T39T (p.Thr39Thr) variant of MAPT (P10636)
T39T (p.Thr39Thr) 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.
T39T (p.Thr39Thr) variant details
- p.Thr39Thr
- rs63750529
- gnomAD 17-45962454-G-A
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.0901
- CADD 1.34
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available
- Literature evidence available