N33S (p.Asn33Ser) variant of HAVCR2 (Q8TDQ0)
N33S (p.Asn33Ser) in HAVCR2 (Q8TDQ0) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.23 / 1. The record also includes population frequency data.
N33S (p.Asn33Ser) variant details
- p.Asn33Ser
- Ensembl rs1757261776
- Missense
- Variant Prioritization Score for Impact Estimate 0.228
- REVEL 0.12
- CADD 14.70
- PolyPhen-2 0.04
- SIFT 0.19
- Most common in the Non-Finnish European population (allele frequency 9e-07)