V109I (p.Val109Ile) variant of CHD8 (Q9HCK8)
V109I (p.Val109Ile) 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.
V109I (p.Val109Ile) variant details
- p.Val109Ile
- rs2502015972
- ClinGen CA388889475
- ClinVar RCV003031431
- Uncertain significance
- not provided
- Missense
- ClinVar: Uncertain significance (not provided)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance