L20I (p.Leu20Ile) variant of FGG (Fibrinogen gamma chain)
L20I (p.Leu20Ile) in FGG (Fibrinogen gamma chain) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.08 / 1. The record also includes population frequency data and structural context.
L20I (p.Leu20Ile) variant details
- p.Leu20Ile
- NCI-TCGA Cosmic COSV6019
- cosmic curated COSV60194
- TOPMed rs992441964
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.0754
- REVEL 0.04
- CADD 8.48
- PolyPhen-2 0.01
- SIFT 0.09
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available