V38I (p.Val38Ile) variant of MYH11 (Myosin-11)
V38I (p.Val38Ile) in MYH11 (Myosin-11) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.22 / 1. The record also includes population frequency data and structural context.
V38I (p.Val38Ile) variant details
- p.Val38Ile
- cosmic curated COSV55565
- gnomAD rs1226021715
- Missense
- Variant Prioritization Score for Impact Estimate 0.224
- REVEL 0.20
- CADD 14.30
- PolyPhen-2 0.06
- SIFT 0.29
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available