Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.148081384T>GCA358425248NR3C2c.2915A>C (p.Glu972Ala)
c.*298A>C (n.*298A>C)
c.2927A>C (p.Glu976Ala)
c.2564A>C (p.Glu855Ala)
n.2782A>C
n.2676A>C
dbSNP
4g.148081384T>CCA119757NR3C2c.2915A>G (p.Glu972Gly)
c.*298A>G (n.*298A>G)
c.2927A>G (p.Glu976Gly)
c.2564A>G (p.Glu855Gly)
n.2782A>G
n.2676A>G
ClinVar dbSNP
4g.148081384T=CA1502331469NR3C2c.2915A= (p.Glu972=)
c.*298A= (n.*298A=)
c.2927A= (p.Glu976=)
c.2564A= (p.Glu855=)
n.2782A=
n.2676A=
dbSNP

Number of alleles fetched