| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S3644 | missense_variant | NRP1 | NM_003873.6:c.2197G>A | G/G | isolated CHD: TOF |
| S3645 | missense_variant | NRP1 | NM_003873.6:c.2197G>A | A/G | isolated CHD: TOF |
| S3646 | missense_variant | NRP1 | NM_003873.6:c.2197G>A | A/A | isolated CHD: TOF |
| S3647 | missense_variant | NRP1 | NM_003873.6:c.2197G>A | A | isolated CHD: TOF |