Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.38070872C>A | CA346327061 | CYP1B1 | c.1482G>T (p.Arg494Ser) c.369G>T (p.Arg123Ser) | |
2 | g.38070872C>G | CA346327062 | CYP1B1 | c.1482G>C (p.Arg494Ser) c.369G>C (p.Arg123Ser) | |
2 | g.38070872C>T | CA425864433 | CYP1B1 | c.1482G>A (p.Arg494=) c.369G>A (p.Arg123=) | gnomAD v4 |
2 | g.38070873C>A | CA346327064 | CYP1B1 | c.1481G>T (p.Arg494Met) c.368G>T (p.Arg123Met) | |
2 | g.38070873C>G | CA346327065 | CYP1B1 | c.1481G>C (p.Arg494Thr) c.368G>C (p.Arg123Thr) | gnomAD v4 |
2 | g.38070873C>T | CA346327063 | CYP1B1 | c.1481G>A (p.Arg494Lys) c.368G>A (p.Arg123Lys) | COSMIC |
2 | g.38070874T>A | CA346327066 | CYP1B1 | c.1480A>T (p.Arg494Trp) c.367A>T (p.Arg123Trp) | |
2 | g.38070874T>C | CA346327067 | CYP1B1 | c.1480A>G (p.Arg494Gly) c.367A>G (p.Arg123Gly) | gnomAD v4 |
2 | g.38070874T>G | CA425864434 | CYP1B1 | c.1480A>C (p.Arg494=) c.367A>C (p.Arg123=) | gnomAD v4 |
2 | g.38070875G>A | CA425864436 | CYP1B1 | c.1479C>T (p.Phe493=) c.366C>T (p.Phe122=) | |
2 | g.38070875G>C | CA346327068 | CYP1B1 | c.1479C>G (p.Phe493Leu) c.366C>G (p.Phe122Leu) | |
2 | g.38070875G>T | CA346327069 | CYP1B1 | c.1479C>A (p.Phe493Leu) c.366C>A (p.Phe122Leu) | |
2 | g.38070876A>C | CA346327070 | CYP1B1 | c.1478T>G (p.Phe493Cys) c.365T>G (p.Phe122Cys) | |
2 | g.38070876A>G | CA346327071 | CYP1B1 | c.1478T>C (p.Phe493Ser) c.365T>C (p.Phe122Ser) | gnomAD v3 gnomAD v4 |
2 | g.38070876A>T | CA346327072 | CYP1B1 | c.1478T>A (p.Phe493Tyr) c.365T>A (p.Phe122Tyr) | |
2 | g.38070877A>C | CA346327073 | CYP1B1 | c.1477T>G (p.Phe493Val) c.364T>G (p.Phe122Val) | |
2 | g.38070877A>G | CA346327074 | CYP1B1 | c.1477T>C (p.Phe493Leu) c.364T>C (p.Phe122Leu) | |
2 | g.38070877A>T | CA346327075 | CYP1B1 | c.1477T>A (p.Phe493Ile) c.364T>A (p.Phe122Ile) | |
2 | g.38070878A= | CA1245625993 | CYP1B1 | c.1476T= (p.Asp492=) c.363T= (p.Asp121=) | |
2 | g.38070878A>C | CA346327076 | CYP1B1 | c.1476T>G (p.Asp492Glu) c.363T>G (p.Asp121Glu) | |
2 | g.38070878A>G | CA1619772 | CYP1B1 | c.1476T>C (p.Asp492=) c.363T>C (p.Asp121=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.38070878A>T | CA346327077 | CYP1B1 | c.1476T>A (p.Asp492Glu) c.363T>A (p.Asp121Glu) | |
2 | g.38070879T>A | CA346327080 | CYP1B1 | c.1475A>T (p.Asp492Val) c.362A>T (p.Asp121Val) | |
2 | g.38070879T>C | CA346327079 | CYP1B1 | c.1475A>G (p.Asp492Gly) c.362A>G (p.Asp121Gly) | |
2 | g.38070879T>G | CA346327078 | CYP1B1 | c.1475A>C (p.Asp492Ala) c.362A>C (p.Asp121Ala) | |
2 | g.38070880C>A | CA346327081 | CYP1B1 | c.1474G>T (p.Asp492Tyr) c.361G>T (p.Asp121Tyr) | gnomAD v4 |
2 | g.38070880C= | CA1245625994 | CYP1B1 | c.1474G= (p.Asp492=) c.361G= (p.Asp121=) | |
2 | g.38070880C>G | CA346327082 | CYP1B1 | c.1474G>C (p.Asp492His) c.361G>C (p.Asp121His) | dbSNP |
2 | g.38070880C>T | CA1619773 | CYP1B1 | c.1474G>A (p.Asp492Asn) c.361G>A (p.Asp121Asn) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
2 | g.38070881G>A | CA1619774 | CYP1B1 | c.1473C>T (p.Cys491=) c.360C>T (p.Cys120=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.38070881G>C | CA346327083 | CYP1B1 | c.1473C>G (p.Cys491Trp) c.360C>G (p.Cys120Trp) | |
2 | g.38070881G= | CA1245625995 | CYP1B1 | c.1473C= (p.Cys491=) c.360C= (p.Cys120=) | |
2 | g.38070881G>T | CA346327084 | CYP1B1 | c.1473C>A (p.Cys491Ter) c.360C>A (p.Cys120Ter) | dbSNP gnomAD v2 gnomAD v4 |
2 | g.38070882C>A | CA346327085 | CYP1B1 | c.1472G>T (p.Cys491Phe) c.359G>T (p.Cys120Phe) | |
2 | g.38070882C= | CA1245625996 | CYP1B1 | c.1472G= (p.Cys491=) c.359G= (p.Cys120=) | |
2 | g.38070882C>G | CA346327086 | CYP1B1 | c.1472G>C (p.Cys491Ser) c.359G>C (p.Cys120Ser) | dbSNP |
2 | g.38070882C>T | CA346327087 | CYP1B1 | c.1472G>A (p.Cys491Tyr) c.359G>A (p.Cys120Tyr) | |
2 | g.38070883A= | CA1245625997 | CYP1B1 | c.1471T= (p.Cys491=) c.358T= (p.Cys120=) | |
2 | g.38070883A>C | CA346327088 | CYP1B1 | c.1471T>G (p.Cys491Gly) c.358T>G (p.Cys120Gly) | gnomAD v4 |
2 | g.38070883A>G | CA45505911 | CYP1B1 | c.1471T>C (p.Cys491Arg) c.358T>C (p.Cys120Arg) | dbSNP gnomAD v4 |
2 | g.38070883A>T | CA346327089 | CYP1B1 | c.1471T>A (p.Cys491Ser) c.358T>A (p.Cys120Ser) | |
2 | g.38070884C>A | CA346327090 | CYP1B1 | c.1470G>T (p.Gln490His) c.357G>T (p.Gln119His) | |
2 | g.38070884C= | CA1245625998 | CYP1B1 | c.1470G= (p.Gln490=) c.357G= (p.Gln119=) | |
2 | g.38070884C>G | CA346327091 | CYP1B1 | c.1470G>C (p.Gln490His) c.357G>C (p.Gln119His) | |
2 | g.38070884C>T | CA1619775 | CYP1B1 | c.1470G>A (p.Gln490=) c.357G>A (p.Gln119=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.38070885T>A | CA1619776 | CYP1B1 | c.1469A>T (p.Gln490Leu) c.356A>T (p.Gln119Leu) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.38070885T>C | CA346327093 | CYP1B1 | c.1469A>G (p.Gln490Arg) c.356A>G (p.Gln119Arg) | |
2 | g.38070885T>G | CA346327092 | CYP1B1 | c.1469A>C (p.Gln490Pro) c.356A>C (p.Gln119Pro) | |
2 | g.38070885T= | CA1245625999 | CYP1B1 | c.1469A= (p.Gln490=) c.356A= (p.Gln119=) | |
2 | g.38070885dup | CA768461758 | CYP1B1 | c.1469dup (p.Cys491ValfsTer9) c.356dup (p.Cys120ValfsTer9) | dbSNP |