| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S4785 | missense_variant | KAT2B | NM_003884.5:c.1157A>G | A/A | isolated CHD: VSD/ASD/PDA/TOF/PS/other |
| S4786 | missense_variant | KAT2B | NM_003884.5:c.1157A>G | A/G | isolated CHD: VSD/ASD/PDA/TOF/PS/other |
| S4787 | missense_variant | KAT2B | NM_003884.5:c.1157A>G | G/G | isolated CHD: VSD/ASD/PDA/TOF/PS/other |
| S4788 | missense_variant | KAT2B | NM_003884.5:c.1157A>G | A | isolated CHD: VSD/ASD/PDA/TOF/PS/other |
| S4789 | missense_variant | KAT2B | NM_003884.5:c.1157A>G | G | isolated CHD: VSD/ASD/PDA/TOF/PS/other |