G16G (p.Gly16Gly) variant of SPG7 (Q9UQ90)
G16G (p.Gly16Gly) in SPG7 (Q9UQ90) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.09 / 1. The record also includes population frequency data, published literature, and structural context.
G16G (p.Gly16Gly) variant details
- p.Gly16Gly
- gnomAD 16-89508465-C-A
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.0899
- CADD 1.31
- Most common in the HGDP:FRENCH population (allele frequency 0.019)
- Structural context available
- Literature evidence available