A79G (p.Ala79Gly) variant of FLT3 (P36888)
A79G (p.Ala79Gly) in FLT3 (P36888) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.23 / 1. The record also includes population frequency data and structural context.
A79G (p.Ala79Gly) variant details
- p.Ala79Gly
- ExAC rs746082684
- TOPMed rs746082684
- gnomAD rs746082684
- Missense
- Variant Prioritization Score for Impact Estimate 0.226
- REVEL 0.07
- MetaLR 0.23
- MetaSVM -0.89
- CADD 9.88
- PolyPhen-2 0.02
- SIFT 0.57
- Most common in the East Asian population (allele frequency 0.00019)
- Structural context available