P28T (p.Pro28Thr) variant of MYLK (Q15746)
P28T (p.Pro28Thr) in MYLK (Q15746) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
P28T (p.Pro28Thr) variant details
- p.Pro28Thr
- NCI-TCGA Cosmic COSV1006
- cosmic curated COSV10065
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available