Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.73207352C>T | CA13690657 | LINC02444 | n.386-95C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.73207352C>A | CA691674464 | LINC02444 | n.386-95C>A | dbSNP |
12 | g.73207352C= | CA2046136554 | LINC02444 | n.386-95C= | dbSNP |