A87T (p.Ala87Thr) variant of FLT3 (P36888)
A87T (p.Ala87Thr) in FLT3 (P36888) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.24 / 1. The record also includes population frequency data and structural context.
A87T (p.Ala87Thr) variant details
- p.Ala87Thr
- rs753172215
- NCI-TCGA Cosmic COSV9905
- ExAC rs753172215
- TOPMed rs753172215
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.242
- REVEL 0.07
- MetaLR 0.07
- MetaSVM -1.06
- CADD 13.30
- PolyPhen-2 0.23
- SIFT 0.12
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available