D21G (p.Asp21Gly) variant of DYSF (Dysferlin)
D21G (p.Asp21Gly) in DYSF (Dysferlin) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.68 / 1. The record also includes population frequency data, published literature, and structural context.
D21G (p.Asp21Gly) variant details
- p.Asp21Gly
- gnomAD 2-71454060-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.675
- CADD 32.00
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available