N29S (p.Asn29Ser) variant of ALDH2 (P05091)
N29S (p.Asn29Ser) in ALDH2 (P05091) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.29 / 1. The record also includes population frequency data and structural context.
N29S (p.Asn29Ser) variant details
- p.Asn29Ser
- ExAC rs756057023
- TOPMed rs756057023
- gnomAD rs756057023
- Missense
- Variant Prioritization Score for Impact Estimate 0.292
- REVEL 0.26
- CADD 14.50
- PolyPhen-2 0.00
- SIFT 0.77
- Most common in the Latino/Admixed American population (allele frequency 0.00013)
- Structural context available