Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.112838793C>TCA008153APCc.2864C>T (n.2864C>T)
c.3253C>T (p.Gln1085Ter)
c.*3205C>T (n.*3205C>T)
c.3145C>T (p.Gln1049Ter)
c.3199C>T (p.Gln1067Ter)
c.1552C>T
c.*2521C>T (n.*2521C>T)
c.230+9821C>T
c.3229C>T (p.Gln1077Ter)
c.3124C>T (p.Gln1042Ter)
c.3115C>T (p.Gln1039Ter)
c.3076C>T (p.Gln1026Ter)
c.3022C>T (p.Gln1008Ter)
c.2926C>T (p.Gln976Ter)
c.2896C>T (p.Gln966Ter)
c.2821C>T (p.Gln941Ter)
c.2719C>T (p.Gln907Ter)
c.2350C>T (p.Gln784Ter)
ClinVar dbSNP COSMIC
5g.112838793C>ACA16028350APCc.2864C>A (n.2864C>A)
c.3253C>A (p.Gln1085Lys)
c.*3205C>A (n.*3205C>A)
c.3145C>A (p.Gln1049Lys)
c.3199C>A (p.Gln1067Lys)
c.1552C>A
c.*2521C>A (n.*2521C>A)
c.230+9821C>A
c.3229C>A (p.Gln1077Lys)
c.3124C>A (p.Gln1042Lys)
c.3115C>A (p.Gln1039Lys)
c.3076C>A (p.Gln1026Lys)
c.3022C>A (p.Gln1008Lys)
c.2926C>A (p.Gln976Lys)
c.2896C>A (p.Gln966Lys)
c.2821C>A (p.Gln941Lys)
c.2719C>A (p.Gln907Lys)
c.2350C>A (p.Gln784Lys)
dbSNP

Number of alleles fetched