N93S (p.Asn93Ser) variant of FSHR (P23945)
N93S (p.Asn93Ser) in FSHR (P23945) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.26 / 1. The record also includes population frequency data and structural context.
N93S (p.Asn93Ser) variant details
- p.Asn93Ser
- TOPMed rs1667635909
- gnomAD rs1667635909
- Missense
- Variant Prioritization Score for Impact Estimate 0.26
- REVEL 0.19
- MetaLR 0.34
- MetaSVM -0.78
- CADD 14.90
- PolyPhen-2 0.00
- SIFT 0.43
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available