N47D (p.Asn47Asp) variant of HAVCR2 (Q8TDQ0)
N47D (p.Asn47Asp) in HAVCR2 (Q8TDQ0) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.10 / 1. The record also includes population frequency data.
N47D (p.Asn47Asp) variant details
- p.Asn47Asp
- gnomAD rs1316059430
- Missense
- Variant Prioritization Score for Impact Estimate 0.0991
- REVEL 0.11
- CADD 0.07
- Most common in the Non-Finnish European population (allele frequency 4.4e-05)