G21D (p.Gly21Asp) variant of KCNJ3 (P48549)
G21D (p.Gly21Asp) in KCNJ3 (P48549) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.48 / 1. The record also includes population frequency data, published literature, and structural context.
G21D (p.Gly21Asp) variant details
- p.Gly21Asp
- gnomAD 2-154698837-G-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.483
- REVEL 0.30
- CADD 23.20
- PolyPhen-2 0.00
- SIFT 0.24
- Most common in the Non-Finnish European population (allele frequency 8.8e-05)
- Structural context available
- Literature evidence available