N39S (p.Asn39Ser) variant of FLT3 (P36888)
N39S (p.Asn39Ser) in FLT3 (P36888) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.14 / 1. The record also includes population frequency data and structural context.
N39S (p.Asn39Ser) variant details
- p.Asn39Ser
- ESP rs376280703
- TOPMed rs376280703
- gnomAD rs376280703
- Missense
- Variant Prioritization Score for Impact Estimate 0.141
- REVEL 0.13
- MetaLR 0.17
- MetaSVM -0.99
- CADD 3.08
- PolyPhen-2 0.00
- SIFT 1.00
- Most common in the African/African-American population (allele frequency 7.2e-05)
- Structural context available