R75M (p.Arg75Met) variant of TGFB2 (P61812)
R75M (p.Arg75Met) in TGFB2 (P61812) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
R75M (p.Arg75Met) variant details
- p.Arg75Met
- NCI-TCGA Cosmic COSV1008
- cosmic curated COSV10085
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available