Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.117540097_117540344delinsTAGAACAGAACTGAAACTGACTCGGAAGGCAGCCTATGTGAGATACTTCAATAGCTCAGCCTTCTTCTTCTCAGGGTTCTTTGTGGTGTTTTTATCTGTGCTTCCCTATGCACTAATCAAAGGAATCATCCTCCGGAAAATATTCACCACCATCTCATTCTGCATTGTTCTGCGCATGGCGGTCACTCGGCAATTTCCCTGGGCTGTACAAACATGGTATGACTCTCTTGGAGCAATAAACAAAATACCA1737331753CFTRc.870-3_1114delinsTAGAACAGAACTGAAACTGACTCGGAAGGCAGCCTATGTGAGATACTTCAATAGCTCAGCCTTCTTCTTCTCAGGGTTCTTTGTGGTGTTTTTATCTGTGCTTCCCTATGCACTAATCAAAGGAATCATCCTCCGGAAAATATTCACCACCATCTCATTCTGCATTGTTCTGCGCATGGCGGTCACTCGGCAATTTCCCTGGGCTGTACAAACATGGTATGACTCTCTTGGAGCAATAAACAAAATAC
c.*767-3_*1011delinsTAGAACAGAACTGAAACTGACTCGGAAGGCAGCCTATGTGAGATACTTCAATAGCTCAGCCTTCTTCTTCTCAGGGTTCTTTGTGGTGTTTTTATCTGTGCTTCCCTATGCACTAATCAAAGGAATCATCCTCCGGAAAATATTCACCACCATCTCATTCTGCATTGTTCTGCGCATGGCGGTCACTCGGCAATTTCCCTGGGCTGTACAAACATGGTATGACTCTCTTGGAGCAATAAACAAAATAC
c.*694-3_*938delinsTAGAACAGAACTGAAACTGACTCGGAAGGCAGCCTATGTGAGATACTTCAATAGCTCAGCCTTCTTCTTCTCAGGGTTCTTTGTGGTGTTTTTATCTGTGCTTCCCTATGCACTAATCAAAGGAATCATCCTCCGGAAAATATTCACCACCATCTCATTCTGCATTGTTCTGCGCATGGCGGTCACTCGGCAATTTCCCTGGGCTGTACAAACATGGTATGACTCTCTTGGAGCAATAAACAAAATAC
c.627-3_871delinsTAGAACAGAACTGAAACTGACTCGGAAGGCAGCCTATGTGAGATACTTCAATAGCTCAGCCTTCTTCTTCTCAGGGTTCTTTGTGGTGTTTTTATCTGTGCTTCCCTATGCACTAATCAAAGGAATCATCCTCCGGAAAATATTCACCACCATCTCATTCTGCATTGTTCTGCGCATGGCGGTCACTCGGCAATTTCCCTGGGCTGTACAAACATGGTATGACTCTCTTGGAGCAATAAACAAAATAC
c.780-3_1024delinsTAGAACAGAACTGAAACTGACTCGGAAGGCAGCCTATGTGAGATACTTCAATAGCTCAGCCTTCTTCTTCTCAGGGTTCTTTGTGGTGTTTTTATCTGTGCTTCCCTATGCACTAATCAAAGGAATCATCCTCCGGAAAATATTCACCACCATCTCATTCTGCATTGTTCTGCGCATGGCGGTCACTCGGCAATTTCCCTGGGCTGTACAAACATGGTATGACTCTCTTGGAGCAATAAACAAAATAC
c.960-3_1204delinsTAGAACAGAACTGAAACTGACTCGGAAGGCAGCCTATGTGAGATACTTCAATAGCTCAGCCTTCTTCTTCTCAGGGTTCTTTGTGGTGTTTTTATCTGTGCTTCCCTATGCACTAATCAAAGGAATCATCCTCCGGAAAATATTCACCACCATCTCATTCTGCATTGTTCTGCGCATGGCGGTCACTCGGCAATTTCCCTGGGCTGTACAAACATGGTATGACTCTCTTGGAGCAATAAACAAAATAC
7g.117540100_117540346delCA913189992CFTRc.870_1116del
c.*767_*1013del
c.*694_*940del
c.627_873del
c.780_1026del
c.960_1206del
ClinVar dbSNP
7g.117540238_117540249dupCA326363CFTRc.1008_1019dup (p.Ile340_Ser341insPheThrThrIle)
c.*905_*916dup (n.*905_*916dup)
c.*832_*843dup (n.*832_*843dup)
c.765_776dup (p.Ile259_Ser260insPheThrThrIle)
c.918_929dup (p.Ile310_Ser311insPheThrThrIle)
c.1098_1109dup (p.Ile370_Ser371insPheThrThrIle)
ClinVar dbSNP
7g.117540246_117540248delCA2695208309CFTRc.1016_1018del (p.Thr339del)
c.*913_*915del (n.*913_*915del)
c.*840_*842del (n.*840_*842del)
c.773_775del (p.Thr258del)
c.926_928del (p.Thr309del)
c.1106_1108del (p.Thr369del)
7g.117540245A>CCA368978783CFTRc.1015A>C (p.Thr339Pro)
c.*912A>C (n.*912A>C)
c.*839A>C (n.*839A>C)
c.772A>C (p.Thr258Pro)
c.925A>C (p.Thr309Pro)
c.1105A>C (p.Thr369Pro)
7g.117540245A>GCA368978785CFTRc.1015A>G (p.Thr339Ala)
c.*912A>G (n.*912A>G)
c.*839A>G (n.*839A>G)
c.772A>G (p.Thr258Ala)
c.925A>G (p.Thr309Ala)
c.1105A>G (p.Thr369Ala)
7g.117540245A>TCA368978787CFTRc.1015A>T (p.Thr339Ser)
c.*912A>T (n.*912A>T)
c.*839A>T (n.*839A>T)
c.772A>T (p.Thr258Ser)
c.925A>T (p.Thr309Ser)
c.1105A>T (p.Thr369Ser)
7g.117540246C>ACA368978788CFTRc.1016C>A (p.Thr339Asn)
c.*913C>A (n.*913C>A)
c.*840C>A (n.*840C>A)
c.773C>A (p.Thr258Asn)
c.926C>A (p.Thr309Asn)
c.1106C>A (p.Thr369Asn)
ClinVar
7g.117540246C>GCA368978789CFTRc.1016C>G (p.Thr339Ser)
c.*913C>G (n.*913C>G)
c.*840C>G (n.*840C>G)
c.773C>G (p.Thr258Ser)
c.926C>G (p.Thr309Ser)
c.1106C>G (p.Thr369Ser)
ClinVar
7g.117540246C>TCA368978791CFTRc.1016C>T (p.Thr339Ile)
c.*913C>T (n.*913C>T)
c.*840C>T (n.*840C>T)
c.773C>T (p.Thr258Ile)
c.926C>T (p.Thr309Ile)
c.1106C>T (p.Thr369Ile)
7g.117540247C>ACA457448754CFTRc.1017C>A (p.Thr339=)
c.*914C>A (n.*914C>A)
c.*841C>A (n.*841C>A)
c.774C>A (p.Thr258=)
c.927C>A (p.Thr309=)
c.1107C>A (p.Thr369=)
dbSNP
7g.117540247C=CA1737332211CFTRc.1017C= (p.Thr339=)
c.*914C= (n.*914C=)
c.*841C= (n.*841C=)
c.774C= (p.Thr258=)
c.927C= (p.Thr309=)
c.1107C= (p.Thr369=)
7g.117540247C>GCA457448755CFTRc.1017C>G (p.Thr339=)
c.*914C>G (n.*914C>G)
c.*841C>G (n.*841C>G)
c.774C>G (p.Thr258=)
c.927C>G (p.Thr309=)
c.1107C>G (p.Thr369=)
7g.117540247C>TCA457448756CFTRc.1017C>T (p.Thr339=)
c.*914C>T (n.*914C>T)
c.*841C>T (n.*841C>T)
c.774C>T (p.Thr258=)
c.927C>T (p.Thr309=)
c.1107C>T (p.Thr369=)
ClinVar dbSNP
7g.117540247_117540248delinsCACA1737332212CFTRc.1017_1018delinsCA (p.Thr339=)
c.*914_*915delinsCA (n.*914_*915delinsCA)
c.*841_*842delinsCA (n.*841_*842delinsCA)
c.774_775delinsCA (p.Thr258=)
c.927_928delinsCA (p.Thr309=)
c.1107_1108delinsCA (p.Thr369=)
7g.117540248delCA326369CFTRc.1018del (p.Ile340SerfsTer29)
c.*915del (n.*915del)
c.*842del (n.*842del)
c.775del (p.Ile259SerfsTer29)
c.928del (p.Ile310SerfsTer29)
c.1108del (p.Ile370SerfsTer29)
dbSNP
7g.117540248A=CA1737332217CFTRc.1018A= (p.Ile340=)
c.*915A= (n.*915A=)
c.*842A= (n.*842A=)
c.775A= (p.Ile259=)
c.928A= (p.Ile310=)
c.1108A= (p.Ile370=)
7g.117540248A>CCA368978795CFTRc.1018A>C (p.Ile340Leu)
c.*915A>C (n.*915A>C)
c.*842A>C (n.*842A>C)
c.775A>C (p.Ile259Leu)
c.928A>C (p.Ile310Leu)
c.1108A>C (p.Ile370Leu)
7g.117540248A>GCA164953763CFTRc.1018A>G (p.Ile340Val)
c.*915A>G (n.*915A>G)
c.*842A>G (n.*842A>G)
c.775A>G (p.Ile259Val)
c.928A>G (p.Ile310Val)
c.1108A>G (p.Ile370Val)
ClinVar dbSNP gnomAD v2 gnomAD v4
7g.117540248A>TCA368978793CFTRc.1018A>T (p.Ile340Phe)
c.*915A>T (n.*915A>T)
c.*842A>T (n.*842A>T)
c.775A>T (p.Ile259Phe)
c.928A>T (p.Ile310Phe)
c.1108A>T (p.Ile370Phe)
7g.117540249T>ACA368978798CFTRc.1019T>A (p.Ile340Asn)
c.*916T>A (n.*916T>A)
c.*843T>A (n.*843T>A)
c.776T>A (p.Ile259Asn)
c.929T>A (p.Ile310Asn)
c.1109T>A (p.Ile370Asn)
ClinVar dbSNP gnomAD v4
7g.117540249T>CCA368978799CFTRc.1019T>C (p.Ile340Thr)
c.*916T>C (n.*916T>C)
c.*843T>C (n.*843T>C)
c.776T>C (p.Ile259Thr)
c.929T>C (p.Ile310Thr)
c.1109T>C (p.Ile370Thr)
7g.117540249T>GCA368978801CFTRc.1019T>G (p.Ile340Ser)
c.*916T>G (n.*916T>G)
c.*843T>G (n.*843T>G)
c.776T>G (p.Ile259Ser)
c.929T>G (p.Ile310Ser)
c.1109T>G (p.Ile370Ser)
7g.117540249T=CA1737332226CFTRc.1019T= (p.Ile340=)
c.*916T= (n.*916T=)
c.*843T= (n.*843T=)
c.776T= (p.Ile259=)
c.929T= (p.Ile310=)
c.1109T= (p.Ile370=)
7g.117540251_117540252dupCA340640CFTRc.1021_1022dup (p.Phe342HisfsTer28)
c.*918_*919dup (n.*918_*919dup)
c.*845_*846dup (n.*845_*846dup)
c.778_779dup (p.Phe261HisfsTer28)
c.931_932dup (p.Phe312HisfsTer28)
c.1111_1112dup (p.Phe372HisfsTer28)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.117540250C>ACA457448758CFTRc.1020C>A (p.Ile340=)
c.*917C>A (n.*917C>A)
c.*844C>A (n.*844C>A)
c.777C>A (p.Ile259=)
c.930C>A (p.Ile310=)
c.1110C>A (p.Ile370=)
7g.117540250C>GCA368978803CFTRc.1020C>G (p.Ile340Met)
c.*917C>G (n.*917C>G)
c.*844C>G (n.*844C>G)
c.777C>G (p.Ile259Met)
c.930C>G (p.Ile310Met)
c.1110C>G (p.Ile370Met)
dbSNP
7g.117540250C>TCA457448757CFTRc.1020C>T (p.Ile340=)
c.*917C>T (n.*917C>T)
c.*844C>T (n.*844C>T)
c.777C>T (p.Ile259=)
c.930C>T (p.Ile310=)
c.1110C>T (p.Ile370=)
7g.117540251T>ACA368978805CFTRc.1021T>A (p.Ser341Thr)
c.*918T>A (n.*918T>A)
c.*845T>A (n.*845T>A)
c.778T>A (p.Ser260Thr)
c.931T>A (p.Ser311Thr)
c.1111T>A (p.Ser371Thr)
7g.117540251T>CCA328077CFTRc.1021T>C (p.Ser341Pro)
c.*918T>C (n.*918T>C)
c.*845T>C (n.*845T>C)
c.778T>C (p.Ser260Pro)
c.931T>C (p.Ser311Pro)
c.1111T>C (p.Ser371Pro)
ClinVar dbSNP gnomAD v4
7g.117540251T>GCA368978807CFTRc.1021T>G (p.Ser341Ala)
c.*918T>G (n.*918T>G)
c.*845T>G (n.*845T>G)
c.778T>G (p.Ser260Ala)
c.931T>G (p.Ser311Ala)
c.1111T>G (p.Ser371Ala)
7g.117540251T=CA1737332236CFTRc.1021T= (p.Ser341=)
c.*918T= (n.*918T=)
c.*845T= (n.*845T=)
c.778T= (p.Ser260=)
c.931T= (p.Ser311=)
c.1111T= (p.Ser371=)
7g.117540252C>ACA368978808CFTRc.1022C>A (p.Ser341Ter)
c.*919C>A (n.*919C>A)
c.*846C>A (n.*846C>A)
c.779C>A (p.Ser260Ter)
c.932C>A (p.Ser311Ter)
c.1112C>A (p.Ser371Ter)
7g.117540252C>GCA368978809CFTRc.1022C>G (p.Ser341Ter)
c.*919C>G (n.*919C>G)
c.*846C>G (n.*846C>G)
c.779C>G (p.Ser260Ter)
c.932C>G (p.Ser311Ter)
c.1112C>G (p.Ser371Ter)
7g.117540252C>TCA368978810CFTRc.1022C>T (p.Ser341Leu)
c.*919C>T (n.*919C>T)
c.*846C>T (n.*846C>T)
c.779C>T (p.Ser260Leu)
c.932C>T (p.Ser311Leu)
c.1112C>T (p.Ser371Leu)
7g.117540252dupCA1737332247CFTRc.1022dup (p.Phe342IlefsTer22)
c.*919dup (n.*919dup)
c.*846dup (n.*846dup)
c.779dup (p.Phe261IlefsTer22)
c.932dup (p.Phe312IlefsTer22)
c.1112dup (p.Phe372IlefsTer22)
dbSNP
7g.117540253A=CA1737332250CFTRc.1023A= (p.Ser341=)
c.*920A= (n.*920A=)
c.*847A= (n.*847A=)
c.780A= (p.Ser260=)
c.933A= (p.Ser311=)
c.1113A= (p.Ser371=)
7g.117540253A>CCA457448759CFTRc.1023A>C (p.Ser341=)
c.*920A>C (n.*920A>C)
c.*847A>C (n.*847A>C)
c.780A>C (p.Ser260=)
c.933A>C (p.Ser311=)
c.1113A>C (p.Ser371=)
dbSNP gnomAD v4
7g.117540253A>GCA164953797CFTRc.1023A>G (p.Ser341=)
c.*920A>G (n.*920A>G)
c.*847A>G (n.*847A>G)
c.780A>G (p.Ser260=)
c.933A>G (p.Ser311=)
c.1113A>G (p.Ser371=)
dbSNP
7g.117540253A>TCA457448760CFTRc.1023A>T (p.Ser341=)
c.*920A>T (n.*920A>T)
c.*847A>T (n.*847A>T)
c.780A>T (p.Ser260=)
c.933A>T (p.Ser311=)
c.1113A>T (p.Ser371=)
7g.117540254T>ACA368978815CFTRc.1024T>A (p.Phe342Ile)
c.*921T>A (n.*921T>A)
c.*848T>A (n.*848T>A)
c.781T>A (p.Phe261Ile)
c.934T>A (p.Phe312Ile)
c.1114T>A (p.Phe372Ile)
7g.117540254T>CCA368978813CFTRc.1024T>C (p.Phe342Leu)
c.*921T>C (n.*921T>C)
c.*848T>C (n.*848T>C)
c.781T>C (p.Phe261Leu)
c.934T>C (p.Phe312Leu)
c.1114T>C (p.Phe372Leu)
7g.117540254T>GCA368978814CFTRc.1024T>G (p.Phe342Val)
c.*921T>G (n.*921T>G)
c.*848T>G (n.*848T>G)
c.781T>G (p.Phe261Val)
c.934T>G (p.Phe312Val)
c.1114T>G (p.Phe372Val)
7g.117540255T>ACA368978817CFTRc.1025T>A (p.Phe342Tyr)
c.*922T>A (n.*922T>A)
c.*849T>A (n.*849T>A)
c.782T>A (p.Phe261Tyr)
c.935T>A (p.Phe312Tyr)
c.1115T>A (p.Phe372Tyr)
7g.117540255T>CCA368978818CFTRc.1025T>C (p.Phe342Ser)
c.*922T>C (n.*922T>C)
c.*849T>C (n.*849T>C)
c.782T>C (p.Phe261Ser)
c.935T>C (p.Phe312Ser)
c.1115T>C (p.Phe372Ser)
7g.117540255T>GCA368978820CFTRc.1025T>G (p.Phe342Cys)
c.*922T>G (n.*922T>G)
c.*849T>G (n.*849T>G)
c.782T>G (p.Phe261Cys)
c.935T>G (p.Phe312Cys)
c.1115T>G (p.Phe372Cys)
7g.117540256_117540257dupCA2573332342CFTRc.1026_1027dup (p.Cys343SerfsTer27)
c.*923_*924dup (n.*923_*924dup)
c.*850_*851dup (n.*850_*851dup)
c.783_784dup (p.Cys262SerfsTer27)
c.936_937dup (p.Cys313SerfsTer27)
c.1116_1117dup (p.Cys373SerfsTer27)
7g.117540256C>ACA368978822CFTRc.1026C>A (p.Phe342Leu)
c.*923C>A (n.*923C>A)
c.*850C>A (n.*850C>A)
c.783C>A (p.Phe261Leu)
c.936C>A (p.Phe312Leu)
c.1116C>A (p.Phe372Leu)
7g.117540256C=CA1737332253CFTRc.1026C= (p.Phe342=)
c.*923C= (n.*923C=)
c.*850C= (n.*850C=)
c.783C= (p.Phe261=)
c.936C= (p.Phe312=)
c.1116C= (p.Phe372=)
7g.117540256C>GCA368978823CFTRc.1026C>G (p.Phe342Leu)
c.*923C>G (n.*923C>G)
c.*850C>G (n.*850C>G)
c.783C>G (p.Phe261Leu)
c.936C>G (p.Phe312Leu)
c.1116C>G (p.Phe372Leu)

Number of alleles fetched