Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.20077705A>G | CA13643677 | LINC02398 | n.410-21047A>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.20077705A>T | CA2020449102 | LINC02398 | n.410-21047A>T | dbSNP |
12 | g.20077705A= | CA2020449101 | LINC02398 | n.410-21047A= | dbSNP |