D38D (p.Asp38Asp) variant of MAPT (P10636)
D38D (p.Asp38Asp) in MAPT (P10636) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.12 / 1. The record also includes population frequency data, published literature, and structural context.
D38D (p.Asp38Asp) variant details
- p.Asp38Asp
- gnomAD 17-45962451-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.115
- CADD 4.88
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available
- Literature evidence available