A36T (p.Ala36Thr) variant of GNA11 (P29992)
A36T (p.Ala36Thr) in GNA11 (P29992) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.57 / 1. The record also includes population frequency data and structural context.
A36T (p.Ala36Thr) variant details
- p.Ala36Thr
- ExAC rs773203722
- gnomAD rs773203722
- Missense
- Variant Prioritization Score for Impact Estimate 0.573
- REVEL 0.52
- CADD 23.30
- PolyPhen-2 0.19
- SIFT 0.20
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available