Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.3734467C>T | CA10897518 | TP73 | c.*1388C>T (n.*1388C>T) c.*1705C>T (n.*1705C>T) c.*1722C>T (n.*1722C>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.3734467C>A | CA17105446 | TP73 | c.*1388C>A (n.*1388C>A) c.*1705C>A (n.*1705C>A) c.*1722C>A (n.*1722C>A) | dbSNP |