P74T (p.Pro74Thr) variant of MYL2 (P10916)
P74T (p.Pro74Thr) in MYL2 (P10916) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
P74T (p.Pro74Thr) variant details
- p.Pro74Thr
- NCI-TCGA Cosmic COSV5740
- cosmic curated COSV57406
- NCI-TCGA Cosmic COSV9996
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available