Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.109862649T>A | CA1188273390 | LINC01768 | n.845+29234T>A | dbSNP |
1 | g.109862649T>G | CA1188273389 | LINC01768 | n.845+29234T>G | dbSNP |
1 | g.109862649T>C | CA15147293 | LINC01768 | n.845+29234T>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |