| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S2011 | missense_variant | TFAP2B | NM_003221.4:c.(854G>A) | A | isolated CHD: PDA |
| S2012 | missense_variant | TFAP2B | NM_003221.4:c.(854G>A) | A | isolated CHD: PDA |
| S2013 | missense_variant | TFAP2B | NM_003221.4:c.(854G>A) | A | isolated CHD: PDA |
| S2014 | missense_variant | TFAP2B | NM_003221.4:c.(854G>A) | A | isolated CHD: PDA |