Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.72007071T>C | CA13593559 | TPH2 | c.1068+12506T>C (n.1068+12506T>C) c.474+12506T>C (n.474+12506T>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.72007071T= | CA2045544698 | TPH2 | c.1068+12506T= (n.1068+12506T=) c.474+12506T= (n.474+12506T=) | dbSNP |