G99V (p.Gly99Val) variant of ADH1B (P00325)
G99V (p.Gly99Val) in ADH1B (P00325) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.42 / 1. The record also includes population frequency data and structural context.
G99V (p.Gly99Val) variant details
- p.Gly99Val
- gnomAD rs1191282382
- Missense
- Variant Prioritization Score for Impact Estimate 0.415
- REVEL 0.26
- CADD 27.10
- PolyPhen-2 0.97
- SIFT 0.01
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available