| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S0812 | missense_variant | AFAP1L2 | NM_001001936.3:c.2174G>A | A | isolated CHD: ASD |
| S0833 | missense_variant | AFAP1L2 | NM_001001936.3:c.2174G>A | A | isolated CHD: ASD |
| S0842 | missense_variant | AFAP1L2 | NM_001001936.3:c.2174G>A | A | isolated CHD: ASD |
| S0863 | missense_variant | AFAP1L2 | NM_001001936.3:c.2174G>A | A | isolated CHD: ASD |