Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.118476863G>ACA382823739KMT2Ac.3314G>A (p.Cys1105Tyr)
c.797G>A (p.Cys266Tyr)
c.698G>A (p.Cys233Tyr)
c.1022G>A (p.Cys341Tyr)
c.196G>A
c.3215G>A (p.Cys1072Tyr)
c.467G>A (p.Cys156Tyr)
c.1985G>A (p.Cys662Tyr)
c.449G>A (p.Cys150Tyr)
c.1121G>A (p.Cys374Tyr)
dbSNP
11g.118476863G>CCA382823741KMT2Ac.3314G>C (p.Cys1105Ser)
c.797G>C (p.Cys266Ser)
c.698G>C (p.Cys233Ser)
c.1022G>C (p.Cys341Ser)
c.196G>C
c.3215G>C (p.Cys1072Ser)
c.467G>C (p.Cys156Ser)
c.1985G>C (p.Cys662Ser)
c.449G>C (p.Cys150Ser)
c.1121G>C (p.Cys374Ser)
dbSNP
11g.118476863G>TCA382823738KMT2Ac.3314G>T (p.Cys1105Phe)
c.797G>T (p.Cys266Phe)
c.698G>T (p.Cys233Phe)
c.1022G>T (p.Cys341Phe)
c.196G>T
c.3215G>T (p.Cys1072Phe)
c.467G>T (p.Cys156Phe)
c.1985G>T (p.Cys662Phe)
c.449G>T (p.Cys150Phe)
c.1121G>T (p.Cys374Phe)
ClinVar dbSNP

Number of alleles fetched