E37G (p.Glu37Gly) variant of NPM1 (Nucleophosmin)
E37G (p.Glu37Gly) in NPM1 (Nucleophosmin) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.44 / 1. The record also includes population frequency data and structural context.
E37G (p.Glu37Gly) variant details
- p.Glu37Gly
- cosmic curated COSV99744
- Missense
- Variant Prioritization Score for Impact Estimate 0.44
- REVEL 0.27
- CADD 32.00
- PolyPhen-2 0.63
- SIFT 0.04
- Most common in the Non-Finnish European population (allele frequency 9.1e-07)
- Structural context available