A19T (p.Ala19Thr) variant of MAP2K2 (P36507)
A19T (p.Ala19Thr) in MAP2K2 (P36507) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.29 / 1. The record also includes population frequency data and structural context.
A19T (p.Ala19Thr) variant details
- p.Ala19Thr
- Ensembl rs2145089839
- Missense
- Variant Prioritization Score for Impact Estimate 0.294
- REVEL 0.17
- CADD 19.60
- PolyPhen-2 0.00
- SIFT 0.50
- Most common in the Finnish in Finland (FIN) population (allele frequency 2.2e-05)
- Structural context available