T41N (p.Thr41Asn) variant of HAVCR2 (Q8TDQ0)
T41N (p.Thr41Asn) in HAVCR2 (Q8TDQ0) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.06 / 1. The record also includes population frequency data.
T41N (p.Thr41Asn) variant details
- p.Thr41Asn
- ExAC rs751807490
- TOPMed rs751807490
- gnomAD rs751807490
- Missense
- Variant Prioritization Score for Impact Estimate 0.0618
- REVEL 0.03
- CADD 6.88
- PolyPhen-2 0.13
- SIFT 0.02
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)