The record also includes population frequency data and structural context.
A20G (p.Ala20Gly) variant details
- p.Ala20Gly
- ExAC rs779003828
- TOPMed rs779003828
- gnomAD rs779003828
- Missense
- Variant Prioritization Score for Impact Estimate 0.403
- REVEL 0.35
- AlphaMissense 0.09
- MetaLR 0.89
- MetaSVM 0.73
- CADD 10.50
- PolyPhen-2 0.01
- Most common in the East Asian population (allele frequency 0.00019)
- Structural context available