M1I (p.Met1Ile) variant of CHD8 (Q9HCK8)
M1I (p.Met1Ile) in CHD8 (Q9HCK8) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of not provided.
M1I (p.Met1Ile) variant details
- p.Met1Ile
- rs2502017323
- ClinGen CA388891692
- ClinVar RCV003020877
- Uncertain significance
- not provided
- Missense
- ClinVar: Uncertain significance (not provided)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance