Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.112839693C>GCA16030308APCc.3764C>G (n.3764C>G)
c.4153C>G (p.Gln1385Glu)
c.*4105C>G (n.*4105C>G)
c.4045C>G (p.Gln1349Glu)
c.4099C>G (p.Gln1367Glu)
c.2452C>G
c.*3421C>G (n.*3421C>G)
c.230+10721C>G
c.4129C>G (p.Gln1377Glu)
c.4024C>G (p.Gln1342Glu)
c.4015C>G (p.Gln1339Glu)
c.3976C>G (p.Gln1326Glu)
c.3922C>G (p.Gln1308Glu)
c.3826C>G (p.Gln1276Glu)
c.3796C>G (p.Gln1266Glu)
c.3721C>G (p.Gln1241Glu)
c.3619C>G (p.Gln1207Glu)
c.3250C>G (p.Gln1084Glu)
dbSNP COSMIC
5g.112839693C>TCA16030309APCc.3764C>T (n.3764C>T)
c.4153C>T (p.Gln1385Ter)
c.*4105C>T (n.*4105C>T)
c.4045C>T (p.Gln1349Ter)
c.4099C>T (p.Gln1367Ter)
c.2452C>T
c.*3421C>T (n.*3421C>T)
c.230+10721C>T
c.4129C>T (p.Gln1377Ter)
c.4024C>T (p.Gln1342Ter)
c.4015C>T (p.Gln1339Ter)
c.3976C>T (p.Gln1326Ter)
c.3922C>T (p.Gln1308Ter)
c.3826C>T (p.Gln1276Ter)
c.3796C>T (p.Gln1266Ter)
c.3721C>T (p.Gln1241Ter)
c.3619C>T (p.Gln1207Ter)
c.3250C>T (p.Gln1084Ter)
ClinVar dbSNP COSMIC

Number of alleles fetched