T17S (p.Thr17Ser) variant of FGFR2 (P21802)
T17S (p.Thr17Ser) in FGFR2 (P21802) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.22 / 1. The record also includes population frequency data and structural context.
T17S (p.Thr17Ser) variant details
- p.Thr17Ser
- ExAC rs766435280
- TOPMed rs766435280
- gnomAD rs766435280
- Missense
- Variant Prioritization Score for Impact Estimate 0.224
- REVEL 0.12
- CADD 16.20
- Most common in the 1KG:GIH population (allele frequency 0.0053)
- Structural context available