Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.1234209A>T | CA12553356 | UNCX | c.450+514A>T (n.450+514A>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.1234209A>C | CA1682451657 | UNCX | c.450+514A>C (n.450+514A>C) | dbSNP |
7 | g.1234209A= | CA1682451658 | UNCX | c.450+514A= (n.450+514A=) | dbSNP |