| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S1531 | missense_variant | ACTC1 | NM_005159.5:c.532A>T | T | isolated CHD: ASD |
| S1532 | missense_variant | ACTC1 | NM_005159.5:c.532A>T | T | isolated CHD: ASD |
| S1533 | missense_variant | ACTC1 | NM_005159.5:c.532A>T | T | isolated CHD: ASD |
| S1534 | missense_variant | ACTC1 | NM_005159.5:c.532A>T | T | isolated CHD: ASD |
| S1535 | missense_variant | ACTC1 | NM_005159.5:c.532A>T | T | isolated CHD: ASD |