Q39* (p.Gln39Ter) variant of COMP (P49747)
Q39* (p.Gln39Ter) in COMP (P49747) is a protein-truncating change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.81 / 1. The record also includes population frequency data and structural context.
Q39* (p.Gln39Ter) variant details
- p.Gln39Ter
- gnomAD rs866594232
- Stop Gained
- Variant Prioritization Score for Impact Estimate 0.812
- CADD 35.00
- Most common in the African/African-American population (allele frequency 3.1e-05)
- Structural context available