Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.112453274C>T | CA123050 | PTPN11 | c.412C>T (p.Arg138Ter) c.409C>T (p.Arg137Ter) | ClinVar dbSNP gnomAD v2 |
12 | g.112453274C>A | CA481882496 | PTPN11 | c.412C>A (p.Arg138=) c.409C>A (p.Arg137=) | dbSNP |
12 | g.112453274C>G | CA386781157 | PTPN11 | c.412C>G (p.Arg138Gly) c.409C>G (p.Arg137Gly) | dbSNP |