G19G (p.Gly19Gly) variant of MAPT (P10636)
G19G (p.Gly19Gly) in MAPT (P10636) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.24 / 1. The record also includes population frequency data, published literature, and structural context.
G19G (p.Gly19Gly) variant details
- p.Gly19Gly
- gnomAD 17-45962394-G-A
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.242
- CADD 4.47
- Most common in the Non-Finnish European population (allele frequency 2.3e-05)
- Structural context available
- Literature evidence available