| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 1 | g.206841127A>T | CA528577113 | IL19 | c.438+49A>T (n.438+49A>T) c.552+49A>T (n.552+49A>T) n.701T>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.206841127A>C | CA1364097 | IL19 | c.438+49A>C (n.438+49A>C) c.552+49A>C (n.552+49A>C) n.701T>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |