Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.68363778_68363795dupCA2614711311LRP5c.718_735dup (p.Leu245_Ser246insProPheAlaLeuThrLeu)
c.-1048_-1031dup (n.-1048_-1031dup)
c.745_762dup (p.Leu254_Ser255insProPheAlaLeuThrLeu)
n.760_777dup
 gnomAD v4
11g.68363784G>ACA118097LRP5c.724G>A (p.Ala242Thr)
c.-1042G>A (n.-1042G>A)
c.751G>A (p.Ala251Thr)
n.766G>A
 ClinVar dbSNP gnomAD v4 COSMIC
11g.68363784G>CCA381610977LRP5c.724G>C (p.Ala242Pro)
c.-1042G>C (n.-1042G>C)
c.751G>C (p.Ala251Pro)
n.766G>C
11g.68363784G=CA1980645800LRP5c.724G= (p.Ala242=)
c.-1042G= (n.-1042G=)
c.751G= (p.Ala251=)
n.766G=
11g.68363784G>TCA381610978LRP5c.724G>T (p.Ala242Ser)
c.-1042G>T (n.-1042G>T)
c.751G>T (p.Ala251Ser)
n.766G>T
 gnomAD v4
11g.68363785C>ACA381610979LRP5c.725C>A (p.Ala242Asp)
c.-1041C>A (n.-1041C>A)
c.752C>A (p.Ala251Asp)
n.767C>A
11g.68363785C>GCA381610980LRP5c.725C>G (p.Ala242Gly)
c.-1041C>G (n.-1041C>G)
c.752C>G (p.Ala251Gly)
n.767C>G
11g.68363785C>TCA381610981LRP5c.725C>T (p.Ala242Val)
c.-1041C>T (n.-1041C>T)
c.752C>T (p.Ala251Val)
n.767C>T
11g.68363786C>ACA475460247LRP5c.726C>A (p.Ala242=)
c.-1040C>A (n.-1040C>A)
c.753C>A (p.Ala251=)
n.768C>A
11g.68363786C>GCA475460248LRP5c.726C>G (p.Ala242=)
c.-1040C>G (n.-1040C>G)
c.753C>G (p.Ala251=)
n.768C>G
11g.68363786C>TCA475460249LRP5c.726C>T (p.Ala242=)
c.-1040C>T (n.-1040C>T)
c.753C>T (p.Ala251=)
n.768C>T
11g.68363787C>ACA381610982LRP5c.727C>A (p.Leu243Met)
c.-1039C>A (n.-1039C>A)
c.754C>A (p.Leu252Met)
n.769C>A
11g.68363787C>GCA381610983LRP5c.727C>G (p.Leu243Val)
c.-1039C>G (n.-1039C>G)
c.754C>G (p.Leu252Val)
n.769C>G
11g.68363787C>TCA475460250LRP5c.727C>T (p.Leu243=)
c.-1039C>T (n.-1039C>T)
c.754C>T (p.Leu252=)
n.769C>T
11g.68363788T>ACA381610984LRP5c.728T>A (p.Leu243Gln)
c.-1038T>A (n.-1038T>A)
c.755T>A (p.Leu252Gln)
n.770T>A
11g.68363788T>CCA381610985LRP5c.728T>C (p.Leu243Pro)
c.-1038T>C (n.-1038T>C)
c.755T>C (p.Leu252Pro)
n.770T>C
11g.68363788T>GCA381610986LRP5c.728T>G (p.Leu243Arg)
c.-1038T>G (n.-1038T>G)
c.755T>G (p.Leu252Arg)
n.770T>G
11g.68363789G>ACA475460251LRP5c.729G>A (p.Leu243=)
c.-1037G>A (n.-1037G>A)
c.756G>A (p.Leu252=)
n.771G>A
 gnomAD v4
11g.68363789G>CCA475460252LRP5c.729G>C (p.Leu243=)
c.-1037G>C (n.-1037G>C)
c.756G>C (p.Leu252=)
n.771G>C
11g.68363789G>TCA475460253LRP5c.729G>T (p.Leu243=)
c.-1037G>T (n.-1037G>T)
c.756G>T (p.Leu252=)
n.771G>T
11g.68363790A>CCA381610987LRP5c.730A>C (p.Thr244Pro)
c.-1036A>C (n.-1036A>C)
c.757A>C (p.Thr253Pro)
n.772A>C
11g.68363790A>GCA381610989LRP5c.730A>G (p.Thr244Ala)
c.-1036A>G (n.-1036A>G)
c.757A>G (p.Thr253Ala)
n.772A>G
11g.68363790A>TCA381610988LRP5c.730A>T (p.Thr244Ser)
c.-1036A>T (n.-1036A>T)
c.757A>T (p.Thr253Ser)
n.772A>T
11g.68363791C>ACA381610990LRP5c.731C>A (p.Thr244Lys)
c.-1035C>A (n.-1035C>A)
c.758C>A (p.Thr253Lys)
n.773C>A
11g.68363791C=CA1980645814LRP5c.731C= (p.Thr244=)
c.-1035C= (n.-1035C=)
c.758C= (p.Thr253=)
n.773C=
11g.68363791C>GCA381610991LRP5c.731C>G (p.Thr244Arg)
c.-1035C>G (n.-1035C>G)
c.758C>G (p.Thr253Arg)
n.773C>G
 dbSNP gnomAD v3 gnomAD v4
11g.68363791C>TCA130818LRP5c.731C>T (p.Thr244Met)
c.-1035C>T (n.-1035C>T)
c.758C>T (p.Thr253Met)
n.773C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
11g.68363792G>ACA475460254LRP5c.732G>A (p.Thr244=)
c.-1034G>A (n.-1034G>A)
c.759G>A (p.Thr253=)
n.774G>A
 ClinVar dbSNP gnomAD v3 gnomAD v4
11g.68363792G>CCA475460255LRP5c.732G>C (p.Thr244=)
c.-1034G>C (n.-1034G>C)
c.759G>C (p.Thr253=)
n.774G>C
11g.68363792G=CA1980645817LRP5c.732G= (p.Thr244=)
c.-1034G= (n.-1034G=)
c.759G= (p.Thr253=)
n.774G=
11g.68363792G>TCA475460256LRP5c.732G>T (p.Thr244=)
c.-1034G>T (n.-1034G>T)
c.759G>T (p.Thr253=)
n.774G>T
11g.68363793C>ACA381610992LRP5c.733C>A (p.Leu245Ile)
c.-1033C>A (n.-1033C>A)
c.760C>A (p.Leu254Ile)
n.775C>A
11g.68363793C>GCA381610994LRP5c.733C>G (p.Leu245Val)
c.-1033C>G (n.-1033C>G)
c.760C>G (p.Leu254Val)
n.775C>G
11g.68363793C>TCA381610993LRP5c.733C>T (p.Leu245Phe)
c.-1033C>T (n.-1033C>T)
c.760C>T (p.Leu254Phe)
n.775C>T
11g.68363794T>ACA381610995LRP5c.734T>A (p.Leu245His)
c.-1032T>A (n.-1032T>A)
c.761T>A (p.Leu254His)
n.776T>A
11g.68363794T>CCA381610996LRP5c.734T>C (p.Leu245Pro)
c.-1032T>C (n.-1032T>C)
c.761T>C (p.Leu254Pro)
n.776T>C
11g.68363794T>GCA381610997LRP5c.734T>G (p.Leu245Arg)
c.-1032T>G (n.-1032T>G)
c.761T>G (p.Leu254Arg)
n.776T>G
11g.68363795C>ACA475460257LRP5c.735C>A (p.Leu245=)
c.-1031C>A (n.-1031C>A)
c.762C>A (p.Leu254=)
n.777C>A
11g.68363795C=CA1980645823LRP5c.735C= (p.Leu245=)
c.-1031C= (n.-1031C=)
c.762C= (p.Leu254=)
n.777C=
11g.68363795C>GCA475460258LRP5c.735C>G (p.Leu245=)
c.-1031C>G (n.-1031C>G)
c.762C>G (p.Leu254=)
n.777C>G
11g.68363795C>TCA475460259LRP5c.735C>T (p.Leu245=)
c.-1031C>T (n.-1031C>T)
c.762C>T (p.Leu254=)
n.777C>T
 dbSNP gnomAD v3 gnomAD v4
11g.68363796T>ACA381610998LRP5c.736T>A (p.Ser246Thr)
c.-1030T>A (n.-1030T>A)
c.763T>A (p.Ser255Thr)
n.778T>A
11g.68363796T>CCA381610999LRP5c.736T>C (p.Ser246Pro)
c.-1030T>C (n.-1030T>C)
c.763T>C (p.Ser255Pro)
n.778T>C
11g.68363796T>GCA381611000LRP5c.736T>G (p.Ser246Ala)
c.-1030T>G (n.-1030T>G)
c.763T>G (p.Ser255Ala)
n.778T>G
11g.68363797C>ACA381611001LRP5c.737C>A (p.Ser246Tyr)
c.-1029C>A (n.-1029C>A)
c.764C>A (p.Ser255Tyr)
n.779C>A
11g.68363797C>GCA381611002LRP5c.737C>G (p.Ser246Cys)
c.-1029C>G (n.-1029C>G)
c.764C>G (p.Ser255Cys)
n.779C>G
11g.68363797C>TCA381611003LRP5c.737C>T (p.Ser246Phe)
c.-1029C>T (n.-1029C>T)
c.764C>T (p.Ser255Phe)
n.779C>T
11g.68363798C>ACA475460260LRP5c.738C>A (p.Ser246=)
c.-1028C>A (n.-1028C>A)
c.765C>A (p.Ser255=)
n.780C>A
 gnomAD v4
11g.68363798C=CA1980645825LRP5c.738C= (p.Ser246=)
c.-1028C= (n.-1028C=)
c.765C= (p.Ser255=)
n.780C=
11g.68363798C>GCA475460261LRP5c.738C>G (p.Ser246=)
c.-1028C>G (n.-1028C>G)
c.765C>G (p.Ser255=)
n.780C>G
11g.68363798C>TCA6149098LRP5c.738C>T (p.Ser246=)
c.-1028C>T (n.-1028C>T)
c.765C>T (p.Ser255=)
n.780C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.68363799G>ACA6149099LRP5c.739G>A (p.Gly247Arg)
c.-1027G>A (n.-1027G>A)
c.766G>A (p.Gly256Arg)
n.781G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.68363799G>CCA381611005LRP5c.739G>C (p.Gly247Arg)
c.-1027G>C (n.-1027G>C)
c.766G>C (p.Gly256Arg)
n.781G>C
11g.68363799G=CA1980645829LRP5c.739G= (p.Gly247=)
c.-1027G= (n.-1027G=)
c.766G= (p.Gly256=)
n.781G=
11g.68363799G>TCA381611004LRP5c.739G>T (p.Gly247Trp)
c.-1027G>T (n.-1027G>T)
c.766G>T (p.Gly256Trp)
n.781G>T
 gnomAD v4
11g.68363800G>ACA6149100LRP5c.740G>A (p.Gly247Glu)
c.-1026G>A (n.-1026G>A)
c.767G>A (p.Gly256Glu)
n.782G>A
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.68363800G>CCA381611006LRP5c.740G>C (p.Gly247Ala)
c.-1026G>C (n.-1026G>C)
c.767G>C (p.Gly256Ala)
n.782G>C
11g.68363800G=CA1980645835LRP5c.740G= (p.Gly247=)
c.-1026G= (n.-1026G=)
c.767G= (p.Gly256=)
n.782G=
11g.68363800G>TCA381611007LRP5c.740G>T (p.Gly247Val)
c.-1026G>T (n.-1026G>T)
c.767G>T (p.Gly256Val)
n.782G>T
11g.68363801G>ACA475460262LRP5c.741G>A (p.Gly247=)
c.-1025G>A (n.-1025G>A)
c.768G>A (p.Gly256=)
n.783G>A
 ClinVar dbSNP gnomAD v4
11g.68363801G>CCA475460263LRP5c.741G>C (p.Gly247=)
c.-1025G>C (n.-1025G>C)
c.768G>C (p.Gly256=)
n.783G>C
 dbSNP gnomAD v3 gnomAD v4
11g.68363801G=CA1980645837LRP5c.741G= (p.Gly247=)
c.-1025G= (n.-1025G=)
c.768G= (p.Gly256=)
n.783G=
11g.68363801G>TCA475460264LRP5c.741G>T (p.Gly247=)
c.-1025G>T (n.-1025G>T)
c.768G>T (p.Gly256=)
n.783G>T
11g.68363802G>ACA381611008LRP5c.742G>A (p.Asp248Asn)
c.-1024G>A (n.-1024G>A)
c.769G>A (p.Asp257Asn)
n.784G>A
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.68363802G>CCA381611009LRP5c.742G>C (p.Asp248His)
c.-1024G>C (n.-1024G>C)
c.769G>C (p.Asp257His)
n.784G>C
11g.68363802G=CA1980645839LRP5c.742G= (p.Asp248=)
c.-1024G= (n.-1024G=)
c.769G= (p.Asp257=)
n.784G=
11g.68363802G>TCA381611010LRP5c.742G>T (p.Asp248Tyr)
c.-1024G>T (n.-1024G>T)
c.769G>T (p.Asp257Tyr)
n.784G>T
11g.68363803A>CCA381611011LRP5c.743A>C (p.Asp248Ala)
c.-1023A>C (n.-1023A>C)
c.770A>C (p.Asp257Ala)
n.785A>C
11g.68363803A>GCA381611012LRP5c.743A>G (p.Asp248Gly)
c.-1023A>G (n.-1023A>G)
c.770A>G (p.Asp257Gly)
n.785A>G
11g.68363803A>TCA381611013LRP5c.743A>T (p.Asp248Val)
c.-1023A>T (n.-1023A>T)
c.770A>T (p.Asp257Val)
n.785A>T
 gnomAD v4
11g.68363804C>ACA381611014LRP5c.744C>A (p.Asp248Glu)
c.-1022C>A (n.-1022C>A)
c.771C>A (p.Asp257Glu)
n.786C>A
 dbSNP gnomAD v4
11g.68363804C=CA1980645842LRP5c.744C= (p.Asp248=)
c.-1022C= (n.-1022C=)
c.771C= (p.Asp257=)
n.786C=
11g.68363804C>GCA381611015LRP5c.744C>G (p.Asp248Glu)
c.-1022C>G (n.-1022C>G)
c.771C>G (p.Asp257Glu)
n.786C>G
11g.68363804C>TCA475460265LRP5c.744C>T (p.Asp248=)
c.-1022C>T (n.-1022C>T)
c.771C>T (p.Asp257=)
n.786C>T
 ClinVar dbSNP gnomAD v4
11g.68363805A>CCA381611017LRP5c.745A>C (p.Thr249Pro)
c.-1021A>C (n.-1021A>C)
c.772A>C (p.Thr258Pro)
n.787A>C
 gnomAD v4
11g.68363805A>GCA381611018LRP5c.745A>G (p.Thr249Ala)
c.-1021A>G (n.-1021A>G)
c.772A>G (p.Thr258Ala)
n.787A>G
 ClinVar
11g.68363805A>TCA381611016LRP5c.745A>T (p.Thr249Ser)
c.-1021A>T (n.-1021A>T)
c.772A>T (p.Thr258Ser)
n.787A>T
11g.68363805_68363807delinsACTCA1980645846LRP5c.745_747delinsACT (p.Thr249=)
c.-1021_-1019delinsACT (n.-1021_-1019delinsACT)
c.772_774delinsACT (p.Thr258=)
n.787_789delinsACT
11g.68363806C>ACA381611019LRP5c.746C>A (p.Thr249Asn)
c.-1020C>A (n.-1020C>A)
c.773C>A (p.Thr258Asn)
n.788C>A
11g.68363806C=CA1980645848LRP5c.746C= (p.Thr249=)
c.-1020C= (n.-1020C=)
c.773C= (p.Thr258=)
n.788C=
11g.68363806C>GCA381611020LRP5c.746C>G (p.Thr249Ser)
c.-1020C>G (n.-1020C>G)
c.773C>G (p.Thr258Ser)
n.788C>G
11g.68363806C>TCA6149102LRP5c.746C>T (p.Thr249Ile)
c.-1020C>T (n.-1020C>T)
c.773C>T (p.Thr258Ile)
n.788C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.68363808_68363809delCA6149101LRP5c.748_749del (p.Leu250ValfsTer?)
c.-1018_-1017del (n.-1018_-1017del)
c.775_776del (p.Leu259ValfsTer?)
n.790_791del
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.68363807T>ACA6149103LRP5c.747T>A (p.Thr249=)
c.-1019T>A (n.-1019T>A)
c.774T>A (p.Thr258=)
n.789T>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.68363807T>CCA475460266LRP5c.747T>C (p.Thr249=)
c.-1019T>C (n.-1019T>C)
c.774T>C (p.Thr258=)
n.789T>C
11g.68363807T>GCA475460267LRP5c.747T>G (p.Thr249=)
c.-1019T>G (n.-1019T>G)
c.774T>G (p.Thr258=)
n.789T>G
 gnomAD v4
11g.68363807T=CA1980645851LRP5c.747T= (p.Thr249=)
c.-1019T= (n.-1019T=)
c.774T= (p.Thr258=)
n.789T=
11g.68363808C>ACA381611022LRP5c.748C>A (p.Leu250Met)
c.-1018C>A (n.-1018C>A)
c.775C>A (p.Leu259Met)
n.790C>A
11g.68363808C>GCA381611021LRP5c.748C>G (p.Leu250Val)
c.-1018C>G (n.-1018C>G)
c.775C>G (p.Leu259Val)
n.790C>G
11g.68363808C>TCA475460268LRP5c.748C>T (p.Leu250=)
c.-1018C>T (n.-1018C>T)
c.775C>T (p.Leu259=)
n.790C>T
11g.68363809T>ACA381611023LRP5c.749T>A (p.Leu250Gln)
c.-1017T>A (n.-1017T>A)
c.776T>A (p.Leu259Gln)
n.791T>A
11g.68363809T>CCA381611024LRP5c.749T>C (p.Leu250Pro)
c.-1017T>C (n.-1017T>C)
c.776T>C (p.Leu259Pro)
n.791T>C
11g.68363809T>GCA381611025LRP5c.749T>G (p.Leu250Arg)
c.-1017T>G (n.-1017T>G)
c.776T>G (p.Leu259Arg)
n.791T>G
11g.68363810G>ACA475460269LRP5c.750G>A (p.Leu250=)
c.-1016G>A (n.-1016G>A)
c.777G>A (p.Leu259=)
n.792G>A
11g.68363810G>CCA475460270LRP5c.750G>C (p.Leu250=)
c.-1016G>C (n.-1016G>C)
c.777G>C (p.Leu259=)
n.792G>C
11g.68363810G>TCA475460271LRP5c.750G>T (p.Leu250=)
c.-1016G>T (n.-1016G>T)
c.777G>T (p.Leu259=)
n.792G>T
11g.68363811T>ACA381611026LRP5c.751T>A (p.Tyr251Asn)
c.-1015T>A (n.-1015T>A)
c.778T>A (p.Tyr260Asn)
n.793T>A
11g.68363811T>CCA381611027LRP5c.751T>C (p.Tyr251His)
c.-1015T>C (n.-1015T>C)
c.778T>C (p.Tyr260His)
n.793T>C
11g.68363811T>GCA381611028LRP5c.751T>G (p.Tyr251Asp)
c.-1015T>G (n.-1015T>G)
c.778T>G (p.Tyr260Asp)
n.793T>G
11g.68363812A>CCA381611029LRP5c.752A>C (p.Tyr251Ser)
c.-1014A>C (n.-1014A>C)
c.779A>C (p.Tyr260Ser)
n.794A>C
 gnomAD v4
11g.68363812A>GCA381611031LRP5c.752A>G (p.Tyr251Cys)
c.-1014A>G (n.-1014A>G)
c.779A>G (p.Tyr260Cys)
n.794A>G
 gnomAD v4
11g.68363812A>TCA381611030LRP5c.752A>T (p.Tyr251Phe)
c.-1014A>T (n.-1014A>T)
c.779A>T (p.Tyr260Phe)
n.794A>T
11g.68363813C>ACA381611032LRP5c.753C>A (p.Tyr251Ter)
c.-1013C>A (n.-1013C>A)
c.780C>A (p.Tyr260Ter)
n.795C>A
11g.68363813C=CA1980645855LRP5c.753C= (p.Tyr251=)
c.-1013C= (n.-1013C=)
c.780C= (p.Tyr260=)
n.795C=
11g.68363813C>GCA381611033LRP5c.753C>G (p.Tyr251Ter)
c.-1013C>G (n.-1013C>G)
c.780C>G (p.Tyr260Ter)
n.795C>G
11g.68363813C>TCA6149104LRP5c.753C>T (p.Tyr251=)
c.-1013C>T (n.-1013C>T)
c.780C>T (p.Tyr260=)
n.795C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.68363814T>ACA381611034LRP5c.754T>A (p.Trp252Arg)
c.-1012T>A (n.-1012T>A)
c.781T>A (p.Trp261Arg)
n.796T>A
11g.68363814T>CCA381611035LRP5c.754T>C (p.Trp252Arg)
c.-1012T>C (n.-1012T>C)
c.781T>C (p.Trp261Arg)
n.796T>C
11g.68363814T>GCA6149105LRP5c.754T>G (p.Trp252Gly)
c.-1012T>G (n.-1012T>G)
c.781T>G (p.Trp261Gly)
n.796T>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.68363814T=CA1980645859LRP5c.754T= (p.Trp252=)
c.-1012T= (n.-1012T=)
c.781T= (p.Trp261=)
n.796T=
11g.68363815G>ACA381611036LRP5c.755G>A (p.Trp252Ter)
c.-1011G>A (n.-1011G>A)
c.782G>A (p.Trp261Ter)
n.797G>A
11g.68363815G>CCA381611037LRP5c.755G>C (p.Trp252Ser)
c.-1011G>C (n.-1011G>C)
c.782G>C (p.Trp261Ser)
n.797G>C
11g.68363815G>TCA381611038LRP5c.755G>T (p.Trp252Leu)
c.-1011G>T (n.-1011G>T)
c.782G>T (p.Trp261Leu)
n.797G>T
 COSMIC
11g.68363816G>ACA6149106LRP5c.756G>A (p.Trp252Ter)
c.-1010G>A (n.-1010G>A)
c.783G>A (p.Trp261Ter)
n.798G>A
 dbSNP ExAC gnomAD v2
11g.68363816G>CCA381611039LRP5c.756G>C (p.Trp252Cys)
c.-1010G>C (n.-1010G>C)
c.783G>C (p.Trp261Cys)
n.798G>C
11g.68363816G=CA1980645862LRP5c.756G= (p.Trp252=)
c.-1010G= (n.-1010G=)
c.783G= (p.Trp261=)
n.798G=
11g.68363816G>TCA381611040LRP5c.756G>T (p.Trp252Cys)
c.-1010G>T (n.-1010G>T)
c.783G>T (p.Trp261Cys)
n.798G>T
11g.68363817A>CCA381611043LRP5c.757A>C (p.Thr253Pro)
c.-1009A>C (n.-1009A>C)
c.784A>C (p.Thr262Pro)
n.799A>C
11g.68363817A>GCA381611042LRP5c.757A>G (p.Thr253Ala)
c.-1009A>G (n.-1009A>G)
c.784A>G (p.Thr262Ala)
n.799A>G
11g.68363817A>TCA381611041LRP5c.757A>T (p.Thr253Ser)
c.-1009A>T (n.-1009A>T)
c.784A>T (p.Thr262Ser)
n.799A>T
11g.68363818C>ACA381611045LRP5c.758C>A (p.Thr253Lys)
c.-1008C>A (n.-1008C>A)
c.785C>A (p.Thr262Lys)
n.800C>A
 ClinVar dbSNP
11g.68363818C=CA1980645870LRP5c.758C= (p.Thr253=)
c.-1008C= (n.-1008C=)
c.785C= (p.Thr262=)
n.800C=
11g.68363818C>GCA381611044LRP5c.758C>G (p.Thr253Arg)
c.-1008C>G (n.-1008C>G)
c.785C>G (p.Thr262Arg)
n.800C>G
11g.68363818C>TCA118100LRP5c.758C>T (p.Thr253Ile)
c.-1008C>T (n.-1008C>T)
c.785C>T (p.Thr262Ile)
n.800C>T
 ClinVar dbSNP
11g.68363819A=CA1980645873LRP5c.759A= (p.Thr253=)
c.-1007A= (n.-1007A=)
c.786A= (p.Thr262=)
n.801A=
11g.68363819A>CCA6149107LRP5c.759A>C (p.Thr253=)
c.-1007A>C (n.-1007A>C)
c.786A>C (p.Thr262=)
n.801A>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.68363819A>GCA475460272LRP5c.759A>G (p.Thr253=)
c.-1007A>G (n.-1007A>G)
c.786A>G (p.Thr262=)
n.801A>G
 gnomAD v4
11g.68363819A>TCA475460273LRP5c.759A>T (p.Thr253=)
c.-1007A>T (n.-1007A>T)
c.786A>T (p.Thr262=)
n.801A>T
11g.68363820G>ACA381611046LRP5c.760G>A (p.Asp254Asn)
c.-1006G>A (n.-1006G>A)
c.787G>A (p.Asp263Asn)
n.802G>A
11g.68363820G>CCA381611047LRP5c.760G>C (p.Asp254His)
c.-1006G>C (n.-1006G>C)
c.787G>C (p.Asp263His)
n.802G>C
11g.68363820G>TCA381611048LRP5c.760G>T (p.Asp254Tyr)
c.-1006G>T (n.-1006G>T)
c.787G>T (p.Asp263Tyr)
n.802G>T
11g.68363821A>CCA381611049LRP5c.761A>C (p.Asp254Ala)
c.-1005A>C (n.-1005A>C)
c.788A>C (p.Asp263Ala)
n.803A>C
11g.68363821A>GCA381611050LRP5c.761A>G (p.Asp254Gly)
c.-1005A>G (n.-1005A>G)
c.788A>G (p.Asp263Gly)
n.803A>G
11g.68363821A>TCA381611051LRP5c.761A>T (p.Asp254Val)
c.-1005A>T (n.-1005A>T)
c.788A>T (p.Asp263Val)
n.803A>T
11g.68363822C>ACA381611052LRP5c.762C>A (p.Asp254Glu)
c.-1004C>A (n.-1004C>A)
c.789C>A (p.Asp263Glu)
n.804C>A
11g.68363822C>GCA381611053LRP5c.762C>G (p.Asp254Glu)
c.-1004C>G (n.-1004C>G)
c.789C>G (p.Asp263Glu)
n.804C>G
11g.68363822C>TCA475460274LRP5c.762C>T (p.Asp254=)
c.-1004C>T (n.-1004C>T)
c.789C>T (p.Asp263=)
n.804C>T
 COSMIC
11g.68363823T>ACA381611054LRP5c.763T>A (p.Trp255Arg)
c.-1003T>A (n.-1003T>A)
c.790T>A (p.Trp264Arg)
n.805T>A
11g.68363823T>CCA381611055LRP5c.763T>C (p.Trp255Arg)
c.-1003T>C (n.-1003T>C)
c.790T>C (p.Trp264Arg)
n.805T>C
 COSMIC
11g.68363823T>GCA381611056LRP5c.763T>G (p.Trp255Gly)
c.-1003T>G (n.-1003T>G)
c.790T>G (p.Trp264Gly)
n.805T>G
11g.68363824G>ACA381611059LRP5c.764G>A (p.Trp255Ter)
c.-1002G>A (n.-1002G>A)
c.791G>A (p.Trp264Ter)
n.806G>A
11g.68363824G>CCA381611057LRP5c.764G>C (p.Trp255Ser)
c.-1002G>C (n.-1002G>C)
c.791G>C (p.Trp264Ser)
n.806G>C
11g.68363824G>TCA381611058LRP5c.764G>T (p.Trp255Leu)
c.-1002G>T (n.-1002G>T)
c.791G>T (p.Trp264Leu)
n.806G>T
11g.68363825G>ACA381611060LRP5c.765G>A (p.Trp255Ter)
c.-1001G>A (n.-1001G>A)
c.792G>A (p.Trp264Ter)
n.807G>A
 dbSNP gnomAD v2 COSMIC
11g.68363825G>CCA381611061LRP5c.765G>C (p.Trp255Cys)
c.-1001G>C (n.-1001G>C)
c.792G>C (p.Trp264Cys)
n.807G>C
11g.68363825G=CA1980645876LRP5c.765G= (p.Trp255=)
c.-1001G= (n.-1001G=)
c.792G= (p.Trp264=)
n.807G=
11g.68363825G>TCA381611062LRP5c.765G>T (p.Trp255Cys)
c.-1001G>T (n.-1001G>T)
c.792G>T (p.Trp264Cys)
n.807G>T
11g.68363826delCA2792538267LRP5c.766del (p.Gln256ArgfsTer20)
c.-1000del (n.-1000del)
c.793del (p.Gln265ArgfsTer20)
n.808del
11g.68363826C>ACA381611063LRP5c.766C>A (p.Gln256Lys)
c.-1000C>A (n.-1000C>A)
c.793C>A (p.Gln265Lys)
n.808C>A
11g.68363826C>GCA381611064LRP5c.766C>G (p.Gln256Glu)
c.-1000C>G (n.-1000C>G)
c.793C>G (p.Gln265Glu)
n.808C>G
11g.68363826C>TCA381611065LRP5c.766C>T (p.Gln256Ter)
c.-1000C>T (n.-1000C>T)
c.793C>T (p.Gln265Ter)
n.808C>T
11g.68363827A>CCA381611066LRP5c.767A>C (p.Gln256Pro)
c.-999A>C (n.-999A>C)
c.794A>C (p.Gln265Pro)
n.809A>C
11g.68363827A>GCA381611067LRP5c.767A>G (p.Gln256Arg)
c.-999A>G (n.-999A>G)
c.794A>G (p.Gln265Arg)
n.809A>G
11g.68363827A>TCA381611068LRP5c.767A>T (p.Gln256Leu)
c.-999A>T (n.-999A>T)
c.794A>T (p.Gln265Leu)
n.809A>T
11g.68363828G>ACA475460275LRP5c.768G>A (p.Gln256=)
c.-998G>A (n.-998G>A)
c.795G>A (p.Gln265=)
n.810G>A
11g.68363828G>CCA381611069LRP5c.768G>C (p.Gln256His)
c.-998G>C (n.-998G>C)
c.795G>C (p.Gln265His)
n.810G>C
11g.68363828G>TCA381611070LRP5c.768G>T (p.Gln256His)
c.-998G>T (n.-998G>T)
c.795G>T (p.Gln265His)
n.810G>T
11g.68363829A=CA1980645879LRP5c.769A= (p.Thr257=)
c.-997A= (n.-997A=)
c.796A= (p.Thr266=)
n.811A=
11g.68363829A>CCA381611072LRP5c.769A>C (p.Thr257Pro)
c.-997A>C (n.-997A>C)
c.796A>C (p.Thr266Pro)
n.811A>C
 dbSNP
11g.68363829A>GCA381611073LRP5c.769A>G (p.Thr257Ala)
c.-997A>G (n.-997A>G)
c.796A>G (p.Thr266Ala)
n.811A>G
11g.68363829A>TCA381611071LRP5c.769A>T (p.Thr257Ser)
c.-997A>T (n.-997A>T)
c.796A>T (p.Thr266Ser)
n.811A>T
11g.68363830C>ACA381611074LRP5c.770C>A (p.Thr257Asn)
c.-996C>A (n.-996C>A)
c.797C>A (p.Thr266Asn)
n.812C>A
 dbSNP gnomAD v2 gnomAD v4
11g.68363830C=CA1980645881LRP5c.770C= (p.Thr257=)
c.-996C= (n.-996C=)
c.797C= (p.Thr266=)
n.812C=
11g.68363830C>GCA381611075LRP5c.770C>G (p.Thr257Ser)
c.-996C>G (n.-996C>G)
c.797C>G (p.Thr266Ser)
n.812C>G
11g.68363830C>TCA6149108LRP5c.770C>T (p.Thr257Ile)
c.-996C>T (n.-996C>T)
c.797C>T (p.Thr266Ile)
n.812C>T
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.68363832delCA2573147523LRP5c.772del (p.Arg258AlafsTer18)
c.-994del (n.-994del)
c.799del (p.Arg267AlafsTer18)
n.814del
 ClinVar dbSNP
11g.68363831C>ACA475460276LRP5c.771C>A (p.Thr257=)
c.-995C>A (n.-995C>A)
c.798C>A (p.Thr266=)
n.813C>A
11g.68363831C>GCA475460278LRP5c.771C>G (p.Thr257=)
c.-995C>G (n.-995C>G)
c.798C>G (p.Thr266=)
n.813C>G
11g.68363831C>TCA475460277LRP5c.771C>T (p.Thr257=)
c.-995C>T (n.-995C>T)
c.798C>T (p.Thr266=)
n.813C>T
11g.68363832C>ACA381611076LRP5c.772C>A (p.Arg258Ser)
c.-994C>A (n.-994C>A)
c.799C>A (p.Arg267Ser)
n.814C>A
11g.68363832C=CA1980645885LRP5c.772C= (p.Arg258=)
c.-994C= (n.-994C=)
c.799C= (p.Arg267=)
n.814C=
11g.68363832C>GCA381611077LRP5c.772C>G (p.Arg258Gly)
c.-994C>G (n.-994C>G)
c.799C>G (p.Arg267Gly)
n.814C>G
11g.68363832C>TCA6149109LRP5c.772C>T (p.Arg258Cys)
c.-994C>T (n.-994C>T)
c.799C>T (p.Arg267Cys)
n.814C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.68363833G>ACA381611078LRP5c.773G>A (p.Arg258His)
c.-993G>A (n.-993G>A)
c.800G>A (p.Arg267His)
n.815G>A
 ClinVar dbSNP gnomAD v4
11g.68363833G>CCA381611079LRP5c.773G>C (p.Arg258Pro)
c.-993G>C (n.-993G>C)
c.800G>C (p.Arg267Pro)
n.815G>C
11g.68363833G=CA1980645888LRP5c.773G= (p.Arg258=)
c.-993G= (n.-993G=)
c.800G= (p.Arg267=)
n.815G=
11g.68363833G>TCA381611080LRP5c.773G>T (p.Arg258Leu)
c.-993G>T (n.-993G>T)
c.800G>T (p.Arg267Leu)
n.815G>T
11g.68363834C>ACA475460279LRP5c.774C>A (p.Arg258=)
c.-992C>A (n.-992C>A)
c.801C>A (p.Arg267=)
n.816C>A
11g.68363834C>GCA475460280LRP5c.774C>G (p.Arg258=)
c.-992C>G (n.-992C>G)
c.801C>G (p.Arg267=)
n.816C>G
11g.68363834C>TCA475460281LRP5c.774C>T (p.Arg258=)
c.-992C>T (n.-992C>T)
c.801C>T (p.Arg267=)
n.816C>T
11g.68363835T>ACA381611081LRP5c.775T>A (p.Ser259Thr)
c.-991T>A (n.-991T>A)
c.802T>A (p.Ser268Thr)
n.817T>A
11g.68363835T>CCA381611082LRP5c.775T>C (p.Ser259Pro)
c.-991T>C (n.-991T>C)
c.802T>C (p.Ser268Pro)
n.817T>C
11g.68363835T>GCA381611083LRP5c.775T>G (p.Ser259Ala)
c.-991T>G (n.-991T>G)
c.802T>G (p.Ser268Ala)
n.817T>G
11g.68363836C>ACA381611085LRP5c.776C>A (p.Ser259Tyr)
c.-990C>A (n.-990C>A)
c.803C>A (p.Ser268Tyr)
n.818C>A
11g.68363836C>GCA381611086LRP5c.776C>G (p.Ser259Cys)
c.-990C>G (n.-990C>G)
c.803C>G (p.Ser268Cys)
n.818C>G
11g.68363836C>TCA381611084LRP5c.776C>T (p.Ser259Phe)
c.-990C>T (n.-990C>T)
c.803C>T (p.Ser268Phe)
n.818C>T
11g.68363837C>ACA475460282LRP5c.777C>A (p.Ser259=)
c.-989C>A (n.-989C>A)
c.804C>A (p.Ser268=)
n.819C>A
11g.68363837C>GCA475460284LRP5c.777C>G (p.Ser259=)
c.-989C>G (n.-989C>G)
c.804C>G (p.Ser268=)
n.819C>G
11g.68363837C>TCA475460283LRP5c.777C>T (p.Ser259=)
c.-989C>T (n.-989C>T)
c.804C>T (p.Ser268=)
n.819C>T
11g.68363838A>CCA381611087LRP5c.778A>C (p.Ile260Leu)
c.-988A>C (n.-988A>C)
c.805A>C (p.Ile269Leu)
n.820A>C
11g.68363838A>GCA381611088LRP5c.778A>G (p.Ile260Val)
c.-988A>G (n.-988A>G)
c.805A>G (p.Ile269Val)
n.820A>G
11g.68363838A>TCA381611089LRP5c.778A>T (p.Ile260Phe)
c.-988A>T (n.-988A>T)
c.805A>T (p.Ile269Phe)
n.820A>T
11g.68363839T>ACA381611090LRP5c.779T>A (p.Ile260Asn)
c.-987T>A (n.-987T>A)
c.806T>A (p.Ile269Asn)
n.821T>A
11g.68363839T>CCA381611091LRP5c.779T>C (p.Ile260Thr)
c.-987T>C (n.-987T>C)
c.806T>C (p.Ile269Thr)
n.821T>C
11g.68363839T>GCA381611092LRP5c.779T>G (p.Ile260Ser)
c.-987T>G (n.-987T>G)
c.806T>G (p.Ile269Ser)
n.821T>G
11g.68363840C>ACA475460285LRP5c.780C>A (p.Ile260=)
c.-986C>A (n.-986C>A)
c.807C>A (p.Ile269=)
n.822C>A
11g.68363840C>GCA381611093LRP5c.780C>G (p.Ile260Met)
c.-986C>G (n.-986C>G)
c.807C>G (p.Ile269Met)
n.822C>G
11g.68363840C>TCA475460286LRP5c.780C>T (p.Ile260=)
c.-986C>T (n.-986C>T)
c.807C>T (p.Ile269=)
n.822C>T
11g.68363841C>ACA381611094LRP5c.781C>A (p.His261Asn)
c.-985C>A (n.-985C>A)
c.808C>A (p.His270Asn)
n.823C>A
11g.68363841C>GCA381611096LRP5c.781C>G (p.His261Asp)
c.-985C>G (n.-985C>G)
c.808C>G (p.His270Asp)
n.823C>G
11g.68363841C>TCA381611095LRP5c.781C>T (p.His261Tyr)
c.-985C>T (n.-985C>T)
c.808C>T (p.His270Tyr)
n.823C>T
 COSMIC
11g.68363842A>CCA381611097LRP5c.782A>C (p.His261Pro)
c.-984A>C (n.-984A>C)
c.809A>C (p.His270Pro)
n.824A>C
11g.68363842A>GCA381611098LRP5c.782A>G (p.His261Arg)
c.-984A>G (n.-984A>G)
c.809A>G (p.His270Arg)
n.824A>G
11g.68363842A>TCA381611099LRP5c.782A>T (p.His261Leu)
c.-984A>T (n.-984A>T)
c.809A>T (p.His270Leu)
n.824A>T
11g.68363843T>ACA381611100LRP5c.783T>A (p.His261Gln)
c.-983T>A (n.-983T>A)
c.810T>A (p.His270Gln)
n.825T>A
11g.68363843T>CCA475460287LRP5c.783T>C (p.His261=)
c.-983T>C (n.-983T>C)
c.810T>C (p.His270=)
n.825T>C
11g.68363843T>GCA381611101LRP5c.783T>G (p.His261Gln)
c.-983T>G (n.-983T>G)
c.810T>G (p.His270Gln)
n.825T>G
11g.68363844G>ACA381611103LRP5c.784G>A (p.Ala262Thr)
c.-982G>A (n.-982G>A)
c.811G>A (p.Ala271Thr)
n.826G>A
11g.68363844G>CCA381611104LRP5c.784G>C (p.Ala262Pro)
c.-982G>C (n.-982G>C)
c.811G>C (p.Ala271Pro)
n.826G>C
11g.68363844G>TCA381611102LRP5c.784G>T (p.Ala262Ser)
c.-982G>T (n.-982G>T)
c.811G>T (p.Ala271Ser)
n.826G>T
 gnomAD v4
11g.68363845C>ACA381611105LRP5c.785C>A (p.Ala262Asp)
c.-981C>A (n.-981C>A)
c.812C>A (p.Ala271Asp)
n.827C>A
11g.68363845C=CA1980645893LRP5c.785C= (p.Ala262=)
c.-981C= (n.-981C=)
c.812C= (p.Ala271=)
n.827C=
11g.68363845C>GCA381611107LRP5c.785C>G (p.Ala262Gly)
c.-981C>G (n.-981C>G)
c.812C>G (p.Ala271Gly)
n.827C>G
11g.68363845C>TCA381611106LRP5c.785C>T (p.Ala262Val)
c.-981C>T (n.-981C>T)
c.812C>T (p.Ala271Val)
n.827C>T
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.68363846C>ACA475460289LRP5c.786C>A (p.Ala262=)
c.-980C>A (n.-980C>A)
c.813C>A (p.Ala271=)
n.828C>A
11g.68363846C=CA1980645897LRP5c.786C= (p.Ala262=)
c.-980C= (n.-980C=)
c.813C= (p.Ala271=)
n.828C=
11g.68363846C>GCA475460288LRP5c.786C>G (p.Ala262=)
c.-980C>G (n.-980C>G)
c.813C>G (p.Ala271=)
n.828C>G
11g.68363846C>TCA6149110LRP5c.786C>T (p.Ala262=)
c.-980C>T (n.-980C>T)
c.813C>T (p.Ala271=)
n.828C>T
 dbSNP ExAC gnomAD v2 gnomAD v4
11g.68363847T>ACA381611110LRP5c.787T>A (p.Cys263Ser)
c.-979T>A (n.-979T>A)
c.814T>A (p.Cys272Ser)
n.829T>A
11g.68363847T>CCA381611108LRP5c.787T>C (p.Cys263Arg)
c.-979T>C (n.-979T>C)
c.814T>C (p.Cys272Arg)
n.829T>C
 ClinVar dbSNP
11g.68363847T>GCA381611109LRP5c.787T>G (p.Cys263Gly)
c.-979T>G (n.-979T>G)
c.814T>G (p.Cys272Gly)
n.829T>G
11g.68363848G>ACA381611111LRP5c.788G>A (p.Cys263Tyr)
c.-978G>A (n.-978G>A)
c.815G>A (p.Cys272Tyr)
n.830G>A
 gnomAD v4
11g.68363848G>CCA381611112LRP5c.788G>C (p.Cys263Ser)
c.-978G>C (n.-978G>C)
c.815G>C (p.Cys272Ser)
n.830G>C
11g.68363848G>TCA381611113LRP5c.788G>T (p.Cys263Phe)
c.-978G>T (n.-978G>T)
c.815G>T (p.Cys272Phe)
n.830G>T
11g.68363849C>ACA381611114LRP5c.789C>A (p.Cys263Ter)
c.-977C>A (n.-977C>A)
c.816C>A (p.Cys272Ter)
n.831C>A
11g.68363849C=CA1980645900LRP5c.789C= (p.Cys263=)
c.-977C= (n.-977C=)
c.816C= (p.Cys272=)
n.831C=
11g.68363849C>GCA381611115LRP5c.789C>G (p.Cys263Trp)
c.-977C>G (n.-977C>G)
c.816C>G (p.Cys272Trp)
n.831C>G
11g.68363849C>TCA6149111LRP5c.789C>T (p.Cys263=)
c.-977C>T (n.-977C>T)
c.816C>T (p.Cys272=)
n.831C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.68363850A>CCA381611116LRP5c.790A>C (p.Asn264His)
c.-976A>C (n.-976A>C)
c.817A>C (p.Asn273His)
n.832A>C
11g.68363850A>GCA381611117LRP5c.790A>G (p.Asn264Asp)
c.-976A>G (n.-976A>G)
c.817A>G (p.Asn273Asp)
n.832A>G
11g.68363850A>TCA381611118LRP5c.790A>T (p.Asn264Tyr)
c.-976A>T (n.-976A>T)
c.817A>T (p.Asn273Tyr)
n.832A>T
11g.68363851A>CCA381611121LRP5c.791A>C (p.Asn264Thr)
c.-975A>C (n.-975A>C)
c.818A>C (p.Asn273Thr)
n.833A>C
 gnomAD v4
11g.68363851A>GCA381611119LRP5c.791A>G (p.Asn264Ser)
c.-975A>G (n.-975A>G)
c.818A>G (p.Asn273Ser)
n.833A>G
11g.68363851A>TCA381611120LRP5c.791A>T (p.Asn264Ile)
c.-975A>T (n.-975A>T)
c.818A>T (p.Asn273Ile)
n.833A>T
11g.68363852C>ACA381611122LRP5c.792C>A (p.Asn264Lys)
c.-974C>A (n.-974C>A)
c.819C>A (p.Asn273Lys)
n.834C>A
11g.68363852C=CA1980645903LRP5c.792C= (p.Asn264=)
c.-974C= (n.-974C=)
c.819C= (p.Asn273=)
n.834C=
11g.68363852C>GCA381611123LRP5c.792C>G (p.Asn264Lys)
c.-974C>G (n.-974C>G)
c.819C>G (p.Asn273Lys)
n.834C>G
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.68363852C>TCA475460290LRP5c.792C>T (p.Asn264=)
c.-974C>T (n.-974C>T)
c.819C>T (p.Asn273=)
n.834C>T
11g.68363853A>CCA381611124LRP5c.793A>C (p.Lys265Gln)
c.-973A>C (n.-973A>C)
c.820A>C (p.Lys274Gln)
n.835A>C
11g.68363853A>GCA381611125LRP5c.793A>G (p.Lys265Glu)
c.-973A>G (n.-973A>G)
c.820A>G (p.Lys274Glu)
n.835A>G
11g.68363853A>TCA381611126LRP5c.793A>T (p.Lys265Ter)
c.-973A>T (n.-973A>T)
c.820A>T (p.Lys274Ter)
n.835A>T
11g.68363854A>CCA381611127LRP5c.794A>C (p.Lys265Thr)
c.-972A>C (n.-972A>C)
c.821A>C (p.Lys274Thr)
n.836A>C
11g.68363854A>GCA381611128LRP5c.794A>G (p.Lys265Arg)
c.-972A>G (n.-972A>G)
c.821A>G (p.Lys274Arg)
n.836A>G
11g.68363854A>TCA381611129LRP5c.794A>T (p.Lys265Met)
c.-972A>T (n.-972A>T)
c.821A>T (p.Lys274Met)
n.836A>T
11g.68363855G>ACA475460291LRP5c.795G>A (p.Lys265=)
c.-971G>A (n.-971G>A)
c.822G>A (p.Lys274=)
n.837G>A
11g.68363855G>CCA381611130LRP5c.795G>C (p.Lys265Asn)
c.-971G>C (n.-971G>C)
c.822G>C (p.Lys274Asn)
n.837G>C
11g.68363855G>TCA381611131LRP5c.795G>T (p.Lys265Asn)
c.-971G>T (n.-971G>T)
c.822G>T (p.Lys274Asn)
n.837G>T
11g.68363856C>ACA381611132LRP5c.796C>A (p.Arg266Ser)
c.-970C>A (n.-970C>A)
c.823C>A (p.Arg275Ser)
n.838C>A
 ClinVar dbSNP
11g.68363856C=CA1980645910LRP5c.796C= (p.Arg266=)
c.-970C= (n.-970C=)
c.823C= (p.Arg275=)
n.838C=
11g.68363856C>GCA381611133LRP5c.796C>G (p.Arg266Gly)
c.-970C>G (n.-970C>G)
c.823C>G (p.Arg275Gly)
n.838C>G
11g.68363856C>TCA6149112LRP5c.796C>T (p.Arg266Cys)
c.-970C>T (n.-970C>T)
c.823C>T (p.Arg275Cys)
n.838C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.68363857G>ACA381611134LRP5c.797G>A (p.Arg266His)
c.-969G>A (n.-969G>A)
c.824G>A (p.Arg275His)
n.839G>A
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
11g.68363857G>CCA381611135LRP5c.797G>C (p.Arg266Pro)
c.-969G>C (n.-969G>C)
c.824G>C (p.Arg275Pro)
n.839G>C
11g.68363857G=CA1980645917LRP5c.797G= (p.Arg266=)
c.-969G= (n.-969G=)
c.824G= (p.Arg275=)
n.839G=
11g.68363857G>TCA381611136LRP5c.797G>T (p.Arg266Leu)
c.-969G>T (n.-969G>T)
c.824G>T (p.Arg275Leu)
n.839G>T
 ClinVar gnomAD v4
11g.68363858C>ACA475460292LRP5c.798C>A (p.Arg266=)
c.-968C>A (n.-968C>A)
c.825C>A (p.Arg275=)
n.840C>A
11g.68363858C>GCA475460293LRP5c.798C>G (p.Arg266=)
c.-968C>G (n.-968C>G)
c.825C>G (p.Arg275=)
n.840C>G
11g.68363858C>TCA475460294LRP5c.798C>T (p.Arg266=)
c.-968C>T (n.-968C>T)
c.825C>T (p.Arg275=)
n.840C>T
 gnomAD v4
11g.68363859A>CCA381611137LRP5c.799A>C (p.Thr267Pro)
c.-967A>C (n.-967A>C)
c.826A>C (p.Thr276Pro)
n.841A>C
11g.68363859A>GCA381611138LRP5c.799A>G (p.Thr267Ala)
c.-967A>G (n.-967A>G)
c.826A>G (p.Thr276Ala)
n.841A>G
11g.68363859A>TCA381611139LRP5c.799A>T (p.Thr267Ser)
c.-967A>T (n.-967A>T)
c.826A>T (p.Thr276Ser)
n.841A>T
 gnomAD v4
11g.68363860C>ACA381611140LRP5c.800C>A (p.Thr267Asn)
c.-966C>A (n.-966C>A)
c.827C>A (p.Thr276Asn)
n.842C>A
 dbSNP gnomAD v2 gnomAD v4
11g.68363860C=CA1980645925LRP5c.800C= (p.Thr267=)
c.-966C= (n.-966C=)
c.827C= (p.Thr276=)
n.842C=
11g.68363860C>GCA381611141LRP5c.800C>G (p.Thr267Ser)
c.-966C>G (n.-966C>G)
c.827C>G (p.Thr276Ser)
n.842C>G
11g.68363860C>TCA6149113LRP5c.800C>T (p.Thr267Ile)
c.-966C>T (n.-966C>T)
c.827C>T (p.Thr276Ile)
n.842C>T
 dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
11g.68363861T>ACA475460296LRP5c.801T>A (p.Thr267=)
c.-965T>A (n.-965T>A)
c.828T>A (p.Thr276=)
n.843T>A
11g.68363861T>CCA475460297LRP5c.801T>C (p.Thr267=)
c.-965T>C (n.-965T>C)
c.828T>C (p.Thr276=)
n.843T>C
11g.68363861T>GCA475460295LRP5c.801T>G (p.Thr267=)
c.-965T>G (n.-965T>G)
c.828T>G (p.Thr276=)
n.843T>G
11g.68363861T=CA1980645932LRP5c.801T= (p.Thr267=)
c.-965T= (n.-965T=)
c.828T= (p.Thr276=)
n.843T=
11g.68363861_68363871delinsTGGGGGGAAGACA1980645930LRP5c.801_811delinsTGGGGGGAAGA (p.Thr267=)
c.-965_-955delinsTGGGGGGAAGA (n.-965_-955delinsTGGGGGGAAGA)
c.828_838delinsTGGGGGGAAGA (p.Thr276=)
n.843_853delinsTGGGGGGAAGA
11g.68363862G>ACA381611142LRP5c.802G>A (p.Gly268Arg)
c.-964G>A (n.-964G>A)
c.829G>A (p.Gly277Arg)
n.844G>A
 dbSNP
11g.68363862G>CCA381611143LRP5c.802G>C (p.Gly268Arg)
c.-964G>C (n.-964G>C)
c.829G>C (p.Gly277Arg)
n.844G>C
11g.68363862G=CA1980645941LRP5c.802G= (p.Gly268=)
c.-964G= (n.-964G=)
c.829G= (p.Gly277=)
n.844G=
11g.68363862G>TCA381611144LRP5c.802G>T (p.Gly268Trp)
c.-964G>T (n.-964G>T)
c.829G>T (p.Gly277Trp)
n.844G>T
11g.68363867dupCA600238930LRP5c.807dup (p.Lys270GlufsTer?)
c.-959dup (n.-959dup)
c.834dup (p.Lys279GlufsTer?)
n.849dup
 dbSNP gnomAD v2 gnomAD v4
11g.68363867delCA475460298LRP5c.807del (p.Lys270ArgfsTer6)
c.-959del (n.-959del)
c.834del (p.Lys279ArgfsTer6)
n.849del
 COSMIC
11g.68363864_68363873delCA118110LRP5c.804_813del (p.Gly269ArgfsTer4)
c.-962_-953del (n.-962_-953del)
c.831_840del (p.Gly278ArgfsTer4)
n.846_855del
 ClinVar dbSNP
11g.68363863G>ACA381611146LRP5c.803G>A (p.Gly268Glu)
c.-963G>A (n.-963G>A)
c.830G>A (p.Gly277Glu)
n.845G>A
 ClinVar dbSNP gnomAD v2 gnomAD v4
11g.68363863G>CCA6149114LRP5c.803G>C (p.Gly268Ala)
c.-963G>C (n.-963G>C)
c.830G>C (p.Gly277Ala)
n.845G>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.68363863G=CA1980645946LRP5c.803G= (p.Gly268=)
c.-963G= (n.-963G=)
c.830G= (p.Gly277=)
n.845G=
11g.68363863G>TCA381611145LRP5c.803G>T (p.Gly268Val)
c.-963G>T (n.-963G>T)
c.830G>T (p.Gly277Val)
n.845G>T
 gnomAD v4 COSMIC
11g.68363864G>ACA475460299LRP5c.804G>A (p.Gly268=)
c.-962G>A (n.-962G>A)
c.831G>A (p.Gly277=)
n.846G>A
 dbSNP gnomAD v3 gnomAD v4
11g.68363864G>CCA224239720LRP5c.804G>C (p.Gly268=)
c.-962G>C (n.-962G>C)
c.831G>C (p.Gly277=)
n.846G>C
 ClinVar dbSNP gnomAD v3 gnomAD v4
11g.68363864G=CA1980645950LRP5c.804G= (p.Gly268=)
c.-962G= (n.-962G=)
c.831G= (p.Gly277=)
n.846G=
11g.68363864G>TCA475460300LRP5c.804G>T (p.Gly268=)
c.-962G>T (n.-962G>T)
c.831G>T (p.Gly277=)
n.846G>T
11g.68363865G>ACA381611147LRP5c.805G>A (p.Gly269Arg)
c.-961G>A (n.-961G>A)
c.832G>A (p.Gly278Arg)
n.847G>A
 COSMIC
11g.68363865G>CCA381611148LRP5c.805G>C (p.Gly269Arg)
c.-961G>C (n.-961G>C)
c.832G>C (p.Gly278Arg)
n.847G>C
11g.68363865G>TCA381611149LRP5c.805G>T (p.Gly269Trp)
c.-961G>T (n.-961G>T)
c.832G>T (p.Gly278Trp)
n.847G>T
 gnomAD v4
11g.68363866G>ACA381611150LRP5c.806G>A (p.Gly269Glu)
c.-960G>A (n.-960G>A)
c.833G>A (p.Gly278Glu)
n.848G>A
 gnomAD v4
11g.68363866G>CCA381611151LRP5c.806G>C (p.Gly269Ala)
c.-960G>C (n.-960G>C)
c.833G>C (p.Gly278Ala)
n.848G>C
11g.68363866G>TCA381611152LRP5c.806G>T (p.Gly269Val)
c.-960G>T (n.-960G>T)
c.833G>T (p.Gly278Val)
n.848G>T
11g.68363867G>ACA475460301LRP5c.807G>A (p.Gly269=)
c.-959G>A (n.-959G>A)
c.834G>A (p.Gly278=)
n.849G>A
 dbSNP
11g.68363867G>CCA475460302LRP5c.807G>C (p.Gly269=)
c.-959G>C (n.-959G>C)
c.834G>C (p.Gly278=)
n.849G>C
11g.68363867G=CA1980645955LRP5c.807G= (p.Gly269=)
c.-959G= (n.-959G=)
c.834G= (p.Gly278=)
n.849G=
11g.68363867G>TCA475460303LRP5c.807G>T (p.Gly269=)
c.-959G>T (n.-959G>T)
c.834G>T (p.Gly278=)
n.849G>T
11g.68363868A>CCA381611153LRP5c.808A>C (p.Lys270Gln)
c.-958A>C (n.-958A>C)
c.835A>C (p.Lys279Gln)
n.850A>C
11g.68363868A>GCA381611154LRP5c.808A>G (p.Lys270Glu)
c.-958A>G (n.-958A>G)
c.835A>G (p.Lys279Glu)
n.850A>G
11g.68363868A>TCA381611155LRP5c.808A>T (p.Lys270Ter)
c.-958A>T (n.-958A>T)
c.835A>T (p.Lys279Ter)
n.850A>T
11g.68363869A=CA1980645957LRP5c.809A= (p.Lys270=)
c.-957A= (n.-957A=)
c.836A= (p.Lys279=)
n.851A=
11g.68363869A>CCA381611156LRP5c.809A>C (p.Lys270Thr)
c.-957A>C (n.-957A>C)
c.836A>C (p.Lys279Thr)
n.851A>C
11g.68363869A>GCA381611157LRP5c.809A>G (p.Lys270Arg)
c.-957A>G (n.-957A>G)
c.836A>G (p.Lys279Arg)
n.851A>G
 ClinVar dbSNP gnomAD v3 gnomAD v4
11g.68363869A>TCA381611158LRP5c.809A>T (p.Lys270Met)
c.-957A>T (n.-957A>T)
c.836A>T (p.Lys279Met)
n.851A>T
11g.68363870G>ACA475460304LRP5c.810G>A (p.Lys270=)
c.-956G>A (n.-956G>A)
c.837G>A (p.Lys279=)
n.852G>A
11g.68363870G>CCA381611160LRP5c.810G>C (p.Lys270Asn)
c.-956G>C (n.-956G>C)
c.837G>C (p.Lys279Asn)
n.852G>C
 dbSNP
11g.68363870G=CA1980645962LRP5c.810G= (p.Lys270=)
c.-956G= (n.-956G=)
c.837G= (p.Lys279=)
n.852G=
11g.68363870G>TCA381611159LRP5c.810G>T (p.Lys270Asn)
c.-956G>T (n.-956G>T)
c.837G>T (p.Lys279Asn)
n.852G>T
11g.68363871A>CCA475460305LRP5c.811A>C (p.Arg271=)
c.-955A>C (n.-955A>C)
c.838A>C (p.Arg280=)
n.853A>C
11g.68363871A>GCA381611161LRP5c.811A>G (p.Arg271Gly)
c.-955A>G (n.-955A>G)
c.838A>G (p.Arg280Gly)
n.853A>G
11g.68363871A>TCA381611162LRP5c.811A>T (p.Arg271Trp)
c.-955A>T (n.-955A>T)
c.838A>T (p.Arg280Trp)
n.853A>T
11g.68363872G>ACA381611163LRP5c.812G>A (p.Arg271Lys)
c.-954G>A (n.-954G>A)
c.839G>A (p.Arg280Lys)
n.854G>A
11g.68363872G>CCA381611164LRP5c.812G>C (p.Arg271Thr)
c.-954G>C (n.-954G>C)
c.839G>C (p.Arg280Thr)
n.854G>C
11g.68363872G>TCA381611165LRP5c.812G>T (p.Arg271Met)
c.-954G>T (n.-954G>T)
c.839G>T (p.Arg280Met)
n.854G>T
11g.68363873G>ACA475460306LRP5c.813G>A (p.Arg271=)
c.-953G>A (n.-953G>A)
c.840G>A (p.Arg280=)
n.855G>A
11g.68363873G>CCA381611166LRP5c.813G>C (p.Arg271Ser)
c.-953G>C (n.-953G>C)
c.840G>C (p.Arg280Ser)
n.855G>C
11g.68363873G>TCA381611167LRP5c.813G>T (p.Arg271Ser)
c.-953G>T (n.-953G>T)
c.840G>T (p.Arg280Ser)
n.855G>T
11g.68363874A>CCA381611168LRP5c.814A>C (p.Lys272Gln)
c.-952A>C (n.-952A>C)
c.841A>C (p.Lys281Gln)
n.856A>C
11g.68363874A>GCA381611169LRP5c.814A>G (p.Lys272Glu)
c.-952A>G (n.-952A>G)
c.841A>G (p.Lys281Glu)
n.856A>G
11g.68363874A>TCA381611170LRP5c.814A>T (p.Lys272Ter)
c.-952A>T (n.-952A>T)
c.841A>T (p.Lys281Ter)
n.856A>T
11g.68363875A>CCA381611171LRP5c.815A>C (p.Lys272Thr)
c.-951A>C (n.-951A>C)
c.842A>C (p.Lys281Thr)
n.857A>C
11g.68363875A>GCA381611172LRP5c.815A>G (p.Lys272Arg)
c.-951A>G (n.-951A>G)
c.842A>G (p.Lys281Arg)
n.857A>G
11g.68363875A>TCA381611173LRP5c.815A>T (p.Lys272Met)
c.-951A>T (n.-951A>T)
c.842A>T (p.Lys281Met)
n.857A>T
11g.68363876G>ACA475460307LRP5c.816G>A (p.Lys272=)
c.-950G>A (n.-950G>A)
c.843G>A (p.Lys281=)
n.858G>A
11g.68363876G>CCA381611174LRP5c.816G>C (p.Lys272Asn)
c.-950G>C (n.-950G>C)
c.843G>C (p.Lys281Asn)
n.858G>C
11g.68363876G>TCA381611175LRP5c.816G>T (p.Lys272Asn)
c.-950G>T (n.-950G>T)
c.843G>T (p.Lys281Asn)
n.858G>T
11g.68363877G>ACA381611178LRP5c.817G>A (p.Glu273Lys)
c.-949G>A (n.-949G>A)
c.844G>A (p.Glu282Lys)
n.859G>A
11g.68363877G>CCA381611176LRP5c.817G>C (p.Glu273Gln)
c.-949G>C (n.-949G>C)
c.844G>C (p.Glu282Gln)
n.859G>C
11g.68363877G>TCA381611177LRP5c.817G>T (p.Glu273Ter)
c.-949G>T (n.-949G>T)
c.844G>T (p.Glu282Ter)
n.859G>T
11g.68363878A>CCA381611179LRP5c.818A>C (p.Glu273Ala)
c.-948A>C (n.-948A>C)
c.845A>C (p.Glu282Ala)
n.860A>C
11g.68363878A>GCA381611180LRP5c.818A>G (p.Glu273Gly)
c.-948A>G (n.-948A>G)
c.845A>G (p.Glu282Gly)
n.860A>G
11g.68363878A>TCA381611181LRP5c.818A>T (p.Glu273Val)
c.-948A>T (n.-948A>T)
c.845A>T (p.Glu282Val)
n.860A>T
11g.68363879G>ACA475460308LRP5c.819G>A (p.Glu273=)
c.-947G>A (n.-947G>A)
c.846G>A (p.Glu282=)
n.861G>A
11g.68363879G>CCA381611182LRP5c.819G>C (p.Glu273Asp)
c.-947G>C (n.-947G>C)
c.846G>C (p.Glu282Asp)
n.861G>C
11g.68363879G>TCA381611183LRP5c.819G>T (p.Glu273Asp)
c.-947G>T (n.-947G>T)
c.846G>T (p.Glu282Asp)
n.861G>T
11g.68363880A>CCA381611184LRP5c.820A>C (p.Ile274Leu)
c.-946A>C (n.-946A>C)
c.847A>C (p.Ile283Leu)
n.862A>C
11g.68363880A>GCA381611185LRP5c.820A>G (p.Ile274Val)
c.-946A>G (n.-946A>G)
c.847A>G (p.Ile283Val)
n.862A>G
 COSMIC
11g.68363880A>TCA381611186LRP5c.820A>T (p.Ile274Phe)
c.-946A>T (n.-946A>T)
c.847A>T (p.Ile283Phe)
n.862A>T
11g.68363881T>ACA381611187LRP5c.821T>A (p.Ile274Asn)
c.-945T>A (n.-945T>A)
c.848T>A (p.Ile283Asn)
n.863T>A
11g.68363881T>CCA381611188LRP5c.821T>C (p.Ile274Thr)
c.-945T>C (n.-945T>C)
c.848T>C (p.Ile283Thr)
n.863T>C
11g.68363881T>GCA381611189LRP5c.821T>G (p.Ile274Ser)
c.-945T>G (n.-945T>G)
c.848T>G (p.Ile283Ser)
n.863T>G
11g.68363882C>ACA224239724LRP5c.822C>A (p.Ile274=)
c.-944C>A (n.-944C>A)
c.849C>A (p.Ile283=)
n.864C>A
 dbSNP gnomAD v3 gnomAD v4
11g.68363882C=CA1980645965LRP5c.822C= (p.Ile274=)
c.-944C= (n.-944C=)
c.849C= (p.Ile283=)
n.864C=
11g.68363882C>GCA381611190LRP5c.822C>G (p.Ile274Met)
c.-944C>G (n.-944C>G)
c.849C>G (p.Ile283Met)
n.864C>G
11g.68363882C>TCA475460309LRP5c.822C>T (p.Ile274=)
c.-944C>T (n.-944C>T)
c.849C>T (p.Ile283=)
n.864C>T
11g.68363883C>ACA381611191LRP5c.823C>A (p.Leu275Met)
c.-943C>A (n.-943C>A)
c.850C>A (p.Leu284Met)
n.865C>A
11g.68363883C>GCA381611192LRP5c.823C>G (p.Leu275Val)
c.-943C>G (n.-943C>G)
c.850C>G (p.Leu284Val)
n.865C>G
11g.68363883C>TCA475460310LRP5c.823C>T (p.Leu275=)
c.-943C>T (n.-943C>T)
c.850C>T (p.Leu284=)
n.865C>T
11g.68363884T>ACA6149115LRP5c.824T>A (p.Leu275Gln)
c.-942T>A (n.-942T>A)
c.851T>A (p.Leu284Gln)
n.866T>A
 dbSNP ExAC gnomAD v2 gnomAD v4
11g.68363884T>CCA381611193LRP5c.824T>C (p.Leu275Pro)
c.-942T>C (n.-942T>C)
c.851T>C (p.Leu284Pro)
n.866T>C
11g.68363884T>GCA381611194LRP5c.824T>G (p.Leu275Arg)
c.-942T>G (n.-942T>G)
c.851T>G (p.Leu284Arg)
n.866T>G
11g.68363884T=CA1980645969LRP5c.824T= (p.Leu275=)
c.-942T= (n.-942T=)
c.851T= (p.Leu284=)
n.866T=

Number of alleles fetched