P99L (p.Pro99Leu) variant of MYH7 (Myosin-7)
P99L (p.Pro99Leu) in MYH7 (Myosin-7) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
P99L (p.Pro99Leu) variant details
- p.Pro99Leu
- NCI-TCGA Cosmic COSV6252
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available