Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.44927769G>T | CA2494526734 | LINC01833 | n.378-4190C>A | dbSNP |
2 | g.44927769G>C | CA2494526736 | LINC01833 | n.378-4190C>G | dbSNP |
2 | g.44927769G>A | CA15156752 | LINC01833 | n.378-4190C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |