A18T (p.Ala18Thr) variant of BDNF (P23560)
A18T (p.Ala18Thr) in BDNF (P23560) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.06 / 1. The record also includes population frequency data and published literature.
A18T (p.Ala18Thr) variant details
- p.Ala18Thr
- rs1312832856
- gnomAD 11-27674275-C-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.0617
- CADD 0.06
- SIFT 0.53
- Most common in the Non-Finnish European population (allele frequency 2.8e-06)
- Literature evidence available