T17T (p.Thr17Thr) variant of MAPT (P10636)
T17T (p.Thr17Thr) in MAPT (P10636) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.09 / 1. The record also includes population frequency data, published literature, and structural context.
T17T (p.Thr17Thr) variant details
- p.Thr17Thr
- rs369969350
- gnomAD 17-45962388-G-A
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.0868
- CADD 0.87
- Most common in the 1KG:GIH population (allele frequency 0.0053)
- Structural context available
- Literature evidence available