G46W (p.Gly46Trp) variant of HAVCR2 (Q8TDQ0)
G46W (p.Gly46Trp) in HAVCR2 (Q8TDQ0) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.33 / 1. The record also includes population frequency data.
G46W (p.Gly46Trp) variant details
- p.Gly46Trp
- cosmic curated COSV57154
- TOPMed rs1190700485
- gnomAD rs1190700485
- Missense
- Variant Prioritization Score for Impact Estimate 0.329
- REVEL 0.05
- AlphaMissense 0.17
- MetaLR 0.04
- MetaSVM -1.03
- CADD 21.80
- PolyPhen-2 0.22
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)