N9S (p.Asn9Ser) variant of CD28 (P10747)
N9S (p.Asn9Ser) in CD28 (P10747) 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 and structural context.
N9S (p.Asn9Ser) variant details
- p.Asn9Ser
- TOPMed rs1303625960
- gnomAD rs1303625960
- Missense
- Variant Prioritization Score for Impact Estimate 0.253
- REVEL 0.23
- MetaLR 0.39
- MetaSVM -0.73
- CADD 8.72
- SIFT 0.95
- Most common in the Latino/Admixed American population (allele frequency 6.5e-05)
- Structural context available