T41P (p.Thr41Pro) variant of HAVCR2 (Q8TDQ0)
T41P (p.Thr41Pro) 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.
T41P (p.Thr41Pro) variant details
- p.Thr41Pro
- TOPMed rs1488560271
- gnomAD rs1488560271
- Missense
- Variant Prioritization Score for Impact Estimate 0.119
- REVEL 0.07
- CADD 15.80
- PolyPhen-2 0.47
- SIFT 0.03
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)