G21G (p.Gly21Gly) variant of MAPT (P10636)
G21G (p.Gly21Gly) 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.
G21G (p.Gly21Gly) variant details
- p.Gly21Gly
- rs200084740
- gnomAD 17-45962400-G-A
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.236
- CADD 8.30
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available
- Literature evidence available