G39W (p.Gly39Trp) variant of ABL2 (Tyrosine-protein kinase ABL2)
G39W (p.Gly39Trp) in ABL2 (Tyrosine-protein kinase ABL2) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of not specified. The available variant effect predictions contribute to a CATVariant prioritization score of 0.56 / 1. The record also includes population frequency data.
G39W (p.Gly39Trp) variant details
- p.Gly39Trp
- cosmic curated COSV10085
- ExAC rs772415670
- TOPMed rs772415670
- gnomAD rs772415670
- Uncertain significance
- not specified
- Missense
- Variant Prioritization Score for Impact Estimate 0.559
- REVEL 0.41
- CADD 27.30
- PolyPhen-2 0.74
- SIFT 0.01
- ClinVar: Uncertain significance (not specified)
- UniProt: Uncertain significance
- Population evidence available