A16T (p.Ala16Thr) variant of FGFR1 (P11362)
A16T (p.Ala16Thr) in FGFR1 (P11362) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.56 / 1. The record also includes population frequency data and structural context.
A16T (p.Ala16Thr) variant details
- p.Ala16Thr
- Ensembl rs1833149044
- Missense
- Variant Prioritization Score for Impact Estimate 0.561
- REVEL 0.41
- CADD 25.80
- PolyPhen-2 0.23
- SIFT 0.04
- Most common in the REMAINING population (allele frequency 1.7e-05)
- Structural context available