| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S3297 | missense_variant | MTHFD1 | NM_001364837.1:c.1958G>A | G | isolated CHD: VSD |
| S3298 | missense_variant | MTHFD1 | NM_001364837.1:c.1958G>A | G | isolated CHD: VSD |
| S3299 | missense_variant | MTHFD1 | NM_001364837.1:c.1958G>A | A | isolated CHD: VSD |
| S3300 | missense_variant | MTHFD1 | NM_001364837.1:c.1958G>A | A | isolated CHD: VSD |