A21G (p.Ala21Gly) variant of FGFR1 (P11362)
A21G (p.Ala21Gly) in FGFR1 (P11362) is a missense change. 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.
A21G (p.Ala21Gly) variant details
- p.Ala21Gly
- Ensembl rs2151343110
- Missense
- Variant Prioritization Score for Impact Estimate 0.295
- CADD 6.48
- Most common in the REMAINING population (allele frequency 0.0001)
- Structural context available