Chr Mutation (hg38) CAid Gene Transcript Linkouts
15g.40931691T>ACA391807073DLL4c.583T>A (p.Phe195Ile)
n.812T>A
15g.40931691T>CCA204440DLL4c.583T>C (p.Phe195Leu)
n.812T>C
ClinVar dbSNP
15g.40931691T>GCA391807072DLL4c.583T>G (p.Phe195Val)
n.812T>G
15g.40931691T=CA2172012891DLL4c.583T= (p.Phe195=)
n.812T=
15g.40931692T>ACA391807074DLL4c.584T>A (p.Phe195Tyr)
n.813T>A
15g.40931692T>CCA391807075DLL4c.584T>C (p.Phe195Ser)
n.813T>C
15g.40931692T>GCA391807076DLL4c.584T>G (p.Phe195Cys)
n.813T>G
15g.40931693C>ACA391807077DLL4c.585C>A (p.Phe195Leu)
n.814C>A
15g.40931693C=CA2172012892DLL4c.585C= (p.Phe195=)
n.814C=
15g.40931693C>GCA391807078DLL4c.585C>G (p.Phe195Leu)
n.814C>G
15g.40931693C>TCA7487707DLL4c.585C>T (p.Phe195=)
n.814C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.40931694G>ACA391807079DLL4c.586G>A (p.Gly196Ser)
n.815G>A
15g.40931694G>CCA391807080DLL4c.586G>C (p.Gly196Arg)
n.815G>C
15g.40931694G>TCA391807081DLL4c.586G>T (p.Gly196Cys)
n.815G>T
15g.40931695G>ACA391807082DLL4c.587G>A (p.Gly196Asp)
n.816G>A
15g.40931695G>CCA391807083DLL4c.587G>C (p.Gly196Ala)
n.816G>C
15g.40931695G>TCA391807084DLL4c.587G>T (p.Gly196Val)
n.816G>T
15g.40931696C>ACA489781772DLL4c.588C>A (p.Gly196=)
n.817C>A
15g.40931696C>GCA489781773DLL4c.588C>G (p.Gly196=)
n.817C>G
15g.40931696C>TCA489781774DLL4c.588C>T (p.Gly196=)
n.817C>T
15g.40931697C>ACA391807085DLL4c.589C>A (p.His197Asn)
n.818C>A
15g.40931697C>GCA391807087DLL4c.589C>G (p.His197Asp)
n.818C>G
15g.40931697C>TCA391807086DLL4c.589C>T (p.His197Tyr)
n.818C>T
15g.40931698A>CCA391807088DLL4c.590A>C (p.His197Pro)
n.819A>C
15g.40931698A>GCA391807090DLL4c.590A>G (p.His197Arg)
n.819A>G
15g.40931698A>TCA391807089DLL4c.590A>T (p.His197Leu)
n.819A>T
15g.40931699C>ACA391807091DLL4c.591C>A (p.His197Gln)
n.820C>A
15g.40931699C>GCA391807092DLL4c.591C>G (p.His197Gln)
n.820C>G
15g.40931699C>TCA489781775DLL4c.591C>T (p.His197=)
n.820C>T
15g.40931700T>ACA391807093DLL4c.592T>A (p.Tyr198Asn)
n.821T>A
15g.40931700T>CCA391807094DLL4c.592T>C (p.Tyr198His)
n.821T>C
15g.40931700T>GCA391807095DLL4c.592T>G (p.Tyr198Asp)
n.821T>G
15g.40931701A>CCA391807096DLL4c.593A>C (p.Tyr198Ser)
n.822A>C
15g.40931701A>GCA391807097DLL4c.593A>G (p.Tyr198Cys)
n.822A>G
15g.40931701A>TCA391807098DLL4c.593A>T (p.Tyr198Phe)
n.822A>T
15g.40931702T>ACA391807099DLL4c.594T>A (p.Tyr198Ter)
n.823T>A
15g.40931702T>CCA7487708DLL4c.594T>C (p.Tyr198=)
n.823T>C
dbSNP ExAC gnomAD v2 gnomAD v4
15g.40931702T>GCA391807100DLL4c.594T>G (p.Tyr198Ter)
n.823T>G
15g.40931702T=CA2172012893DLL4c.594T= (p.Tyr198=)
n.823T=
15g.40931703G>ACA7487709DLL4c.595G>A (p.Val199Met)
n.824G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.40931703G>CCA7487710DLL4c.595G>C (p.Val199Leu)
n.824G>C
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.40931703G=CA2172012894DLL4c.595G= (p.Val199=)
n.824G=
15g.40931703G>TCA391807101DLL4c.595G>T (p.Val199Leu)
n.824G>T
15g.40931704T>ACA391807102DLL4c.596T>A (p.Val199Glu)
n.825T>A
15g.40931704T>CCA391807103DLL4c.596T>C (p.Val199Ala)
n.825T>C
15g.40931704T>GCA391807104DLL4c.596T>G (p.Val199Gly)
n.825T>G
15g.40931705G>ACA489781776DLL4c.597G>A (p.Val199=)
n.826G>A
15g.40931705G>CCA489781777DLL4c.597G>C (p.Val199=)
n.826G>C
15g.40931705G=CA2172012895DLL4c.597G= (p.Val199=)
n.826G=
15g.40931705G>TCA489781778DLL4c.597G>T (p.Val199=)
n.826G>T
dbSNP gnomAD v4

Number of alleles fetched