M19T (p.Met19Thr) variant of SETD5 (Q9C0A6)
M19T (p.Met19Thr) in SETD5 (Q9C0A6) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
M19T (p.Met19Thr) variant details
- p.Met19Thr
- NCI-TCGA Cosmic COSV5670
- cosmic curated COSV56709
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available