| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S1061 | synonymous_variant | NKX2-5 | NM_004387.4:c.606G>C | C | isolated CHD: VSD |
| S1062 | synonymous_variant | NKX2-5 | NM_004387.4:c.606G>C | C | isolated CHD: PDA |
| S1063 | synonymous_variant | NKX2-5 | NM_004387.4:c.606G>C | C | isolated CHD: ASD |
| S1064 | synonymous_variant | NKX2-5 | NM_004387.4:c.606G>C | C | non-isolated CHD: ASD, PDA |
| S1065 | synonymous_variant | NKX2-5 | NM_004387.4:c.606G>C | C | isolated CHD: PTA |