W68G (p.Trp68Gly) variant of KCNJ11 (Q14654)
W68G (p.Trp68Gly) in KCNJ11 (Q14654) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.86 / 1. The record also includes population frequency data and structural context.
W68G (p.Trp68Gly) variant details
- p.Trp68Gly
- gnomAD rs1474444717
- Missense
- Variant Prioritization Score for Impact Estimate 0.861
- REVEL 0.99
- CADD 32.00
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available