| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 4 | g.139842970G>T | CA11662621 | MAML3 | c.111-112303C>A c.2079+46387C>A (n.2079+46387C>A) c.2067+46387C>A (n.2067+46387C>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.139842970G>A | CA1498539385 | MAML3 | c.111-112303C>T c.2079+46387C>T (n.2079+46387C>T) c.2067+46387C>T (n.2067+46387C>T) | dbSNP |