V37D (p.Val37Asp) variant of BDNF (P23560)
V37D (p.Val37Asp) in BDNF (P23560) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.46 / 1. The record also includes population frequency data and published literature.
V37D (p.Val37Asp) variant details
- p.Val37Asp
- gnomAD 11-27674193-A-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.464
- CADD 24.50
- SIFT 0.00
- Most common in the REMAINING population (allele frequency 3.3e-05)
- Literature evidence available