Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
9 | g.99132634C>T | CA16612807 | TGFBR1 | c.262C>T (p.Arg88Ter) c.274C>T (p.Arg92Ter) c.136+3534C>T (n.136+3534C>T) c.*265C>T (n.*265C>T) c.469C>T (p.Arg157Ter) c.343+3534C>T (n.343+3534C>T) c.481C>T (p.Arg161Ter) | ClinVar dbSNP gnomAD v4 COSMIC |
9 | g.99132634C= | CA1867274582 | TGFBR1 | c.262C= (p.Arg88=) c.274C= (p.Arg92=) c.136+3534C= (n.136+3534C=) c.*265C= (n.*265C=) c.469C= (p.Arg157=) c.343+3534C= (n.343+3534C=) c.481C= (p.Arg161=) | dbSNP |