A20G (p.Ala20Gly) variant of TRMU (O75648)
A20G (p.Ala20Gly) in TRMU (O75648) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.67 / 1. The record also includes population frequency data and structural context.
A20G (p.Ala20Gly) variant details
- p.Ala20Gly
- TOPMed rs1329491402
- gnomAD rs1329491402
- Missense
- Variant Prioritization Score for Impact Estimate 0.67
- REVEL 0.62
- ESM-1b 1.00
- AlphaMissense 0.41
- CADD 29.10
- PolyPhen-2 0.94
- SIFT 0.01
- Most common in the HGDP:SINDHI population (allele frequency 0.023)
- Structural context available