G16G (p.Gly16Gly) variant of CLCN5 (P51795)
G16G (p.Gly16Gly) in CLCN5 (P51795) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.15 / 1. The record also includes population frequency data, published literature, and structural context.
G16G (p.Gly16Gly) variant details
- p.Gly16Gly
- rs1932251426
- gnomAD X-50042347-G-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.152
- CADD 10.10
- Most common in the South Asian population (allele frequency 6.4e-05)
- Structural context available
- Literature evidence available