M79I (p.Met79Ile) variant of MYH11 (Myosin-11)
M79I (p.Met79Ile) in MYH11 (Myosin-11) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.71 / 1. The record also includes population frequency data and structural context.
M79I (p.Met79Ile) variant details
- p.Met79Ile
- NCI-TCGA Cosmic COSV5556
- cosmic curated COSV55568
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.71
- REVEL 0.67
- CADD 25.40
- PolyPhen-2 0.83
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available