M9T (p.Met9Thr) variant of NPM1 (Nucleophosmin)
M9T (p.Met9Thr) in NPM1 (Nucleophosmin) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.33 / 1. The record also includes population frequency data, published literature, and structural context.
M9T (p.Met9Thr) variant details
- p.Met9Thr
- gnomAD 5-171387974-T-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.328
- REVEL 0.15
- CADD 22.90
- PolyPhen-2 0.03
- SIFT 0.19
- Most common in the Non-Finnish European population (allele frequency 3.6e-06)
- Structural context available
- Literature evidence available