Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.21196677C>T | CA233550149 | SLCO1B1 | c.728-269C>T (n.728-269C>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.21196677C>G | CA686364539 | SLCO1B1 | c.728-269C>G (n.728-269C>G) | dbSNP |
12 | g.21196677C= | CA2020999735 | SLCO1B1 | c.728-269C= (n.728-269C=) | dbSNP |