| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S4014 | missense_variant | TGFβ1 | NM_000660.7:c.29C>T | C/C | non-isolated CHD: TS, VSD |
| S4015 | missense_variant | TGFβ1 | NM_000660.7:c.29C>T | C/T | non-isolated CHD: TS, VSD |
| S4016 | missense_variant | TGFβ1 | NM_000660.7:c.29C>T | T/T | non-isolated CHD: TS, VSD |
| S4017 | missense_variant | TGFβ1 | NM_000660.7:c.29C>T | C | non-isolated CHD: TS, VSD |
| S4018 | missense_variant | TGFβ1 | NM_000660.7:c.29C>T | T | non-isolated CHD: TS, VSD |