E26G (p.Glu26Gly) variant of GNA11 (P29992)
E26G (p.Glu26Gly) in GNA11 (P29992) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.69 / 1. The record also includes population frequency data, published literature, and structural context.
E26G (p.Glu26Gly) variant details
- p.Glu26Gly
- gnomAD 19-3094728-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.687
- REVEL 0.81
- AlphaMissense 0.56
- MetaLR 0.67
- MetaSVM 0.17
- CADD 31.00
- PolyPhen-2 0.59
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available
- Literature evidence available