S11G (p.Ser11Gly) variant of BDNF (P23560)
S11G (p.Ser11Gly) in BDNF (P23560) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.28 / 1. The record also includes population frequency data and published literature.
S11G (p.Ser11Gly) variant details
- p.Ser11Gly
- gnomAD 11-27674269-T-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.278
- CADD 17.50
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 9.2e-07)
- Literature evidence available