P56S (p.Pro56Ser) variant of MMACHC (Q9Y4U1)
P56S (p.Pro56Ser) in MMACHC (Q9Y4U1) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
P56S (p.Pro56Ser) variant details
- p.Pro56Ser
- NCI-TCGA Cosmic COSV5311
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available