| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S0820 | missense_variant | TLE1 | NM_001303103.1:c.962C>T | T | isolated CHD: ASD |
| S0835 | missense_variant | TLE1 | NM_001303103.1:c.962C>T | T | isolated CHD: ASD |
| S0850 | missense_variant | TLE1 | NM_001303103.1:c.962C>T | T | isolated CHD: ASD |
| S0871 | missense_variant | TLE1 | NM_001303103.1:c.962C>T | T | isolated CHD: ASD |