P59P (p.Pro59Pro) variant of MAPT (P10636)
P59P (p.Pro59Pro) 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.
P59P (p.Pro59Pro) variant details
- p.Pro59Pro
- rs370131551
- gnomAD 17-45971902-G-A
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.0969
- CADD 2.30
- Most common in the REMAINING population (allele frequency 1.7e-05)
- Structural context available
- Literature evidence available