| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S0821 | missense_variant | FCN1 | NM_002003.5:c.449C>T | T | isolated CHD: ASD |
| S0851 | missense_variant | FCN1 | NM_002003.5:c.449C>T | T | isolated CHD: ASD |
| S0872 | missense_variant | FCN1 | NM_002003.5:c.449C>T | T | isolated CHD: ASD |
| S0884 | missense_variant | FCN1 | NM_002003.5:c.449C>T | T | isolated CHD: ASD |