T38I (p.Thr38Ile) variant of CD8A (P01732)
T38I (p.Thr38Ile) in CD8A (P01732) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.25 / 1. The record also includes population frequency data.
T38I (p.Thr38Ile) variant details
- p.Thr38Ile
- ExAC rs769109914
- gnomAD rs769109914
- Missense
- Variant Prioritization Score for Impact Estimate 0.254
- REVEL 0.36
- MetaLR 0.30
- MetaSVM -0.40
- CADD 0.69
- PolyPhen-2 0.48
- SIFT 0.03
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00019)