M28T (p.Met28Thr) variant of CD28 (P10747)
M28T (p.Met28Thr) in CD28 (P10747) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.16 / 1. The record also includes population frequency data, published literature, and structural context.
M28T (p.Met28Thr) variant details
- p.Met28Thr
- gnomAD 2-203706567-T-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.165
- CADD 4.40
- SIFT 0.04
- Most common in the Non-Finnish European population (allele frequency 9.1e-07)
- Structural context available
- Literature evidence available