R27M (p.Arg27Met) variant of NTRK2 (Q16620)
R27M (p.Arg27Met) in NTRK2 (Q16620) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
R27M (p.Arg27Met) variant details
- p.Arg27Met
- NCI-TCGA Cosmic COSV9945
- cosmic curated COSV99453
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available