A21S (p.Ala21Ser) variant of FGFR1 (P11362)
A21S (p.Ala21Ser) in FGFR1 (P11362) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The available variant effect predictions contribute to a CATVariant prioritization score of 0.29 / 1. The record also includes population frequency data and structural context.
A21S (p.Ala21Ser) variant details
- p.Ala21Ser
- gnomAD rs1383262590
- Uncertain significance
- Missense
- Variant Prioritization Score for Impact Estimate 0.287
- CADD 7.51
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Population evidence available
- Structural context available