H98R (p.His98Arg) variant of FSHR (P23945)
H98R (p.His98Arg) in FSHR (P23945) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.35 / 1. The record also includes population frequency data and structural context.
H98R (p.His98Arg) variant details
- p.His98Arg
- ESP rs377550562
- ExAC rs377550562
- TOPMed rs377550562
- gnomAD rs377550562
- Missense
- Variant Prioritization Score for Impact Estimate 0.348
- REVEL 0.32
- MetaLR 0.36
- MetaSVM -0.44
- CADD 19.90
- PolyPhen-2 0.01
- SIFT 0.19
- Most common in the REMAINING population (allele frequency 3.3e-05)
- Structural context available