Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.118476863G>A | CA382823739 | KMT2A | c.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 |
11 | g.118476863G>C | CA382823741 | KMT2A | c.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 |
11 | g.118476863G>T | CA382823738 | KMT2A | c.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 |