Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.44901174T>G | CA2338163797 | TOMM40 | c.844-34T>G (n.844-34T>G) c.360-34T>G | dbSNP |
19 | g.44901174T>C | CA9505817 | TOMM40 | c.844-34T>C (n.844-34T>C) c.360-34T>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.44901174T= | CA2338163796 | TOMM40 | c.844-34T= (n.844-34T=) c.360-34T= | dbSNP |