I19M (p.Ile19Met) variant of MLH3 (DNA mismatch repair protein Mlh3)
I19M (p.Ile19Met) in MLH3 (DNA mismatch repair protein Mlh3) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
I19M (p.Ile19Met) variant details
- p.Ile19Met
- rs2503338803
- ClinGen CA390451834
- ClinVar RCV004054108
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available