A96V (p.Ala96Val) variant of DNMT1 (P26358)
A96V (p.Ala96Val) in DNMT1 (P26358) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.31 / 1. The record also includes population frequency data and structural context.
A96V (p.Ala96Val) variant details
- p.Ala96Val
- TOPMed rs2039026701
- gnomAD rs2039026701
- Missense
- Variant Prioritization Score for Impact Estimate 0.311
- REVEL 0.09
- CADD 21.30
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00019)
- Structural context available