S26N (p.Ser26Asn) variant of FGFR2 (P21802)
S26N (p.Ser26Asn) in FGFR2 (P21802) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.12 / 1. The record also includes population frequency data and structural context.
S26N (p.Ser26Asn) variant details
- p.Ser26Asn
- gnomAD rs1379302733
- Missense
- Variant Prioritization Score for Impact Estimate 0.12
- REVEL 0.11
- CADD 9.00
- PolyPhen-2 0.00
- SIFT 0.50
- Most common in the East Asian population (allele frequency 2.8e-05)
- Structural context available