Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.209794570A>G | CA10932369 | IRF6 | c.508+720T>C (n.508+720T>C) c.223+720T>C (n.223+720T>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.209794570A>T | CA2484366971 | IRF6 | c.508+720T>A (n.508+720T>A) c.223+720T>A (n.223+720T>A) | dbSNP |