A33V (p.Ala33Val) variant of BDNF (P23560)
A33V (p.Ala33Val) in BDNF (P23560) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.33 / 1. The record also includes population frequency data.
A33V (p.Ala33Val) variant details
- p.Ala33Val
- NCI-TCGA TCGA novel
- gnomAD rs1852858181
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.329
- REVEL 0.11
- CADD 21.90
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the REMAINING population (allele frequency 0.00048)