Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.117527502_117531824delCA2580076333CFTRc.274-3397_489+710del
c.*171-3397_*386+710del
c.*98-3397_*313+710del
c.31-3397_246+710del
c.364-3397_579+710del
ClinVar
7g.117530896_117531112delinsTAGGAAGTCACCAAAGCAGTACAGCCTCTCTTACTGGGAAGAATCATAGCTTCCTATGACCCGGATAACAAGGAGGAACGCTCTATCGCGATTTATCTAGGCATAGGCTTATGCCTTCTCTTTATTGTGAGGACACTGCTCCTACACCCAGCCATTTTTGGCCTTCATCACATTGGAATGCAGATGAGAATAGCTATGTTTAGTTTGATTTATAAGACA1737359079CFTRc.274-3_487delinsTAGGAAGTCACCAAAGCAGTACAGCCTCTCTTACTGGGAAGAATCATAGCTTCCTATGACCCGGATAACAAGGAGGAACGCTCTATCGCGATTTATCTAGGCATAGGCTTATGCCTTCTCTTTATTGTGAGGACACTGCTCCTACACCCAGCCATTTTTGGCCTTCATCACATTGGAATGCAGATGAGAATAGCTATGTTTAGTTTGATTTATAAGA
c.*171-3_*384delinsTAGGAAGTCACCAAAGCAGTACAGCCTCTCTTACTGGGAAGAATCATAGCTTCCTATGACCCGGATAACAAGGAGGAACGCTCTATCGCGATTTATCTAGGCATAGGCTTATGCCTTCTCTTTATTGTGAGGACACTGCTCCTACACCCAGCCATTTTTGGCCTTCATCACATTGGAATGCAGATGAGAATAGCTATGTTTAGTTTGATTTATAAGA
c.*98-3_*311delinsTAGGAAGTCACCAAAGCAGTACAGCCTCTCTTACTGGGAAGAATCATAGCTTCCTATGACCCGGATAACAAGGAGGAACGCTCTATCGCGATTTATCTAGGCATAGGCTTATGCCTTCTCTTTATTGTGAGGACACTGCTCCTACACCCAGCCATTTTTGGCCTTCATCACATTGGAATGCAGATGAGAATAGCTATGTTTAGTTTGATTTATAAGA
c.31-3_244delinsTAGGAAGTCACCAAAGCAGTACAGCCTCTCTTACTGGGAAGAATCATAGCTTCCTATGACCCGGATAACAAGGAGGAACGCTCTATCGCGATTTATCTAGGCATAGGCTTATGCCTTCTCTTTATTGTGAGGACACTGCTCCTACACCCAGCCATTTTTGGCCTTCATCACATTGGAATGCAGATGAGAATAGCTATGTTTAGTTTGATTTATAAGA
c.364-3_577delinsTAGGAAGTCACCAAAGCAGTACAGCCTCTCTTACTGGGAAGAATCATAGCTTCCTATGACCCGGATAACAAGGAGGAACGCTCTATCGCGATTTATCTAGGCATAGGCTTATGCCTTCTCTTTATTGTGAGGACACTGCTCCTACACCCAGCCATTTTTGGCCTTCATCACATTGGAATGCAGATGAGAATAGCTATGTTTAGTTTGATTTATAAGA
7g.117530900_117531115delCA913189986CFTRc.275_489+1del
c.*172_*386+1del
c.*99_*313+1del
c.32_246+1del
c.365_579+1del
ClinVar dbSNP
7g.117530900_117534366delCA913189987CFTRc.275_579+1del
c.*172_*476+1del
c.*99_*403+1del
c.32_336+1del
c.275_490-882del
c.365_669+1del
ClinVar
7g.117530919_117530960delCA2695208292CFTRc.294_335del (p.Gln98_Asp112delinsHis)
c.*191_*232del (n.*191_*232del)
c.*118_*159del (n.*118_*159del)
c.51_92del (p.Gln17_Asp31delinsHis)
c.384_425del (p.Gln128_Asp142delinsHis)
7g.117530925_117530926delCA2580617092CFTRc.300_301del (p.Leu101ThrfsTer9)
c.*197_*198del (n.*197_*198del)
c.*124_*125del (n.*124_*125del)
c.57_58del (p.Leu20ThrfsTer9)
c.390_391del (p.Leu131ThrfsTer9)
ClinVar dbSNP
7g.117530923C>ACA368974270CFTRc.298C>A (p.Leu100Ile)
c.*195C>A (n.*195C>A)
c.*122C>A (n.*122C>A)
c.55C>A (p.Leu19Ile)
c.388C>A (p.Leu130Ile)
7g.117530923C=CA1737359169CFTRc.298C= (p.Leu100=)
c.*195C= (n.*195C=)
c.*122C= (n.*122C=)
c.55C= (p.Leu19=)
c.388C= (p.Leu130=)
7g.117530923C>GCA4450701CFTRc.298C>G (p.Leu100Val)
c.*195C>G (n.*195C>G)
c.*122C>G (n.*122C>G)
c.55C>G (p.Leu19Val)
c.388C>G (p.Leu130Val)
dbSNP ExAC gnomAD v2 gnomAD v4
7g.117530923C>TCA368974272CFTRc.298C>T (p.Leu100Phe)
c.*195C>T (n.*195C>T)
c.*122C>T (n.*122C>T)
c.55C>T (p.Leu19Phe)
c.388C>T (p.Leu130Phe)
ClinVar dbSNP
7g.117530924delCA2695208293CFTRc.299del (p.Leu100ProfsTer7)
c.*196del (n.*196del)
c.*123del (n.*123del)
c.56del (p.Leu19ProfsTer7)
c.389del (p.Leu130ProfsTer7)
7g.117530924T>ACA368974274CFTRc.299T>A (p.Leu100His)
c.*196T>A (n.*196T>A)
c.*123T>A (n.*123T>A)
c.56T>A (p.Leu19His)
c.389T>A (p.Leu130His)
ClinVar
7g.117530924T>CCA368974276CFTRc.299T>C (p.Leu100Pro)
c.*196T>C (n.*196T>C)
c.*123T>C (n.*123T>C)
c.56T>C (p.Leu19Pro)
c.389T>C (p.Leu130Pro)
7g.117530924T>GCA368974277CFTRc.299T>G (p.Leu100Arg)
c.*196T>G (n.*196T>G)
c.*123T>G (n.*123T>G)
c.56T>G (p.Leu19Arg)
c.389T>G (p.Leu130Arg)
dbSNP gnomAD v3 gnomAD v4 COSMIC
7g.117530924T=CA1737359172CFTRc.299T= (p.Leu100=)
c.*196T= (n.*196T=)
c.*123T= (n.*123T=)
c.56T= (p.Leu19=)
c.389T= (p.Leu130=)
7g.117530925C>ACA457448555CFTRc.300C>A (p.Leu100=)
c.*197C>A (n.*197C>A)
c.*124C>A (n.*124C>A)
c.57C>A (p.Leu19=)
c.390C>A (p.Leu130=)
7g.117530925C=CA1737359174CFTRc.300C= (p.Leu100=)
c.*197C= (n.*197C=)
c.*124C= (n.*124C=)
c.57C= (p.Leu19=)
c.390C= (p.Leu130=)
7g.117530925C>GCA457448557CFTRc.300C>G (p.Leu100=)
c.*197C>G (n.*197C>G)
c.*124C>G (n.*124C>G)
c.57C>G (p.Leu19=)
c.390C>G (p.Leu130=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.117530925C>TCA457448559CFTRc.300C>T (p.Leu100=)
c.*197C>T (n.*197C>T)
c.*124C>T (n.*124C>T)
c.57C>T (p.Leu19=)
c.390C>T (p.Leu130=)
ClinVar dbSNP
7g.117530926T>ACA368974280CFTRc.301T>A (p.Leu101Ile)
c.*198T>A (n.*198T>A)
c.*125T>A (n.*125T>A)
c.58T>A (p.Leu20Ile)
c.391T>A (p.Leu131Ile)
7g.117530926T>CCA457448561CFTRc.301T>C (p.Leu101=)
c.*198T>C (n.*198T>C)
c.*125T>C (n.*125T>C)
c.58T>C (p.Leu20=)
c.391T>C (p.Leu131=)
7g.117530926T>GCA368974282CFTRc.301T>G (p.Leu101Val)
c.*198T>G (n.*198T>G)
c.*125T>G (n.*125T>G)
c.58T>G (p.Leu20Val)
c.391T>G (p.Leu131Val)
7g.117530927T>ACA368974284CFTRc.302T>A (p.Leu101Ter)
c.*199T>A (n.*199T>A)
c.*126T>A (n.*126T>A)
c.59T>A (p.Leu20Ter)
c.392T>A (p.Leu131Ter)
7g.117530927T>CCA327018CFTRc.302T>C (p.Leu101Ser)
c.*199T>C (n.*199T>C)
c.*126T>C (n.*126T>C)
c.59T>C (p.Leu20Ser)
c.392T>C (p.Leu131Ser)
dbSNP
7g.117530927T>GCA327020CFTRc.302T>G (p.Leu101Ter)
c.*199T>G (n.*199T>G)
c.*126T>G (n.*126T>G)
c.59T>G (p.Leu20Ter)
c.392T>G (p.Leu131Ter)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
7g.117530927T=CA1737359183CFTRc.302T= (p.Leu101=)
c.*199T= (n.*199T=)
c.*126T= (n.*126T=)
c.59T= (p.Leu20=)
c.392T= (p.Leu131=)
7g.117530928A>CCA368974287CFTRc.303A>C (p.Leu101Phe)
c.*200A>C (n.*200A>C)
c.*127A>C (n.*127A>C)
c.60A>C (p.Leu20Phe)
c.393A>C (p.Leu131Phe)
gnomAD v4
7g.117530928A>GCA457448562CFTRc.303A>G (p.Leu101=)
c.*200A>G (n.*200A>G)
c.*127A>G (n.*127A>G)
c.60A>G (p.Leu20=)
c.393A>G (p.Leu131=)
ClinVar
7g.117530928A>TCA368974289CFTRc.303A>T (p.Leu101Phe)
c.*200A>T (n.*200A>T)
c.*127A>T (n.*127A>T)
c.60A>T (p.Leu20Phe)
c.393A>T (p.Leu131Phe)
COSMIC
7g.117530928dupCA327025CFTRc.303dup (p.Leu102ThrfsTer9)
c.*200dup (n.*200dup)
c.*127dup (n.*127dup)
c.60dup (p.Leu21ThrfsTer9)
c.393dup (p.Leu132ThrfsTer9)
ClinVar dbSNP
7g.117530929C>ACA368974291CFTRc.304C>A (p.Leu102Met)
c.*201C>A (n.*201C>A)
c.*128C>A (n.*128C>A)
c.61C>A (p.Leu21Met)
c.394C>A (p.Leu132Met)
7g.117530929C=CA1737359194CFTRc.304C= (p.Leu102=)
c.*201C= (n.*201C=)
c.*128C= (n.*128C=)
c.61C= (p.Leu21=)
c.394C= (p.Leu132=)
7g.117530929C>GCA368974293CFTRc.304C>G (p.Leu102Val)
c.*201C>G (n.*201C>G)
c.*128C>G (n.*128C>G)
c.61C>G (p.Leu21Val)
c.394C>G (p.Leu132Val)
dbSNP
7g.117530929C>TCA457448564CFTRc.304C>T (p.Leu102=)
c.*201C>T (n.*201C>T)
c.*128C>T (n.*128C>T)
c.61C>T (p.Leu21=)
c.394C>T (p.Leu132=)
ClinVar dbSNP
7g.117530930T>ACA368974295CFTRc.305T>A (p.Leu102Gln)
c.*202T>A (n.*202T>A)
c.*129T>A (n.*129T>A)
c.62T>A (p.Leu21Gln)
c.395T>A (p.Leu132Gln)
7g.117530930T>CCA327031CFTRc.305T>C (p.Leu102Pro)
c.*202T>C (n.*202T>C)
c.*129T>C (n.*129T>C)
c.62T>C (p.Leu21Pro)
c.395T>C (p.Leu132Pro)
ClinVar dbSNP
7g.117530930T>GCA4450702CFTRc.305T>G (p.Leu102Arg)
c.*202T>G (n.*202T>G)
c.*129T>G (n.*129T>G)
c.62T>G (p.Leu21Arg)
c.395T>G (p.Leu132Arg)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
7g.117530930T=CA1737359197CFTRc.305T= (p.Leu102=)
c.*202T= (n.*202T=)
c.*129T= (n.*129T=)
c.62T= (p.Leu21=)
c.395T= (p.Leu132=)
7g.117530930_117530931delinsTGCA1737359200CFTRc.305_306delinsTG (p.Leu102=)
c.*202_*203delinsTG (n.*202_*203delinsTG)
c.*129_*130delinsTG (n.*129_*130delinsTG)
c.62_63delinsTG (p.Leu21=)
c.395_396delinsTG (p.Leu132=)
7g.117530931G>ACA457448568CFTRc.306G>A (p.Leu102=)
c.*203G>A (n.*203G>A)
c.*130G>A (n.*130G>A)
c.63G>A (p.Leu21=)
c.396G>A (p.Leu132=)
7g.117530931G>CCA457448567CFTRc.306G>C (p.Leu102=)
c.*203G>C (n.*203G>C)
c.*130G>C (n.*130G>C)
c.63G>C (p.Leu21=)
c.396G>C (p.Leu132=)
7g.117530931G=CA1737359205CFTRc.306G= (p.Leu102=)
c.*203G= (n.*203G=)
c.*130G= (n.*130G=)
c.63G= (p.Leu21=)
c.396G= (p.Leu132=)
7g.117530931G>TCA457448566CFTRc.306G>T (p.Leu102=)
c.*203G>T (n.*203G>T)
c.*130G>T (n.*130G>T)
c.63G>T (p.Leu21=)
c.396G>T (p.Leu132=)
ClinVar dbSNP
7g.117530933delCA1737359204CFTRc.308del (p.Gly103GlufsTer4)
c.*205del (n.*205del)
c.*132del (n.*132del)
c.65del (p.Gly22GlufsTer4)
c.398del (p.Gly133GlufsTer4)
ClinVar dbSNP
7g.117530932G>ACA368974299CFTRc.307G>A (p.Gly103Arg)
c.*204G>A (n.*204G>A)
c.*131G>A (n.*131G>A)
c.64G>A (p.Gly22Arg)
c.397G>A (p.Gly133Arg)
ClinVar dbSNP
7g.117530932G>CCA368974301CFTRc.307G>C (p.Gly103Arg)
c.*204G>C (n.*204G>C)
c.*131G>C (n.*131G>C)
c.64G>C (p.Gly22Arg)
c.397G>C (p.Gly133Arg)
7g.117530932G=CA1737359208CFTRc.307G= (p.Gly103=)
c.*204G= (n.*204G=)
c.*131G= (n.*131G=)
c.64G= (p.Gly22=)
c.397G= (p.Gly133=)
7g.117530932G>TCA368974303CFTRc.307G>T (p.Gly103Ter)
c.*204G>T (n.*204G>T)
c.*131G>T (n.*131G>T)
c.64G>T (p.Gly22Ter)
c.397G>T (p.Gly133Ter)
ClinVar dbSNP
7g.117530933G>ACA368974305CFTRc.308G>A (p.Gly103Glu)
c.*205G>A (n.*205G>A)
c.*132G>A (n.*132G>A)
c.65G>A (p.Gly22Glu)
c.398G>A (p.Gly133Glu)
COSMIC
7g.117530933G>CCA368974307CFTRc.308G>C (p.Gly103Ala)
c.*205G>C (n.*205G>C)
c.*132G>C (n.*132G>C)
c.65G>C (p.Gly22Ala)
c.398G>C (p.Gly133Ala)

Number of alleles fetched