H98D (p.His98Asp) variant of FSHR (P23945)
H98D (p.His98Asp) in FSHR (P23945) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.44 / 1. The record also includes population frequency data and structural context.
H98D (p.His98Asp) variant details
- p.His98Asp
- gnomAD rs1384040967
- Missense
- Variant Prioritization Score for Impact Estimate 0.443
- REVEL 0.47
- MetaLR 0.44
- MetaSVM -0.28
- CADD 22.90
- PolyPhen-2 0.57
- SIFT 0.15
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available