Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.112453274C>TCA123050PTPN11c.412C>T (p.Arg138Ter)
c.409C>T (p.Arg137Ter)
ClinVar dbSNP gnomAD v2
12g.112453274C>ACA481882496PTPN11c.412C>A (p.Arg138=)
c.409C>A (p.Arg137=)
dbSNP
12g.112453274C>GCA386781157PTPN11c.412C>G (p.Arg138Gly)
c.409C>G (p.Arg137Gly)
dbSNP

Number of alleles fetched