S76T (p.Ser76Thr) variant of ADH1B (P00325)
S76T (p.Ser76Thr) in ADH1B (P00325) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.37 / 1. The record also includes population frequency data and structural context.
S76T (p.Ser76Thr) variant details
- p.Ser76Thr
- gnomAD rs1278530780
- Missense
- Variant Prioritization Score for Impact Estimate 0.371
- REVEL 0.20
- CADD 23.50
- PolyPhen-2 0.69
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available