| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S3494 | missense_variant | CBS | NM_000071.2:c.919G>A | G | isolated CHD: NA |
| S3495 | missense_variant | CBS | NM_000071.2:c.919G>A | A | isolated CHD: NA |
| S3496 | missense_variant | CBS | NM_000071.2:c.919G>A | G | isolated CHD: NA |
| S3497 | missense_variant | CBS | NM_000071.2:c.919G>A | A | isolated CHD: NA |
| S3498 | missense_variant | CBS | NM_000071.2:c.919G>A | G | isolated CHD: NA |
| S3499 | missense_variant | CBS | NM_000071.2:c.919G>A | A | isolated CHD: NA |