| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S3114 | intron_variant | CUBN | NC_000010.11:g.17088694A>G | A | NA: NA |
| S3115 | intron_variant | CUBN | NC_000010.11:g.17088694A>G | G | NA: NA |
| S3116 | intron_variant | CUBN | NC_000010.11:g.17088694A>G | A | NA: NA |
| S3117 | intron_variant | CUBN | NC_000010.11:g.17088694A>G | G | NA: NA |
| S3118 | intron_variant | CUBN | NC_000010.11:g.17088694A>G | A | NA: NA |
| S3119 | intron_variant | CUBN | NC_000010.11:g.17088694A>G | G | NA: NA |