R6G (p.Arg6Gly) variant of MTHFR (P42898)
R6G (p.Arg6Gly) in MTHFR (P42898) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
R6G (p.Arg6Gly) variant details
- p.Arg6Gly
- NCI-TCGA Cosmic COSV5673
- cosmic curated COSV56739
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available