G33W (p.Gly33Trp) variant of TRMU (O75648)
G33W (p.Gly33Trp) in TRMU (O75648) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.82 / 1. The record also includes population frequency data, published literature, and structural context.
G33W (p.Gly33Trp) variant details
- p.Gly33Trp
- gnomAD 22-46337793-G-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.824
- REVEL 0.82
- ESM-1b 1.00
- AlphaMissense 0.99
- MetaLR 0.63
- MetaSVM 0.67
- CADD 32.00
- Most common in the 1KG:FIN population (allele frequency 0.071)
- Structural context available
- Literature evidence available