N35Y (p.Asn35Tyr) variant of LHCGR (P22888)
N35Y (p.Asn35Tyr) in LHCGR (P22888) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.21 / 1. The record also includes population frequency data and structural context.
N35Y (p.Asn35Tyr) variant details
- p.Asn35Tyr
- TOPMed rs1474245717
- Missense
- Variant Prioritization Score for Impact Estimate 0.211
- REVEL 0.18
- CADD 22.50
- PolyPhen-2 0.05
- SIFT 0.01
- Population evidence available
- Structural context available