| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 11 | g.64807677A>G | CA381185239 | MEN1 | c.673T>C (p.Trp225Arg) c.644T>C (p.Leu215Pro) c.658T>C (p.Trp220Arg) c.405T>C c.9T>C n.690T>C n.620T>C n.318T>C n.698T>C n.935T>C c.384T>C c.553T>C (p.Trp185Arg) | ClinVar dbSNP |
| 11 | g.64807677A= | CA1978892248 | MEN1 | c.673T= (p.Trp225=) c.644T= (p.Leu215=) c.658T= (p.Trp220=) c.405T= c.9T= n.690T= n.620T= n.318T= n.698T= n.935T= c.384T= c.553T= (p.Trp185=) | dbSNP |