| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S1066 | 3_Prime_UTR_variant | NKX2-5 | NM_004387.4:c.*61G>T | T | isolated CHD: PDA |
| S1067 | 3_Prime_UTR_variant | NKX2-5 | NM_004387.4:c.*61G>T | T | isolated CHD: VSD |
| S1068 | 3_Prime_UTR_variant | NKX2-5 | NM_004387.4:c.*61G>T | T | isolated CHD: ASD |
| S1069 | 3_Prime_UTR_variant | NKX2-5 | NM_004387.4:c.*61G>T | T | isolated CHD: AVSD |
| S1070 | 3_Prime_UTR_variant | NKX2-5 | NM_004387.4:c.*61G>T | T | non-isolated CHD: VSD, PDA |
| S1071 | 3_Prime_UTR_variant | NKX2-5 | NM_004387.4:c.*61G>T | T | isolated CHD: TOF |
| S1072 | 3_Prime_UTR_variant | NKX2-5 | NM_004387.4:c.*61G>T | T | isolated CHD: PTA |