Y26F (p.Tyr26Phe) variant of HAVCR2 (Q8TDQ0)
Y26F (p.Tyr26Phe) in HAVCR2 (Q8TDQ0) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.12 / 1. The record also includes population frequency data.
Y26F (p.Tyr26Phe) variant details
- p.Tyr26Phe
- TOPMed rs1247312085
- gnomAD rs1247312085
- Missense
- Variant Prioritization Score for Impact Estimate 0.123
- REVEL 0.09
- CADD 13.30
- PolyPhen-2 0.86
- SIFT 0.14
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)