Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
9 | g.112035757G>A | CA198811530 | LINC02977 | n.2186+2422C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.112035757G>C | CA466833021 | LINC02977 | n.2186+2422C>G | dbSNP |
9 | g.112035757G= | CA1872767535 | LINC02977 | n.2186+2422C= | dbSNP |