T97N (p.Thr97Asn) variant of CD8A (P01732)
T97N (p.Thr97Asn) in CD8A (P01732) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.13 / 1. The record also includes population frequency data and structural context.
T97N (p.Thr97Asn) variant details
- p.Thr97Asn
- TOPMed rs1472696905
- gnomAD rs1472696905
- Missense
- Variant Prioritization Score for Impact Estimate 0.131
- REVEL 0.08
- AlphaMissense 0.10
- MetaLR 0.32
- MetaSVM -0.65
- CADD 0.00
- PolyPhen-2 0.00
- Most common in the African/African-American population (allele frequency 0.00041)
- Structural context available