| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 1 | g.209633134C>T | CA344595004 | LAMB3 | c.565-1G>A (n.565-1G>A) c.373-1G>A (n.373-1G>A) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 1 | g.209633134C>A | CA16040702 | LAMB3 | c.565-1G>T (n.565-1G>T) c.373-1G>T (n.373-1G>T) | ClinVar dbSNP |