G39D (p.Gly39Asp) variant of FGB (Fibrinogen beta chain)
G39D (p.Gly39Asp) in FGB (Fibrinogen beta 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 0.29 / 1. The record also includes structural context.
G39D (p.Gly39Asp) variant details
- p.Gly39Asp
- rs1560816739
- NCI-TCGA Cosmic COSV5741
- Ensembl rs1560816739
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.286
- AlphaMissense 0.06
- MetaLR 0.05
- MetaSVM -1.06
- PolyPhen-2 0.00
- SIFT 0.93
- EVE 0.08
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available