S25T (p.Ser25Thr) variant of FGFR4 (P22455)
S25T (p.Ser25Thr) in FGFR4 (P22455) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.34 / 1. The record also includes population frequency data and structural context.
S25T (p.Ser25Thr) variant details
- p.Ser25Thr
- TOPMed rs968495498
- gnomAD rs968495498
- Missense
- Variant Prioritization Score for Impact Estimate 0.342
- REVEL 0.29
- CADD 23.00
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available