N107S (p.Asn107Ser) variant of FSHR (P23945)
N107S (p.Asn107Ser) in FSHR (P23945) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.29 / 1. The record also includes population frequency data and structural context.
N107S (p.Asn107Ser) variant details
- p.Asn107Ser
- TOPMed rs1336738341
- gnomAD rs1336738341
- Missense
- Variant Prioritization Score for Impact Estimate 0.287
- REVEL 0.21
- MetaLR 0.37
- MetaSVM -0.44
- CADD 15.80
- PolyPhen-2 0.00
- SIFT 0.46
- Most common in the East Asian population (allele frequency 2.5e-05)
- Structural context available