Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.74192430T>G | CA239777150 | LINC02882 | n.553+1644A>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.74192430T>C | CA2739313587 | LINC02882 | n.553+1644A>G | dbSNP |
12 | g.74192430T>A | CA2739313586 | LINC02882 | n.553+1644A>T | dbSNP |
12 | g.74192430T= | CA2046626577 | LINC02882 | n.553+1644A= | dbSNP |