| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.44899959C>G | CA308877289 | TOMM40 | c.644-771C>G (n.644-771C>G) c.160-771C>G | dbSNP |
| 19 | g.44899959C>T | CA14690424 | TOMM40 | c.644-771C>T (n.644-771C>T) c.160-771C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.44899959C= | CA2338163210 | TOMM40 | c.644-771C= (n.644-771C=) c.160-771C= | dbSNP |