D29G (p.Asp29Gly) variant of FAS (P25445)
D29G (p.Asp29Gly) in FAS (P25445) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.09 / 1. The record also includes population frequency data and structural context.
D29G (p.Asp29Gly) variant details
- p.Asp29Gly
- ExAC rs758551688
- TOPMed rs758551688
- gnomAD rs758551688
- Missense
- Variant Prioritization Score for Impact Estimate 0.0906
- CADD 1.40
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available