Y13C (p.Tyr13Cys) variant of FGG (Fibrinogen gamma chain)
Y13C (p.Tyr13Cys) in FGG (Fibrinogen gamma chain) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.07 / 1. The record also includes population frequency data and structural context.
Y13C (p.Tyr13Cys) variant details
- p.Tyr13Cys
- cosmic curated COSV10966
- TOPMed rs773024285
- Missense
- Variant Prioritization Score for Impact Estimate 0.0651
- REVEL 0.07
- CADD 0.19
- PolyPhen-2 0.00
- SIFT 0.19
- Most common in the East Asian population (allele frequency 2.5e-05)
- Structural context available