A69T (p.Ala69Thr) variant of CD2 (T-cell surface antigen CD2)
A69T (p.Ala69Thr) in CD2 (T-cell surface antigen CD2) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.23 / 1. The record also includes population frequency data and structural context.
A69T (p.Ala69Thr) variant details
- p.Ala69Thr
- NCI-TCGA Cosmic COSV6564
- cosmic curated COSV65643
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.229
- REVEL 0.09
- MetaLR 0.25
- MetaSVM -0.84
- CADD 21.90
- PolyPhen-2 0.93
- SIFT 0.03
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available