M55I (p.Met55Ile) variant of ITGB4 (Integrin beta-4)
M55I (p.Met55Ile) in ITGB4 (Integrin beta-4) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of Inborn genetic diseases. The record also includes structural context.
M55I (p.Met55Ile) variant details
- p.Met55Ile
- Ensembl rs2148462610
- Uncertain significance
- Inborn genetic diseases
- Missense
- ClinVar: Uncertain significance (Inborn genetic diseases)
- UniProt: Uncertain significance
- Structural context available