M77T (p.Met77Thr) variant of MYH7 (Myosin-7)
M77T (p.Met77Thr) in MYH7 (Myosin-7) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.44 / 1. The record also includes population frequency data and structural context.
M77T (p.Met77Thr) variant details
- p.Met77Thr
- TOPMed rs1380485301
- gnomAD rs1380485301
- Missense
- Variant Prioritization Score for Impact Estimate 0.436
- REVEL 0.33
- CADD 20.40
- Most common in the Ashkenazi Jewish population (allele frequency 5.1e-05)
- Structural context available