Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.155461450T>G | CA1754594071 | EN2 | c.686-921T>G (n.686-921T>G) | dbSNP |
7 | g.155461450T>C | CA126742 | EN2 | c.686-921T>C (n.686-921T>C) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.155461450T>A | CA1754594070 | EN2 | c.686-921T>A (n.686-921T>A) | dbSNP |