I117M (p.Ile117Met) variant of HAVCR2 (Q8TDQ0)
I117M (p.Ile117Met) 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.
I117M (p.Ile117Met) variant details
- p.Ile117Met
- TOPMed rs1757256066
- Missense
- Variant Prioritization Score for Impact Estimate 0.0968
- REVEL 0.10
- CADD 4.02
- PolyPhen-2 0.33
- SIFT 0.22
- Most common in the Latino/Admixed American population (allele frequency 2.2e-05)