Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.115893327C>T | CA229845914 | LINC02698 | n.469-7409C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.115893327C= | CA2002310785 | LINC02698 | n.469-7409C= | dbSNP |
11 | g.115893327C>G | CA2838157850 | LINC02698 | n.469-7409C>G | dbSNP |
11 | g.115893327C>A | CA2838157851 | LINC02698 | n.469-7409C>A | dbSNP |