V38A (p.Val38Ala) variant of NUDT15 (Q9NV35)
V38A (p.Val38Ala) in NUDT15 (Q9NV35) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.20 / 1. The record also includes population frequency data and structural context.
V38A (p.Val38Ala) variant details
- p.Val38Ala
- TOPMed rs1427452470
- gnomAD rs1427452470
- Missense
- Variant Prioritization Score for Impact Estimate 0.199
- REVEL 0.08
- MetaLR 0.02
- MetaSVM -0.95
- CADD 16.90
- PolyPhen-2 0.01
- SIFT 0.55
- Most common in the Latino/Admixed American population (allele frequency 0.0029)
- Structural context available