Y91H (p.Tyr91His) variant of GABRB3 (P28472)
Y91H (p.Tyr91His) in GABRB3 (P28472) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.54 / 1. The record also includes population frequency data and structural context.
Y91H (p.Tyr91His) variant details
- p.Tyr91His
- 1000Genomes rs1423283107
- TOPMed rs1423283107
- Missense
- Variant Prioritization Score for Impact Estimate 0.54
- REVEL 0.50
- CADD 22.90
- PolyPhen-2 0.21
- SIFT 0.17
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available