| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S2995 | missense_variant | NKX2-5 | NM_004387.4:c.533C>T | T | isolated CHD: ASD, AV block |
| S2996 | missense_variant | NKX2-5 | NM_004387.4:c.533C>T | T | isolated CHD: ASD, AV block |
| S2997 | missense_variant | NKX2-5 | NM_004387.4:c.533C>T | T | isolated CHD: ASD, AV block |
| S2998 | missense_variant | NKX2-5 | NM_004387.4:c.533C>T | T | isolated CHD: ASD, AV block |
| S2999 | missense_variant | NKX2-5 | NM_004387.4:c.533C>T | T | isolated CHD: ASD, AV block |