G36D (p.Gly36Asp) variant of BDNF (P23560)
G36D (p.Gly36Asp) 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.
G36D (p.Gly36Asp) variant details
- p.Gly36Asp
- TOPMed rs1037807065
- gnomAD rs1037807065
- Missense
- Variant Prioritization Score for Impact Estimate 0.283
- REVEL 0.21
- CADD 19.40
- PolyPhen-2 0.26
- SIFT 0.13
- Most common in the South Asian population (allele frequency 2.3e-05)