Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
5 | g.136163522T>G | CA1584849668 | SMAD5 | c.775+131T>G (n.775+131T>G) c.242+131T>G n.60-8912T>G | dbSNP gnomAD v4 |
5 | g.136163522T>A | CA12074181 | SMAD5 | c.775+131T>A (n.775+131T>A) c.242+131T>A n.60-8912T>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |