Chr Mutation (hg38) CAid Gene Transcript Linkouts
6g.136898142_136898241delCA2695207084PEX7c.804_903del
c.*69_*168del
c.492_591del
c.690_789del
c.684_783del
c.510_609del
c.527_*26del
6g.136898155delCA658823309PEX7c.817del (p.Ser273GlnfsTer20)
c.*82del (n.*82del)
c.505del
c.703del (p.Ser235GlnfsTer20)
c.697del (p.Ser233GlnfsTer20)
c.523del (p.Ser175GlnfsTer20)
c.540del (p.Gln181LysfsTer3)
ClinVar dbSNP
6g.136898153T>ACA365766550PEX7c.815T>A (p.Phe272Tyr)
c.*80T>A (n.*80T>A)
c.503T>A
c.701T>A (p.Phe234Tyr)
c.695T>A (p.Phe232Tyr)
c.521T>A (p.Phe174Tyr)
c.538T>A (p.Phe180Ile)
6g.136898153T>CCA365766551PEX7c.815T>C (p.Phe272Ser)
c.*80T>C (n.*80T>C)
c.503T>C
c.701T>C (p.Phe234Ser)
c.695T>C (p.Phe232Ser)
c.521T>C (p.Phe174Ser)
c.538T>C (p.Phe180Leu)
6g.136898153T>GCA365766552PEX7c.815T>G (p.Phe272Cys)
c.*80T>G (n.*80T>G)
c.503T>G
c.701T>G (p.Phe234Cys)
c.695T>G (p.Phe232Cys)
c.521T>G (p.Phe174Cys)
c.538T>G (p.Phe180Val)
6g.136898154T>ACA365766553PEX7c.816T>A (p.Phe272Leu)
c.*81T>A (n.*81T>A)
c.504T>A
c.702T>A (p.Phe234Leu)
c.696T>A (p.Phe232Leu)
c.522T>A (p.Phe174Leu)
c.539T>A (p.Phe180Tyr)
6g.136898154T>CCA452231776PEX7c.816T>C (p.Phe272=)
c.*81T>C (n.*81T>C)
c.504T>C
c.702T>C (p.Phe234=)
c.696T>C (p.Phe232=)
c.522T>C (p.Phe174=)
c.539T>C (p.Phe180Ser)
6g.136898154T>GCA365766554PEX7c.816T>G (p.Phe272Leu)
c.*81T>G (n.*81T>G)
c.504T>G
c.702T>G (p.Phe234Leu)
c.696T>G (p.Phe232Leu)
c.522T>G (p.Phe174Leu)
c.539T>G (p.Phe180Cys)
6g.136898155T>ACA365766555PEX7c.817T>A (p.Ser273Thr)
c.*82T>A (n.*82T>A)
c.505T>A
c.703T>A (p.Ser235Thr)
c.697T>A (p.Ser233Thr)
c.523T>A (p.Ser175Thr)
c.540T>A (p.Phe180Leu)
6g.136898155T>CCA365766556PEX7c.817T>C (p.Ser273Pro)
c.*82T>C (n.*82T>C)
c.505T>C
c.703T>C (p.Ser235Pro)
c.697T>C (p.Ser233Pro)
c.523T>C (p.Ser175Pro)
c.540T>C (p.Phe180=)
6g.136898155T>GCA365766557PEX7c.817T>G (p.Ser273Ala)
c.*82T>G (n.*82T>G)
c.505T>G
c.703T>G (p.Ser235Ala)
c.697T>G (p.Ser233Ala)
c.523T>G (p.Ser175Ala)
c.540T>G (p.Phe180Leu)
6g.136898156C>ACA365766560PEX7c.818C>A (p.Ser273Ter)
c.*83C>A (n.*83C>A)
c.506C>A
c.704C>A (p.Ser235Ter)
c.698C>A (p.Ser233Ter)
c.524C>A (p.Ser175Ter)
c.541C>A (p.Gln181Lys)
6g.136898156C>GCA365766558PEX7c.818C>G (p.Ser273Ter)
c.*83C>G (n.*83C>G)
c.506C>G
c.704C>G (p.Ser235Ter)
c.698C>G (p.Ser233Ter)
c.524C>G (p.Ser175Ter)
c.541C>G (p.Gln181Glu)
ClinVar dbSNP gnomAD v2 gnomAD v4
6g.136898156C>TCA365766559PEX7c.818C>T (p.Ser273Leu)
c.*83C>T (n.*83C>T)
c.506C>T
c.704C>T (p.Ser235Leu)
c.698C>T (p.Ser233Leu)
c.524C>T (p.Ser175Leu)
c.541C>T (p.Gln181Ter)
6g.136898157A>CCA452231777PEX7c.819A>C (p.Ser273=)
c.*84A>C (n.*84A>C)
c.507A>C
c.705A>C (p.Ser235=)
c.699A>C (p.Ser233=)
c.525A>C (p.Ser175=)
c.542A>C (p.Gln181Pro)
6g.136898157A>GCA452231778PEX7c.819A>G (p.Ser273=)
c.*84A>G (n.*84A>G)
c.507A>G
c.705A>G (p.Ser235=)
c.699A>G (p.Ser233=)
c.525A>G (p.Ser175=)
c.542A>G (p.Gln181Arg)
dbSNP gnomAD v2 gnomAD v4
6g.136898157A>TCA452231779PEX7c.819A>T (p.Ser273=)
c.*84A>T (n.*84A>T)
c.507A>T
c.705A>T (p.Ser235=)
c.699A>T (p.Ser233=)
c.525A>T (p.Ser175=)
c.542A>T (p.Gln181Leu)
6g.136898158A>CCA365766561PEX7c.820A>C (p.Lys274Gln)
c.*85A>C (n.*85A>C)
c.508A>C
c.706A>C (p.Lys236Gln)
c.700A>C (p.Lys234Gln)
c.526A>C (p.Lys176Gln)
c.543A>C (p.Gln181His)
6g.136898158A>GCA365766562PEX7c.820A>G (p.Lys274Glu)
c.*85A>G (n.*85A>G)
c.508A>G
c.706A>G (p.Lys236Glu)
c.700A>G (p.Lys234Glu)
c.526A>G (p.Lys176Glu)
c.543A>G (p.Gln181=)
6g.136898158A>TCA365766563PEX7c.820A>T (p.Lys274Ter)
c.*85A>T (n.*85A>T)
c.508A>T
c.706A>T (p.Lys236Ter)
c.700A>T (p.Lys234Ter)
c.526A>T (p.Lys176Ter)
c.543A>T (p.Gln181His)
6g.136898159A>CCA365766564PEX7c.821A>C (p.Lys274Thr)
c.*86A>C (n.*86A>C)
c.509A>C
c.707A>C (p.Lys236Thr)
c.701A>C (p.Lys234Thr)
c.527A>C (p.Lys176Thr)
c.544A>C (p.Ser182Arg)
6g.136898159A>GCA365766565PEX7c.821A>G (p.Lys274Arg)
c.*86A>G (n.*86A>G)
c.509A>G
c.707A>G (p.Lys236Arg)
c.701A>G (p.Lys234Arg)
c.527A>G (p.Lys176Arg)
c.544A>G (p.Ser182Gly)
6g.136898159A>TCA365766566PEX7c.821A>T (p.Lys274Met)
c.*86A>T (n.*86A>T)
c.509A>T
c.707A>T (p.Lys236Met)
c.701A>T (p.Lys234Met)
c.527A>T (p.Lys176Met)
c.544A>T (p.Ser182Cys)
6g.136898160G>ACA452231780PEX7c.822G>A (p.Lys274=)
c.*87G>A (n.*87G>A)
c.510G>A
c.708G>A (p.Lys236=)
c.702G>A (p.Lys234=)
c.528G>A (p.Lys176=)
c.545G>A (p.Ser182Asn)
ClinVar dbSNP
6g.136898160G>CCA365766567PEX7c.822G>C (p.Lys274Asn)
c.*87G>C (n.*87G>C)
c.510G>C
c.708G>C (p.Lys236Asn)
c.702G>C (p.Lys234Asn)
c.528G>C (p.Lys176Asn)
c.545G>C (p.Ser182Thr)
6g.136898160G>TCA365766568PEX7c.822G>T (p.Lys274Asn)
c.*87G>T (n.*87G>T)
c.510G>T
c.708G>T (p.Lys236Asn)
c.702G>T (p.Lys234Asn)
c.528G>T (p.Lys176Asn)
c.545G>T (p.Ser182Ile)
6g.136898161C>ACA365766569PEX7c.823C>A (p.Pro275Thr)
c.*88C>A (n.*88C>A)
c.511C>A
c.709C>A (p.Pro237Thr)
c.703C>A (p.Pro235Thr)
c.529C>A (p.Pro177Thr)
c.546C>A (p.Ser182Arg)
gnomAD v4
6g.136898161C>GCA365766570PEX7c.823C>G (p.Pro275Ala)
c.*88C>G (n.*88C>G)
c.511C>G
c.709C>G (p.Pro237Ala)
c.703C>G (p.Pro235Ala)
c.529C>G (p.Pro177Ala)
c.546C>G (p.Ser182Arg)
gnomAD v4
6g.136898161C>TCA4017780PEX7c.823C>T (p.Pro275Ser)
c.*88C>T (n.*88C>T)
c.511C>T
c.709C>T (p.Pro237Ser)
c.703C>T (p.Pro235Ser)
c.529C>T (p.Pro177Ser)
c.546C>T (p.Ser182=)
dbSNP ExAC gnomAD v2 gnomAD v4
6g.136898162C>ACA365766573PEX7c.824C>A (p.Pro275His)
c.*89C>A (n.*89C>A)
c.512C>A
c.710C>A (p.Pro237His)
c.704C>A (p.Pro235His)
c.530C>A (p.Pro177His)
c.547C>A (p.Leu183Met)
6g.136898162C>GCA365766572PEX7c.824C>G (p.Pro275Arg)
c.*89C>G (n.*89C>G)
c.512C>G
c.710C>G (p.Pro237Arg)
c.704C>G (p.Pro235Arg)
c.530C>G (p.Pro177Arg)
c.547C>G (p.Leu183Val)
6g.136898162C>TCA365766571PEX7c.824C>T (p.Pro275Leu)
c.*89C>T (n.*89C>T)
c.512C>T
c.710C>T (p.Pro237Leu)
c.704C>T (p.Pro235Leu)
c.530C>T (p.Pro177Leu)
c.547C>T (p.Leu183=)
6g.136898163T>ACA452231781PEX7c.825T>A (p.Pro275=)
c.*90T>A (n.*90T>A)
c.513T>A
c.711T>A (p.Pro237=)
c.705T>A (p.Pro235=)
c.531T>A (p.Pro177=)
c.548T>A (p.Leu183Gln)
6g.136898163T>CCA452231782PEX7c.825T>C (p.Pro275=)
c.*90T>C (n.*90T>C)
c.513T>C
c.711T>C (p.Pro237=)
c.705T>C (p.Pro235=)
c.531T>C (p.Pro177=)
c.548T>C (p.Leu183Pro)
6g.136898163T>GCA452231783PEX7c.825T>G (p.Pro275=)
c.*90T>G (n.*90T>G)
c.513T>G
c.711T>G (p.Pro237=)
c.705T>G (p.Pro235=)
c.531T>G (p.Pro177=)
c.548T>G (p.Leu183Arg)
6g.136898164G>ACA365766574PEX7c.826G>A (p.Asp276Asn)
c.*91G>A (n.*91G>A)
c.514G>A
c.712G>A (p.Asp238Asn)
c.706G>A (p.Asp236Asn)
c.532G>A (p.Asp178Asn)
c.549G>A (p.Leu183=)
6g.136898164G>CCA365766575PEX7c.826G>C (p.Asp276His)
c.*91G>C (n.*91G>C)
c.514G>C
c.712G>C (p.Asp238His)
c.706G>C (p.Asp236His)
c.532G>C (p.Asp178His)
c.549G>C (p.Leu183=)
6g.136898164G>TCA365766577PEX7c.826G>T (p.Asp276Tyr)
c.*91G>T (n.*91G>T)
c.514G>T
c.712G>T (p.Asp238Tyr)
c.706G>T (p.Asp236Tyr)
c.532G>T (p.Asp178Tyr)
c.549G>T (p.Leu183=)
6g.136898165A>CCA365766579PEX7c.827A>C (p.Asp276Ala)
c.*92A>C (n.*92A>C)
c.515A>C
c.713A>C (p.Asp238Ala)
c.707A>C (p.Asp236Ala)
c.533A>C (p.Asp178Ala)
c.550A>C (p.Thr184Pro)
6g.136898165A>GCA365766581PEX7c.827A>G (p.Asp276Gly)
c.*92A>G (n.*92A>G)
c.515A>G
c.713A>G (p.Asp238Gly)
c.707A>G (p.Asp236Gly)
c.533A>G (p.Asp178Gly)
c.550A>G (p.Thr184Ala)
6g.136898165A>TCA365766582PEX7c.827A>T (p.Asp276Val)
c.*92A>T (n.*92A>T)
c.515A>T
c.713A>T (p.Asp238Val)
c.707A>T (p.Asp236Val)
c.533A>T (p.Asp178Val)
c.550A>T (p.Thr184Ser)
6g.136898166C>ACA365766586PEX7c.828C>A (p.Asp276Glu)
c.*93C>A (n.*93C>A)
c.516C>A
c.714C>A (p.Asp238Glu)
c.708C>A (p.Asp236Glu)
c.534C>A (p.Asp178Glu)
c.551C>A (p.Thr184Asn)
6g.136898166C>GCA365766584PEX7c.828C>G (p.Asp276Glu)
c.*93C>G (n.*93C>G)
c.516C>G
c.714C>G (p.Asp238Glu)
c.708C>G (p.Asp236Glu)
c.534C>G (p.Asp178Glu)
c.551C>G (p.Thr184Ser)
gnomAD v4 COSMIC
6g.136898166C>TCA452231784PEX7c.828C>T (p.Asp276=)
c.*93C>T (n.*93C>T)
c.516C>T
c.714C>T (p.Asp238=)
c.708C>T (p.Asp236=)
c.534C>T (p.Asp178=)
c.551C>T (p.Thr184Ile)
ClinVar
6g.136898170_136898171delCA645549445PEX7c.832_833del (p.Leu278SerfsTer2)
c.*97_*98del (n.*97_*98del)
c.520_521del
c.718_719del (p.Leu240SerfsTer2)
c.712_713del (p.Leu238SerfsTer2)
c.538_539del (p.Leu180SerfsTer2)
c.555_556del (p.Phe186LeufsTer?)
COSMIC
6g.136898167T>ACA365766588PEX7c.829T>A (p.Ser277Thr)
c.*94T>A (n.*94T>A)
c.517T>A
c.715T>A (p.Ser239Thr)
c.709T>A (p.Ser237Thr)
c.535T>A (p.Ser179Thr)
c.552T>A (p.Thr184=)
6g.136898167T>CCA365766589PEX7c.829T>C (p.Ser277Pro)
c.*94T>C (n.*94T>C)
c.517T>C
c.715T>C (p.Ser239Pro)
c.709T>C (p.Ser237Pro)
c.535T>C (p.Ser179Pro)
c.552T>C (p.Thr184=)
gnomAD v4
6g.136898167T>GCA365766591PEX7c.829T>G (p.Ser277Ala)
c.*94T>G (n.*94T>G)
c.517T>G
c.715T>G (p.Ser239Ala)
c.709T>G (p.Ser237Ala)
c.535T>G (p.Ser179Ala)
c.552T>G (p.Thr184=)
6g.136898168C>ACA365766592PEX7c.830C>A (p.Ser277Tyr)
c.*95C>A (n.*95C>A)
c.518C>A
c.716C>A (p.Ser239Tyr)
c.710C>A (p.Ser237Tyr)
c.536C>A (p.Ser179Tyr)
c.553C>A (p.Leu185Ile)
6g.136898168C>GCA365766594PEX7c.830C>G (p.Ser277Cys)
c.*95C>G (n.*95C>G)
c.518C>G
c.716C>G (p.Ser239Cys)
c.710C>G (p.Ser237Cys)
c.536C>G (p.Ser179Cys)
c.553C>G (p.Leu185Val)
ClinVar

Number of alleles fetched