N99S (p.Asn99Ser) variant of HAVCR2 (Q8TDQ0)
N99S (p.Asn99Ser) in HAVCR2 (Q8TDQ0) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.18 / 1. The record also includes population frequency data.
N99S (p.Asn99Ser) variant details
- p.Asn99Ser
- gnomAD rs1183555178
- Missense
- Variant Prioritization Score for Impact Estimate 0.183
- REVEL 0.10
- CADD 16.50
- PolyPhen-2 0.17
- SIFT 0.04
- Most common in the South Asian population (allele frequency 1.2e-05)