Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.112839777A>TCA008937APCc.3848A>T (n.3848A>T)
c.4237A>T (p.Ser1413Cys)
c.*4189A>T (n.*4189A>T)
c.4129A>T (p.Ser1377Cys)
c.4183A>T (p.Ser1395Cys)
c.2536A>T
c.*3505A>T (n.*3505A>T)
c.230+10805A>T
c.4213A>T (p.Ser1405Cys)
c.4108A>T (p.Ser1370Cys)
c.4099A>T (p.Ser1367Cys)
c.4060A>T (p.Ser1354Cys)
c.4006A>T (p.Ser1336Cys)
c.3910A>T (p.Ser1304Cys)
c.3880A>T (p.Ser1294Cys)
c.3805A>T (p.Ser1269Cys)
c.3703A>T (p.Ser1235Cys)
c.3334A>T (p.Ser1112Cys)
ClinVar dbSNP COSMIC
5g.112839777A>GCA16030496APCc.3848A>G (n.3848A>G)
c.4237A>G (p.Ser1413Gly)
c.*4189A>G (n.*4189A>G)
c.4129A>G (p.Ser1377Gly)
c.4183A>G (p.Ser1395Gly)
c.2536A>G
c.*3505A>G (n.*3505A>G)
c.230+10805A>G
c.4213A>G (p.Ser1405Gly)
c.4108A>G (p.Ser1370Gly)
c.4099A>G (p.Ser1367Gly)
c.4060A>G (p.Ser1354Gly)
c.4006A>G (p.Ser1336Gly)
c.3910A>G (p.Ser1304Gly)
c.3880A>G (p.Ser1294Gly)
c.3805A>G (p.Ser1269Gly)
c.3703A>G (p.Ser1235Gly)
c.3334A>G (p.Ser1112Gly)
ClinVar dbSNP
5g.112839777A=CA1573466750APCc.3848A= (n.3848A=)
c.4237A= (p.Ser1413=)
c.*4189A= (n.*4189A=)
c.4129A= (p.Ser1377=)
c.4183A= (p.Ser1395=)
c.2536A=
c.*3505A= (n.*3505A=)
c.230+10805A=
c.4213A= (p.Ser1405=)
c.4108A= (p.Ser1370=)
c.4099A= (p.Ser1367=)
c.4060A= (p.Ser1354=)
c.4006A= (p.Ser1336=)
c.3910A= (p.Ser1304=)
c.3880A= (p.Ser1294=)
c.3805A= (p.Ser1269=)
c.3703A= (p.Ser1235=)
c.3334A= (p.Ser1112=)
dbSNP

Number of alleles fetched