Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
9 | g.94606845A>C | CA466099963 | FBP1 | c.835T>G (n.835T>G) c.675T>G (p.Thr225=) c.480T>G (p.Thr160=) c.423T>G (p.Thr141=) c.429T>G (p.Thr143=) | |
9 | g.94606845A>G | CA466099964 | FBP1 | c.835T>C (n.835T>C) c.675T>C (p.Thr225=) c.480T>C (p.Thr160=) c.423T>C (p.Thr141=) c.429T>C (p.Thr143=) | |
9 | g.94606845A>T | CA466099965 | FBP1 | c.835T>A (n.835T>A) c.675T>A (p.Thr225=) c.480T>A (p.Thr160=) c.423T>A (p.Thr141=) c.429T>A (p.Thr143=) | |
9 | g.94606846G>A | CA374106683 | FBP1 | c.834C>T (n.834C>T) c.674C>T (p.Thr225Ile) c.479C>T (p.Thr160Ile) c.422C>T (p.Thr141Ile) c.428C>T (p.Thr143Ile) | |
9 | g.94606846G>C | CA374106685 | FBP1 | c.834C>G (n.834C>G) c.674C>G (p.Thr225Ser) c.479C>G (p.Thr160Ser) c.422C>G (p.Thr141Ser) c.428C>G (p.Thr143Ser) | |
9 | g.94606846G>T | CA374106687 | FBP1 | c.834C>A (n.834C>A) c.674C>A (p.Thr225Asn) c.479C>A (p.Thr160Asn) c.422C>A (p.Thr141Asn) c.428C>A (p.Thr143Asn) | |
9 | g.94606847T>A | CA374106693 | FBP1 | c.833A>T (n.833A>T) c.673A>T (p.Thr225Ser) c.478A>T (p.Thr160Ser) c.421A>T (p.Thr141Ser) c.427A>T (p.Thr143Ser) | |
9 | g.94606847T>C | CA374106691 | FBP1 | c.833A>G (n.833A>G) c.673A>G (p.Thr225Ala) c.478A>G (p.Thr160Ala) c.421A>G (p.Thr141Ala) c.427A>G (p.Thr143Ala) | |
9 | g.94606847T>G | CA374106689 | FBP1 | c.833A>C (n.833A>C) c.673A>C (p.Thr225Pro) c.478A>C (p.Thr160Pro) c.421A>C (p.Thr141Pro) c.427A>C (p.Thr143Pro) | |
9 | g.94606848G>A | CA5136169 | FBP1 | c.832C>T (n.832C>T) c.672C>T (p.Val224=) c.477C>T (p.Val159=) c.420C>T (p.Val140=) c.426C>T (p.Val142=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.94606848G>C | CA466099966 | FBP1 | c.832C>G (n.832C>G) c.672C>G (p.Val224=) c.477C>G (p.Val159=) c.420C>G (p.Val140=) c.426C>G (p.Val142=) | |
9 | g.94606848G= | CA1865226631 | FBP1 | c.832C= (n.832C=) c.672C= (p.Val224=) c.477C= (p.Val159=) c.420C= (p.Val140=) c.426C= (p.Val142=) | |
9 | g.94606848G>T | CA466099967 | FBP1 | c.832C>A (n.832C>A) c.672C>A (p.Val224=) c.477C>A (p.Val159=) c.420C>A (p.Val140=) c.426C>A (p.Val142=) | |
9 | g.94606849A= | CA1865226632 | FBP1 | c.831T= (n.831T=) c.671T= (p.Val224=) c.476T= (p.Val159=) c.419T= (p.Val140=) c.425T= (p.Val142=) | |
9 | g.94606849A>C | CA374106695 | FBP1 | c.831T>G (n.831T>G) c.671T>G (p.Val224Gly) c.476T>G (p.Val159Gly) c.419T>G (p.Val140Gly) c.425T>G (p.Val142Gly) | |
9 | g.94606849A>G | CA196553530 | FBP1 | c.831T>C (n.831T>C) c.671T>C (p.Val224Ala) c.476T>C (p.Val159Ala) c.419T>C (p.Val140Ala) c.425T>C (p.Val142Ala) | dbSNP |
9 | g.94606849A>T | CA374106697 | FBP1 | c.831T>A (n.831T>A) c.671T>A (p.Val224Asp) c.476T>A (p.Val159Asp) c.419T>A (p.Val140Asp) c.425T>A (p.Val142Asp) | dbSNP |
9 | g.94606850C>A | CA374106701 | FBP1 | c.830G>T (n.830G>T) c.670G>T (p.Val224Phe) c.475G>T (p.Val159Phe) c.418G>T (p.Val140Phe) c.424G>T (p.Val142Phe) | |
9 | g.94606850C= | CA1865226633 | FBP1 | c.830G= (n.830G=) c.670G= (p.Val224=) c.475G= (p.Val159=) c.418G= (p.Val140=) c.424G= (p.Val142=) | |
9 | g.94606850C>G | CA374106702 | FBP1 | c.830G>C (n.830G>C) c.670G>C (p.Val224Leu) c.475G>C (p.Val159Leu) c.418G>C (p.Val140Leu) c.424G>C (p.Val142Leu) | |
9 | g.94606850C>T | CA323535 | FBP1 | c.830G>A (n.830G>A) c.670G>A (p.Val224Ile) c.475G>A (p.Val159Ile) c.418G>A (p.Val140Ile) c.424G>A (p.Val142Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.94606851G>A | CA196553536 | FBP1 | c.829C>T (n.829C>T) c.669C>T (p.Ala223=) c.474C>T (p.Ala158=) c.417C>T (p.Ala139=) c.423C>T (p.Ala141=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.94606851G>C | CA466099969 | FBP1 | c.829C>G (n.829C>G) c.669C>G (p.Ala223=) c.474C>G (p.Ala158=) c.417C>G (p.Ala139=) c.423C>G (p.Ala141=) | |
9 | g.94606851G= | CA1865226634 | FBP1 | c.829C= (n.829C=) c.669C= (p.Ala223=) c.474C= (p.Ala158=) c.417C= (p.Ala139=) c.423C= (p.Ala141=) | |
9 | g.94606851G>T | CA466099970 | FBP1 | c.829C>A (n.829C>A) c.669C>A (p.Ala223=) c.474C>A (p.Ala158=) c.417C>A (p.Ala139=) c.423C>A (p.Ala141=) | |
9 | g.94606852G>A | CA374106704 | FBP1 | c.828C>T (n.828C>T) c.668C>T (p.Ala223Val) c.473C>T (p.Ala158Val) c.416C>T (p.Ala139Val) c.422C>T (p.Ala141Val) | |
9 | g.94606852G>C | CA374106706 | FBP1 | c.828C>G (n.828C>G) c.668C>G (p.Ala223Gly) c.473C>G (p.Ala158Gly) c.416C>G (p.Ala139Gly) c.422C>G (p.Ala141Gly) | gnomAD v4 |
9 | g.94606852G= | CA1865226635 | FBP1 | c.828C= (n.828C=) c.668C= (p.Ala223=) c.473C= (p.Ala158=) c.416C= (p.Ala139=) c.422C= (p.Ala141=) | |
9 | g.94606852G>T | CA320998 | FBP1 | c.828C>A (n.828C>A) c.668C>A (p.Ala223Asp) c.473C>A (p.Ala158Asp) c.416C>A (p.Ala139Asp) c.422C>A (p.Ala141Asp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.94606853C>A | CA374106709 | FBP1 | c.827G>T (n.827G>T) c.667G>T (p.Ala223Ser) c.472G>T (p.Ala158Ser) c.415G>T (p.Ala139Ser) c.421G>T (p.Ala141Ser) | |
9 | g.94606853C>G | CA374106711 | FBP1 | c.827G>C (n.827G>C) c.667G>C (p.Ala223Pro) c.472G>C (p.Ala158Pro) c.415G>C (p.Ala139Pro) c.421G>C (p.Ala141Pro) | |
9 | g.94606853C>T | CA374106712 | FBP1 | c.827G>A (n.827G>A) c.667G>A (p.Ala223Thr) c.472G>A (p.Ala158Thr) c.415G>A (p.Ala139Thr) c.421G>A (p.Ala141Thr) | dbSNP |
9 | g.94606854A= | CA1865226636 | FBP1 | c.826T= (n.826T=) c.666T= (p.Pro222=) c.471T= (p.Pro157=) c.414T= (p.Pro138=) c.420T= (p.Pro140=) | |
9 | g.94606854A>C | CA466099972 | FBP1 | c.826T>G (n.826T>G) c.666T>G (p.Pro222=) c.471T>G (p.Pro157=) c.414T>G (p.Pro138=) c.420T>G (p.Pro140=) | |
9 | g.94606854A>G | CA466099973 | FBP1 | c.826T>C (n.826T>C) c.666T>C (p.Pro222=) c.471T>C (p.Pro157=) c.414T>C (p.Pro138=) c.420T>C (p.Pro140=) | gnomAD v4 |
9 | g.94606854A>T | CA466099974 | FBP1 | c.826T>A (n.826T>A) c.666T>A (p.Pro222=) c.471T>A (p.Pro157=) c.414T>A (p.Pro138=) c.420T>A (p.Pro140=) | dbSNP gnomAD v2 gnomAD v4 |
9 | g.94606855G>A | CA374106714 | FBP1 | c.825C>T (n.825C>T) c.665C>T (p.Pro222Leu) c.470C>T (p.Pro157Leu) c.413C>T (p.Pro138Leu) c.419C>T (p.Pro140Leu) | dbSNP gnomAD v2 |
9 | g.94606855G>C | CA374106716 | FBP1 | c.825C>G (n.825C>G) c.665C>G (p.Pro222Arg) c.470C>G (p.Pro157Arg) c.413C>G (p.Pro138Arg) c.419C>G (p.Pro140Arg) | |
9 | g.94606855G= | CA1865226637 | FBP1 | c.825C= (n.825C=) c.665C= (p.Pro222=) c.470C= (p.Pro157=) c.413C= (p.Pro138=) c.419C= (p.Pro140=) | |
9 | g.94606855G>T | CA374106718 | FBP1 | c.825C>A (n.825C>A) c.665C>A (p.Pro222His) c.470C>A (p.Pro157His) c.413C>A (p.Pro138His) c.419C>A (p.Pro140His) | |
9 | g.94606856G>A | CA374106724 | FBP1 | c.824C>T (n.824C>T) c.664C>T (p.Pro222Ser) c.469C>T (p.Pro157Ser) c.412C>T (p.Pro138Ser) c.418C>T (p.Pro140Ser) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.94606856G>C | CA374106722 | FBP1 | c.824C>G (n.824C>G) c.664C>G (p.Pro222Ala) c.469C>G (p.Pro157Ala) c.412C>G (p.Pro138Ala) c.418C>G (p.Pro140Ala) | |
9 | g.94606856G= | CA1865226638 | FBP1 | c.824C= (n.824C=) c.664C= (p.Pro222=) c.469C= (p.Pro157=) c.412C= (p.Pro138=) c.418C= (p.Pro140=) | |
9 | g.94606856G>T | CA374106720 | FBP1 | c.824C>A (n.824C>A) c.664C>A (p.Pro222Thr) c.469C>A (p.Pro157Thr) c.412C>A (p.Pro138Thr) c.418C>A (p.Pro140Thr) | |
9 | g.94606857G>A | CA5136170 | FBP1 | c.823C>T (n.823C>T) c.663C>T (p.Asp221=) c.468C>T (p.Asp156=) c.411C>T (p.Asp137=) c.417C>T (p.Asp139=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.94606857G>C | CA374106726 | FBP1 | c.823C>G (n.823C>G) c.663C>G (p.Asp221Glu) c.468C>G (p.Asp156Glu) c.411C>G (p.Asp137Glu) c.417C>G (p.Asp139Glu) | |
9 | g.94606857G= | CA1865226639 | FBP1 | c.823C= (n.823C=) c.663C= (p.Asp221=) c.468C= (p.Asp156=) c.411C= (p.Asp137=) c.417C= (p.Asp139=) | |
9 | g.94606857G>T | CA374106727 | FBP1 | c.823C>A (n.823C>A) c.663C>A (p.Asp221Glu) c.468C>A (p.Asp156Glu) c.411C>A (p.Asp137Glu) c.417C>A (p.Asp139Glu) | |
9 | g.94606858T>A | CA374106729 | FBP1 | c.822A>T (n.822A>T) c.662A>T (p.Asp221Val) c.467A>T (p.Asp156Val) c.410A>T (p.Asp137Val) c.416A>T (p.Asp139Val) | |
9 | g.94606858T>C | CA374106731 | FBP1 | c.822A>G (n.822A>G) c.662A>G (p.Asp221Gly) c.467A>G (p.Asp156Gly) c.410A>G (p.Asp137Gly) c.416A>G (p.Asp139Gly) | |
9 | g.94606858T>G | CA5136171 | FBP1 | c.822A>C (n.822A>C) c.662A>C (p.Asp221Ala) c.467A>C (p.Asp156Ala) c.410A>C (p.Asp137Ala) c.416A>C (p.Asp139Ala) | dbSNP ExAC gnomAD v2 |
9 | g.94606858T= | CA1865226640 | FBP1 | c.822A= (n.822A=) c.662A= (p.Asp221=) c.467A= (p.Asp156=) c.410A= (p.Asp137=) c.416A= (p.Asp139=) | |
9 | g.94606859C>A | CA374106734 | FBP1 | c.821G>T (n.821G>T) c.661G>T (p.Asp221Tyr) c.466G>T (p.Asp156Tyr) c.409G>T (p.Asp137Tyr) c.415G>T (p.Asp139Tyr) | |
9 | g.94606859C>G | CA374106736 | FBP1 | c.821G>C (n.821G>C) c.661G>C (p.Asp221His) c.466G>C (p.Asp156His) c.409G>C (p.Asp137His) c.415G>C (p.Asp139His) | |
9 | g.94606859C>T | CA374106738 | FBP1 | c.821G>A (n.821G>A) c.661G>A (p.Asp221Asn) c.466G>A (p.Asp156Asn) c.409G>A (p.Asp137Asn) c.415G>A (p.Asp139Asn) | |
9 | g.94606860A>C | CA374106740 | FBP1 | c.820T>G (n.820T>G) c.660T>G (p.Phe220Leu) c.465T>G (p.Phe155Leu) c.408T>G (p.Phe136Leu) c.414T>G (p.Phe138Leu) | |
9 | g.94606860A>G | CA466099975 | FBP1 | c.820T>C (n.820T>C) c.660T>C (p.Phe220=) c.465T>C (p.Phe155=) c.408T>C (p.Phe136=) c.414T>C (p.Phe138=) | |
9 | g.94606860A>T | CA374106741 | FBP1 | c.820T>A (n.820T>A) c.660T>A (p.Phe220Leu) c.465T>A (p.Phe155Leu) c.408T>A (p.Phe136Leu) c.414T>A (p.Phe138Leu) | |
9 | g.94606862del | CA2695210723 | FBP1 | c.820del (n.820del) c.660del (p.Phe220LeufsTer?) c.465del (p.Phe155LeufsTer?) c.408del (p.Phe136LeufsTer?) c.414del (p.Phe138LeufsTer?) | |
9 | g.94606861A>C | CA374106746 | FBP1 | c.819T>G (n.819T>G) c.659T>G (p.Phe220Cys) c.464T>G (p.Phe155Cys) c.407T>G (p.Phe136Cys) c.413T>G (p.Phe138Cys) | |
9 | g.94606861A>G | CA374106747 | FBP1 | c.819T>C (n.819T>C) c.659T>C (p.Phe220Ser) c.464T>C (p.Phe155Ser) c.407T>C (p.Phe136Ser) c.413T>C (p.Phe138Ser) | |
9 | g.94606861A>T | CA374106744 | FBP1 | c.819T>A (n.819T>A) c.659T>A (p.Phe220Tyr) c.464T>A (p.Phe155Tyr) c.407T>A (p.Phe136Tyr) c.413T>A (p.Phe138Tyr) | |
9 | g.94606862A= | CA1865226641 | FBP1 | c.818T= (n.818T=) c.658T= (p.Phe220=) c.463T= (p.Phe155=) c.406T= (p.Phe136=) c.412T= (p.Phe138=) | |
9 | g.94606862A>C | CA374106748 | FBP1 | c.818T>G (n.818T>G) c.658T>G (p.Phe220Val) c.463T>G (p.Phe155Val) c.406T>G (p.Phe136Val) c.412T>G (p.Phe138Val) | gnomAD v4 |
9 | g.94606862A>G | CA374106750 | FBP1 | c.818T>C (n.818T>C) c.658T>C (p.Phe220Leu) c.463T>C (p.Phe155Leu) c.406T>C (p.Phe136Leu) c.412T>C (p.Phe138Leu) | dbSNP gnomAD v2 |
9 | g.94606862A>T | CA374106752 | FBP1 | c.818T>A (n.818T>A) c.658T>A (p.Phe220Ile) c.463T>A (p.Phe155Ile) c.406T>A (p.Phe136Ile) c.412T>A (p.Phe138Ile) | |
9 | g.94606863G>A | CA466099983 | FBP1 | c.817C>T (n.817C>T) c.657C>T (p.Asp219=) c.462C>T (p.Asp154=) c.405C>T (p.Asp135=) c.411C>T (p.Asp137=) | |
9 | g.94606863G>C | CA374106753 | FBP1 | c.817C>G (n.817C>G) c.657C>G (p.Asp219Glu) c.462C>G (p.Asp154Glu) c.405C>G (p.Asp135Glu) c.411C>G (p.Asp137Glu) | |
9 | g.94606863G>T | CA374106755 | FBP1 | c.817C>A (n.817C>A) c.657C>A (p.Asp219Glu) c.462C>A (p.Asp154Glu) c.405C>A (p.Asp135Glu) c.411C>A (p.Asp137Glu) | |
9 | g.94606864T>A | CA374106761 | FBP1 | c.816A>T (n.816A>T) c.656A>T (p.Asp219Val) c.461A>T (p.Asp154Val) c.404A>T (p.Asp135Val) c.410A>T (p.Asp137Val) | |
9 | g.94606864T>C | CA374106757 | FBP1 | c.816A>G (n.816A>G) c.656A>G (p.Asp219Gly) c.461A>G (p.Asp154Gly) c.404A>G (p.Asp135Gly) c.410A>G (p.Asp137Gly) | |
9 | g.94606864T>G | CA374106759 | FBP1 | c.816A>C (n.816A>C) c.656A>C (p.Asp219Ala) c.461A>C (p.Asp154Ala) c.404A>C (p.Asp135Ala) c.410A>C (p.Asp137Ala) | |
9 | g.94606865C>A | CA374106764 | FBP1 | c.815G>T (n.815G>T) c.655G>T (p.Asp219Tyr) c.460G>T (p.Asp154Tyr) c.403G>T (p.Asp135Tyr) c.409G>T (p.Asp137Tyr) | |
9 | g.94606865C>G | CA374106766 | FBP1 | c.815G>C (n.815G>C) c.655G>C (p.Asp219His) c.460G>C (p.Asp154His) c.403G>C (p.Asp135His) c.409G>C (p.Asp137His) | |
9 | g.94606865C>T | CA374106768 | FBP1 | c.815G>A (n.815G>A) c.655G>A (p.Asp219Asn) c.460G>A (p.Asp154Asn) c.403G>A (p.Asp135Asn) c.409G>A (p.Asp137Asn) | gnomAD v4 |
9 | g.94606866C>A | CA374106769 | FBP1 | c.814G>T (n.814G>T) c.654G>T (p.Arg218Ser) c.459G>T (p.Arg153Ser) c.402G>T (p.Arg134Ser) c.408G>T (p.Arg136Ser) | |
9 | g.94606866C>G | CA374106770 | FBP1 | c.814G>C (n.814G>C) c.654G>C (p.Arg218Ser) c.459G>C (p.Arg153Ser) c.402G>C (p.Arg134Ser) c.408G>C (p.Arg136Ser) | |
9 | g.94606866C>T | CA466099987 | FBP1 | c.814G>A (n.814G>A) c.654G>A (p.Arg218=) c.459G>A (p.Arg153=) c.402G>A (p.Arg134=) c.408G>A (p.Arg136=) | |
9 | g.94606867C>A | CA374106773 | FBP1 | c.813G>T (n.813G>T) c.653G>T (p.Arg218Met) c.458G>T (p.Arg153Met) c.401G>T (p.Arg134Met) c.407G>T (p.Arg136Met) | dbSNP |
9 | g.94606867C= | CA1865226642 | FBP1 | c.813G= (n.813G=) c.653G= (p.Arg218=) c.458G= (p.Arg153=) c.401G= (p.Arg134=) c.407G= (p.Arg136=) | |
9 | g.94606867C>G | CA374106775 | FBP1 | c.813G>C (n.813G>C) c.653G>C (p.Arg218Thr) c.458G>C (p.Arg153Thr) c.401G>C (p.Arg134Thr) c.407G>C (p.Arg136Thr) | dbSNP |
9 | g.94606867C>T | CA5136172 | FBP1 | c.813G>A (n.813G>A) c.653G>A (p.Arg218Lys) c.458G>A (p.Arg153Lys) c.401G>A (p.Arg134Lys) c.407G>A (p.Arg136Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.94606867_94606869delinsCTG | CA1865226643 | FBP1 | c.811_813delinsCAG (n.811_813delinsCAG) c.651_653delinsCAG (p.Ala217=) c.456_458delinsCAG (p.Ala152=) c.399_401delinsCAG (p.Ala133=) c.405_407delinsCAG (p.Ala135=) | |
9 | g.94606867_94606869delinsTTA | CA196553557 | FBP1 | c.811_813delinsTAA (n.811_813delinsTAA) c.651_653delinsTAA (p.Arg218Lys) c.456_458delinsTAA (p.Arg153Lys) c.399_401delinsTAA (p.Arg134Lys) c.405_407delinsTAA (p.Arg136Lys) | ClinVar dbSNP |
9 | g.94606868T>A | CA374106777 | FBP1 | c.812A>T (n.812A>T) c.652A>T (p.Arg218Trp) c.457A>T (p.Arg153Trp) c.400A>T (p.Arg134Trp) c.406A>T (p.Arg136Trp) | |
9 | g.94606868T>C | CA374106779 | FBP1 | c.812A>G (n.812A>G) c.652A>G (p.Arg218Gly) c.457A>G (p.Arg153Gly) c.400A>G (p.Arg134Gly) c.406A>G (p.Arg136Gly) | |
9 | g.94606868T>G | CA466099993 | FBP1 | c.812A>C (n.812A>C) c.652A>C (p.Arg218=) c.457A>C (p.Arg153=) c.400A>C (p.Arg134=) c.406A>C (p.Arg136=) | |
9 | g.94606869G>A | CA5136173 | FBP1 | c.811C>T (n.811C>T) c.651C>T (p.Ala217=) c.456C>T (p.Ala152=) c.399C>T (p.Ala133=) c.405C>T (p.Ala135=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
9 | g.94606869G>C | CA466099995 | FBP1 | c.811C>G (n.811C>G) c.651C>G (p.Ala217=) c.456C>G (p.Ala152=) c.399C>G (p.Ala133=) c.405C>G (p.Ala135=) | dbSNP |
9 | g.94606869G= | CA1630847869 | FBP1 | c.811C= (n.811C=) c.651C= (p.Ala217=) c.456C= (p.Ala152=) c.399C= (p.Ala133=) c.405C= (p.Ala135=) | |
9 | g.94606869G>T | CA196553571 | FBP1 | c.811C>A (n.811C>A) c.651C>A (p.Ala217=) c.456C>A (p.Ala152=) c.399C>A (p.Ala133=) c.405C>A (p.Ala135=) | dbSNP |
9 | g.94606870G>A | CA374106782 | FBP1 | c.810C>T (n.810C>T) c.650C>T (p.Ala217Val) c.455C>T (p.Ala152Val) c.398C>T (p.Ala133Val) c.404C>T (p.Ala135Val) | |
9 | g.94606870G>C | CA374106784 | FBP1 | c.810C>G (n.810C>G) c.650C>G (p.Ala217Gly) c.455C>G (p.Ala152Gly) c.398C>G (p.Ala133Gly) c.404C>G (p.Ala135Gly) | dbSNP gnomAD v3 gnomAD v4 |
9 | g.94606870G= | CA1865226644 | FBP1 | c.810C= (n.810C=) c.650C= (p.Ala217=) c.455C= (p.Ala152=) c.398C= (p.Ala133=) c.404C= (p.Ala135=) | |
9 | g.94606870G>T | CA374106786 | FBP1 | c.810C>A (n.810C>A) c.650C>A (p.Ala217Asp) c.455C>A (p.Ala152Asp) c.398C>A (p.Ala133Asp) c.404C>A (p.Ala135Asp) | |
9 | g.94606871C>A | CA374106788 | FBP1 | c.809G>T (n.809G>T) c.649G>T (p.Ala217Ser) c.454G>T (p.Ala152Ser) c.397G>T (p.Ala133Ser) c.403G>T (p.Ala135Ser) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.94606871C= | CA1865226645 | FBP1 | c.809G= (n.809G=) c.649G= (p.Ala217=) c.454G= (p.Ala152=) c.397G= (p.Ala133=) c.403G= (p.Ala135=) | |
9 | g.94606871C>G | CA374106790 | FBP1 | c.809G>C (n.809G>C) c.649G>C (p.Ala217Pro) c.454G>C (p.Ala152Pro) c.397G>C (p.Ala133Pro) c.403G>C (p.Ala135Pro) | |
9 | g.94606871C>T | CA5136174 | FBP1 | c.809G>A (n.809G>A) c.649G>A (p.Ala217Thr) c.454G>A (p.Ala152Thr) c.397G>A (p.Ala133Thr) c.403G>A (p.Ala135Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.94606872G>A | CA5136175 | FBP1 | c.808C>T (n.808C>T) c.648C>T (p.Tyr216=) c.453C>T (p.Tyr151=) c.396C>T (p.Tyr132=) c.402C>T (p.Tyr134=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
9 | g.94606872G>C | CA374106794 | FBP1 | c.808C>G (n.808C>G) c.648C>G (p.Tyr216Ter) c.453C>G (p.Tyr151Ter) c.396C>G (p.Tyr132Ter) c.402C>G (p.Tyr134Ter) | |
9 | g.94606872G= | CA1865226646 | FBP1 | c.808C= (n.808C=) c.648C= (p.Tyr216=) c.453C= (p.Tyr151=) c.396C= (p.Tyr132=) c.402C= (p.Tyr134=) | |
9 | g.94606872G>T | CA374106796 | FBP1 | c.808C>A (n.808C>A) c.648C>A (p.Tyr216Ter) c.453C>A (p.Tyr151Ter) c.396C>A (p.Tyr132Ter) c.402C>A (p.Tyr134Ter) | |
9 | g.94606873T>A | CA374106799 | FBP1 | c.807A>T (n.807A>T) c.647A>T (p.Tyr216Phe) c.452A>T (p.Tyr151Phe) c.395A>T (p.Tyr132Phe) c.401A>T (p.Tyr134Phe) | |
9 | g.94606873T>C | CA374106801 | FBP1 | c.807A>G (n.807A>G) c.647A>G (p.Tyr216Cys) c.452A>G (p.Tyr151Cys) c.395A>G (p.Tyr132Cys) c.401A>G (p.Tyr134Cys) | dbSNP gnomAD v4 COSMIC |
9 | g.94606873T>G | CA374106797 | FBP1 | c.807A>C (n.807A>C) c.647A>C (p.Tyr216Ser) c.452A>C (p.Tyr151Ser) c.395A>C (p.Tyr132Ser) c.401A>C (p.Tyr134Ser) | |
9 | g.94606873T= | CA1865226647 | FBP1 | c.807A= (n.807A=) c.647A= (p.Tyr216=) c.452A= (p.Tyr151=) c.395A= (p.Tyr132=) c.401A= (p.Tyr134=) | |
9 | g.94606874A>C | CA374106807 | FBP1 | c.806T>G (n.806T>G) c.646T>G (p.Tyr216Asp) c.451T>G (p.Tyr151Asp) c.394T>G (p.Tyr132Asp) c.400T>G (p.Tyr134Asp) | |
9 | g.94606874A>G | CA374106803 | FBP1 | c.806T>C (n.806T>C) c.646T>C (p.Tyr216His) c.451T>C (p.Tyr151His) c.394T>C (p.Tyr132His) c.400T>C (p.Tyr134His) | |
9 | g.94606874A>T | CA374106805 | FBP1 | c.806T>A (n.806T>A) c.646T>A (p.Tyr216Asn) c.451T>A (p.Tyr151Asn) c.394T>A (p.Tyr132Asn) c.400T>A (p.Tyr134Asn) | |
9 | g.94606875G>A | CA466100007 | FBP1 | c.805C>T (n.805C>T) c.645C>T (p.Gly215=) c.450C>T (p.Gly150=) c.393C>T (p.Gly131=) c.399C>T (p.Gly133=) | gnomAD v4 |
9 | g.94606875G>C | CA466100008 | FBP1 | c.805C>G (n.805C>G) c.645C>G (p.Gly215=) c.450C>G (p.Gly150=) c.393C>G (p.Gly131=) c.399C>G (p.Gly133=) | gnomAD v4 |
9 | g.94606875G>T | CA466100010 | FBP1 | c.805C>A (n.805C>A) c.645C>A (p.Gly215=) c.450C>A (p.Gly150=) c.393C>A (p.Gly131=) c.399C>A (p.Gly133=) | |
9 | g.94606876C>A | CA374106809 | FBP1 | c.804G>T (n.804G>T) c.644G>T (p.Gly215Val) c.449G>T (p.Gly150Val) c.392G>T (p.Gly131Val) c.398G>T (p.Gly133Val) | |
9 | g.94606876C>G | CA374106811 | FBP1 | c.804G>C (n.804G>C) c.644G>C (p.Gly215Ala) c.449G>C (p.Gly150Ala) c.392G>C (p.Gly131Ala) c.398G>C (p.Gly133Ala) | |
9 | g.94606876C>T | CA374106813 | FBP1 | c.804G>A (n.804G>A) c.644G>A (p.Gly215Asp) c.449G>A (p.Gly150Asp) c.392G>A (p.Gly131Asp) c.398G>A (p.Gly133Asp) | |
9 | g.94606877C>A | CA374106816 | FBP1 | c.803G>T (n.803G>T) c.643G>T (p.Gly215Cys) c.448G>T (p.Gly150Cys) c.391G>T (p.Gly131Cys) c.397G>T (p.Gly133Cys) | |
9 | g.94606877C>G | CA374106818 | FBP1 | c.803G>C (n.803G>C) c.643G>C (p.Gly215Arg) c.448G>C (p.Gly150Arg) c.391G>C (p.Gly131Arg) c.397G>C (p.Gly133Arg) | |
9 | g.94606877C>T | CA374106820 | FBP1 | c.803G>A (n.803G>A) c.643G>A (p.Gly215Ser) c.448G>A (p.Gly150Ser) c.391G>A (p.Gly131Ser) c.397G>A (p.Gly133Ser) | |
9 | g.94606878C>A | CA374106822 | FBP1 | c.802G>T (n.802G>T) c.642G>T (p.Glu214Asp) c.447G>T (p.Glu149Asp) c.390G>T (p.Glu130Asp) c.396G>T (p.Glu132Asp) | |
9 | g.94606878C>G | CA374106824 | FBP1 | c.802G>C (n.802G>C) c.642G>C (p.Glu214Asp) c.447G>C (p.Glu149Asp) c.390G>C (p.Glu130Asp) c.396G>C (p.Glu132Asp) | |
9 | g.94606878C>T | CA466100017 | FBP1 | c.802G>A (n.802G>A) c.642G>A (p.Glu214=) c.447G>A (p.Glu149=) c.390G>A (p.Glu130=) c.396G>A (p.Glu132=) | |
9 | g.94606879T>A | CA374106826 | FBP1 | c.801A>T (n.801A>T) c.641A>T (p.Glu214Val) c.446A>T (p.Glu149Val) c.389A>T (p.Glu130Val) c.395A>T (p.Glu132Val) | |
9 | g.94606879T>C | CA374106828 | FBP1 | c.801A>G (n.801A>G) c.641A>G (p.Glu214Gly) c.446A>G (p.Glu149Gly) c.389A>G (p.Glu130Gly) c.395A>G (p.Glu132Gly) | |
9 | g.94606879T>G | CA374106830 | FBP1 | c.801A>C (n.801A>C) c.641A>C (p.Glu214Ala) c.446A>C (p.Glu149Ala) c.389A>C (p.Glu130Ala) c.395A>C (p.Glu132Ala) | |
9 | g.94606880C>A | CA374106832 | FBP1 | c.800G>T (n.800G>T) c.640G>T (p.Glu214Ter) c.445G>T (p.Glu149Ter) c.388G>T (p.Glu130Ter) c.394G>T (p.Glu132Ter) | |
9 | g.94606880C= | CA1865226648 | FBP1 | c.800G= (n.800G=) c.640G= (p.Glu214=) c.445G= (p.Glu149=) c.388G= (p.Glu130=) c.394G= (p.Glu132=) | |
9 | g.94606880C>G | CA374106836 | FBP1 | c.800G>C (n.800G>C) c.640G>C (p.Glu214Gln) c.445G>C (p.Glu149Gln) c.388G>C (p.Glu130Gln) c.394G>C (p.Glu132Gln) | |
9 | g.94606880C>T | CA374106834 | FBP1 | c.800G>A (n.800G>A) c.640G>A (p.Glu214Lys) c.445G>A (p.Glu149Lys) c.388G>A (p.Glu130Lys) c.394G>A (p.Glu132Lys) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.94606881G>A | CA466100024 | FBP1 | c.799C>T (n.799C>T) c.639C>T (p.Asn213=) c.444C>T (p.Asn148=) c.387C>T (p.Asn129=) c.393C>T (p.Asn131=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.94606881G>C | CA196553595 | FBP1 | c.799C>G (n.799C>G) c.639C>G (p.Asn213Lys) c.444C>G (p.Asn148Lys) c.387C>G (p.Asn129Lys) c.393C>G (p.Asn131Lys) | dbSNP gnomAD v4 |
9 | g.94606881G= | CA1865226649 | FBP1 | c.799C= (n.799C=) c.639C= (p.Asn213=) c.444C= (p.Asn148=) c.387C= (p.Asn129=) c.393C= (p.Asn131=) | |
9 | g.94606881G>T | CA374106838 | FBP1 | c.799C>A (n.799C>A) c.639C>A (p.Asn213Lys) c.444C>A (p.Asn148Lys) c.387C>A (p.Asn129Lys) c.393C>A (p.Asn131Lys) | ClinVar |
9 | g.94606882T>A | CA374106840 | FBP1 | c.798A>T (n.798A>T) c.638A>T (p.Asn213Ile) c.443A>T (p.Asn148Ile) c.386A>T (p.Asn129Ile) c.392A>T (p.Asn131Ile) | |
9 | g.94606882T>C | CA374106842 | FBP1 | c.798A>G (n.798A>G) c.638A>G (p.Asn213Ser) c.443A>G (p.Asn148Ser) c.386A>G (p.Asn129Ser) c.392A>G (p.Asn131Ser) | gnomAD v4 |
9 | g.94606882T>G | CA374106844 | FBP1 | c.798A>C (n.798A>C) c.638A>C (p.Asn213Thr) c.443A>C (p.Asn148Thr) c.386A>C (p.Asn129Thr) c.392A>C (p.Asn131Thr) | |
9 | g.94606883T>A | CA374106846 | FBP1 | c.797A>T (n.797A>T) c.637A>T (p.Asn213Tyr) c.442A>T (p.Asn148Tyr) c.385A>T (p.Asn129Tyr) c.391A>T (p.Asn131Tyr) | |
9 | g.94606883T>C | CA374106847 | FBP1 | c.797A>G (n.797A>G) c.637A>G (p.Asn213Asp) c.442A>G (p.Asn148Asp) c.385A>G (p.Asn129Asp) c.391A>G (p.Asn131Asp) | |
9 | g.94606883T>G | CA374106850 | FBP1 | c.797A>C (n.797A>C) c.637A>C (p.Asn213His) c.442A>C (p.Asn148His) c.385A>C (p.Asn129His) c.391A>C (p.Asn131His) | |
9 | g.94606884A= | CA1865226650 | FBP1 | c.796T= (n.796T=) c.636T= (p.Leu212=) c.441T= (p.Leu147=) c.384T= (p.Leu128=) c.390T= (p.Leu130=) | |
9 | g.94606884A>C | CA466100027 | FBP1 | c.796T>G (n.796T>G) c.636T>G (p.Leu212=) c.441T>G (p.Leu147=) c.384T>G (p.Leu128=) c.390T>G (p.Leu130=) | |
9 | g.94606884A>G | CA466100029 | FBP1 | c.796T>C (n.796T>C) c.636T>C (p.Leu212=) c.441T>C (p.Leu147=) c.384T>C (p.Leu128=) c.390T>C (p.Leu130=) | |
9 | g.94606884A>T | CA466100031 | FBP1 | c.796T>A (n.796T>A) c.636T>A (p.Leu212=) c.441T>A (p.Leu147=) c.384T>A (p.Leu128=) c.390T>A (p.Leu130=) | dbSNP gnomAD v2 gnomAD v4 |
9 | g.94606885A>C | CA374106852 | FBP1 | c.795T>G (n.795T>G) c.635T>G (p.Leu212Arg) c.440T>G (p.Leu147Arg) c.383T>G (p.Leu128Arg) c.389T>G (p.Leu130Arg) | |
9 | g.94606885A>G | CA374106854 | FBP1 | c.795T>C (n.795T>C) c.635T>C (p.Leu212Pro) c.440T>C (p.Leu147Pro) c.383T>C (p.Leu128Pro) c.389T>C (p.Leu130Pro) | |
9 | g.94606885A>T | CA374106856 | FBP1 | c.795T>A (n.795T>A) c.635T>A (p.Leu212His) c.440T>A (p.Leu147His) c.383T>A (p.Leu128His) c.389T>A (p.Leu130His) | |
9 | g.94606886G>A | CA374106860 | FBP1 | c.794C>T (n.794C>T) c.634C>T (p.Leu212Phe) c.439C>T (p.Leu147Phe) c.382C>T (p.Leu128Phe) c.388C>T (p.Leu130Phe) | |
9 | g.94606886G>C | CA374106862 | FBP1 | c.794C>G (n.794C>G) c.634C>G (p.Leu212Val) c.439C>G (p.Leu147Val) c.382C>G (p.Leu128Val) c.388C>G (p.Leu130Val) | |
9 | g.94606886G>T | CA374106858 | FBP1 | c.794C>A (n.794C>A) c.634C>A (p.Leu212Ile) c.439C>A (p.Leu147Ile) c.382C>A (p.Leu128Ile) c.388C>A (p.Leu130Ile) | |
9 | g.94606887G>A | CA466100036 | FBP1 | c.793C>T (n.793C>T) c.633C>T (p.Ser211=) c.438C>T (p.Ser146=) c.381C>T (p.Ser127=) c.387C>T (p.Ser129=) | ClinVar dbSNP gnomAD v2 |
9 | g.94606887G>C | CA374106864 | FBP1 | c.793C>G (n.793C>G) c.633C>G (p.Ser211Arg) c.438C>G (p.Ser146Arg) c.381C>G (p.Ser127Arg) c.387C>G (p.Ser129Arg) | |
9 | g.94606887G= | CA1865226651 | FBP1 | c.793C= (n.793C=) c.633C= (p.Ser211=) c.438C= (p.Ser146=) c.381C= (p.Ser127=) c.387C= (p.Ser129=) | |
9 | g.94606887G>T | CA374106865 | FBP1 | c.793C>A (n.793C>A) c.633C>A (p.Ser211Arg) c.438C>A (p.Ser146Arg) c.381C>A (p.Ser127Arg) c.387C>A (p.Ser129Arg) | |
9 | g.94606888C>A | CA374106867 | FBP1 | c.792G>T (n.792G>T) c.632G>T (p.Ser211Ile) c.437G>T (p.Ser146Ile) c.380G>T (p.Ser127Ile) c.386G>T (p.Ser129Ile) | |
9 | g.94606888C= | CA1865226652 | FBP1 | c.792G= (n.792G=) c.632G= (p.Ser211=) c.437G= (p.Ser146=) c.380G= (p.Ser127=) c.386G= (p.Ser129=) | |
9 | g.94606888C>G | CA374106869 | FBP1 | c.792G>C (n.792G>C) c.632G>C (p.Ser211Thr) c.437G>C (p.Ser146Thr) c.380G>C (p.Ser127Thr) c.386G>C (p.Ser129Thr) | gnomAD v4 |
9 | g.94606888C>T | CA374106871 | FBP1 | c.792G>A (n.792G>A) c.632G>A (p.Ser211Asn) c.437G>A (p.Ser146Asn) c.380G>A (p.Ser127Asn) c.386G>A (p.Ser129Asn) | dbSNP gnomAD v3 gnomAD v4 |
9 | g.94606889T>A | CA374106873 | FBP1 | c.791A>T (n.791A>T) c.631A>T (p.Ser211Cys) c.436A>T (p.Ser146Cys) c.379A>T (p.Ser127Cys) c.385A>T (p.Ser129Cys) | |
9 | g.94606889T>C | CA374106875 | FBP1 | c.791A>G (n.791A>G) c.631A>G (p.Ser211Gly) c.436A>G (p.Ser146Gly) c.379A>G (p.Ser127Gly) c.385A>G (p.Ser129Gly) | |
9 | g.94606889T>G | CA374106877 | FBP1 | c.791A>C (n.791A>C) c.631A>C (p.Ser211Arg) c.436A>C (p.Ser146Arg) c.379A>C (p.Ser127Arg) c.385A>C (p.Ser129Arg) | |
9 | g.94606890G>A | CA466100042 | FBP1 | c.790C>T (n.790C>T) c.630C>T (p.Tyr210=) c.435C>T (p.Tyr145=) c.378C>T (p.Tyr126=) c.384C>T (p.Tyr128=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.94606890G>C | CA374106878 | FBP1 | c.790C>G (n.790C>G) c.630C>G (p.Tyr210Ter) c.435C>G (p.Tyr145Ter) c.378C>G (p.Tyr126Ter) c.384C>G (p.Tyr128Ter) | |
9 | g.94606890G= | CA1865226653 | FBP1 | c.790C= (n.790C=) c.630C= (p.Tyr210=) c.435C= (p.Tyr145=) c.378C= (p.Tyr126=) c.384C= (p.Tyr128=) | |
9 | g.94606890G>T | CA374106879 | FBP1 | c.790C>A (n.790C>A) c.630C>A (p.Tyr210Ter) c.435C>A (p.Tyr145Ter) c.378C>A (p.Tyr126Ter) c.384C>A (p.Tyr128Ter) | |
9 | g.94606891T>A | CA374106881 | FBP1 | c.789A>T (n.789A>T) c.629A>T (p.Tyr210Phe) c.434A>T (p.Tyr145Phe) c.377A>T (p.Tyr126Phe) c.383A>T (p.Tyr128Phe) | |
9 | g.94606891T>C | CA374106883 | FBP1 | c.789A>G (n.789A>G) c.629A>G (p.Tyr210Cys) c.434A>G (p.Tyr145Cys) c.377A>G (p.Tyr126Cys) c.383A>G (p.Tyr128Cys) | |
9 | g.94606891T>G | CA374106885 | FBP1 | c.789A>C (n.789A>C) c.629A>C (p.Tyr210Ser) c.434A>C (p.Tyr145Ser) c.377A>C (p.Tyr126Ser) c.383A>C (p.Tyr128Ser) | |
9 | g.94606892A>C | CA374106889 | FBP1 | c.788T>G (n.788T>G) c.628T>G (p.Tyr210Asp) c.433T>G (p.Tyr145Asp) c.376T>G (p.Tyr126Asp) c.382T>G (p.Tyr128Asp) | |
9 | g.94606892A>G | CA374106891 | FBP1 | c.788T>C (n.788T>C) c.628T>C (p.Tyr210His) c.433T>C (p.Tyr145His) c.376T>C (p.Tyr126His) c.382T>C (p.Tyr128His) | |
9 | g.94606892A>T | CA374106887 | FBP1 | c.788T>A (n.788T>A) c.628T>A (p.Tyr210Asn) c.433T>A (p.Tyr145Asn) c.376T>A (p.Tyr126Asn) c.382T>A (p.Tyr128Asn) | |
9 | g.94606893G>A | CA466100048 | FBP1 | c.787C>T (n.787C>T) c.627C>T (p.Ile209=) c.432C>T (p.Ile144=) c.375C>T (p.Ile125=) c.381C>T (p.Ile127=) | COSMIC |
9 | g.94606893G>C | CA374106893 | FBP1 | c.787C>G (n.787C>G) c.627C>G (p.Ile209Met) c.432C>G (p.Ile144Met) c.375C>G (p.Ile125Met) c.381C>G (p.Ile127Met) | |
9 | g.94606893G>T | CA466100051 | FBP1 | c.787C>A (n.787C>A) c.627C>A (p.Ile209=) c.432C>A (p.Ile144=) c.375C>A (p.Ile125=) c.381C>A (p.Ile127=) | COSMIC |
9 | g.94606894A>C | CA374106895 | FBP1 | c.786T>G (n.786T>G) c.626T>G (p.Ile209Ser) c.431T>G (p.Ile144Ser) c.374T>G (p.Ile125Ser) c.380T>G (p.Ile127Ser) | |
9 | g.94606894A>G | CA374106896 | FBP1 | c.786T>C (n.786T>C) c.626T>C (p.Ile209Thr) c.431T>C (p.Ile144Thr) c.374T>C (p.Ile125Thr) c.380T>C (p.Ile127Thr) | |
9 | g.94606894A>T | CA374106898 | FBP1 | c.786T>A (n.786T>A) c.626T>A (p.Ile209Asn) c.431T>A (p.Ile144Asn) c.374T>A (p.Ile125Asn) c.380T>A (p.Ile127Asn) | |
9 | g.94606895T>A | CA374106901 | FBP1 | c.785A>T (n.785A>T) c.625A>T (p.Ile209Phe) c.430A>T (p.Ile144Phe) c.373A>T (p.Ile125Phe) c.379A>T (p.Ile127Phe) | |
9 | g.94606895T>C | CA374106902 | FBP1 | c.785A>G (n.785A>G) c.625A>G (p.Ile209Val) c.430A>G (p.Ile144Val) c.373A>G (p.Ile125Val) c.379A>G (p.Ile127Val) | |
9 | g.94606895T>G | CA374106904 | FBP1 | c.785A>C (n.785A>C) c.625A>C (p.Ile209Leu) c.430A>C (p.Ile144Leu) c.373A>C (p.Ile125Leu) c.379A>C (p.Ile127Leu) | |
9 | g.94606896T>A | CA374106906 | FBP1 | c.784A>T (n.784A>T) c.624A>T (p.Lys208Asn) c.429A>T (p.Lys143Asn) c.372A>T (p.Lys124Asn) c.378A>T (p.Lys126Asn) | gnomAD v4 |
9 | g.94606896T>C | CA466100057 | FBP1 | c.784A>G (n.784A>G) c.624A>G (p.Lys208=) c.429A>G (p.Lys143=) c.372A>G (p.Lys124=) c.378A>G (p.Lys126=) | |
9 | g.94606896T>G | CA374106908 | FBP1 | c.784A>C (n.784A>C) c.624A>C (p.Lys208Asn) c.429A>C (p.Lys143Asn) c.372A>C (p.Lys124Asn) c.378A>C (p.Lys126Asn) | |
9 | g.94606897T>A | CA374106909 | FBP1 | c.783A>T (n.783A>T) c.623A>T (p.Lys208Ile) c.428A>T (p.Lys143Ile) c.371A>T (p.Lys124Ile) c.377A>T (p.Lys126Ile) | |
9 | g.94606897T>C | CA374106911 | FBP1 | c.783A>G (n.783A>G) c.623A>G (p.Lys208Arg) c.428A>G (p.Lys143Arg) c.371A>G (p.Lys124Arg) c.377A>G (p.Lys126Arg) | |
9 | g.94606897T>G | CA374106913 | FBP1 | c.783A>C (n.783A>C) c.623A>C (p.Lys208Thr) c.428A>C (p.Lys143Thr) c.371A>C (p.Lys124Thr) c.377A>C (p.Lys126Thr) | |
9 | g.94606898T>A | CA374106915 | FBP1 | c.782A>T (n.782A>T) c.622A>T (p.Lys208Ter) c.427A>T (p.Lys143Ter) c.370A>T (p.Lys124Ter) c.376A>T (p.Lys126Ter) | |
9 | g.94606898T>C | CA374106917 | FBP1 | c.782A>G (n.782A>G) c.622A>G (p.Lys208Glu) c.427A>G (p.Lys143Glu) c.370A>G (p.Lys124Glu) c.376A>G (p.Lys126Glu) | |
9 | g.94606898T>G | CA374106918 | FBP1 | c.782A>C (n.782A>C) c.622A>C (p.Lys208Gln) c.427A>C (p.Lys143Gln) c.370A>C (p.Lys124Gln) c.376A>C (p.Lys126Gln) | |
9 | g.94606899A>C | CA466100067 | FBP1 | c.781T>G (n.781T>G) c.621T>G (p.Gly207=) c.426T>G (p.Gly142=) c.369T>G (p.Gly123=) c.375T>G (p.Gly125=) | gnomAD v3 gnomAD v4 |
9 | g.94606899A>G | CA466100065 | FBP1 | c.781T>C (n.781T>C) c.621T>C (p.Gly207=) c.426T>C (p.Gly142=) c.369T>C (p.Gly123=) c.375T>C (p.Gly125=) | |
9 | g.94606899A>T | CA466100064 | FBP1 | c.781T>A (n.781T>A) c.621T>A (p.Gly207=) c.426T>A (p.Gly142=) c.369T>A (p.Gly123=) c.375T>A (p.Gly125=) | |
9 | g.94606900C>A | CA374106922 | FBP1 | c.780G>T (n.780G>T) c.620G>T (p.Gly207Val) c.425G>T (p.Gly142Val) c.368G>T (p.Gly123Val) c.374G>T (p.Gly125Val) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.94606900C= | CA1865226654 | FBP1 | c.780G= (n.780G=) c.620G= (p.Gly207=) c.425G= (p.Gly142=) c.368G= (p.Gly123=) c.374G= (p.Gly125=) | |
9 | g.94606900C>G | CA374106924 | FBP1 | c.780G>C (n.780G>C) c.620G>C (p.Gly207Ala) c.425G>C (p.Gly142Ala) c.368G>C (p.Gly123Ala) c.374G>C (p.Gly125Ala) | |
9 | g.94606900C>T | CA374106920 | FBP1 | c.780G>A (n.780G>A) c.620G>A (p.Gly207Asp) c.425G>A (p.Gly142Asp) c.368G>A (p.Gly123Asp) c.374G>A (p.Gly125Asp) | |
9 | g.94606901C>A | CA374106926 | FBP1 | c.779G>T (n.779G>T) c.619G>T (p.Gly207Cys) c.424G>T (p.Gly142Cys) c.367G>T (p.Gly123Cys) c.373G>T (p.Gly125Cys) | |
9 | g.94606901C= | CA1865226655 | FBP1 | c.779G= (n.779G=) c.619G= (p.Gly207=) c.424G= (p.Gly142=) c.367G= (p.Gly123=) c.373G= (p.Gly125=) | |
9 | g.94606901C>G | CA5136176 | FBP1 | c.779G>C (n.779G>C) c.619G>C (p.Gly207Arg) c.424G>C (p.Gly142Arg) c.367G>C (p.Gly123Arg) c.373G>C (p.Gly125Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.94606901C>T | CA374106928 | FBP1 | c.779G>A (n.779G>A) c.619G>A (p.Gly207Ser) c.424G>A (p.Gly142Ser) c.367G>A (p.Gly123Ser) c.373G>A (p.Gly125Ser) | |
9 | g.94606905_94606908del | CA2695210724 | FBP1 | c.776_779del (n.776_779del) c.616_619del (p.Lys206ValfsTer?) c.421_424del (p.Lys141ValfsTer?) c.364_367del (p.Lys122ValfsTer?) c.370_373del (p.Lys124ValfsTer?) | |
9 | g.94606902T>A | CA374106931 | FBP1 | c.778A>T (n.778A>T) c.618A>T (p.Lys206Asn) c.423A>T (p.Lys141Asn) c.366A>T (p.Lys122Asn) c.372A>T (p.Lys124Asn) | |
9 | g.94606902T>C | CA466100073 | FBP1 | c.778A>G (n.778A>G) c.618A>G (p.Lys206=) c.423A>G (p.Lys141=) c.366A>G (p.Lys122=) c.372A>G (p.Lys124=) | |
9 | g.94606902T>G | CA374106932 | FBP1 | c.778A>C (n.778A>C) c.618A>C (p.Lys206Asn) c.423A>C (p.Lys141Asn) c.366A>C (p.Lys122Asn) c.372A>C (p.Lys124Asn) | |
9 | g.94606904del | CA2579387244 | FBP1 | c.778del (n.778del) c.618del (p.Gly207ValfsTer?) c.423del (p.Gly142ValfsTer?) c.366del (p.Gly123ValfsTer?) c.372del (p.Gly125ValfsTer?) | gnomAD v4 |
9 | g.94606903T>A | CA374106933 | FBP1 | c.777A>T (n.777A>T) c.617A>T (p.Lys206Ile) c.422A>T (p.Lys141Ile) c.365A>T (p.Lys122Ile) c.371A>T (p.Lys124Ile) | |
9 | g.94606903T>C | CA374106937 | FBP1 | c.777A>G (n.777A>G) c.617A>G (p.Lys206Arg) c.422A>G (p.Lys141Arg) c.365A>G (p.Lys122Arg) c.371A>G (p.Lys124Arg) | |
9 | g.94606903T>G | CA374106935 | FBP1 | c.777A>C (n.777A>C) c.617A>C (p.Lys206Thr) c.422A>C (p.Lys141Thr) c.365A>C (p.Lys122Thr) c.371A>C (p.Lys124Thr) | |
9 | g.94606904T>A | CA374106939 | FBP1 | c.776A>T (n.776A>T) c.616A>T (p.Lys206Ter) c.421A>T (p.Lys141Ter) c.364A>T (p.Lys122Ter) c.370A>T (p.Lys124Ter) | |
9 | g.94606904T>C | CA374106940 | FBP1 | c.776A>G (n.776A>G) c.616A>G (p.Lys206Glu) c.421A>G (p.Lys141Glu) c.364A>G (p.Lys122Glu) c.370A>G (p.Lys124Glu) | |
9 | g.94606904T>G | CA374106942 | FBP1 | c.776A>C (n.776A>C) c.616A>C (p.Lys206Gln) c.421A>C (p.Lys141Gln) c.364A>C (p.Lys122Gln) c.370A>C (p.Lys124Gln) | |
9 | g.94606905C>A | CA374106944 | FBP1 | c.775G>T (n.775G>T) c.615G>T (p.Lys205Asn) c.420G>T (p.Lys140Asn) c.363G>T (p.Lys121Asn) c.369G>T (p.Lys123Asn) | |
9 | g.94606905C>G | CA374106945 | FBP1 | c.775G>C (n.775G>C) c.615G>C (p.Lys205Asn) c.420G>C (p.Lys140Asn) c.363G>C (p.Lys121Asn) c.369G>C (p.Lys123Asn) | |
9 | g.94606905C>T | CA466100081 | FBP1 | c.775G>A (n.775G>A) c.615G>A (p.Lys205=) c.420G>A (p.Lys140=) c.363G>A (p.Lys121=) c.369G>A (p.Lys123=) | |
9 | g.94606905_94606909delinsCTTTT | CA1865226656 | FBP1 | c.771_775delinsAAAAG (n.771_775delinsAAAAG) c.611_615delinsAAAAG (p.Lys204=) c.416_420delinsAAAAG (p.Lys139=) c.359_363delinsAAAAG (p.Lys120=) c.365_369delinsAAAAG (p.Lys122=) | |
9 | g.94606906T>A | CA374106947 | FBP1 | c.774A>T (n.774A>T) c.614A>T (p.Lys205Met) c.419A>T (p.Lys140Met) c.362A>T (p.Lys121Met) c.368A>T (p.Lys123Met) | |
9 | g.94606906T>C | CA374106949 | FBP1 | c.774A>G (n.774A>G) c.614A>G (p.Lys205Arg) c.419A>G (p.Lys140Arg) c.362A>G (p.Lys121Arg) c.368A>G (p.Lys123Arg) | gnomAD v4 |
9 | g.94606906T>G | CA374106951 | FBP1 | c.774A>C (n.774A>C) c.614A>C (p.Lys205Thr) c.419A>C (p.Lys140Thr) c.362A>C (p.Lys121Thr) c.368A>C (p.Lys123Thr) | |
9 | g.94606911dup | CA2690769343 | FBP1 | c.774dup (n.774dup) c.614dup (p.Lys206GlufsTer3) c.419dup (p.Lys141GlufsTer3) c.362dup (p.Lys122GlufsTer3) c.368dup (p.Lys124GlufsTer3) | gnomAD v4 |
9 | g.94606911del | CA2690769344 | FBP1 | c.774del (n.774del) c.614del (p.Lys205ArgfsTer?) c.419del (p.Lys140ArgfsTer?) c.362del (p.Lys121ArgfsTer?) c.368del (p.Lys123ArgfsTer?) | gnomAD v4 |
9 | g.94606908_94606911del | CA5136177 | FBP1 | c.771_774del (n.771_774del) c.611_614del (p.Lys204ArgfsTer?) c.416_419del (p.Lys139ArgfsTer?) c.359_362del (p.Lys120ArgfsTer?) c.365_368del (p.Lys122ArgfsTer?) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.94606907T>A | CA374106954 | FBP1 | c.773A>T (n.773A>T) c.613A>T (p.Lys205Ter) c.418A>T (p.Lys140Ter) c.361A>T (p.Lys121Ter) c.367A>T (p.Lys123Ter) | |
9 | g.94606907T>C | CA374106956 | FBP1 | c.773A>G (n.773A>G) c.613A>G (p.Lys205Glu) c.418A>G (p.Lys140Glu) c.361A>G (p.Lys121Glu) c.367A>G (p.Lys123Glu) | |
9 | g.94606907T>G | CA374106957 | FBP1 | c.773A>C (n.773A>C) c.613A>C (p.Lys205Gln) c.418A>C (p.Lys140Gln) c.361A>C (p.Lys121Gln) c.367A>C (p.Lys123Gln) | |
9 | g.94606908T>A | CA374106960 | FBP1 | c.772A>T (n.772A>T) c.612A>T (p.Lys204Asn) c.417A>T (p.Lys139Asn) c.360A>T (p.Lys120Asn) c.366A>T (p.Lys122Asn) | |
9 | g.94606908T>C | CA466100089 | FBP1 | c.772A>G (n.772A>G) c.612A>G (p.Lys204=) c.417A>G (p.Lys139=) c.360A>G (p.Lys120=) c.366A>G (p.Lys122=) | |
9 | g.94606908T>G | CA374106962 | FBP1 | c.772A>C (n.772A>C) c.612A>C (p.Lys204Asn) c.417A>C (p.Lys139Asn) c.360A>C (p.Lys120Asn) c.366A>C (p.Lys122Asn) | dbSNP |
9 | g.94606908T= | CA1865226657 | FBP1 | c.772A= (n.772A=) c.612A= (p.Lys204=) c.417A= (p.Lys139=) c.360A= (p.Lys120=) c.366A= (p.Lys122=) | |
9 | g.94606909T>A | CA374106963 | FBP1 | c.771A>T (n.771A>T) c.611A>T (p.Lys204Ile) c.416A>T (p.Lys139Ile) c.359A>T (p.Lys120Ile) c.365A>T (p.Lys122Ile) | |
9 | g.94606909T>C | CA374106965 | FBP1 | c.771A>G (n.771A>G) c.611A>G (p.Lys204Arg) c.416A>G (p.Lys139Arg) c.359A>G (p.Lys120Arg) c.365A>G (p.Lys122Arg) | |
9 | g.94606909T>G | CA374106967 | FBP1 | c.771A>C (n.771A>C) c.611A>C (p.Lys204Thr) c.416A>C (p.Lys139Thr) c.359A>C (p.Lys120Thr) c.365A>C (p.Lys122Thr) | |
9 | g.94606910T>A | CA374106969 | FBP1 | c.770A>T (n.770A>T) c.610A>T (p.Lys204Ter) c.415A>T (p.Lys139Ter) c.358A>T (p.Lys120Ter) c.364A>T (p.Lys122Ter) | gnomAD v4 |
9 | g.94606910T>C | CA374106971 | FBP1 | c.770A>G (n.770A>G) c.610A>G (p.Lys204Glu) c.415A>G (p.Lys139Glu) c.358A>G (p.Lys120Glu) c.364A>G (p.Lys122Glu) | |
9 | g.94606910T>G | CA374106973 | FBP1 | c.770A>C (n.770A>C) c.610A>C (p.Lys204Gln) c.415A>C (p.Lys139Gln) c.358A>C (p.Lys120Gln) c.364A>C (p.Lys122Gln) | |
9 | g.94606911T>A | CA466100095 | FBP1 | c.769A>T (n.769A>T) c.609A>T (p.Ile203=) c.414A>T (p.Ile138=) c.357A>T (p.Ile119=) c.363A>T (p.Ile121=) | |
9 | g.94606911T>C | CA374106974 | FBP1 | c.769A>G (n.769A>G) c.609A>G (p.Ile203Met) c.414A>G (p.Ile138Met) c.357A>G (p.Ile119Met) c.363A>G (p.Ile121Met) | gnomAD v4 |
9 | g.94606911T>G | CA466100097 | FBP1 | c.769A>C (n.769A>C) c.609A>C (p.Ile203=) c.414A>C (p.Ile138=) c.357A>C (p.Ile119=) c.363A>C (p.Ile121=) | |
9 | g.94606912A>C | CA374106975 | FBP1 | c.768T>G (n.768T>G) c.608T>G (p.Ile203Arg) c.413T>G (p.Ile138Arg) c.356T>G (p.Ile119Arg) c.362T>G (p.Ile121Arg) | |
9 | g.94606912A>G | CA374106977 | FBP1 | c.768T>C (n.768T>C) c.608T>C (p.Ile203Thr) c.413T>C (p.Ile138Thr) c.356T>C (p.Ile119Thr) c.362T>C (p.Ile121Thr) | gnomAD v4 |
9 | g.94606912A>T | CA374106979 | FBP1 | c.768T>A (n.768T>A) c.608T>A (p.Ile203Lys) c.413T>A (p.Ile138Lys) c.356T>A (p.Ile119Lys) c.362T>A (p.Ile121Lys) | |
9 | g.94606913T>A | CA374106983 | FBP1 | c.767A>T (n.767A>T) c.607A>T (p.Ile203Leu) c.412A>T (p.Ile138Leu) c.355A>T (p.Ile119Leu) c.361A>T (p.Ile121Leu) | |
9 | g.94606913T>C | CA374106986 | FBP1 | c.767A>G (n.767A>G) c.607A>G (p.Ile203Val) c.412A>G (p.Ile138Val) c.355A>G (p.Ile119Val) c.361A>G (p.Ile121Val) | |
9 | g.94606913T>G | CA374106981 | FBP1 | c.767A>C (n.767A>C) c.607A>C (p.Ile203Leu) c.412A>C (p.Ile138Leu) c.355A>C (p.Ile119Leu) c.361A>C (p.Ile121Leu) | |
9 | g.94606914C>A | CA374106988 | FBP1 | c.766G>T (n.766G>T) c.606G>T (p.Lys202Asn) c.411G>T (p.Lys137Asn) c.354G>T (p.Lys118Asn) c.360G>T (p.Lys120Asn) | |
9 | g.94606914C= | CA1865226658 | FBP1 | c.766G= (n.766G=) c.606G= (p.Lys202=) c.411G= (p.Lys137=) c.354G= (p.Lys118=) c.360G= (p.Lys120=) | |
9 | g.94606914C>G | CA374106990 | FBP1 | c.766G>C (n.766G>C) c.606G>C (p.Lys202Asn) c.411G>C (p.Lys137Asn) c.354G>C (p.Lys118Asn) c.360G>C (p.Lys120Asn) | |
9 | g.94606914C>T | CA5136178 | FBP1 | c.766G>A (n.766G>A) c.606G>A (p.Lys202=) c.411G>A (p.Lys137=) c.354G>A (p.Lys118=) c.360G>A (p.Lys120=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.94606915T>A | CA374106992 | FBP1 | c.765A>T (n.765A>T) c.605A>T (p.Lys202Met) c.410A>T (p.Lys137Met) c.353A>T (p.Lys118Met) c.359A>T (p.Lys120Met) | |
9 | g.94606915T>C | CA374106994 | FBP1 | c.765A>G (n.765A>G) c.605A>G (p.Lys202Arg) c.410A>G (p.Lys137Arg) c.353A>G (p.Lys118Arg) c.359A>G (p.Lys120Arg) | |
9 | g.94606915T>G | CA374106995 | FBP1 | c.765A>C (n.765A>C) c.605A>C (p.Lys202Thr) c.410A>C (p.Lys137Thr) c.353A>C (p.Lys118Thr) c.359A>C (p.Lys120Thr) | dbSNP |
9 | g.94606915T= | CA1865226659 | FBP1 | c.765A= (n.765A=) c.605A= (p.Lys202=) c.410A= (p.Lys137=) c.353A= (p.Lys118=) c.359A= (p.Lys120=) | |
9 | g.94606916del | CA2690769345 | FBP1 | c.765del (n.765del) c.605del (p.Lys202ArgfsTer2) c.410del (p.Lys137ArgfsTer2) c.353del (p.Lys118ArgfsTer2) c.359del (p.Lys120ArgfsTer2) | gnomAD v4 |
9 | g.94606916T>A | CA374106998 | FBP1 | c.764A>T (n.764A>T) c.604A>T (p.Lys202Ter) c.409A>T (p.Lys137Ter) c.352A>T (p.Lys118Ter) c.358A>T (p.Lys120Ter) | |
9 | g.94606916T>C | CA374107000 | FBP1 | c.764A>G (n.764A>G) c.604A>G (p.Lys202Glu) c.409A>G (p.Lys137Glu) c.352A>G (p.Lys118Glu) c.358A>G (p.Lys120Glu) | |
9 | g.94606916T>G | CA374107001 | FBP1 | c.764A>C (n.764A>C) c.604A>C (p.Lys202Gln) c.409A>C (p.Lys137Gln) c.352A>C (p.Lys118Gln) c.358A>C (p.Lys120Gln) | |
9 | g.94606917del | CA2695210725 | FBP1 | c.763del (n.763del) c.603del (p.Lys202ArgfsTer2) c.408del (p.Lys137ArgfsTer2) c.351del (p.Lys118ArgfsTer2) c.357del (p.Lys120ArgfsTer2) | |
9 | g.94606917C>A | CA466100110 | FBP1 | c.763G>T (n.763G>T) c.603G>T (p.Val201=) c.408G>T (p.Val136=) c.351G>T (p.Val117=) c.357G>T (p.Val119=) | |
9 | g.94606917C>G | CA466100111 | FBP1 | c.763G>C (n.763G>C) c.603G>C (p.Val201=) c.408G>C (p.Val136=) c.351G>C (p.Val117=) c.357G>C (p.Val119=) | |
9 | g.94606917C>T | CA466100112 | FBP1 | c.763G>A (n.763G>A) c.603G>A (p.Val201=) c.408G>A (p.Val136=) c.351G>A (p.Val117=) c.357G>A (p.Val119=) | |
9 | g.94606918A= | CA1865226660 | FBP1 | c.762T= (n.762T=) c.602T= (p.Val201=) c.407T= (p.Val136=) c.350T= (p.Val117=) c.356T= (p.Val119=) | |
9 | g.94606918A>C | CA374107004 | FBP1 | c.762T>G (n.762T>G) c.602T>G (p.Val201Gly) c.407T>G (p.Val136Gly) c.350T>G (p.Val117Gly) c.356T>G (p.Val119Gly) | |
9 | g.94606918A>G | CA374107005 | FBP1 | c.762T>C (n.762T>C) c.602T>C (p.Val201Ala) c.407T>C (p.Val136Ala) c.350T>C (p.Val117Ala) c.356T>C (p.Val119Ala) | dbSNP |
9 | g.94606918A>T | CA374107007 | FBP1 | c.762T>A (n.762T>A) c.602T>A (p.Val201Glu) c.407T>A (p.Val136Glu) c.350T>A (p.Val117Glu) c.356T>A (p.Val119Glu) | |
9 | g.94606919C>A | CA374107011 | FBP1 | c.761G>T (n.761G>T) c.601G>T (p.Val201Leu) c.406G>T (p.Val136Leu) c.349G>T (p.Val117Leu) c.355G>T (p.Val119Leu) | |
9 | g.94606919C>G | CA374107012 | FBP1 | c.761G>C (n.761G>C) c.601G>C (p.Val201Leu) c.406G>C (p.Val136Leu) c.349G>C (p.Val117Leu) c.355G>C (p.Val119Leu) | |
9 | g.94606919C>T | CA374107009 | FBP1 | c.761G>A (n.761G>A) c.601G>A (p.Val201Met) c.406G>A (p.Val136Met) c.349G>A (p.Val117Met) c.355G>A (p.Val119Met) | |
9 | g.94606920A= | CA1865226661 | FBP1 | c.760T= (n.760T=) c.600T= (p.Asp200=) c.405T= (p.Asp135=) c.348T= (p.Asp116=) c.354T= (p.Asp118=) | |
9 | g.94606920A>C | CA196553612 | FBP1 | c.760T>G (n.760T>G) c.600T>G (p.Asp200Glu) c.405T>G (p.Asp135Glu) c.348T>G (p.Asp116Glu) c.354T>G (p.Asp118Glu) | dbSNP |
9 | g.94606920A>G | CA466100118 | FBP1 | c.760T>C (n.760T>C) c.600T>C (p.Asp200=) c.405T>C (p.Asp135=) c.348T>C (p.Asp116=) c.354T>C (p.Asp118=) | |
9 | g.94606920A>T | CA374107014 | FBP1 | c.760T>A (n.760T>A) c.600T>A (p.Asp200Glu) c.405T>A (p.Asp135Glu) c.348T>A (p.Asp116Glu) c.354T>A (p.Asp118Glu) | |
9 | g.94606921T>A | CA374107017 | FBP1 | c.759A>T (n.759A>T) c.599A>T (p.Asp200Val) c.404A>T (p.Asp135Val) c.347A>T (p.Asp116Val) c.353A>T (p.Asp118Val) | gnomAD v4 |
9 | g.94606921T>C | CA374107018 | FBP1 | c.759A>G (n.759A>G) c.599A>G (p.Asp200Gly) c.404A>G (p.Asp135Gly) c.347A>G (p.Asp116Gly) c.353A>G (p.Asp118Gly) | |
9 | g.94606921T>G | CA374107020 | FBP1 | c.759A>C (n.759A>C) c.599A>C (p.Asp200Ala) c.404A>C (p.Asp135Ala) c.347A>C (p.Asp116Ala) c.353A>C (p.Asp118Ala) | |
9 | g.94606922C>A | CA374107025 | FBP1 | c.758G>T (n.758G>T) c.598G>T (p.Asp200Tyr) c.403G>T (p.Asp135Tyr) c.346G>T (p.Asp116Tyr) c.352G>T (p.Asp118Tyr) | gnomAD v4 |
9 | g.94606922C= | CA1865226662 | FBP1 | c.758G= (n.758G=) c.598G= (p.Asp200=) c.403G= (p.Asp135=) c.346G= (p.Asp116=) c.352G= (p.Asp118=) | |
9 | g.94606922C>G | CA374107022 | FBP1 | c.758G>C (n.758G>C) c.598G>C (p.Asp200His) c.403G>C (p.Asp135His) c.346G>C (p.Asp116His) c.352G>C (p.Asp118His) | |
9 | g.94606922C>T | CA5136179 | FBP1 | c.758G>A (n.758G>A) c.598G>A (p.Asp200Asn) c.403G>A (p.Asp135Asn) c.346G>A (p.Asp116Asn) c.352G>A (p.Asp118Asn) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
9 | g.94606923C>A | CA374107027 | FBP1 | c.757G>T (n.757G>T) c.597G>T (p.Lys199Asn) c.402G>T (p.Lys134Asn) c.345G>T (p.Lys115Asn) c.351G>T (p.Lys117Asn) | |
9 | g.94606923C= | CA1865226663 | FBP1 | c.757G= (n.757G=) c.597G= (p.Lys199=) c.402G= (p.Lys134=) c.345G= (p.Lys115=) c.351G= (p.Lys117=) | |
9 | g.94606923C>G | CA374107029 | FBP1 | c.757G>C (n.757G>C) c.597G>C (p.Lys199Asn) c.402G>C (p.Lys134Asn) c.345G>C (p.Lys115Asn) c.351G>C (p.Lys117Asn) | |
9 | g.94606923C>T | CA466100126 | FBP1 | c.757G>A (n.757G>A) c.597G>A (p.Lys199=) c.402G>A (p.Lys134=) c.345G>A (p.Lys115=) c.351G>A (p.Lys117=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
9 | g.94606924T>A | CA374107032 | FBP1 | c.756A>T (n.756A>T) c.596A>T (p.Lys199Met) c.401A>T (p.Lys134Met) c.344A>T (p.Lys115Met) c.350A>T (p.Lys117Met) | |
9 | g.94606924T>C | CA374107033 | FBP1 | c.756A>G (n.756A>G) c.596A>G (p.Lys199Arg) c.401A>G (p.Lys134Arg) c.344A>G (p.Lys115Arg) c.350A>G (p.Lys117Arg) | |
9 | g.94606924T>G | CA374107035 | FBP1 | c.756A>C (n.756A>C) c.596A>C (p.Lys199Thr) c.401A>C (p.Lys134Thr) c.344A>C (p.Lys115Thr) c.350A>C (p.Lys117Thr) | |
9 | g.94606925T>A | CA374107040 | FBP1 | c.755A>T (n.755A>T) c.595A>T (p.Lys199Ter) c.400A>T (p.Lys134Ter) c.343A>T (p.Lys115Ter) c.349A>T (p.Lys117Ter) | |
9 | g.94606925T>C | CA374107038 | FBP1 | c.755A>G (n.755A>G) c.595A>G (p.Lys199Glu) c.400A>G (p.Lys134Glu) c.343A>G (p.Lys115Glu) c.349A>G (p.Lys117Glu) | |
9 | g.94606925T>G | CA374107037 | FBP1 | c.755A>C (n.755A>C) c.595A>C (p.Lys199Gln) c.400A>C (p.Lys134Gln) c.343A>C (p.Lys115Gln) c.349A>C (p.Lys117Gln) | |
9 | g.94606926G>A | CA466100132 | FBP1 | c.754C>T (n.754C>T) c.594C>T (p.Asp198=) c.399C>T (p.Asp133=) c.342C>T (p.Asp114=) c.348C>T (p.Asp116=) | dbSNP gnomAD v2 gnomAD v4 |
9 | g.94606926G>C | CA374107042 | FBP1 | c.754C>G (n.754C>G) c.594C>G (p.Asp198Glu) c.399C>G (p.Asp133Glu) c.342C>G (p.Asp114Glu) c.348C>G (p.Asp116Glu) | |
9 | g.94606926G= | CA1865226664 | FBP1 | c.754C= (n.754C=) c.594C= (p.Asp198=) c.399C= (p.Asp133=) c.342C= (p.Asp114=) c.348C= (p.Asp116=) | |
9 | g.94606926G>T | CA374107044 | FBP1 | c.754C>A (n.754C>A) c.594C>A (p.Asp198Glu) c.399C>A (p.Asp133Glu) c.342C>A (p.Asp114Glu) c.348C>A (p.Asp116Glu) | |
9 | g.94606927T>A | CA374107046 | FBP1 | c.753A>T (n.753A>T) c.593A>T (p.Asp198Val) c.398A>T (p.Asp133Val) c.341A>T (p.Asp114Val) c.347A>T (p.Asp116Val) | |
9 | g.94606927T>C | CA374107048 | FBP1 | c.753A>G (n.753A>G) c.593A>G (p.Asp198Gly) c.398A>G (p.Asp133Gly) c.341A>G (p.Asp114Gly) c.347A>G (p.Asp116Gly) | |
9 | g.94606927T>G | CA374107049 | FBP1 | c.753A>C (n.753A>C) c.593A>C (p.Asp198Ala) c.398A>C (p.Asp133Ala) c.341A>C (p.Asp114Ala) c.347A>C (p.Asp116Ala) | |
9 | g.94606928C>A | CA374107051 | FBP1 | c.752G>T (n.752G>T) c.592G>T (p.Asp198Tyr) c.397G>T (p.Asp133Tyr) c.340G>T (p.Asp114Tyr) c.346G>T (p.Asp116Tyr) | |
9 | g.94606928C= | CA1865226665 | FBP1 | c.752G= (n.752G=) c.592G= (p.Asp198=) c.397G= (p.Asp133=) c.340G= (p.Asp114=) c.346G= (p.Asp116=) | |
9 | g.94606928C>G | CA374107053 | FBP1 | c.752G>C (n.752G>C) c.592G>C (p.Asp198His) c.397G>C (p.Asp133His) c.340G>C (p.Asp114His) c.346G>C (p.Asp116His) | |
9 | g.94606928C>T | CA374107055 | FBP1 | c.752G>A (n.752G>A) c.592G>A (p.Asp198Asn) c.397G>A (p.Asp133Asn) c.340G>A (p.Asp114Asn) c.346G>A (p.Asp116Asn) | dbSNP gnomAD v2 gnomAD v4 |
9 | g.94606929C>A | CA466100139 | FBP1 | c.751G>T (n.751G>T) c.591G>T (p.Val197=) c.396G>T (p.Val132=) c.339G>T (p.Val113=) c.345G>T (p.Val115=) | |
9 | g.94606929C>G | CA466100140 | FBP1 | c.751G>C (n.751G>C) c.591G>C (p.Val197=) c.396G>C (p.Val132=) c.339G>C (p.Val113=) c.345G>C (p.Val115=) | |
9 | g.94606929C>T | CA466100141 | FBP1 | c.751G>A (n.751G>A) c.591G>A (p.Val197=) c.396G>A (p.Val132=) c.339G>A (p.Val113=) c.345G>A (p.Val115=) | |
9 | g.94606930A>C | CA374107056 | FBP1 | c.750T>G (n.750T>G) c.590T>G (p.Val197Gly) c.395T>G (p.Val132Gly) c.338T>G (p.Val113Gly) c.344T>G (p.Val115Gly) | |
9 | g.94606930A>G | CA374107058 | FBP1 | c.750T>C (n.750T>C) c.590T>C (p.Val197Ala) c.395T>C (p.Val132Ala) c.338T>C (p.Val113Ala) c.344T>C (p.Val115Ala) | COSMIC |
9 | g.94606930A>T | CA374107060 | FBP1 | c.750T>A (n.750T>A) c.590T>A (p.Val197Glu) c.395T>A (p.Val132Glu) c.338T>A (p.Val113Glu) c.344T>A (p.Val115Glu) | |
9 | g.94606931C>A | CA374107062 | FBP1 | c.749G>T (n.749G>T) c.589G>T (p.Val197Leu) c.394G>T (p.Val132Leu) c.337G>T (p.Val113Leu) c.343G>T (p.Val115Leu) | |
9 | g.94606931C>G | CA374107064 | FBP1 | c.749G>C (n.749G>C) c.589G>C (p.Val197Leu) c.394G>C (p.Val132Leu) c.337G>C (p.Val113Leu) c.343G>C (p.Val115Leu) | |
9 | g.94606931C>T | CA374107066 | FBP1 | c.749G>A (n.749G>A) c.589G>A (p.Val197Met) c.394G>A (p.Val132Met) c.337G>A (p.Val113Met) c.343G>A (p.Val115Met) | gnomAD v4 |
9 | g.94606932C>A | CA374107069 | FBP1 | c.748G>T (n.748G>T) c.588G>T (p.Leu196Phe) c.393G>T (p.Leu131Phe) c.336G>T (p.Leu112Phe) c.342G>T (p.Leu114Phe) | |
9 | g.94606932C= | CA1865226666 | FBP1 | c.748G= (n.748G=) c.588G= (p.Leu196=) c.393G= (p.Leu131=) c.336G= (p.Leu112=) c.342G= (p.Leu114=) | |
9 | g.94606932C>G | CA374107067 | FBP1 | c.748G>C (n.748G>C) c.588G>C (p.Leu196Phe) c.393G>C (p.Leu131Phe) c.336G>C (p.Leu112Phe) c.342G>C (p.Leu114Phe) | |
9 | g.94606932C>T | CA466100147 | FBP1 | c.748G>A (n.748G>A) c.588G>A (p.Leu196=) c.393G>A (p.Leu131=) c.336G>A (p.Leu112=) c.342G>A (p.Leu114=) | dbSNP |
9 | g.94606933A>C | CA374107071 | FBP1 | c.747T>G (n.747T>G) c.587T>G (p.Leu196Trp) c.392T>G (p.Leu131Trp) c.335T>G (p.Leu112Trp) c.341T>G (p.Leu114Trp) | |
9 | g.94606933A>G | CA374107073 | FBP1 | c.747T>C (n.747T>C) c.587T>C (p.Leu196Ser) c.392T>C (p.Leu131Ser) c.335T>C (p.Leu112Ser) c.341T>C (p.Leu114Ser) | |
9 | g.94606933A>T | CA374107075 | FBP1 | c.747T>A (n.747T>A) c.587T>A (p.Leu196Ter) c.392T>A (p.Leu131Ter) c.335T>A (p.Leu112Ter) c.341T>A (p.Leu114Ter) | gnomAD v4 |
9 | g.94606936del | CA2690769346 | FBP1 | c.747del (n.747del) c.587del (p.Leu196TrpfsTer6) c.392del (p.Leu131TrpfsTer6) c.335del (p.Leu112TrpfsTer6) c.341del (p.Leu114TrpfsTer6) | gnomAD v4 |
9 | g.94606934A= | CA1865226667 | FBP1 | c.746T= (n.746T=) c.586T= (p.Leu196=) c.391T= (p.Leu131=) c.334T= (p.Leu112=) c.340T= (p.Leu114=) | |
9 | g.94606934A>C | CA374107077 | FBP1 | c.746T>G (n.746T>G) c.586T>G (p.Leu196Val) c.391T>G (p.Leu131Val) c.334T>G (p.Leu112Val) c.340T>G (p.Leu114Val) | |
9 | g.94606934A>G | CA466100151 | FBP1 | c.746T>C (n.746T>C) c.586T>C (p.Leu196=) c.391T>C (p.Leu131=) c.334T>C (p.Leu112=) c.340T>C (p.Leu114=) | ClinVar dbSNP gnomAD v4 |
9 | g.94606934A>T | CA374107079 | FBP1 | c.746T>A (n.746T>A) c.586T>A (p.Leu196Met) c.391T>A (p.Leu131Met) c.334T>A (p.Leu112Met) c.340T>A (p.Leu114Met) | COSMIC |
9 | g.94606935A>C | CA374107081 | FBP1 | c.745T>G (n.745T>G) c.585T>G (p.Ile195Met) c.390T>G (p.Ile130Met) c.333T>G (p.Ile111Met) c.339T>G (p.Ile113Met) | |
9 | g.94606935A>G | CA466100155 | FBP1 | c.745T>C (n.745T>C) c.585T>C (p.Ile195=) c.390T>C (p.Ile130=) c.333T>C (p.Ile111=) c.339T>C (p.Ile113=) | |
9 | g.94606935A>T | CA466100153 | FBP1 | c.745T>A (n.745T>A) c.585T>A (p.Ile195=) c.390T>A (p.Ile130=) c.333T>A (p.Ile111=) c.339T>A (p.Ile113=) | |
9 | g.94606935_94606936insCACACCCAACAC | CA2785154757 | FBP1 | c.744_745insGTGTTGGGTGTG (n.744_745insGTGTTGGGTGTG) c.584_585insGTGTTGGGTGTG (p.Ile195delinsMetCysTrpValCys) c.389_390insGTGTTGGGTGTG (p.Ile130delinsMetCysTrpValCys) c.332_333insGTGTTGGGTGTG (p.Ile111delinsMetCysTrpValCys) c.338_339insGTGTTGGGTGTG (p.Ile113delinsMetCysTrpValCys) | |
9 | g.94606935_94606936insCAACCAAACACACCCAACAC | CA2785154756 | FBP1 | c.744_745insGTGTTGGGTGTGTTTGGTTG (n.744_745insGTGTTGGGTGTGTTTGGTTG) c.584_585insGTGTTGGGTGTGTTTGGTTG (p.Ile195MetfsTer14) c.389_390insGTGTTGGGTGTGTTTGGTTG (p.Ile130MetfsTer14) c.332_333insGTGTTGGGTGTGTTTGGTTG (p.Ile111MetfsTer14) c.338_339insGTGTTGGGTGTGTTTGGTTG (p.Ile113MetfsTer14) | |
9 | g.94606936A>C | CA374107082 | FBP1 | c.744T>G (n.744T>G) c.584T>G (p.Ile195Ser) c.389T>G (p.Ile130Ser) c.332T>G (p.Ile111Ser) c.338T>G (p.Ile113Ser) | |
9 | g.94606936A>G | CA374107084 | FBP1 | c.744T>C (n.744T>C) c.584T>C (p.Ile195Thr) c.389T>C (p.Ile130Thr) c.332T>C (p.Ile111Thr) c.338T>C (p.Ile113Thr) | |
9 | g.94606936A>T | CA374107085 | FBP1 | c.744T>A (n.744T>A) c.584T>A (p.Ile195Asn) c.389T>A (p.Ile130Asn) c.332T>A (p.Ile111Asn) c.338T>A (p.Ile113Asn) | |
9 | g.94606937T>A | CA374107088 | FBP1 | c.743A>T (n.743A>T) c.583A>T (p.Ile195Phe) c.388A>T (p.Ile130Phe) c.331A>T (p.Ile111Phe) c.337A>T (p.Ile113Phe) | |
9 | g.94606937T>C | CA374107090 | FBP1 | c.743A>G (n.743A>G) c.583A>G (p.Ile195Val) c.388A>G (p.Ile130Val) c.331A>G (p.Ile111Val) c.337A>G (p.Ile113Val) | |
9 | g.94606937T>G | CA374107091 | FBP1 | c.743A>C (n.743A>C) c.583A>C (p.Ile195Leu) c.388A>C (p.Ile130Leu) c.331A>C (p.Ile111Leu) c.337A>C (p.Ile113Leu) | |
9 | g.94606938G>A | CA466100160 | FBP1 | c.742C>T (n.742C>T) c.582C>T (p.Phe194=) c.387C>T (p.Phe129=) c.330C>T (p.Phe110=) c.336C>T (p.Phe112=) | |
9 | g.94606938G>C | CA374107095 | FBP1 | c.742C>G (n.742C>G) c.582C>G (p.Phe194Leu) c.387C>G (p.Phe129Leu) c.330C>G (p.Phe110Leu) c.336C>G (p.Phe112Leu) | |
9 | g.94606938G>T | CA374107093 | FBP1 | c.742C>A (n.742C>A) c.582C>A (p.Phe194Leu) c.387C>A (p.Phe129Leu) c.330C>A (p.Phe110Leu) c.336C>A (p.Phe112Leu) | |
9 | g.94606939A= | CA1865226668 | FBP1 | c.741T= (n.741T=) c.581T= (p.Phe194=) c.386T= (p.Phe129=) c.329T= (p.Phe110=) c.335T= (p.Phe112=) | |
9 | g.94606939A>C | CA374107097 | FBP1 | c.741T>G (n.741T>G) c.581T>G (p.Phe194Cys) c.386T>G (p.Phe129Cys) c.329T>G (p.Phe110Cys) c.335T>G (p.Phe112Cys) | |
9 | g.94606939A>G | CA114590 | FBP1 | c.741T>C (n.741T>C) c.581T>C (p.Phe194Ser) c.386T>C (p.Phe129Ser) c.329T>C (p.Phe110Ser) c.335T>C (p.Phe112Ser) | ClinVar dbSNP gnomAD v4 |
9 | g.94606939A>T | CA374107099 | FBP1 | c.741T>A (n.741T>A) c.581T>A (p.Phe194Tyr) c.386T>A (p.Phe129Tyr) c.329T>A (p.Phe110Tyr) c.335T>A (p.Phe112Tyr) | |
9 | g.94606940A>C | CA374107102 | FBP1 | c.740T>G (n.740T>G) c.580T>G (p.Phe194Val) c.385T>G (p.Phe129Val) c.328T>G (p.Phe110Val) c.334T>G (p.Phe112Val) | |
9 | g.94606940A>G | CA374107104 | FBP1 | c.740T>C (n.740T>C) c.580T>C (p.Phe194Leu) c.385T>C (p.Phe129Leu) c.328T>C (p.Phe110Leu) c.334T>C (p.Phe112Leu) | |
9 | g.94606940A>T | CA374107106 | FBP1 | c.740T>A (n.740T>A) c.580T>A (p.Phe194Ile) c.385T>A (p.Phe129Ile) c.328T>A (p.Phe110Ile) c.334T>A (p.Phe112Ile) | |
9 | g.94606941C>A | CA374107110 | FBP1 | c.739G>T (n.739G>T) c.579G>T (p.Glu193Asp) c.384G>T (p.Glu128Asp) c.327G>T (p.Glu109Asp) c.333G>T (p.Glu111Asp) | |
9 | g.94606941C>G | CA374107108 | FBP1 | c.739G>C (n.739G>C) c.579G>C (p.Glu193Asp) c.384G>C (p.Glu128Asp) c.327G>C (p.Glu109Asp) c.333G>C (p.Glu111Asp) | |
9 | g.94606941C>T | CA466100169 | FBP1 | c.739G>A (n.739G>A) c.579G>A (p.Glu193=) c.384G>A (p.Glu128=) c.327G>A (p.Glu109=) c.333G>A (p.Glu111=) | dbSNP |
9 | g.94606942T>A | CA374107112 | FBP1 | c.738A>T (n.738A>T) c.578A>T (p.Glu193Val) c.383A>T (p.Glu128Val) c.326A>T (p.Glu109Val) c.332A>T (p.Glu111Val) | |
9 | g.94606942T>C | CA374107114 | FBP1 | c.738A>G (n.738A>G) c.578A>G (p.Glu193Gly) c.383A>G (p.Glu128Gly) c.326A>G (p.Glu109Gly) c.332A>G (p.Glu111Gly) | |
9 | g.94606942T>G | CA374107116 | FBP1 | c.738A>C (n.738A>C) c.578A>C (p.Glu193Ala) c.383A>C (p.Glu128Ala) c.326A>C (p.Glu109Ala) c.332A>C (p.Glu111Ala) | |
9 | g.94606942_94606943delinsTC | CA1865226669 | FBP1 | c.737_738delinsGA (n.737_738delinsGA) c.577_578delinsGA (p.Glu193=) c.382_383delinsGA (p.Glu128=) c.325_326delinsGA (p.Glu109=) c.331_332delinsGA (p.Glu111=) | |
9 | g.94606943C>A | CA374107118 | FBP1 | c.737G>T (n.737G>T) c.577G>T (p.Glu193Ter) c.382G>T (p.Glu128Ter) c.325G>T (p.Glu109Ter) c.331G>T (p.Glu111Ter) | ClinVar dbSNP |
9 | g.94606943C= | CA1865226670 | FBP1 | c.737G= (n.737G=) c.577G= (p.Glu193=) c.382G= (p.Glu128=) c.325G= (p.Glu109=) c.331G= (p.Glu111=) | |
9 | g.94606943C>G | CA374107119 | FBP1 | c.737G>C (n.737G>C) c.577G>C (p.Glu193Gln) c.382G>C (p.Glu128Gln) c.325G>C (p.Glu109Gln) c.331G>C (p.Glu111Gln) | |
9 | g.94606943C>T | CA374107120 | FBP1 | c.737G>A (n.737G>A) c.577G>A (p.Glu193Lys) c.382G>A (p.Glu128Lys) c.325G>A (p.Glu109Lys) c.331G>A (p.Glu111Lys) | |
9 | g.94606946dup | CA2695210726 | FBP1 | c.737dup (n.737dup) c.577dup (p.Glu193GlyfsTer16) c.382dup (p.Glu128GlyfsTer16) c.325dup (p.Glu109GlyfsTer16) c.331dup (p.Glu111GlyfsTer16) | |
9 | g.94606946del | CA589255093 | FBP1 | c.737del (n.737del) c.577del (p.Glu193SerfsTer9) c.382del (p.Glu128SerfsTer9) c.325del (p.Glu109SerfsTer9) c.331del (p.Glu111SerfsTer9) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.94606944C>A | CA466100175 | FBP1 | c.736G>T (n.736G>T) c.576G>T (p.Gly192=) c.381G>T (p.Gly127=) c.324G>T (p.Gly108=) c.330G>T (p.Gly110=) | |
9 | g.94606944C= | CA1865226671 | FBP1 | c.736G= (n.736G=) c.576G= (p.Gly192=) c.381G= (p.Gly127=) c.324G= (p.Gly108=) c.330G= (p.Gly110=) | |
9 | g.94606944C>G | CA466100176 | FBP1 | c.736G>C (n.736G>C) c.576G>C (p.Gly192=) c.381G>C (p.Gly127=) c.324G>C (p.Gly108=) c.330G>C (p.Gly110=) | |
9 | g.94606944C>T | CA466100178 | FBP1 | c.736G>A (n.736G>A) c.576G>A (p.Gly192=) c.381G>A (p.Gly127=) c.324G>A (p.Gly108=) c.330G>A (p.Gly110=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
9 | g.94606945C>A | CA374107123 | FBP1 | c.735G>T (n.735G>T) c.575G>T (p.Gly192Val) c.380G>T (p.Gly127Val) c.323G>T (p.Gly108Val) c.329G>T (p.Gly110Val) | |
9 | g.94606945C>G | CA374107127 | FBP1 | c.735G>C (n.735G>C) c.575G>C (p.Gly192Ala) c.380G>C (p.Gly127Ala) c.323G>C (p.Gly108Ala) c.329G>C (p.Gly110Ala) | |
9 | g.94606945C>T | CA374107125 | FBP1 | c.735G>A (n.735G>A) c.575G>A (p.Gly192Glu) c.380G>A (p.Gly127Glu) c.323G>A (p.Gly108Glu) c.329G>A (p.Gly110Glu) |