Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.42258378C>T | CA16141330 | CCK | c.215-147G>A (n.215-147G>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.42258378C>G | CA907237382 | CCK | c.215-147G>C (n.215-147G>C) | dbSNP gnomAD v4 |
3 | g.42258378C= | CA1360257906 | CCK | c.215-147G= (n.215-147G=) | dbSNP |
3 | g.42258378C>A | CA2580587489 | CCK | c.215-147G>T (n.215-147G>T) | dbSNP |