G26V (p.Gly26Val) variant of DDC (P20711)
G26V (p.Gly26Val) in DDC (P20711) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.18 / 1. The record also includes population frequency data and structural context.
G26V (p.Gly26Val) variant details
- p.Gly26Val
- TOPMed rs1303408405
- gnomAD rs1303408405
- Missense
- Variant Prioritization Score for Impact Estimate 0.176
- REVEL 0.13
- CADD 13.40
- PolyPhen-2 0.03
- SIFT 0.04
- Most common in the Latino/Admixed American population (allele frequency 2.2e-05)
- Structural context available