Q9Q (p.Gln9Gln) variant of CHD2 (O14647)
Q9Q (p.Gln9Gln) in CHD2 (O14647) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.39 / 1. The record also includes population frequency data, published literature, and structural context.
Q9Q (p.Gln9Gln) variant details
- p.Gln9Gln
- gnomAD 15-92901264-A-G
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.386
- CADD 12.90
- Most common in the REMAINING population (allele frequency 1.7e-05)
- Structural context available
- Literature evidence available