Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.68357670_68357675dupCA2695214911LRP5c.509_514dup (p.Gly171_Glu172insGlyGly)
c.-1257_-1252dup (n.-1257_-1252dup)
c.536_541dup (p.Gly180_Glu181insGlyGly)
n.551_556dup
11g.68357672_68357677delCA2695214912LRP5c.511_516del (p.Gly171_Glu172del)
c.-1255_-1250del (n.-1255_-1250del)
c.538_543del (p.Gly180_Glu181del)
n.553_558del
11g.68357672G>ACA381611681LRP5c.511G>A (p.Gly171Ser)
c.-1255G>A (n.-1255G>A)
c.538G>A (p.Gly180Ser)
n.553G>A
11g.68357672G>CCA118096LRP5c.511G>C (p.Gly171Arg)
c.-1255G>C (n.-1255G>C)
c.538G>C (p.Gly180Arg)
n.553G>C
ClinVar dbSNP
11g.68357672G=CA1980639659LRP5c.511G= (p.Gly171=)
c.-1255G= (n.-1255G=)
c.538G= (p.Gly180=)
n.553G=
11g.68357672G>TCA381611682LRP5c.511G>T (p.Gly171Cys)
c.-1255G>T (n.-1255G>T)
c.538G>T (p.Gly180Cys)
n.553G>T
11g.68357673G>ACA381611684LRP5c.512G>A (p.Gly171Asp)
c.-1254G>A (n.-1254G>A)
c.539G>A (p.Gly180Asp)
n.554G>A
gnomAD v4
11g.68357673G>CCA381611683LRP5c.512G>C (p.Gly171Ala)
c.-1254G>C (n.-1254G>C)
c.539G>C (p.Gly180Ala)
n.554G>C
ClinVar
11g.68357673G=CA1980639662LRP5c.512G= (p.Gly171=)
c.-1254G= (n.-1254G=)
c.539G= (p.Gly180=)
n.554G=
11g.68357673G>TCA118095LRP5c.512G>T (p.Gly171Val)
c.-1254G>T (n.-1254G>T)
c.539G>T (p.Gly180Val)
n.554G>T
ClinVar dbSNP gnomAD v4
11g.68357674T>ACA475460116LRP5c.513T>A (p.Gly171=)
c.-1253T>A (n.-1253T>A)
c.540T>A (p.Gly180=)
n.555T>A
gnomAD v4
11g.68357674T>CCA475460117LRP5c.513T>C (p.Gly171=)
c.-1253T>C (n.-1253T>C)
c.540T>C (p.Gly180=)
n.555T>C
11g.68357674T>GCA475460118LRP5c.513T>G (p.Gly171=)
c.-1253T>G (n.-1253T>G)
c.540T>G (p.Gly180=)
n.555T>G
dbSNP
11g.68357674T=CA1980639666LRP5c.513T= (p.Gly171=)
c.-1253T= (n.-1253T=)
c.540T= (p.Gly180=)
n.555T=
11g.68357675G>ACA381611685LRP5c.514G>A (p.Glu172Lys)
c.-1252G>A (n.-1252G>A)
c.541G>A (p.Glu181Lys)
n.556G>A
11g.68357675G>CCA381611686LRP5c.514G>C (p.Glu172Gln)
c.-1252G>C (n.-1252G>C)
c.541G>C (p.Glu181Gln)
n.556G>C
11g.68357675G=CA1980639669LRP5c.514G= (p.Glu172=)
c.-1252G= (n.-1252G=)
c.541G= (p.Glu181=)
n.556G=
11g.68357675G>TCA381611687LRP5c.514G>T (p.Glu172Ter)
c.-1252G>T (n.-1252G>T)
c.541G>T (p.Glu181Ter)
n.556G>T
11g.68357676A>CCA381611688LRP5c.515A>C (p.Glu172Ala)
c.-1251A>C (n.-1251A>C)
c.542A>C (p.Glu181Ala)
n.557A>C
11g.68357676A>GCA381611689LRP5c.515A>G (p.Glu172Gly)
c.-1251A>G (n.-1251A>G)
c.542A>G (p.Glu181Gly)
n.557A>G
11g.68357676A>TCA381611690LRP5c.515A>T (p.Glu172Val)
c.-1251A>T (n.-1251A>T)
c.542A>T (p.Glu181Val)
n.557A>T
11g.68357676dupCA1980639671LRP5c.515dup (p.Thr173AspfsTer5)
c.-1251dup (n.-1251dup)
c.542dup (p.Thr182AspfsTer5)
n.557dup
dbSNP
11g.68357677G>ACA475460119LRP5c.516G>A (p.Glu172=)
c.-1250G>A (n.-1250G>A)
c.543G>A (p.Glu181=)
n.558G>A
11g.68357677G>CCA381611691LRP5c.516G>C (p.Glu172Asp)
c.-1250G>C (n.-1250G>C)
c.543G>C (p.Glu181Asp)
n.558G>C
11g.68357677G>TCA381611692LRP5c.516G>T (p.Glu172Asp)
c.-1250G>T (n.-1250G>T)
c.543G>T (p.Glu181Asp)
n.558G>T
11g.68357678A=CA1980639673LRP5c.517A= (p.Thr173=)
c.-1249A= (n.-1249A=)
c.544A= (p.Thr182=)
n.559A=
11g.68357678A>CCA381611693LRP5c.517A>C (p.Thr173Pro)
c.-1249A>C (n.-1249A>C)
c.544A>C (p.Thr182Pro)
n.559A>C
11g.68357678A>GCA381611694LRP5c.517A>G (p.Thr173Ala)
c.-1249A>G (n.-1249A>G)
c.544A>G (p.Thr182Ala)
n.559A>G
dbSNP gnomAD v3 gnomAD v4
11g.68357678A>TCA381611695LRP5c.517A>T (p.Thr173Ser)
c.-1249A>T (n.-1249A>T)
c.544A>T (p.Thr182Ser)
n.559A>T
11g.68357679C>ACA381611696LRP5c.518C>A (p.Thr173Lys)
c.-1248C>A (n.-1248C>A)
c.545C>A (p.Thr182Lys)
n.560C>A
11g.68357679C=CA1980639679LRP5c.518C= (p.Thr173=)
c.-1248C= (n.-1248C=)
c.545C= (p.Thr182=)
n.560C=
11g.68357679C>GCA381611697LRP5c.518C>G (p.Thr173Arg)
c.-1248C>G (n.-1248C>G)
c.545C>G (p.Thr182Arg)
n.560C>G
11g.68357679C>TCA6149038LRP5c.518C>T (p.Thr173Met)
c.-1248C>T (n.-1248C>T)
c.545C>T (p.Thr182Met)
n.560C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.68357680G>ACA6149039LRP5c.519G>A (p.Thr173=)
c.-1247G>A (n.-1247G>A)
c.546G>A (p.Thr182=)
n.561G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
11g.68357680G>CCA475460121LRP5c.519G>C (p.Thr173=)
c.-1247G>C (n.-1247G>C)
c.546G>C (p.Thr182=)
n.561G>C
11g.68357680G=CA1980639682LRP5c.519G= (p.Thr173=)
c.-1247G= (n.-1247G=)
c.546G= (p.Thr182=)
n.561G=
11g.68357680G>TCA475460120LRP5c.519G>T (p.Thr173=)
c.-1247G>T (n.-1247G>T)
c.546G>T (p.Thr182=)
n.561G>T
11g.68357681C>ACA381611698LRP5c.520C>A (p.Pro174Thr)
c.-1246C>A (n.-1246C>A)
c.547C>A (p.Pro183Thr)
n.562C>A
11g.68357681C>GCA381611699LRP5c.520C>G (p.Pro174Ala)
c.-1246C>G (n.-1246C>G)
c.547C>G (p.Pro183Ala)
n.562C>G
11g.68357681C>TCA381611700LRP5c.520C>T (p.Pro174Ser)
c.-1246C>T (n.-1246C>T)
c.547C>T (p.Pro183Ser)
n.562C>T
11g.68357682C>ACA381611701LRP5c.521C>A (p.Pro174His)
c.-1245C>A (n.-1245C>A)
c.548C>A (p.Pro183His)
n.563C>A
11g.68357682C>GCA381611702LRP5c.521C>G (p.Pro174Arg)
c.-1245C>G (n.-1245C>G)
c.548C>G (p.Pro183Arg)
n.563C>G
11g.68357682C>TCA381611703LRP5c.521C>T (p.Pro174Leu)
c.-1245C>T (n.-1245C>T)
c.548C>T (p.Pro183Leu)
n.563C>T
11g.68357683C>ACA475460122LRP5c.522C>A (p.Pro174=)
c.-1244C>A (n.-1244C>A)
c.549C>A (p.Pro183=)
n.564C>A
11g.68357683C=CA1980639684LRP5c.522C= (p.Pro174=)
c.-1244C= (n.-1244C=)
c.549C= (p.Pro183=)
n.564C=
11g.68357683C>GCA475460123LRP5c.522C>G (p.Pro174=)
c.-1244C>G (n.-1244C>G)
c.549C>G (p.Pro183=)
n.564C>G
dbSNP gnomAD v3 gnomAD v4
11g.68357683C>TCA475460124LRP5c.522C>T (p.Pro174=)
c.-1244C>T (n.-1244C>T)
c.549C>T (p.Pro183=)
n.564C>T
11g.68357684C>ACA475460125LRP5c.523C>A (p.Arg175=)
c.-1243C>A (n.-1243C>A)
c.550C>A (p.Arg184=)
n.565C>A
11g.68357684C=CA1980639687LRP5c.523C= (p.Arg175=)
c.-1243C= (n.-1243C=)
c.550C= (p.Arg184=)
n.565C=
11g.68357684C>GCA6149040LRP5c.523C>G (p.Arg175Gly)
c.-1243C>G (n.-1243C>G)
c.550C>G (p.Arg184Gly)
n.565C>G
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4

Number of alleles fetched