Y13H (p.Tyr13His) variant of FGG (Fibrinogen gamma chain)
Y13H (p.Tyr13His) in FGG (Fibrinogen gamma chain) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.13 / 1. The record also includes population frequency data and structural context.
Y13H (p.Tyr13His) variant details
- p.Tyr13His
- cosmic curated COSV10814
- 1000Genomes rs200241886
- ExAC rs200241886
- TOPMed rs200241886
- Missense
- Variant Prioritization Score for Impact Estimate 0.134
- REVEL 0.13
- CADD 5.80
- PolyPhen-2 0.26
- SIFT 0.53
- Most common in the HGDP:HAZARA population (allele frequency 0.031)
- Structural context available