V37M (p.Val37Met) variant of BDNF (P23560)
V37M (p.Val37Met) in BDNF (P23560) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.16 / 1. The record also includes population frequency data.
V37M (p.Val37Met) variant details
- p.Val37Met
- ExAC rs759834365
- TOPMed rs759834365
- gnomAD rs759834365
- Missense
- Variant Prioritization Score for Impact Estimate 0.16
- REVEL 0.04
- CADD 17.00
- PolyPhen-2 0.00
- SIFT 0.12
- Most common in the Latino/Admixed American population (allele frequency 2.2e-05)