Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.28608338C>TCA16042696WACc.400C>T (p.Gln134Ter)
c.1060C>T (p.Gln354Ter)
c.1072C>T (p.Gln358Ter)
c.937C>T (p.Gln313Ter)
c.*986C>T (n.*986C>T)
c.*81C>T (n.*81C>T)
c.*498C>T (n.*498C>T)
c.*1067C>T (n.*1067C>T)
c.943C>T (p.Gln315Ter)
c.*925C>T (n.*925C>T)
n.870C>T
c.763C>T (p.Gln255Ter)
c.628C>T (p.Gln210Ter)
c.*1080C>T (n.*1080C>T)
n.268C>T
c.1090C>T (p.Gln364Ter)
n.992C>T
n.1027C>T
ClinVar dbSNP COSMIC COSMIC
10g.28608338C=CA1898519668WACc.400C= (p.Gln134=)
c.1060C= (p.Gln354=)
c.1072C= (p.Gln358=)
c.937C= (p.Gln313=)
c.*986C= (n.*986C=)
c.*81C= (n.*81C=)
c.*498C= (n.*498C=)
c.*1067C= (n.*1067C=)
c.943C= (p.Gln315=)
c.*925C= (n.*925C=)
n.870C=
c.763C= (p.Gln255=)
c.628C= (p.Gln210=)
c.*1080C= (n.*1080C=)
n.268C=
c.1090C= (p.Gln364=)
n.992C=
n.1027C=
dbSNP dbSNP

Number of alleles fetched