G16G (p.Gly16Gly) variant of KCNQ4 (P56696)
G16G (p.Gly16Gly) in KCNQ4 (P56696) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.29 / 1. The record also includes population frequency data, published literature, and structural context.
G16G (p.Gly16Gly) variant details
- p.Gly16Gly
- rs1276675997
- gnomAD 1-40784141-G-A
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.295
- CADD 13.60
- Most common in the Amish population (allele frequency 0.0011)
- Structural context available
- Literature evidence available