Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.45405641A>T | CA1906912050 | ALOX5 | c.432-6550A>T (n.432-6550A>T) c.350-6548A>T (n.350-6548A>T) c.-4-6550A>T (n.-4-6550A>T) n.499-6550A>T | dbSNP |
10 | g.45405641A>G | CA16388078 | ALOX5 | c.432-6550A>G (n.432-6550A>G) c.350-6548A>G (n.350-6548A>G) c.-4-6550A>G (n.-4-6550A>G) n.499-6550A>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |