Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
14 | g.52322041G>C | CA963156452 | PTGER2 | c.844-5180G>C (n.844-5180G>C) c.79-5180G>C (n.79-5180G>C) | dbSNP gnomAD v3 gnomAD v4 |
14 | g.52322041G>A | CA15823554 | PTGER2 | c.844-5180G>A (n.844-5180G>A) c.79-5180G>A (n.79-5180G>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |