Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.3069774G>A | CA11394782 | IL5RA | c.*451C>T (n.*451C>T) c.*492C>T (n.*492C>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.3069774G>C | CA1341430276 | IL5RA | c.*451C>G (n.*451C>G) c.*492C>G (n.*492C>G) | dbSNP |