S13G (p.Ser13Gly) variant of FGFR4 (P22455)
S13G (p.Ser13Gly) in FGFR4 (P22455) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.21 / 1. The record also includes population frequency data and structural context.
S13G (p.Ser13Gly) variant details
- p.Ser13Gly
- ExAC rs746965870
- TOPMed rs746965870
- gnomAD rs746965870
- Missense
- Variant Prioritization Score for Impact Estimate 0.207
- REVEL 0.16
- CADD 9.55
- PolyPhen-2 0.00
- SIFT 0.52
- Most common in the African/African-American population (allele frequency 3e-05)
- Structural context available