F19L (p.Phe19Leu) variant of GABRG2 (P18507)
F19L (p.Phe19Leu) in GABRG2 (P18507) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.15 / 1. The record also includes population frequency data, published literature, and structural context.
F19L (p.Phe19Leu) variant details
- p.Phe19Leu
- rs957456458
- gnomAD 5-162036884-T-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.152
- CADD 7.61
- SIFT 0.11
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available
- Literature evidence available