N49S (p.Asn49Ser) variant of CD8A (P01732)
N49S (p.Asn49Ser) in CD8A (P01732) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.09 / 1. The record also includes population frequency data and structural context.
N49S (p.Asn49Ser) variant details
- p.Asn49Ser
- 1000Genomes rs572196668
- Missense
- Variant Prioritization Score for Impact Estimate 0.0897
- REVEL 0.05
- MetaLR 0.11
- MetaSVM -1.01
- CADD 0.00
- PolyPhen-2 0.01
- SIFT 1.00
- Most common in the Non-Finnish European population (allele frequency 8.8e-05)
- Structural context available