V67M (p.Val67Met) variant of HAVCR2 (Q8TDQ0)
V67M (p.Val67Met) 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.
V67M (p.Val67Met) variant details
- p.Val67Met
- ESP rs377032621
- ExAC rs377032621
- TOPMed rs377032621
- gnomAD rs377032621
- Missense
- Variant Prioritization Score for Impact Estimate 0.0999
- REVEL 0.07
- CADD 8.01
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)