I111M (p.Ile111Met) variant of FSHR (P23945)
I111M (p.Ile111Met) 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.
I111M (p.Ile111Met) variant details
- p.Ile111Met
- ExAC rs774057514
- TOPMed rs774057514
- gnomAD rs774057514
- Missense
- Variant Prioritization Score for Impact Estimate 0.347
- REVEL 0.40
- MetaLR 0.38
- MetaSVM -0.44
- CADD 23.00
- PolyPhen-2 1.00
- SIFT 0.12
- Most common in the REMAINING population (allele frequency 6.6e-05)
- Structural context available