N27S (p.Asn27Ser) variant of FSHR (P23945)
N27S (p.Asn27Ser) in FSHR (P23945) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.32 / 1. The record also includes population frequency data and structural context.
N27S (p.Asn27Ser) variant details
- p.Asn27Ser
- Ensembl rs1673168984
- Missense
- Variant Prioritization Score for Impact Estimate 0.323
- REVEL 0.25
- MetaLR 0.70
- MetaSVM 0.04
- CADD 17.80
- PolyPhen-2 0.00
- SIFT 0.67
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available