Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.129810129T>C | CA106257364 | LINC02465 | n.429-1873T>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.129810129T>A | CA787060393 | LINC02465 | n.429-1873T>A | dbSNP |
4 | g.129810129T= | CA1493651071 | LINC02465 | n.429-1873T= | dbSNP |