| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S4780 | synonymous_variant | KAT2B | NM_003884.5:c.309G>A | C/C | isolated CHD: VSD/ASD/PDA/TOF/PS/other |
| S4781 | synonymous_variant | KAT2B | NM_003884.5:c.309G>A | G/A | isolated CHD: VSD/ASD/PDA/TOF/PS/other |
| S4782 | synonymous_variant | KAT2B | NM_003884.5:c.309G>A | A/A | isolated CHD: VSD/ASD/PDA/TOF/PS/other |
| S4783 | synonymous_variant | KAT2B | NM_003884.5:c.309G>A | C | isolated CHD: VSD/ASD/PDA/TOF/PS/other |
| S4784 | synonymous_variant | KAT2B | NM_003884.5:c.309G>A | T | isolated CHD: VSD/ASD/PDA/TOF/PS/other |