Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.177238391C>GCA294866NSD1c.3203C>G (p.Ser1068Ter)
n.892C>G
n.3659C>G
c.3767C>G (p.Ser1256Ter)
n.3473C>G
c.3922-1365C>G (n.3922-1365C>G)
n.4223C>G
c.4076C>G (p.Ser1359Ter)
c.3269C>G (p.Ser1090Ter)
c.333-1365C>G (n.333-1365C>G)
c.3656C>G (p.Ser1219Ter)
c.3020C>G (p.Ser1007Ter)
c.-74-1365C>G (n.-74-1365C>G)
ClinVar dbSNP
5g.177238391C=CA1603482671NSD1c.3203C= (p.Ser1068=)
n.892C=
n.3659C=
c.3767C= (p.Ser1256=)
n.3473C=
c.3922-1365C= (n.3922-1365C=)
n.4223C=
c.4076C= (p.Ser1359=)
c.3269C= (p.Ser1090=)
c.333-1365C= (n.333-1365C=)
c.3656C= (p.Ser1219=)
c.3020C= (p.Ser1007=)
c.-74-1365C= (n.-74-1365C=)
dbSNP

Number of alleles fetched