A97G (p.Ala97Gly) variant of FLT3 (P36888)
A97G (p.Ala97Gly) in FLT3 (P36888) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.28 / 1. The record also includes population frequency data and structural context.
A97G (p.Ala97Gly) variant details
- p.Ala97Gly
- 1000Genomes rs55784328
- ExAC rs55784328
- TOPMed rs55784328
- gnomAD rs55784328
- Missense
- Variant Prioritization Score for Impact Estimate 0.283
- REVEL 0.14
- MetaLR 0.04
- MetaSVM -1.04
- CADD 5.02
- PolyPhen-2 0.00
- SIFT 0.04
- Most common in the 1KG:STU population (allele frequency 0.0051)
- Structural context available