D91G (p.Asp91Gly) variant of CLN3 (Battenin)
D91G (p.Asp91Gly) in CLN3 (Battenin) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.62 / 1. The record also includes population frequency data and structural context.
D91G (p.Asp91Gly) variant details
- p.Asp91Gly
- gnomAD rs1241022940
- Missense
- Variant Prioritization Score for Impact Estimate 0.62
- CADD 27.10
- PolyPhen-2 1.00
- SIFT 0.04
- Most common in the East Asian population (allele frequency 2.5e-05)
- Structural context available