S26P (p.Ser26Pro) variant of MYLK (Q15746)
S26P (p.Ser26Pro) in MYLK (Q15746) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.38 / 1. The record also includes population frequency data and structural context.
S26P (p.Ser26Pro) variant details
- p.Ser26Pro
- TOPMed rs2064878803
- Missense
- Variant Prioritization Score for Impact Estimate 0.38
- REVEL 0.19
- CADD 20.70
- PolyPhen-2 0.01
- SIFT 0.11
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available