C9G (p.Cys9Gly) variant of SERPINE1 (P05121)
C9G (p.Cys9Gly) in SERPINE1 (P05121) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes variant effect predictions and structural context.
C9G (p.Cys9Gly) variant details
- p.Cys9Gly
- NCI-TCGA Cosmic COSV5617
- Variant assessed as somatic; moderate impact.
- Missense
- MetaLR 0.57
- MetaSVM 0.38
- SIFT 0.03
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available