M7T (p.Met7Thr) variant of GNA11 (P29992)
M7T (p.Met7Thr) in GNA11 (P29992) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.63 / 1. The record also includes population frequency data and structural context.
M7T (p.Met7Thr) variant details
- p.Met7Thr
- gnomAD rs1401199158
- Missense
- Variant Prioritization Score for Impact Estimate 0.635
- REVEL 0.70
- CADD 23.90
- PolyPhen-2 0.32
- SIFT 0.02
- Most common in the Latino/Admixed American population (allele frequency 2.6e-05)
- Structural context available