D13D (p.Asp13Asp) variant of MAPT (P10636)
D13D (p.Asp13Asp) in MAPT (P10636) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.10 / 1. The record also includes population frequency data, published literature, and structural context.
D13D (p.Asp13Asp) variant details
- p.Asp13Asp
- rs760999100
- gnomAD 17-45962376-T-C
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.101
- CADD 2.82
- Most common in the Finnish in Finland (FIN) population (allele frequency 3.8e-05)
- Structural context available
- Literature evidence available