G56D (p.Gly56Asp) variant of FAS (P25445)
G56D (p.Gly56Asp) in FAS (P25445) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.06 / 1. The record also includes population frequency data and structural context.
G56D (p.Gly56Asp) variant details
- p.Gly56Asp
- cosmic curated COSV10589
- TOPMed rs1452698941
- gnomAD rs1452698941
- Missense
- Variant Prioritization Score for Impact Estimate 0.0552
- CADD 0.03
- PolyPhen-2 0.06
- SIFT 0.23
- Most common in the East Asian population (allele frequency 0.00013)
- Structural context available