F79L (p.Phe79Leu) variant of SHMT2 (P34897)
F79L (p.Phe79Leu) in SHMT2 (P34897) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
F79L (p.Phe79Leu) variant details
- p.Phe79Leu
- NCI-TCGA Cosmic COSV6107
- cosmic curated COSV61073
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available