S3T (p.Ser3Thr) variant of FGFR2 (P21802)
S3T (p.Ser3Thr) in FGFR2 (P21802) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.31 / 1. The record also includes population frequency data and structural context.
S3T (p.Ser3Thr) variant details
- p.Ser3Thr
- TOPMed rs1271629959
- Missense
- Variant Prioritization Score for Impact Estimate 0.315
- REVEL 0.15
- CADD 18.30
- PolyPhen-2 0.05
- SIFT 0.29
- Most common in the Non-Finnish European population (allele frequency 2.3e-05)
- Structural context available