Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.14294844T>CCA218175344RRAS2c.215A>G (p.Gln72Arg)
c.-17A>G (n.-17A>G)
c.*167A>G (n.*167A>G)
c.158A>G (p.Gln53Arg)
c.*155A>G (n.*155A>G)
c.110A>G (p.Gln37Arg)
c.212A>G (p.Gln71Arg)
c.149A>G (p.Gln50Arg)
dbSNP
11g.14294844T>ACA120437RRAS2c.215A>T (p.Gln72Leu)
c.-17A>T (n.-17A>T)
c.*167A>T (n.*167A>T)
c.158A>T (p.Gln53Leu)
c.*155A>T (n.*155A>T)
c.110A>T (p.Gln37Leu)
c.212A>T (p.Gln71Leu)
c.149A>T (p.Gln50Leu)
ClinVar dbSNP COSMIC
11g.14294844T>GCA379860663RRAS2c.215A>C (p.Gln72Pro)
c.-17A>C (n.-17A>C)
c.*167A>C (n.*167A>C)
c.158A>C (p.Gln53Pro)
c.*155A>C (n.*155A>C)
c.110A>C (p.Gln37Pro)
c.212A>C (p.Gln71Pro)
c.149A>C (p.Gln50Pro)
dbSNP gnomAD v4

Number of alleles fetched