### LOVD-version 3000-30b ### Full data download ### To import, do not remove or alter this header ### ## Filter: (gene_public = NRD1) # 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}}" "NRD1" "nardilysin (N-arginine dibasic convertase)" "1" "p32.2-p32.1" "unknown" "NC_000001.10" "UD_132085265808" "" "https://www.LOVD.nl/NRDC" "" "1" "7995" "4898" "602651" "1" "1" "1" "1" "Alias NRD1.\r\nEstablishment of this gene variant database (LSDB) was performed by Johan den Dunnen, supported by Global Variome." "" "" "" "1" "" "NOTE: gene name changed from NRD1 to NRDC" "-1" "" "-1" "00001" "2013-05-03 00:00:00" "00006" "2026-03-09 21:43:06" "00006" "2026-03-10 14:14:38" ## 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}}" "00026066" "NRD1" "transcript variant 2 (expired, new version available) (expired, new version available)" "001" "NM_001101662.2" "" "NP_001095132.1" "" "" "MANE select" "-322" "3500" "3456" "52344609" "52254864" "00006" "2026-03-09 21:43:33" "" "" ## Diseases ## Do not remove or alter this header ## ## Count = 1 "{{id}}" "{{symbol}}" "{{name}}" "{{inheritance}}" "{{id_omim}}" "{{tissues}}" "{{features}}" "{{remarks}}" "{{created_by}}" "{{created_date}}" "{{edited_by}}" "{{edited_date}}" "05611" "NDD" "neurodevelopmental disorder (NDD)" "" "" "" "" "" "00006" "2019-06-19 12:27:20" "00006" "2024-12-13 11:12:21" ## Genes_To_Diseases ## Do not remove or alter this header ## ## Count = 1 "{{geneid}}" "{{diseaseid}}" "NRD1" "05611" ## Individuals ## Do not remove or alter this header ## ## Count = 14 "{{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}}" "00474059" "" "" "" "2" "" "00006" "{PMID:Pehlivan 2026:41734767}" "2-generation family, 2 affected sisters, unaffected heterozygous carrier parents" "F" "yes" "United States" "4m" "0" "" "" "" "FamAPatII1" "00474060" "" "" "00474059" "1" "" "00006" "{PMID:Pehlivan 2026:41734767}" "sister" "F" "yes" "United States" "1d" "0" "" "" "" "FamAPatII2" "00474061" "" "" "" "1" "" "00006" "{PMID:Pehlivan 2026:41734767}" "2-generation family, 1 affected, unaffected heterozygous carrier parents" "F" "yes" "" "" "0" "" "" "" "FamBPatII4" "00474062" "" "" "" "2" "" "00006" "{PMID:Pehlivan 2026:41734767}" "2-generation family, affected brother/sister, unaffected heterozygous carrier parents" "M" "yes" "" "10d" "0" "" "" "" "FamCPatII1" "00474063" "" "" "00474062" "1" "" "00006" "{PMID:Pehlivan 2026:41734767}" "sister" "F" "yes" "" "10d" "0" "" "" "" "FamCPatII2" "00474064" "" "" "" "2" "" "00006" "{PMID:Pehlivan 2026:41734767}" "2-generation family, affected brother/sister, unaffected heterozygous carrier parents" "M" "yes" "" "6m" "0" "" "" "" "FamDPatII1" "00474065" "" "" "00474064" "1" "" "00006" "{PMID:Pehlivan 2026:41734767}" "sister" "F" "yes" "" "<0d" "0" "" "" "" "FamDPatII2" "00474066" "" "" "" "2" "" "00006" "{PMID:Pehlivan 2026:41734767}" "2-generation family, 2 affected sisters, unaffected heterozygous carrier parents" "F" "yes" "" "" "0" "" "" "" "FamEPatII1" "00474067" "" "" "00474066" "1" "" "00006" "{PMID:Pehlivan 2026:41734767}" "sister" "F" "yes" "" "" "0" "" "" "" "FamEPatII4" "00474068" "" "" "" "1" "" "00006" "{PMID:Pehlivan 2026:41734767}" "2-generation family, 1 affected, unaffected heterozygous carrier parents" "F" "yes" "" "" "0" "" "" "" "FamFPatII1" "00474069" "" "" "" "1" "" "00006" "{PMID:Pehlivan 2026:41734767}" "2-generation family, 1 affected, unaffected heterozygous carrier parents" "F" "yes" "Lebanon" "1y1m" "0" "" "" "" "FamGPatII1" "00474070" "" "" "" "3" "" "00006" "{PMID:Pehlivan 2026:41734767}" "2-generation family, 3 affected (brother/sister/brother), unaffected heterozygous carrier parents" "F" "yes" "" "2y3m" "0" "" "" "" "FamHPatII2" "00474071" "" "" "00474070" "1" "" "00006" "{PMID:Pehlivan 2026:41734767}" "brother" "M" "yes" "" "2y" "0" "" "" "" "FamHPatII3" "00474072" "" "" "" "2" "" "00006" "{PMID:Yoon 2017:28017472}" "2-generation family, affected brother/sister, unaffected parents" "M" "" "United States" "" "0" "" "" "" "FamPatII1/5" ## Individuals_To_Diseases ## Do not remove or alter this header ## ## Count = 14 "{{individualid}}" "{{diseaseid}}" "00474059" "05611" "00474060" "05611" "00474061" "05611" "00474062" "05611" "00474063" "05611" "00474064" "05611" "00474065" "05611" "00474066" "05611" "00474067" "05611" "00474068" "05611" "00474069" "05611" "00474070" "05611" "00474071" "05611" "00474072" "05611" ## Phenotypes ## Do not remove or alter this header ## ## Note: Only showing Phenotype columns active for Diseases 05611 ## Count = 14 "{{id}}" "{{diseaseid}}" "{{individualid}}" "{{owned_by}}" "{{Phenotype/Inheritance}}" "{{Phenotype/Age}}" "{{Phenotype/Additional}}" "{{Phenotype/Age/Onset}}" "{{Phenotype/Age/Diagnosis}}" "{{Phenotype/Onset}}" "{{Phenotype/Enzyme/CPK}}" "{{Phenotype/Heart/Myocardium}}" "{{Phenotype/Lung}}" "{{Phenotype/Diagnosis/Definite}}" "{{Phenotype/Diagnosis/Initial}}" "0000358859" "05611" "00474059" "00006" "Familial, autosomal recessive" "4m" "see paper; .... 4m-deceased; premature birth; birth weight aware gestational age; microcephaly; severe developmental delay/intellectual disability; no seizures; MRI brain normal" "" "" "" "" "" "" "" "neurodevelopmental disorder" "0000358860" "05611" "00474060" "00006" "Familial, autosomal recessive" "1d" "see paper; .... 1d-deceased; premature birth; intrauterine growth restriction; microcephaly; mild contractures; MRI brain normal" "" "" "" "" "" "" "" "neurodevelopmental disorder" "0000358861" "05611" "00474061" "00006" "Familial, autosomal recessive" "7y" "see paper; ..., no premature birth; intrauterine growth restriction; microcephaly; severe developmental delay/intellectual disability; seizures; normal ophthalmology; no musculoskeletal abnormalities; MRI brain normal" "" "" "" "" "" "" "" "neurodevelopmental disorder" "0000358862" "05611" "00474062" "00006" "Familial, autosomal recessive" "10d" "see paper; .... 10d-deceased; premature birth; intrauterine growth restriction; microcephaly; severe developmental delay/intellectual disability; no seizures; arthrogryposis; MRI brain lissencephaly, thick corpus callosum, vermian hypoplasia" "" "" "" "" "" "" "" "neurodevelopmental disorder" "0000358863" "05611" "00474063" "00006" "Familial, autosomal recessive" "10d" "see paper; .... 10d-deceased; premature birth; intrauterine growth restriction; microcephaly; severe developmental delay/intellectual disability; no seizures; arthrogryposis; MRI brain lissencephaly, band heterotopia" "" "" "" "" "" "" "" "neurodevelopmental disorder" "0000358864" "05611" "00474064" "00006" "Familial, autosomal recessive" "6m" "see paper; .... 6m-deceased; no premature birth; intrauterine growth restriction; microcephaly; severe developmental delay/intellectual disability; seizures, concerning episodes; optic atrophy; arthrogryposis; MRI brain cortical dysplasia, severe hypoplasia cerebellum" "" "" "" "" "" "" "" "neurodevelopmental disorder" "0000358865" "05611" "00474065" "00006" "Familial, autosomal recessive" "<0d" "see paper; ..., terminated pregnancyterminated; terminated; intrauterine growth restriction; microcephaly" "" "" "" "" "" "" "" "neurodevelopmental disorder" "0000358866" "05611" "00474066" "00006" "Familial, autosomal recessive" "12y" "see paper; ..., no premature birth; birth weight aware gestational age; microcephaly; severe developmental delay/intellectual disability; seizures; normal ophthalmology; MRI brain diffuse atrophy, T2 signal changes in parietal areas" "" "" "" "" "" "" "" "neurodevelopmental disorder" "0000358867" "05611" "00474067" "00006" "Familial, autosomal recessive" "16y" "see paper; ..., no premature birth; severe developmental delay/intellectual disability; no seizures" "" "" "" "" "" "" "" "neurodevelopmental disorder" "0000358868" "05611" "00474068" "00006" "Familial, autosomal recessive" "3.7y" "see paper; ..., no premature birth; birth weight aware gestational age; microcephaly; global developmental delay; seizures; nystagmus; no musculoskeletal abnormalities; MRI brain features of leukodystrophy" "" "" "" "" "" "" "" "neurodevelopmental disorder" "0000358869" "05611" "00474069" "00006" "Familial, autosomal recessive" "1y1m" "see paper; .... 13m-deceased; no premature birth; intrauterine growth restriction; microcephaly; severe developmental delay/intellectual disability; no musculoskeletal abnormalities" "" "" "" "" "" "" "" "neurodevelopmental disorder" "0000358870" "05611" "00474070" "00006" "Familial, autosomal recessive" "2y3m" "see paper; .... 27m-deceased; no premature birth; intrauterine growth restriction; microcephaly; severe developmental delay/intellectual disability; seizures; optic atrophy; MRI brain diffuse atrophy" "" "" "" "" "" "" "" "neurodevelopmental disorder" "0000358871" "05611" "00474071" "00006" "Familial, autosomal recessive" "2y" "see paper; .... 2y-deceased; no premature birth; intrauterine growth restriction; microcephaly; severe developmental delay/intellectual disability; seizures; visually inattentive; MRI brain diffuse atrophy" "" "" "" "" "" "" "" "neurodevelopmental disorder" "0000358872" "05611" "00474072" "00006" "Familial, autosomal recessive" "15y" "see paper; .... microcephaly; severe developmental delay/intellectual disability; seizures; optic atrophy; no musculoskeletal abnormalities; motor impairment; MRI brain diffuse atrophy; ataxia; hypotonia; language problem; sibling with\r\nsimilar presentation 16m-deceased" "" "" "" "" "" "" "" "global developmental delay, ataxia" ## Screenings ## Do not remove or alter this header ## ## Count = 14 "{{id}}" "{{individualid}}" "{{variants_found}}" "{{owned_by}}" "{{created_by}}" "{{created_date}}" "{{edited_by}}" "{{edited_date}}" "{{Screening/Technique}}" "{{Screening/Template}}" "{{Screening/Tissue}}" "{{Screening/Remarks}}" "0000475729" "00474059" "1" "00006" "00006" "2026-03-10 13:44:25" "" "" "RT-PCR;SEQ;SEQ-NG" "DNA;RNA" "" "WES" "0000475730" "00474060" "1" "00006" "00006" "2026-03-10 13:44:25" "" "" "RT-PCR;SEQ;SEQ-NG" "DNA;RNA" "" "WES" "0000475731" "00474061" "1" "00006" "00006" "2026-03-10 13:44:25" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000475732" "00474062" "1" "00006" "00006" "2026-03-10 13:44:25" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000475733" "00474063" "1" "00006" "00006" "2026-03-10 13:44:25" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000475734" "00474064" "1" "00006" "00006" "2026-03-10 13:44:25" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000475735" "00474065" "1" "00006" "00006" "2026-03-10 13:44:25" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000475736" "00474066" "1" "00006" "00006" "2026-03-10 13:44:25" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000475737" "00474067" "1" "00006" "00006" "2026-03-10 13:44:25" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000475738" "00474068" "1" "00006" "00006" "2026-03-10 13:44:25" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000475739" "00474069" "1" "00006" "00006" "2026-03-10 13:44:25" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000475740" "00474070" "1" "00006" "00006" "2026-03-10 13:44:25" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000475741" "00474071" "1" "00006" "00006" "2026-03-10 13:44:25" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000475742" "00474072" "1" "00006" "00006" "2026-03-10 13:44:25" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" ## Screenings_To_Genes ## Do not remove or alter this header ## ## Count = 0 ## 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 = 15 "{{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}}" "0000717547" "0" "50" "1" "52289399" "52289399" "subst" "0" "01943" "NRD1_000001" "g.52289399A>T" "" "" "" "NRDC(NM_002525.2):c.1300T>A (p.L434M)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "0" "" "" "g.51823727A>T" "" "VUS" "" "0001070277" "3" "90" "1" "52257335" "52257335" "subst" "0" "00006" "NRD1_000005" "g.52257335T>C" "" "{PMID:Pehlivan 2026:41734767}" "" "" "" "Germline" "" "" "0" "" "" "g.51791663T>C" "" "pathogenic (recessive)" "" "0001070278" "3" "90" "1" "52257335" "52257335" "subst" "0" "00006" "NRD1_000005" "g.52257335T>C" "" "{PMID:Pehlivan 2026:41734767}" "" "" "" "Germline" "" "" "0" "" "" "g.51791663T>C" "" "pathogenic (recessive)" "" "0001070279" "3" "90" "1" "52255043" "52255043" "del" "0" "00006" "NRD1_000003" "g.52255043del" "" "{PMID:Pehlivan 2026:41734767}" "" "" "" "Germline" "" "" "0" "" "" "g.51789371del" "" "pathogenic (recessive)" "" "0001070280" "3" "90" "1" "52281983" "52281983" "subst" "0" "00006" "NRD1_000006" "g.52281983C>T" "" "{PMID:Pehlivan 2026:41734767}" "" "" "effect on RNA predicted from in vitro mini-gene splicing assay" "Germline" "" "" "0" "" "" "g.51816311C>T" "" "pathogenic (recessive)" "" "0001070281" "3" "90" "1" "52281983" "52281983" "subst" "0" "00006" "NRD1_000006" "g.52281983C>T" "" "{PMID:Pehlivan 2026:41734767}" "" "" "effect on RNA predicted from in vitro mini-gene splicing assay" "Germline" "" "" "0" "" "" "g.51816311C>T" "" "pathogenic (recessive)" "" "0001070282" "3" "90" "1" "52299690" "52299690" "del" "0" "00006" "NRD1_000008" "g.52299690del" "" "{PMID:Pehlivan 2026:41734767}" "" "" "" "Germline" "" "" "0" "" "" "g.51834018del" "" "pathogenic (recessive)" "" "0001070283" "3" "90" "1" "52299690" "52299690" "del" "0" "00006" "NRD1_000008" "g.52299690del" "" "{PMID:Pehlivan 2026:41734767}" "" "" "" "Germline" "" "" "0" "" "" "g.51834018del" "" "pathogenic (recessive)" "" "0001070284" "3" "90" "1" "52277742" "52277743" "del" "8.1283E-6" "00006" "NRD1_000002" "g.52277742_52277743del" "" "{PMID:Pehlivan 2026:41734767}" "" "1701_1703delAT" "" "Germline" "" "" "0" "" "" "g.51812070_51812071del" "" "pathogenic (recessive)" "" "0001070285" "3" "90" "1" "52277742" "52277743" "del" "8.1283E-6" "00006" "NRD1_000002" "g.52277742_52277743del" "" "{PMID:Pehlivan 2026:41734767}" "" "1702_1703delAT" "" "Germline" "" "" "0" "" "" "g.51812070_51812071del" "" "pathogenic (recessive)" "" "0001070286" "3" "90" "1" "52344286" "52344286" "subst" "0" "00006" "NRD1_000009" "g.52344286A>T" "" "{PMID:Pehlivan 2026:41734767}" "" "" "shorter protein detected in in vitro expression experiment" "Germline" "" "" "0" "" "" "g.51878614A>T" "" "pathogenic (recessive)" "" "0001070287" "3" "90" "1" "52256639" "52256639" "subst" "0" "00006" "NRD1_000004" "g.52256639A>G" "" "{PMID:Pehlivan 2026:41734767}" "" "" "" "Germline" "" "" "0" "" "" "g.51790967A>G" "" "pathogenic (recessive)" "" "0001070288" "3" "90" "1" "52285498" "52285498" "subst" "0" "00006" "NRD1_000007" "g.52285498G>T" "" "{PMID:Pehlivan 2026:41734767}" "" "" "" "Germline" "" "" "0" "" "" "g.51819826G>T" "" "pathogenic (recessive)" "" "0001070289" "3" "90" "1" "52285498" "52285498" "subst" "0" "00006" "NRD1_000007" "g.52285498G>T" "" "{PMID:Pehlivan 2026:41734767}" "" "" "" "Germline" "" "" "0" "" "" "g.51819826G>T" "" "pathogenic (recessive)" "" "0001070290" "3" "90" "1" "52277742" "52277743" "del" "8.1283E-6" "00006" "NRD1_000002" "g.52277742_52277743del" "" "{PMID:Yoon 2017:28017472}, {PMID:Pehlivan 2026:41734767}" "" "1702_1703delAT" "" "Germline" "" "" "0" "" "" "g.51812070_51812071del" "" "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 NRD1 ## Count = 15 "{{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}}" "0000717547" "00026066" "50" "1096" "0" "1096" "0" "c.1096T>A" "r.(?)" "p.(Leu366Met)" "" "0001070277" "00026066" "90" "2877" "-2" "2877" "-2" "c.2877-2A>G" "r.2877_2960del" "Tyr960_Asn987del" "27i" "0001070278" "00026066" "90" "2877" "-2" "2877" "-2" "c.2877-2A>G" "r.2877_2960del" "Tyr960_Asn987del" "27i" "0001070279" "00026066" "90" "3322" "0" "3322" "0" "c.3322del" "r.(?)" "p.(Ser1108LeufsTer5)" "" "0001070280" "00026066" "90" "1439" "1" "1439" "1" "c.1439+1G>A" "r.(1362_1439del)" "p.(Val455_Lys480del)" "11i" "0001070281" "00026066" "90" "1439" "1" "1439" "1" "c.1439+1G>A" "r.(1362_1439del)" "p.(Val455_Lys480del)" "11i" "0001070282" "00026066" "90" "865" "0" "865" "0" "c.865del" "r.(?)" "p.(Arg289AspfsTer10)" "" "0001070283" "00026066" "90" "865" "0" "865" "0" "c.865del" "r.(?)" "p.(Arg289AspfsTer10)" "" "0001070284" "00026066" "90" "1702" "0" "1703" "0" "c.1702_1703del" "r.(?)" "p.(Met568ValfsTer2)" "" "0001070285" "00026066" "90" "1702" "0" "1703" "0" "c.1702_1703del" "r.(?)" "p.(Met568ValfsTer2)" "" "0001070286" "00026066" "90" "2" "0" "2" "0" "c.2T>A" "r.(2T>A)" "p.(Leu2_Met50del)" "" "0001070287" "00026066" "90" "2984" "0" "2984" "0" "c.2984T>C" "r.(?)" "p.(Ile995Thr)" "" "0001070288" "00026066" "90" "1265" "0" "1265" "0" "c.1265C>A" "r.(?)" "p.(Thr422Lys)" "" "0001070289" "00026066" "90" "1265" "0" "1265" "0" "c.1265C>A" "r.(?)" "p.(Thr422Lys)" "" "0001070290" "00026066" "90" "1702" "0" "1703" "0" "c.1702_1703del" "r.(?)" "p.(Met568ValfsTer2)" "" ## Screenings_To_Variants ## Do not remove or alter this header ## ## Count = 14 "{{screeningid}}" "{{variantid}}" "0000475729" "0001070277" "0000475730" "0001070278" "0000475731" "0001070279" "0000475732" "0001070280" "0000475733" "0001070281" "0000475734" "0001070282" "0000475735" "0001070283" "0000475736" "0001070284" "0000475737" "0001070285" "0000475738" "0001070286" "0000475739" "0001070287" "0000475740" "0001070288" "0000475741" "0001070289" "0000475742" "0001070290"