Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.100215693G>A | CA11121357 | LINC01104 | n.567+6873G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.100215693G>C | CA1274236903 | LINC01104 | n.567+6873G>C | dbSNP |
2 | g.100215693G= | CA1274236901 | LINC01104 | n.567+6873G= | dbSNP |