G46G (p.Gly46Gly) variant of CHD7 (Q9P2D1)
G46G (p.Gly46Gly) in CHD7 (Q9P2D1) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.28 / 1. The record also includes population frequency data, published literature, and structural context.
G46G (p.Gly46Gly) variant details
- p.Gly46Gly
- gnomAD 8-60741570-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.283
- CADD 9.82
- Most common in the Latino/Admixed American population (allele frequency 2.2e-05)
- Structural context available
- Literature evidence available