G31S (p.Gly31Ser) variant of HAVCR2 (Q8TDQ0)
G31S (p.Gly31Ser) in HAVCR2 (Q8TDQ0) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.69 / 1. The record also includes population frequency data.
G31S (p.Gly31Ser) variant details
- p.Gly31Ser
- cosmic curated COSV10885
- ExAC rs752806981
- TOPMed rs752806981
- gnomAD rs752806981
- Missense
- Variant Prioritization Score for Impact Estimate 0.691
- REVEL 0.63
- CADD 24.20
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the Amish population (allele frequency 0.0044)