T38A (p.Thr38Ala) variant of FSHR (P23945)
T38A (p.Thr38Ala) in FSHR (P23945) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.63 / 1. The record also includes population frequency data and structural context.
T38A (p.Thr38Ala) variant details
- p.Thr38Ala
- TOPMed rs1673167692
- Missense
- Variant Prioritization Score for Impact Estimate 0.633
- REVEL 0.65
- MetaLR 0.92
- MetaSVM 0.95
- CADD 20.70
- PolyPhen-2 0.05
- SIFT 0.79
- Most common in the REMAINING population (allele frequency 1.7e-05)
- Structural context available