L136F (p.Leu136Phe) variant of FGG (Fibrinogen gamma chain)
L136F (p.Leu136Phe) in FGG (Fibrinogen gamma chain) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.45 / 1. The record also includes population frequency data and structural context.
L136F (p.Leu136Phe) variant details
- p.Leu136Phe
- ExAC rs747889986
- TOPMed rs747889986
- gnomAD rs747889986
- Missense
- Variant Prioritization Score for Impact Estimate 0.454
- REVEL 0.63
- CADD 19.70
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 9.4e-07)
- Structural context available