Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.24917063C>A | CA1159437342 | RUNX3 | c.586+2177G>T (n.586+2177G>T) c.544+2177G>T (n.544+2177G>T) n.318+2177G>T | dbSNP |
1 | g.24917063C>T | CA10977448 | RUNX3 | c.586+2177G>A (n.586+2177G>A) c.544+2177G>A (n.544+2177G>A) n.318+2177G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |