Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.44893408G>T | CA14707526 | TOMM40 | c.436-372G>T (n.436-372G>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.44893408G>A | CA882653582 | TOMM40 | c.436-372G>A (n.436-372G>A) | dbSNP gnomAD v3 gnomAD v4 |
19 | g.44893408G= | CA2338159833 | TOMM40 | c.436-372G= (n.436-372G=) | dbSNP |