Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
5 | g.40703988C>A | CA810609230 | PTGER4,TTC33 | c.221+42810G>T (n.221+42810G>T) c.*37+7225C>A (n.*37+7225C>A) | dbSNP |
5 | g.40703988C>T | CA15403094 | PTGER4,TTC33 | c.221+42810G>A (n.221+42810G>A) c.*37+7225C>T (n.*37+7225C>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |