| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Chopra-Amiel-Gordon syndrome | |
| | | Single nucleotide variant (missense variant) | Chopra-Amiel-Gordon syndrome | |
| | | Duplication (inframe insertion +1 more) | Chopra-Amiel-Gordon syndrome | |
| | | Deletion (inframe_deletion) | Chopra-Amiel-Gordon syndrome | |
Click to view in NCBI Gene