R17G (p.Arg17Gly) variant of FAS (P25445)
R17G (p.Arg17Gly) in FAS (P25445) 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.
R17G (p.Arg17Gly) variant details
- p.Arg17Gly
- TOPMed rs1848019915
- Missense
- Variant Prioritization Score for Impact Estimate 0.21
- CADD 6.20
- PolyPhen-2 0.00
- SIFT 1.00
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available