Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
13 | g.30738041A>C | CA2082040775 | ALOX5AP | c.70+2366A>C (n.70+2366A>C) c.241+2366A>C (n.241+2366A>C) | dbSNP |
13 | g.30738041A>T | CA15793841 | ALOX5AP | c.70+2366A>T (n.70+2366A>T) c.241+2366A>T (n.241+2366A>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |