G56S (p.Gly56Ser) variant of MBP (Myelin basic protein)
G56S (p.Gly56Ser) in MBP (Myelin basic protein) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.09 / 1. The record also includes population frequency data, published literature, and structural context.
G56S (p.Gly56Ser) variant details
- p.Gly56Ser
- rs1490958412
- gnomAD 18-76980416-C-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.0911
- CADD 1.48
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00019)
- Structural context available
- Literature evidence available