p.Arg59 Ala69del variant of ITGB4 (Integrin beta-4)
p.Arg59 Ala69del in ITGB4 (Integrin beta-4) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.48 / 1. The record also includes population frequency data, published literature, and structural context.
p.Arg59 Ala69del variant details
- rs1480399395
- gnomAD 17-75727414-ACCGG
- Inframe Deletion
- Variant Prioritization Score for Impact Estimate 0.477
- CADD 17.70
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available
- Literature evidence available