Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
15 | g.40931691T>A | CA391807073 | DLL4 | c.583T>A (p.Phe195Ile) n.812T>A | |
15 | g.40931691T>C | CA204440 | DLL4 | c.583T>C (p.Phe195Leu) n.812T>C | ClinVar dbSNP |
15 | g.40931691T>G | CA391807072 | DLL4 | c.583T>G (p.Phe195Val) n.812T>G | |
15 | g.40931691T= | CA2172012891 | DLL4 | c.583T= (p.Phe195=) n.812T= | |
15 | g.40931692T>A | CA391807074 | DLL4 | c.584T>A (p.Phe195Tyr) n.813T>A | |
15 | g.40931692T>C | CA391807075 | DLL4 | c.584T>C (p.Phe195Ser) n.813T>C | |
15 | g.40931692T>G | CA391807076 | DLL4 | c.584T>G (p.Phe195Cys) n.813T>G | |
15 | g.40931693C>A | CA391807077 | DLL4 | c.585C>A (p.Phe195Leu) n.814C>A | |
15 | g.40931693C= | CA2172012892 | DLL4 | c.585C= (p.Phe195=) n.814C= | |
15 | g.40931693C>G | CA391807078 | DLL4 | c.585C>G (p.Phe195Leu) n.814C>G | |
15 | g.40931693C>T | CA7487707 | DLL4 | c.585C>T (p.Phe195=) n.814C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.40931694G>A | CA391807079 | DLL4 | c.586G>A (p.Gly196Ser) n.815G>A | |
15 | g.40931694G>C | CA391807080 | DLL4 | c.586G>C (p.Gly196Arg) n.815G>C | |
15 | g.40931694G>T | CA391807081 | DLL4 | c.586G>T (p.Gly196Cys) n.815G>T | |
15 | g.40931695G>A | CA391807082 | DLL4 | c.587G>A (p.Gly196Asp) n.816G>A | |
15 | g.40931695G>C | CA391807083 | DLL4 | c.587G>C (p.Gly196Ala) n.816G>C | |
15 | g.40931695G>T | CA391807084 | DLL4 | c.587G>T (p.Gly196Val) n.816G>T | |
15 | g.40931696C>A | CA489781772 | DLL4 | c.588C>A (p.Gly196=) n.817C>A | |
15 | g.40931696C>G | CA489781773 | DLL4 | c.588C>G (p.Gly196=) n.817C>G | |
15 | g.40931696C>T | CA489781774 | DLL4 | c.588C>T (p.Gly196=) n.817C>T | |
15 | g.40931697C>A | CA391807085 | DLL4 | c.589C>A (p.His197Asn) n.818C>A | |
15 | g.40931697C>G | CA391807087 | DLL4 | c.589C>G (p.His197Asp) n.818C>G | |
15 | g.40931697C>T | CA391807086 | DLL4 | c.589C>T (p.His197Tyr) n.818C>T | |
15 | g.40931698A>C | CA391807088 | DLL4 | c.590A>C (p.His197Pro) n.819A>C | |
15 | g.40931698A>G | CA391807090 | DLL4 | c.590A>G (p.His197Arg) n.819A>G | |
15 | g.40931698A>T | CA391807089 | DLL4 | c.590A>T (p.His197Leu) n.819A>T | |
15 | g.40931699C>A | CA391807091 | DLL4 | c.591C>A (p.His197Gln) n.820C>A | |
15 | g.40931699C>G | CA391807092 | DLL4 | c.591C>G (p.His197Gln) n.820C>G | |
15 | g.40931699C>T | CA489781775 | DLL4 | c.591C>T (p.His197=) n.820C>T | |
15 | g.40931700T>A | CA391807093 | DLL4 | c.592T>A (p.Tyr198Asn) n.821T>A | |
15 | g.40931700T>C | CA391807094 | DLL4 | c.592T>C (p.Tyr198His) n.821T>C | |
15 | g.40931700T>G | CA391807095 | DLL4 | c.592T>G (p.Tyr198Asp) n.821T>G | |
15 | g.40931701A>C | CA391807096 | DLL4 | c.593A>C (p.Tyr198Ser) n.822A>C | |
15 | g.40931701A>G | CA391807097 | DLL4 | c.593A>G (p.Tyr198Cys) n.822A>G | |
15 | g.40931701A>T | CA391807098 | DLL4 | c.593A>T (p.Tyr198Phe) n.822A>T | |
15 | g.40931702T>A | CA391807099 | DLL4 | c.594T>A (p.Tyr198Ter) n.823T>A | |
15 | g.40931702T>C | CA7487708 | DLL4 | c.594T>C (p.Tyr198=) n.823T>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.40931702T>G | CA391807100 | DLL4 | c.594T>G (p.Tyr198Ter) n.823T>G | |
15 | g.40931702T= | CA2172012893 | DLL4 | c.594T= (p.Tyr198=) n.823T= | |
15 | g.40931703G>A | CA7487709 | DLL4 | c.595G>A (p.Val199Met) n.824G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.40931703G>C | CA7487710 | DLL4 | c.595G>C (p.Val199Leu) n.824G>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.40931703G= | CA2172012894 | DLL4 | c.595G= (p.Val199=) n.824G= | |
15 | g.40931703G>T | CA391807101 | DLL4 | c.595G>T (p.Val199Leu) n.824G>T | |
15 | g.40931704T>A | CA391807102 | DLL4 | c.596T>A (p.Val199Glu) n.825T>A | |
15 | g.40931704T>C | CA391807103 | DLL4 | c.596T>C (p.Val199Ala) n.825T>C | |
15 | g.40931704T>G | CA391807104 | DLL4 | c.596T>G (p.Val199Gly) n.825T>G | |
15 | g.40931705G>A | CA489781776 | DLL4 | c.597G>A (p.Val199=) n.826G>A | |
15 | g.40931705G>C | CA489781777 | DLL4 | c.597G>C (p.Val199=) n.826G>C | |
15 | g.40931705G= | CA2172012895 | DLL4 | c.597G= (p.Val199=) n.826G= | |
15 | g.40931705G>T | CA489781778 | DLL4 | c.597G>T (p.Val199=) n.826G>T | dbSNP gnomAD v4 |