A3G (p.Ala3Gly) variant of MET (P08581)
A3G (p.Ala3Gly) in MET (P08581) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The available variant effect predictions contribute to a CATVariant prioritization score of 0.17 / 1. The record also includes population frequency data and structural context.
A3G (p.Ala3Gly) variant details
- p.Ala3Gly
- Ensembl rs1797064164
- Uncertain significance
- Missense
- Variant Prioritization Score for Impact Estimate 0.166
- REVEL 0.09
- MetaLR 0.36
- MetaSVM -0.39
- CADD 7.27
- PolyPhen-2 0.10
- SIFT 0.24
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Most common in the Non-Finnish European population (allele frequency 9.9e-07)
- Structural context available