P99S (p.Pro99Ser) variant of MYH6 (Myosin-6)
P99S (p.Pro99Ser) in MYH6 (Myosin-6) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
P99S (p.Pro99Ser) variant details
- p.Pro99Ser
- NCI-TCGA Cosmic COSV6244
- cosmic curated COSV62447
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available