| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 6 | g.104952962A>G | CA12202975 | LIN28B | c.67+2453A>G (n.67+2453A>G) c.34+2453A>G (n.34+2453A>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 6 | g.104952962A>T | CA1652775745 | LIN28B | c.67+2453A>T (n.67+2453A>T) c.34+2453A>T (n.34+2453A>T) | dbSNP |