V13F (p.Val13Phe) variant of GABRG2 (P18507)
V13F (p.Val13Phe) in GABRG2 (P18507) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.04 / 1. The record also includes population frequency data, published literature, and structural context.
V13F (p.Val13Phe) variant details
- p.Val13Phe
- gnomAD 5-162036881-G-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.0449
- CADD 0.05
- SIFT 0.11
- Population evidence available
- Structural context available
- Literature evidence available