Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.55039931_55039943delinsGAGGACGAGGACGCA1148406183PCSK9c.94_106delinsGAGGACGAGGACG (p.Glu32=)
c.451_463delinsGAGGACGAGGACG (p.Glu151=)
1g.55039938_55039943dupCA045097PCSK9c.101_106dup (p.Asp35_Gly36insGluAsp)
c.458_463dup (p.Asp154_Gly155insGluAsp)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.55039940_55039944delCA2645837444PCSK9c.103_107del (p.Asp35ArgfsTer?)
c.460_464del (p.Asp154ArgfsTer?)
gnomAD v4
1g.55039940G>ACA340482778PCSK9c.103G>A (p.Asp35Asn)
c.460G>A (p.Asp154Asn)
1g.55039940G>CCA340482779PCSK9c.103G>C (p.Asp35His)
c.460G>C (p.Asp154His)
gnomAD v4
1g.55039940G=CA1167976439PCSK9c.103G= (p.Asp35=)
c.460G= (p.Asp154=)
1g.55039940G>TCA034785PCSK9c.103G>T (p.Asp35Tyr)
c.460G>T (p.Asp154Tyr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.55039943_55039948dupCA2697552435PCSK9c.106_111dup (p.Asp37_Tyr38insGlyAsp)
c.463_468dup (p.Asp156_Tyr157insGlyAsp)
ClinVar
1g.55039941A>CCA340482782PCSK9c.104A>C (p.Asp35Ala)
c.461A>C (p.Asp154Ala)
1g.55039941A>GCA340482781PCSK9c.104A>G (p.Asp35Gly)
c.461A>G (p.Asp154Gly)
1g.55039941A>TCA340482780PCSK9c.104A>T (p.Asp35Val)
c.461A>T (p.Asp154Val)
1g.55039942C>ACA340482783PCSK9c.105C>A (p.Asp35Glu)
c.462C>A (p.Asp154Glu)
1g.55039942C=CA1144707896PCSK9c.105C= (p.Asp35=)
c.462C= (p.Asp154=)
1g.55039942C>GCA340482784PCSK9c.105C>G (p.Asp35Glu)
c.462C>G (p.Asp154Glu)
1g.55039942C>TCA034842PCSK9c.105C>T (p.Asp35=)
c.462C>T (p.Asp154=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.55039943G>ACA034887PCSK9c.106G>A (p.Gly36Ser)
c.463G>A (p.Gly155Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.55039943G>CCA340482785PCSK9c.106G>C (p.Gly36Arg)
c.463G>C (p.Gly155Arg)
gnomAD v4
1g.55039943G=CA1167976440PCSK9c.106G= (p.Gly36=)
c.463G= (p.Gly155=)
1g.55039943G>TCA340482786PCSK9c.106G>T (p.Gly36Cys)
c.463G>T (p.Gly155Cys)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
1g.55039944G>ACA340482787PCSK9c.107G>A (p.Gly36Asp)
c.464G>A (p.Gly155Asp)
ClinVar dbSNP gnomAD v2 gnomAD v4
1g.55039944G>CCA340482788PCSK9c.107G>C (p.Gly36Ala)
c.464G>C (p.Gly155Ala)
1g.55039944G=CA1167976441PCSK9c.107G= (p.Gly36=)
c.464G= (p.Gly155=)
1g.55039944G>TCA340482789PCSK9c.107G>T (p.Gly36Val)
c.464G>T (p.Gly155Val)
1g.55039945C>ACA417957357PCSK9c.108C>A (p.Gly36=)
c.465C>A (p.Gly155=)
ClinVar gnomAD v4
1g.55039945C=CA1167976442PCSK9c.108C= (p.Gly36=)
c.465C= (p.Gly155=)
1g.55039945C>GCA417957355PCSK9c.108C>G (p.Gly36=)
c.465C>G (p.Gly155=)
ClinVar
1g.55039945C>TCA417957356PCSK9c.108C>T (p.Gly36=)
c.465C>T (p.Gly155=)
ClinVar dbSNP gnomAD v2 gnomAD v4
1g.55039946G>ACA340482790PCSK9c.109G>A (p.Asp37Asn)
c.466G>A (p.Asp156Asn)
gnomAD v4
1g.55039946G>CCA340482791PCSK9c.109G>C (p.Asp37His)
c.466G>C (p.Asp156His)
1g.55039946G=CA1167976443PCSK9c.109G= (p.Asp37=)
c.466G= (p.Asp156=)
1g.55039946G>TCA340482792PCSK9c.109G>T (p.Asp37Tyr)
c.466G>T (p.Asp156Tyr)
dbSNP gnomAD v4
1g.55039947A>CCA340482795PCSK9c.110A>C (p.Asp37Ala)
c.467A>C (p.Asp156Ala)
1g.55039947A>GCA340482794PCSK9c.110A>G (p.Asp37Gly)
c.467A>G (p.Asp156Gly)
gnomAD v4
1g.55039947A>TCA340482793PCSK9c.110A>T (p.Asp37Val)
c.467A>T (p.Asp156Val)
1g.55039948C>ACA340482796PCSK9c.111C>A (p.Asp37Glu)
c.468C>A (p.Asp156Glu)
ClinVar dbSNP gnomAD v4
1g.55039948C=CA1167976444PCSK9c.111C= (p.Asp37=)
c.468C= (p.Asp156=)
1g.55039948C>GCA340482797PCSK9c.111C>G (p.Asp37Glu)
c.468C>G (p.Asp156Glu)
1g.55039948C>TCA417957361PCSK9c.111C>T (p.Asp37=)
c.468C>T (p.Asp156=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
1g.55039949delCA2743685338PCSK9c.112del (p.Tyr38ThrfsTer6)
c.469del (p.Tyr157ThrfsTer6)
1g.55039949T>ACA340482798PCSK9c.112T>A (p.Tyr38Asn)
c.469T>A (p.Tyr157Asn)
1g.55039949T>CCA22792057PCSK9c.112T>C (p.Tyr38His)
c.469T>C (p.Tyr157His)
dbSNP gnomAD v2 gnomAD v4
1g.55039949T>GCA340482799PCSK9c.112T>G (p.Tyr38Asp)
c.469T>G (p.Tyr157Asp)
1g.55039949T=CA1167976445PCSK9c.112T= (p.Tyr38=)
c.469T= (p.Tyr157=)
1g.55039950A>CCA340482800PCSK9c.113A>C (p.Tyr38Ser)
c.470A>C (p.Tyr157Ser)
1g.55039950A>GCA340482801PCSK9c.113A>G (p.Tyr38Cys)
c.470A>G (p.Tyr157Cys)
ClinVar gnomAD v4
1g.55039950A>TCA340482802PCSK9c.113A>T (p.Tyr38Phe)
c.470A>T (p.Tyr157Phe)
gnomAD v4
1g.55039951C>ACA340482803PCSK9c.114C>A (p.Tyr38Ter)
c.471C>A (p.Tyr157Ter)
gnomAD v4
1g.55039951C>GCA340482804PCSK9c.114C>G (p.Tyr38Ter)
c.471C>G (p.Tyr157Ter)
gnomAD v4
1g.55039951C>TCA417957364PCSK9c.114C>T (p.Tyr38=)
c.471C>T (p.Tyr157=)
ClinVar gnomAD v4
1g.55039952G>ACA035375PCSK9c.115G>A (p.Glu39Lys)
c.472G>A (p.Glu158Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4

Number of alleles fetched