V19G (p.Val19Gly) variant of NUDT15 (Q9NV35)
V19G (p.Val19Gly) in NUDT15 (Q9NV35) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.36 / 1. The record also includes population frequency data, published literature, and structural context.
V19G (p.Val19Gly) variant details
- p.Val19Gly
- gnomAD 13-48037802-T-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.357
- REVEL 0.30
- MetaLR 0.11
- MetaSVM -0.93
- CADD 26.10
- PolyPhen-2 0.98
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 9.1e-07)
- Structural context available
- Literature evidence available