Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.44892962C>T | CA9505650 | TOMM40 | c.435+33C>T (n.435+33C>T) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.44892962C= | CA2338159592 | TOMM40 | c.435+33C= (n.435+33C=) | dbSNP |
19 | g.44892962C>G | CA2580608526 | TOMM40 | c.435+33C>G (n.435+33C>G) | dbSNP |
19 | g.44892962C>A | CA2580608527 | TOMM40 | c.435+33C>A (n.435+33C>A) | dbSNP gnomAD v4 |