M19T (p.Met19Thr) variant of SMARCE1 (Q969G3)
M19T (p.Met19Thr) in SMARCE1 (Q969G3) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes experimental measurements and structural context.
M19T (p.Met19Thr) variant details
- p.Met19Thr
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available
- SMARCE1 High mobility group box domain domainome 1.0: score -0.211