R79= variant of MTHFR (P42898)
R79= in MTHFR (P42898) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; low impact. The record also includes structural context.
R79= variant details
- NCI-TCGA TCGA novel
- Variant assessed as somatic; low impact.
- Missense
- UniProt: Variant assessed as somatic; low impact.
- Structural context available