### LOVD-version 3000-30b ### Full data download ### To import, do not remove or alter this header ### ## Filter: (gene_public = POPDC2) # charset = UTF-8 ## Genes ## Do not remove or alter this header ## ## Count = 1 "{{id}}" "{{name}}" "{{chromosome}}" "{{chrom_band}}" "{{imprinting}}" "{{refseq_genomic}}" "{{refseq_UD}}" "{{reference}}" "{{url_homepage}}" "{{url_external}}" "{{allow_download}}" "{{id_hgnc}}" "{{id_entrez}}" "{{id_omim}}" "{{show_hgmd}}" "{{show_genecards}}" "{{show_genetests}}" "{{show_orphanet}}" "{{note_index}}" "{{note_listing}}" "{{refseq}}" "{{refseq_url}}" "{{disclaimer}}" "{{disclaimer_text}}" "{{header}}" "{{header_align}}" "{{footer}}" "{{footer_align}}" "{{created_by}}" "{{created_date}}" "{{edited_by}}" "{{edited_date}}" "{{updated_by}}" "{{updated_date}}" "POPDC2" "popeye domain containing 2" "3" "q13.33" "unknown" "NC_000003.11" "UD_132610749838" "" "https://www.LOVD.nl/POPDC2" "" "1" "17648" "64091" "605823" "1" "1" "1" "1" "Establishment of this gene variant database (LSDB) was performed by Johan den Dunnen, supported by Global Variome." "" "" "" "1" "" "" "-1" "" "-1" "00001" "2013-05-03 00:00:00" "00006" "2025-07-07 12:11:08" "00000" "2025-07-08 13:22:38" ## Transcripts ## Do not remove or alter this header ## ## Count = 1 "{{id}}" "{{geneid}}" "{{name}}" "{{id_mutalyzer}}" "{{id_ncbi}}" "{{id_ensembl}}" "{{id_protein_ncbi}}" "{{id_protein_ensembl}}" "{{id_protein_uniprot}}" "{{remarks}}" "{{position_c_mrna_start}}" "{{position_c_mrna_end}}" "{{position_c_cds_end}}" "{{position_g_mrna_start}}" "{{position_g_mrna_end}}" "{{created_by}}" "{{created_date}}" "{{edited_by}}" "{{edited_date}}" "00026000" "POPDC2" "transcript variant 3 (removed from reference sequence) (removed from reference sequence) (removed from reference sequence) (removed from reference sequence)" "000" "NM_001369919.2" "" "NP_001356848.1" "" "" "MANE select" "-166" "1656" "1107" "1" "1" "00006" "2025-07-07 11:23:50" "" "" ## Diseases ## Do not remove or alter this header ## ## Count = 2 "{{id}}" "{{symbol}}" "{{name}}" "{{inheritance}}" "{{id_omim}}" "{{tissues}}" "{{features}}" "{{remarks}}" "{{created_by}}" "{{created_date}}" "{{edited_by}}" "{{edited_date}}" "00198" "?" "unclassified / mixed" "" "" "" "" "" "00006" "2013-09-13 14:21:47" "00006" "2024-11-23 09:38:12" "01223" "CCD" "cardiac conduction defect (CCD)" "AD" "115080" "" "" "" "00006" "2014-09-25 23:29:40" "00006" "2021-12-10 21:51:32" ## Genes_To_Diseases ## Do not remove or alter this header ## ## Count = 1 "{{geneid}}" "{{diseaseid}}" "POPDC2" "01223" ## Individuals ## Do not remove or alter this header ## ## Count = 8 "{{id}}" "{{fatherid}}" "{{motherid}}" "{{panelid}}" "{{panel_size}}" "{{license}}" "{{owned_by}}" "{{Individual/Reference}}" "{{Individual/Remarks}}" "{{Individual/Gender}}" "{{Individual/Consanguinity}}" "{{Individual/Origin/Geographic}}" "{{Individual/Age_of_death}}" "{{Individual/VIP}}" "{{Individual/Data_av}}" "{{Individual/Treatment}}" "{{Individual/Origin/Population}}" "{{Individual/Individual_ID}}" "00445371" "" "" "" "2" "" "00006" "{PMID:Rinne 2020:32535041}" "2-generation family, affected twin brothers, unaffected carrier mother" "M" "" "Albania" "" "0" "" "" "" "Fam10031Pat1/4" "00445372" "" "" "" "2" "" "00006" "{PMID:Rinne 2020:32535041}" "2-generation family, affected mother/son" "F;M" "" "Germany" "" "0" "" "" "" "Fam2" "00466008" "" "" "" "1" "" "00006" "{PMID:Nicastro 2025:40409267}, {DOI:Nicastro 2025:10.1016/j.ajhg.2025.04.016}" "2-generation family, 1 affected, unaffected heterozygous carrier parents/relatives" "M" "yes" "" "" "0" "" "" "" "FamAPatII3" "00466009" "" "" "" "2" "" "00006" "{PMID:Nicastro 2025:40409267}, {DOI:Nicastro 2025:10.1016/j.ajhg.2025.04.016}" "2-generation family, affected sister/brother, unaffected parents/relatives" "M" "yes" "" "" "0" "" "" "" "FamBPatII4" "00466010" "" "" "" "3" "" "00006" "{PMID:Nicastro 2025:40409267}, {DOI:Nicastro 2025:10.1016/j.ajhg.2025.04.016}" "2-generation family, 3 affected brothers, unaffected heterozygous carrier parents/relatives" "M" "no" "" "" "0" "" "" "" "FamCPatII1" "00466011" "" "" "00466010" "1" "" "00006" "{PMID:Nicastro 2025:40409267}, {DOI:Nicastro 2025:10.1016/j.ajhg.2025.04.016}" "brother" "M" "no" "" "" "0" "" "" "" "FamCPatII2" "00466012" "" "" "00466010" "1" "" "00006" "{PMID:Nicastro 2025:40409267}, {DOI:Nicastro 2025:10.1016/j.ajhg.2025.04.016}" "brother" "M" "no" "" "" "0" "" "" "" "FamCPatII3" "00466013" "" "" "" "1" "" "00006" "{PMID:Nicastro 2025:40409267}, {DOI:Nicastro 2025:10.1016/j.ajhg.2025.04.016}" "2-generation family, 1 affected, unaffected heterozygous carrier mother" "M" "no" "" "" "0" "" "" "" "FamDPatII1" ## Individuals_To_Diseases ## Do not remove or alter this header ## ## Count = 8 "{{individualid}}" "{{diseaseid}}" "00445371" "00198" "00445372" "00198" "00466008" "01223" "00466009" "01223" "00466010" "01223" "00466011" "01223" "00466012" "01223" "00466013" "01223" ## Phenotypes ## Do not remove or alter this header ## ## Note: Only showing Phenotype columns active for Diseases 00198, 01223 ## Count = 9 "{{id}}" "{{diseaseid}}" "{{individualid}}" "{{owned_by}}" "{{Phenotype/Inheritance}}" "{{Phenotype/Age}}" "{{Phenotype/Additional}}" "{{Phenotype/Age/Onset}}" "{{Phenotype/Age/Diagnosis}}" "{{Phenotype/Onset}}" "{{Phenotype/Protein}}" "{{Phenotype/Tumor/MSI}}" "{{Phenotype/Enzyme/CPK}}" "{{Phenotype/Heart/Myocardium}}" "{{Phenotype/Diagnosis/Definite}}" "{{Phenotype/Diagnosis/Initial}}" "{{Phenotype/Diagnosis/Criteria}}" "0000334606" "00198" "00445371" "00006" "Unknown" "07y" "see paper; ..., severe atrioventricular block; fainting, dizziness, received pacemaker" "" "" "" "" "" "" "" "" "atrioventricular block" "" "0000334607" "00198" "00445372" "00006" "Familial, autosomal dominant" "" "see paper; ..., 1st degree atrioventricular block, mildly increased CK level" "" "" "" "" "" "" "" "" "atrioventricular block" "" "0000334609" "00198" "00445371" "00006" "Unknown" "" "see paper; ..., ventricular premature beats in patients, brother (Pat5) and father (Pat3)" "" "" "" "" "" "" "" "" "ventricular premature beats" "" "0000351393" "01223" "00466008" "00006" "Familial, autosomal recessive" "" "see paper; ..., palpitations; no cardiac arrest; sinus pauses (3 s); AV conduction disease second atrioventricular block (type 1); atrial fibrillation, flutter; monomorphic non-sustained ventricular tachycardia, premature ventricular contractions; hypertrophic cardiomyopathy; cardiac MRI septal hypertrophy (23 mm); no myocarditis" "11y-15y" "" "palpitations" "" "" "" "" "" "cardiac conduction defect" "" "0000351394" "01223" "00466009" "00006" "Familial, autosomal recessive" "" "see paper; ..., palpitations; sinus bradycardia; AV conduction disease PQ time of 200 ms second atrioventricular block; no atrial arrhythmia; no ventricular arrhythmia; hypertrophic cardiomyopathy; cardiac MRI septal hypertrophy (16mm); no myocarditis" "21y-25y" "" "palpitations" "" "" "" "" "" "cardiac conduction defect" "" "0000351395" "01223" "00466010" "00006" "Familial, autosomal recessive" "" "see paper; ..., no cardiac arrest; no sinus node disease; first and second atrioventricular block (type 1 and 2:1); atrial fibrillation, flutter; monomorphic non-sustained ventricular tachycardia; no hypertrophic cardiomyopathy; no myocarditis" "21y-25y" "" "" "" "" "" "" "" "cardiac conduction defect" "" "0000351396" "01223" "00466011" "00006" "Familial, autosomal recessive" "" "see paper; ..., no cardiac arrest; SA-block sinus pauses (5s); AV conduction disease first atrioventricular block; no atrial arrhythmia; no ventricular arrhythmia; no hypertrophic cardiomyopathy; no myocarditis" "21y-25y" "" "" "" "" "" "" "" "cardiac conduction defect" "" "0000351397" "01223" "00466012" "00006" "Familial, autosomal recessive" "" "see paper; ..., cardiac arrest; cardiac arrest following bradycardia; SA block sinus arrest; AV conduction disease first and second atrioventricular block (type 1); episodes of high atrial rate; monomorphic non-sustained ventricular tachycardia; no hypertrophic cardiomyopathy; cardiac MRI possible myocarditis; possible myocarditis" "16y-20y" "" "cardiac arrest" "" "" "" "" "" "cardiac conduction defect" "" "0000351398" "01223" "00466013" "00006" "Familial, autosomal recessive" "" "see paper; ..., chest pain; cardiac arrest following bradycardia; no sinus node disease; AV conduction disease first atrioventricular block; no atrial arrhythmia; ventricular tachycardia; no hypertrophic cardiomyopathy; cardiac MRI significant LV fibrosis, inflammation; clinical myocarditis (not on cardiac histology)" "11y-15y" "" "chest pain" "" "" "" "" "" "cardiac conduction defect" "" ## Screenings ## Do not remove or alter this header ## ## Count = 8 "{{id}}" "{{individualid}}" "{{variants_found}}" "{{owned_by}}" "{{created_by}}" "{{created_date}}" "{{edited_by}}" "{{edited_date}}" "{{Screening/Technique}}" "{{Screening/Template}}" "{{Screening/Tissue}}" "{{Screening/Remarks}}" "0000446942" "00445371" "1" "00006" "00006" "2024-01-10 16:53:03" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000446943" "00445372" "1" "00006" "00006" "2024-01-10 17:26:53" "00006" "2024-01-10 22:07:27" "SEQ" "DNA" "" "" "0000467659" "00466008" "1" "00006" "00006" "2025-07-07 12:08:40" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000467660" "00466009" "1" "00006" "00006" "2025-07-07 12:08:40" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000467661" "00466010" "1" "00006" "00006" "2025-07-07 12:08:40" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000467662" "00466011" "1" "00006" "00006" "2025-07-07 12:08:40" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000467663" "00466012" "1" "00006" "00006" "2025-07-07 12:08:40" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000467664" "00466013" "1" "00006" "00006" "2025-07-07 12:08:40" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" ## Screenings_To_Genes ## Do not remove or alter this header ## ## Count = 1 "{{screeningid}}" "{{geneid}}" "0000446943" "POPDC2" ## Variants_On_Genome ## Do not remove or alter this header ## ## Please note that not necessarily all variants found in the given individuals are shown. This output is restricted to variants in the selected gene. ## Count = 20 "{{id}}" "{{allele}}" "{{effectid}}" "{{chromosome}}" "{{position_g_start}}" "{{position_g_end}}" "{{type}}" "{{average_frequency}}" "{{owned_by}}" "{{VariantOnGenome/DBID}}" "{{VariantOnGenome/DNA}}" "{{VariantOnGenome/Frequency}}" "{{VariantOnGenome/Reference}}" "{{VariantOnGenome/Restriction_site}}" "{{VariantOnGenome/Published_as}}" "{{VariantOnGenome/Remarks}}" "{{VariantOnGenome/Genetic_origin}}" "{{VariantOnGenome/Segregation}}" "{{VariantOnGenome/dbSNP}}" "{{VariantOnGenome/VIP}}" "{{VariantOnGenome/Methylation}}" "{{VariantOnGenome/ISCN}}" "{{VariantOnGenome/DNA/hg38}}" "{{VariantOnGenome/ClinVar}}" "{{VariantOnGenome/ClinicalClassification}}" "{{VariantOnGenome/ClinicalClassification/Method}}" "0000955371" "21" "70" "3" "119373389" "119373389" "subst" "8.94993E-5" "00006" "POPDC2_000001" "g.119373389C>T" "" "{PMID:Rinne 2020:32535041}" "" "" "variant inherited from unaffected mother (reduced penetrance?, sex-specific effects?)" "Germline" "" "" "0" "" "" "g.119654542C>T" "" "likely pathogenic (!)" "" "0000955377" "21" "90" "3" "119373389" "119373389" "subst" "8.94993E-5" "00006" "POPDC2_000001" "g.119373389C>T" "1/82 cases arrhythmias" "{PMID:Rinne 2020:32535041}" "" "" "" "Germline" "yes" "" "0" "" "" "g.119654542C>T" "" "pathogenic (dominant)" "" "0000993176" "0" "10" "3" "119361412" "119361412" "subst" "0.0479702" "02330" "POPDC2_000002" "g.119361412T>C" "" "" "" "POPDC2(NM_001369919.2):c.*44-4A>G" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "0" "" "" "g.119642565T>C" "" "benign" "" "0000993177" "0" "10" "3" "119361415" "119361415" "subst" "0.108139" "02330" "POPDC2_000003" "g.119361415A>G" "" "" "" "POPDC2(NM_001369919.2):c.*44-7T>C" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "0" "" "" "g.119642568A>G" "" "benign" "" "0000993178" "0" "10" "3" "119367390" "119367390" "subst" "0.987725" "02330" "POPDC2_000004" "g.119367390T>C" "" "" "" "POPDC2(NM_001369919.2):c.726A>G (p.S242=)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "benign" "" "0000993179" "0" "50" "3" "119367505" "119367505" "subst" "4.96212E-5" "02330" "POPDC2_000005" "g.119367505G>C" "" "" "" "POPDC2(NM_001369919.2):c.611C>G (p.T204S)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "VUS" "" "0000993180" "0" "10" "3" "119378872" "119378872" "subst" "0.453201" "02330" "POPDC2_000006" "g.119378872G>A" "" "" "" "POPDC2(NM_001369919.2):c.399C>T (p.C133=)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "benign" "" "0000993181" "0" "10" "3" "119378977" "119378977" "subst" "0.156023" "02330" "POPDC2_000007" "g.119378977G>A" "" "" "" "POPDC2(NM_001369919.2):c.294C>T (p.R98=)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "benign" "" "0000993182" "0" "10" "3" "119379186" "119379186" "subst" "0.45312" "02330" "POPDC2_000008" "g.119379186C>T" "" "" "" "POPDC2(NM_001369919.2):c.85G>A (p.V29I)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "benign" "" "0001013799" "0" "50" "3" "119367142" "119367142" "subst" "2.44113E-5" "02330" "POPDC2_000009" "g.119367142C>T" "" "" "" "POPDC2(NM_001369919.2):c.974G>A (p.R325Q)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "VUS" "" "0001013800" "0" "50" "3" "119367329" "119367329" "subst" "7.3097E-5" "02330" "POPDC2_000010" "g.119367329G>A" "" "" "" "POPDC2(NM_001369919.2):c.787C>T (p.R263C)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "VUS" "" "0001024705" "0" "30" "3" "119367043" "119367043" "subst" "0" "02330" "POPDC2_000011" "g.119367043A>G" "" "" "" "POPDC2(NM_001369919.2):c.1073T>C (p.M358T)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "0" "" "" "g.119648196A>G" "" "likely benign" "" "0001033591" "0" "50" "3" "119367340" "119367340" "subst" "9.74572E-5" "02330" "POPDC2_000012" "g.119367340C>T" "" "" "" "POPDC2(NM_001369919.2):c.776G>A (p.R259H)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "VUS" "" "0001045553" "3" "90" "3" "119373426" "119373437" "del" "0" "00006" "POPDC2_000014" "g.119373426_119373437del" "" "{PMID:Nicastro 2025:40409267}, {DOI:Nicastro 2025:10.1016/j.ajhg.2025.04.016}" "" "" "" "Germline" "" "" "0" "" "" "g.119654579_119654590del" "" "likely pathogenic (recessive)" "" "0001045554" "3" "90" "3" "119367328" "119367328" "subst" "4.46719E-5" "00006" "POPDC2_000013" "g.119367328C>T" "" "{PMID:Nicastro 2025:40409267}, {DOI:Nicastro 2025:10.1016/j.ajhg.2025.04.016}" "" "" "" "Germline" "" "" "0" "" "" "g.119648481C>T" "" "likely pathogenic (recessive)" "" "0001045555" "3" "70" "3" "119367329" "119367329" "subst" "7.3097E-5" "00006" "POPDC2_000010" "g.119367329G>A" "" "{PMID:Nicastro 2025:40409267}, {DOI:Nicastro 2025:10.1016/j.ajhg.2025.04.016}" "" "" "" "Germline" "" "" "0" "" "" "g.119648482G>A" "" "likely pathogenic (recessive)" "" "0001045556" "3" "70" "3" "119367329" "119367329" "subst" "7.3097E-5" "00006" "POPDC2_000010" "g.119367329G>A" "" "{PMID:Nicastro 2025:40409267}, {DOI:Nicastro 2025:10.1016/j.ajhg.2025.04.016}" "" "" "" "Germline" "" "" "0" "" "" "g.119648482G>A" "" "likely pathogenic (recessive)" "" "0001045557" "3" "90" "3" "119367329" "119367329" "subst" "7.3097E-5" "00006" "POPDC2_000010" "g.119367329G>A" "" "{PMID:Nicastro 2025:40409267}, {DOI:Nicastro 2025:10.1016/j.ajhg.2025.04.016}" "" "" "" "Germline" "" "" "0" "" "" "g.119648482G>A" "" "likely pathogenic (recessive)" "" "0001045558" "21" "90" "3" "119379160" "119379163" "del" "0" "00006" "POPDC2_000015" "g.119379160_119379163del" "" "{PMID:Nicastro 2025:40409267}, {DOI:Nicastro 2025:10.1016/j.ajhg.2025.04.016}" "" "" "" "Germline" "" "" "0" "" "" "g.119660313_119660316del" "" "likely pathogenic (recessive)" "" "0001045559" "10" "90" "3" "119373389" "119373389" "subst" "8.94993E-5" "00006" "POPDC2_000001" "g.119373389C>T" "" "{PMID:Nicastro 2025:40409267}, {DOI:Nicastro 2025:10.1016/j.ajhg.2025.04.016}" "" "" "" "Germline/De novo (untested)" "" "" "0" "" "" "g.119654542C>T" "" "likely pathogenic (recessive)" "" ## Variants_On_Transcripts ## Do not remove or alter this header ## ## Please note that not necessarily all variants found in the given individuals are shown. This output is restricted to variants in the selected gene. ## Note: Only showing Variants_On_Transcript columns active for Genes POPDC2 ## Count = 20 "{{id}}" "{{transcriptid}}" "{{effectid}}" "{{position_c_start}}" "{{position_c_start_intron}}" "{{position_c_end}}" "{{position_c_end_intron}}" "{{VariantOnTranscript/DNA}}" "{{VariantOnTranscript/RNA}}" "{{VariantOnTranscript/Protein}}" "{{VariantOnTranscript/Exon}}" "0000955371" "00026000" "70" "563" "0" "563" "0" "c.563G>A" "r.(?)" "p.(Trp188Ter)" "" "0000955377" "00026000" "90" "563" "0" "563" "0" "c.563G>A" "r.(?)" "p.(Trp188Ter)" "" "0000993176" "00026000" "10" "1151" "-4" "1151" "-4" "c.*44-4A>G" "r.spl?" "p.?" "" "0000993177" "00026000" "10" "1151" "-7" "1151" "-7" "c.*44-7T>C" "r.(=)" "p.(=)" "" "0000993178" "00026000" "10" "726" "0" "726" "0" "c.726A>G" "r.(?)" "p.(Ser242=)" "" "0000993179" "00026000" "50" "611" "0" "611" "0" "c.611C>G" "r.(?)" "p.(Thr204Ser)" "" "0000993180" "00026000" "10" "399" "0" "399" "0" "c.399C>T" "r.(?)" "p.(Cys133=)" "" "0000993181" "00026000" "10" "294" "0" "294" "0" "c.294C>T" "r.(?)" "p.(Arg98=)" "" "0000993182" "00026000" "10" "85" "0" "85" "0" "c.85G>A" "r.(?)" "p.(Val29Ile)" "" "0001013799" "00026000" "50" "974" "0" "974" "0" "c.974G>A" "r.(?)" "p.(Arg325Gln)" "" "0001013800" "00026000" "50" "787" "0" "787" "0" "c.787C>T" "r.(?)" "p.(Arg263Cys)" "" "0001024705" "00026000" "30" "1073" "0" "1073" "0" "c.1073T>C" "r.(?)" "p.(Met358Thr)" "" "0001033591" "00026000" "50" "776" "0" "776" "0" "c.776G>A" "r.(?)" "p.(Arg259His)" "" "0001045553" "00026000" "90" "516" "0" "527" "0" "c.516_527del" "r.(?)" "p.(Gln172_Tyr176delinsHis)" "" "0001045554" "00026000" "90" "788" "0" "788" "0" "c.788G>A" "r.(?)" "p.(Arg263His)" "" "0001045555" "00026000" "70" "787" "0" "787" "0" "c.787C>T" "r.(?)" "p.(Arg263Cys)" "" "0001045556" "00026000" "70" "787" "0" "787" "0" "c.787C>T" "r.(?)" "p.(Arg263Cys)" "" "0001045557" "00026000" "90" "787" "0" "787" "0" "c.787C>T" "r.(?)" "p.(Arg263Cys)" "" "0001045558" "00026000" "90" "110" "0" "113" "0" "c.110_113del" "r.(?)" "p.(Leu37SerfsTer20)" "" "0001045559" "00026000" "90" "563" "0" "563" "0" "c.563G>A" "r.(?)" "p.(Trp188Ter)" "" ## Screenings_To_Variants ## Do not remove or alter this header ## ## Count = 9 "{{screeningid}}" "{{variantid}}" "0000446942" "0000955371" "0000446943" "0000955377" "0000467659" "0001045553" "0000467660" "0001045554" "0000467661" "0001045555" "0000467662" "0001045556" "0000467663" "0001045557" "0000467664" "0001045558" "0000467664" "0001045559"