V17G (p.Val17Gly) variant of CYP2A6 (Cytochrome P450 2A6)
V17G (p.Val17Gly) in CYP2A6 (Cytochrome P450 2A6) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.25 / 1. The record also includes population frequency data and structural context.
V17G (p.Val17Gly) variant details
- p.Val17Gly
- ESP rs370605094
- ExAC rs370605094
- TOPMed rs370605094
- gnomAD rs370605094
- Missense
- Variant Prioritization Score for Impact Estimate 0.248
- REVEL 0.13
- CADD 17.90
- PolyPhen-2 0.01
- SIFT 0.04
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available