T9I (p.Thr9Ile) variant of GABRG2 (P18507)
T9I (p.Thr9Ile) in GABRG2 (P18507) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.33 / 1. The record also includes population frequency data, published literature, and structural context.
T9I (p.Thr9Ile) variant details
- p.Thr9Ile
- gnomAD 5-162068025-C-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.331
- CADD 15.80
- PolyPhen-2 0.00
- SIFT 0.21
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available