| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.97148976C>A | CA13165897 | SLIT1 | c.413+8842G>T (n.413+8842G>T) c.362+8842G>T (n.362+8842G>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.97148976C= | CA1930307585 | SLIT1 | c.413+8842G= (n.413+8842G=) c.362+8842G= (n.362+8842G=) | dbSNP |