| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 11 | g.96262284T>G | CA1993251656 | MAML2 | c.513+79099A>C (n.513+79099A>C) c.-172+80624A>C (n.-172+80624A>C) | dbSNP |
| 11 | g.96262284T>C | CA1993251655 | MAML2 | c.513+79099A>G (n.513+79099A>G) c.-172+80624A>G (n.-172+80624A>G) | dbSNP |
| 11 | g.96262284T>A | CA13490006 | MAML2 | c.513+79099A>T (n.513+79099A>T) c.-172+80624A>T (n.-172+80624A>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |