T22N (p.Thr22Asn) variant of ALDH2 (P05091)
T22N (p.Thr22Asn) in ALDH2 (P05091) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.21 / 1. The record also includes population frequency data, published literature, and structural context.
T22N (p.Thr22Asn) variant details
- p.Thr22Asn
- gnomAD 12-111767047-C-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.213
- REVEL 0.12
- CADD 12.30
- PolyPhen-2 0.00
- SIFT 0.09
- Population evidence available
- Structural context available
- Literature evidence available