S3G (p.Ser3Gly) variant of FGFR2 (P21802)
S3G (p.Ser3Gly) in FGFR2 (P21802) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.27 / 1. The record also includes population frequency data and structural context.
S3G (p.Ser3Gly) variant details
- p.Ser3Gly
- Ensembl rs2135486526
- Missense
- Variant Prioritization Score for Impact Estimate 0.266
- REVEL 0.17
- CADD 19.60
- Most common in the South Asian population (allele frequency 0.00044)
- Structural context available