M61T (p.Met61Thr) variant of DLG4 (Disks large homolog 4)
M61T (p.Met61Thr) in DLG4 (Disks large homolog 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 population frequency data, experimental measurements, and structural context.
M61T (p.Met61Thr) variant details
- p.Met61Thr
- gnomAD rs1304712290
- Uncertain significance
- Inborn genetic diseases
- Missense
- ClinVar: Uncertain significance (Inborn genetic diseases)
- UniProt: Uncertain significance
- Population evidence available
- Structural context available
- DLG4 PDZ domain domainome 1.0: score -0.0088