G16G (p.Gly16Gly) variant of SDHD (O14521)
G16G (p.Gly16Gly) in SDHD (O14521) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.27 / 1. The record also includes population frequency data, published literature, and structural context.
G16G (p.Gly16Gly) variant details
- p.Gly16Gly
- rs1555186688
- gnomAD 11-112086955-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.268
- CADD 14.30
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available