G28G (p.Gly28Gly) variant of MAPT (P10636)
G28G (p.Gly28Gly) in MAPT (P10636) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.32 / 1. The record also includes population frequency data, published literature, and structural context.
G28G (p.Gly28Gly) variant details
- p.Gly28Gly
- rs2145309593
- gnomAD 17-45962421-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.319
- CADD 7.75
- Most common in the Non-Finnish European population (allele frequency 4.5e-06)
- Structural context available
- Literature evidence available