| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S2004 | missense_variant | NKX2-6 | NM_001136271.2:c.454A>C | C | isolated CHD: VSD |
| S2005 | missense_variant | NKX2-6 | NM_001136271.2:c.454A>C | C | isolated CHD: VSD |
| S2006 | missense_variant | NKX2-6 | NM_001136271.2:c.454A>C | C | isolated CHD: VSD |