### LOVD-version 3000-30b ### Full data download ### To import, do not remove or alter this header ### ## Filter: (gene_public = CWF19L1) # 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}}" "CWF19L1" "CWF19-like 1, cell cycle control (S. pombe)" "10" "q24.31" "unknown" "NC_000010.10" "UD_132319368361" "" "http://www.LOVD.nl/CWF19L1" "" "1" "25613" "55280" "616120" "1" "1" "1" "1" "Establishment of this gene variant database (LSDB) was supported by the Leiden University Medical Center (LUMC), Leiden, Nederland." "" "g" "http://databases.lovd.nl/shared/refseq/CWF19L1_codingDNA.html" "1" "" "" "-1" "" "-1" "00001" "2013-05-03 00:00:00" "00006" "2015-09-06 21:59:37" "00000" "2025-05-05 21:14:00" ## 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}}" "00005909" "CWF19L1" "CWF19-like 1, cell cycle control (S. pombe)" "001" "NM_018294.4" "" "NP_060764.3" "" "" "" "-87" "2546" "1617" "102027437" "101992055" "" "0000-00-00 00:00:00" "" "" ## Diseases ## Do not remove or alter this header ## ## Count = 4 "{{id}}" "{{symbol}}" "{{name}}" "{{inheritance}}" "{{id_omim}}" "{{tissues}}" "{{features}}" "{{remarks}}" "{{created_by}}" "{{created_date}}" "{{edited_by}}" "{{edited_date}}" "00139" "ID" "intellectual disability (ID)" "" "" "" "" "" "00084" "2013-06-04 18:18:07" "00006" "2015-02-09 10:02:49" "04214" "-" "retinal disease" "" "" "" "" "" "00006" "2015-02-27 19:48:07" "00001" "2023-03-09 14:26:26" "04243" "SCAR17" "ataxia, spinocerebellar, autosomal recessive, type 17 (SCAR-17)" "AR" "616127" "" "" "" "00006" "2015-05-01 15:29:36" "00006" "2021-12-10 21:51:32" "04270" "epilepsy" "epilepsy" "" "" "" "" "" "00006" "2015-05-14 16:00:06" "00006" "2017-09-07 14:25:59" ## Genes_To_Diseases ## Do not remove or alter this header ## ## Count = 1 "{{geneid}}" "{{diseaseid}}" "CWF19L1" "04243" ## Individuals ## Do not remove or alter this header ## ## Count = 7 "{{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}}" "00037591" "" "" "" "1" "" "01278" "{PMID:Nguyen 2015:26197978}, {DOI:Nguyen 2015:10.1038/ejhg.2015.158}" "one affected in family, no sibs, parents unaffected heterozygous carriers" "F" "no" "Netherlands" "" "0" "" "" "white" "" "00037743" "" "" "" "2" "" "00006" "{PMID:Yapici 2005:15981765}; {DOI:Yapici 2005:10.1111/j.1651-2227.2005.tb01902.x}" "2-generation family, 2 affected brothers, unaffected heterozygous carrier parents and brother" "M" "yes" "Turkey" "" "0" "" "" "" "" "00275648" "" "" "" "3" "" "00006" "{PMID:Santos-Cortez 2018:30167849}" "4-generation family, 3 affected (F, 2M), unaffected heterozygous carrier parents/relatives" "M" "yes" "Pakistan" "" "0" "" "" "" "FamMR106Pat1" "00275649" "" "" "00275648" "1" "" "00006" "{PMID:Santos-Cortez 2018:30167849}" "" "M" "yes" "Pakistan" "" "0" "" "" "" "FamMR106Pat4" "00362028" "" "" "" "1" "" "00006" "{PMID:Courage 2021:33798445}, {DOI:Courage 2021:10.1016/j.ajhg.2021.03.013}" "" "" "" "" "" "0" "" "" "" "PME54" "00412787" "" "" "" "1" "" "01164" "" "" "M" "yes" "Nepal" "" "0" "" "" "" "199437" "00415262" "" "" "" "1" "" "00000" "{PMID:Alfares 2018:30202406}" "" "M" "" "" "" "0" "" "" "" "17" ## Individuals_To_Diseases ## Do not remove or alter this header ## ## Count = 7 "{{individualid}}" "{{diseaseid}}" "00037591" "04243" "00037743" "04243" "00275648" "00139" "00275649" "00139" "00362028" "04270" "00412787" "04243" "00415262" "04214" ## Phenotypes ## Do not remove or alter this header ## ## Note: Only showing Phenotype columns active for Diseases 00139, 04214, 04243, 04270 ## Count = 7 "{{id}}" "{{diseaseid}}" "{{individualid}}" "{{owned_by}}" "{{Phenotype/Inheritance}}" "{{Phenotype/Age}}" "{{Phenotype/Additional}}" "{{Phenotype/Age/Onset}}" "{{Phenotype/Age/Diagnosis}}" "{{Phenotype/Onset}}" "{{Phenotype/Protein}}" "{{Phenotype/Enzyme/CPK}}" "{{Phenotype/Heart/Myocardium}}" "{{Phenotype/Lung}}" "{{Phenotype/Diagnosis/Definite}}" "{{Phenotype/Diagnosis/Initial}}" "0000028247" "04243" "00037591" "01278" "Familial, autosomal recessive" "" "" "" "" "" "" "" "" "" "" "" "0000028259" "04243" "00037743" "00006" "Isolated (sporadic)" "" "see paper; hypotonia, developmental delay, mental retardation, non-\r\nprogressive truncal and extremity ataxia; MRI demonstrated hypoplasia vermis and cerebellar hemispheres; ..." "" "" "" "" "" "" "" "" "" "0000210259" "00139" "00275648" "00006" "Familial, autosomal recessive" "7y" "OFC 46cm; IQ 40, moderate intellectual disability (HP:0002342); developmental delay" "" "" "" "" "" "" "" "" "intellectual disability" "0000210260" "00139" "00275649" "00006" "Familial, autosomal recessive" "13y" "OFC 50cm; IQ 42, moderate intellectual disability (HP:0002342); developmental delay, seizures, ataxia, MRI-brain cerebellar atrophy" "" "" "" "" "" "" "" "" "intellectual disability" "0000257442" "04270" "00362028" "00006" "Unknown" "" "" "" "" "" "" "" "" "" "" "progressive myoclonus epilepsy" "0000304778" "04243" "00412787" "01164" "Familial, autosomal recessive" "10y" "Global developmental delay, Cerebellar hypoplasia, Dandy-Walker malformation, Hypoplasia of the corpus callosum, Aplasia/Hypoplasia involving the central nervous system, Intellectual disability, Poor fine motor coordination, Delayed gross motor development, Facial grimacing, Bradyphrenia, Behavioral abnormality, Attention deficit hyperactivity disorder" "" "" "" "" "" "" "" "" "" "0000307060" "04214" "00415262" "00000" "Familial, autosomal recessive" "" "OMIM: 616127; developmental delay cerebellar atrophy" "" "" "" "" "" "" "" "Spinocerebellar ataxia type 17" "" ## Screenings ## Do not remove or alter this header ## ## Count = 7 "{{id}}" "{{individualid}}" "{{variants_found}}" "{{owned_by}}" "{{created_by}}" "{{created_date}}" "{{edited_by}}" "{{edited_date}}" "{{Screening/Technique}}" "{{Screening/Template}}" "{{Screening/Tissue}}" "{{Screening/Remarks}}" "0000037685" "00037591" "1" "01278" "01278" "2015-04-28 10:59:44" "01278" "2015-06-11 16:01:48" "PCR;PCRq;SEQ-NG-I" "DNA;RNA" "blood, fibroblasts" "" "0000037975" "00037743" "1" "00006" "00006" "2015-05-01 18:42:34" "" "" "RT-PCR;SEQ;SEQ-NG" "DNA;RNA" "" "" "0000276806" "00275648" "1" "00006" "00006" "2020-01-11 17:34:49" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000276807" "00275649" "1" "00006" "00006" "2020-01-11 17:34:49" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000363256" "00362028" "1" "00006" "00006" "2021-04-14 11:32:13" "" "" "SEQ-NG" "DNA" "" "WES" "0000414057" "00412787" "1" "01164" "01164" "2022-07-04 15:52:03" "" "" "SEQ-NG-I" "DNA" "" "" "0000416544" "00415262" "1" "00000" "03840" "2022-08-10 20:39:58" "" "" "SEQ-NG" "DNA" "" "exome sequencing done at a commercial CAPaccredited laboratory" ## Screenings_To_Genes ## Do not remove or alter this header ## ## Count = 6 "{{screeningid}}" "{{geneid}}" "0000037685" "CWF19L1" "0000037975" "CWF19L1" "0000276806" "CWF19L1" "0000276807" "CWF19L1" "0000414057" "CWF19L1" "0000416544" "CWF19L1" ## 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 = 23 "{{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}}" "0000064839" "11" "70" "10" "102021807" "102021807" "subst" "0" "01278" "CWF19L1_000002" "g.102021807C>G" "" "{PMID:Nguyen 2015:26197978}, {DOI:Nguyen 2015:10.1038/ejhg.2015.158}" "" "" "whole exome sequencing; RNA analysis fibroblasts, nonsense mediated mRNA decay" "Germline" "yes" "" "0" "" "" "g.100262050C>G" "" "likely pathogenic" "" "0000064840" "21" "90" "10" "102005574" "102005574" "subst" "0" "01278" "CWF19L1_000001" "g.102005574T>A" "" "{PMID:Nguyen 2015:26197978}, {DOI:Nguyen 2015:10.1038/ejhg.2015.158}" "" "" "whole exome sequencing; RNA analysis fibroblasts, nonsense mediated mRNA decay" "Germline" "yes" "" "0" "" "" "g.100245817T>A" "" "pathogenic" "" "0000065285" "3" "90" "10" "102005555" "102005555" "subst" "0.00013408" "00006" "CWF19L1_000003" "g.102005555C>T" "1/65 families" "{PMID:Burns 2014:25361784}; {DOI:Burns 2014:10.1212/WNL.0000000000001053}, {OMIM616120:0001}" "" "" "homozygosity mapping, whole exome sequencing; not in 400 control chromosomes; RNA analysis LCL cells, 6-fold reduced expression; no protein on Western blot; functionally tested by morpholino knock-down in zebra fish" "Germline" "yes" "rs587780326" "0" "" "" "g.100245798C>T" "" "pathogenic" "" "0000321727" "0" "50" "10" "102010057" "102010057" "subst" "0" "01804" "CWF19L1_000004" "g.102010057T>C" "" "" "" "CWF19L1(NM_018294.4):c.656A>G (p.(His219Arg))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "0" "" "" "g.100250300T>C" "" "VUS" "" "0000538867" "0" "30" "10" "101996733" "101996733" "subst" "0.00165501" "01943" "CWF19L1_000006" "g.101996733G>T" "" "" "" "CWF19L1(NM_001303405.1):c.844-7C>A" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "g.100236976G>T" "" "likely benign" "" "0000538868" "0" "30" "10" "101997869" "101997869" "subst" "4.8729E-5" "01943" "CWF19L1_000007" "g.101997869A>G" "" "" "" "CWF19L1(NM_001303405.1):c.753T>C (p.Y251=)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "g.100238112A>G" "" "likely benign" "" "0000538869" "0" "30" "10" "102016106" "102016106" "subst" "8.12876E-6" "01943" "CWF19L1_000008" "g.102016106C>T" "" "" "" "CWF19L1(NM_001303405.1):c.6G>A (p.M2I)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "g.100256349C>T" "" "likely benign" "" "0000538870" "0" "70" "10" "102021809" "102021809" "subst" "0" "01943" "CWF19L1_000009" "g.102021809C>T" "" "" "" "CWF19L1(NM_018294.5):c.35G>A (p.G12E)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "g.100262052C>T" "" "likely pathogenic" "" "0000630945" "3" "90" "10" "102005571" "102005571" "subst" "0" "00006" "CWF19L1_000010" "g.102005571G>A" "" "{PMID:Santos-Cortez 2018:30167849}" "" "" "" "Germline" "" "" "0" "" "" "g.100245814G>A" "" "pathogenic (recessive)" "" "0000630946" "3" "90" "10" "102005571" "102005571" "subst" "0" "00006" "CWF19L1_000010" "g.102005571G>A" "" "{PMID:Santos-Cortez 2018:30167849}" "" "" "" "Germline" "" "" "0" "" "" "g.100245814G>A" "" "pathogenic (recessive)" "" "0000656401" "0" "50" "10" "102016086" "102016086" "subst" "0.000361656" "01943" "CWF19L1_000011" "g.102016086A>T" "" "" "" "CWF19L1(NM_001303405.1):c.26T>A (p.F9Y)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "g.100256329A>T" "" "VUS" "" "0000690628" "0" "30" "10" "102016035" "102016035" "subst" "0" "01943" "CWF19L1_000012" "g.102016035T>C" "" "" "" "CWF19L1(NM_001303405.1):c.77A>G (p.N26S)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely benign" "" "0000722636" "0" "30" "10" "101995477" "101995477" "subst" "0.000898392" "01943" "CWF19L1_000013" "g.101995477T>G" "" "" "" "CWF19L1(NM_001303405.1):c.1008A>C (p.T336=)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely benign" "" "0000763822" "3" "50" "10" "101996698" "101996698" "subst" "4.19294E-6" "00006" "CWF19L1_000014" "g.101996698G>A" "" "{PMID:Courage 2021:33798445}, {DOI:Courage 2021:10.1016/j.ajhg.2021.03.013}" "" "1283C>T (Thr428Ile)" "ACMG PM2, BP4" "Germline" "" "" "0" "" "" "g.100236941G>A" "" "VUS" "ACMG" "0000804260" "0" "50" "10" "102005676" "102005676" "subst" "0" "01943" "CWF19L1_000015" "g.102005676A>C" "" "" "" "CWF19L1(NM_001303405.1):c.439-6T>G" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "VUS" "" "0000804261" "0" "70" "10" "102019970" "102019970" "subst" "4.25528E-6" "02327" "CWF19L1_000016" "g.102019970C>T" "" "" "" "" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely pathogenic" "" "0000871647" "3" "90" "10" "102013196" "102013196" "dup" "0" "01164" "CWF19L1_000017" "g.102013196dup" "" "PMID: 30202406" "" "" "ACMG: PVS1, PM2_SUP, PM3_SUP" "Germline" "?" "" "0" "" "" "g.100253439dup" "VCV000800879.1" "pathogenic (recessive)" "ACMG" "0000874672" "3" "70" "10" "102013196" "102013196" "dup" "0" "00000" "CWF19L1_000017" "g.102013196dup" "frequency in 1500 in-house samples: 0" "{PMID:Alfares 2018:30202406}" "" "CWF19L1, NM_018294.5, c.605dup, p.Tyr202*" "homozygous" "Unknown" "?" "" "0" "" "" "g.100253439dup" "" "likely pathogenic" "ACMG" "0000925097" "0" "30" "10" "101989172" "101989172" "subst" "0.00127199" "02326" "CHUK_000012" "g.101989172C>T" "" "" "" "CHUK(NM_001278.5):c.105+13G>A" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely benign" "" "0000949330" "0" "30" "10" "101989173" "101989173" "subst" "0.00128894" "02326" "CHUK_000013" "g.101989173G>A" "" "" "" "CHUK(NM_001278.5):c.105+12C>T" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely benign" "" "0000998043" "0" "90" "10" "102005555" "102005555" "subst" "0.00013408" "02327" "CWF19L1_000003" "g.102005555C>T" "" "" "" "CWF19L1(NM_018294.6):c.964+1G>A" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "pathogenic" "" "0001025699" "0" "50" "10" "102020047" "102020047" "subst" "1.22E-5" "01943" "CWF19L1_000019" "g.102020047T>C" "" "" "" "CWF19L1(NM_018294.5):c.217A>G (p.N73D)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "VUS" "" "0001037672" "0" "90" "10" "102005555" "102005555" "subst" "0.00013408" "01804" "CWF19L1_000003" "g.102005555C>T" "" "" "" "CWF19L1(NM_018294.6):c.964+1G>A" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "pathogenic" "" ## 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 CWF19L1 ## Count = 23 "{{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}}" "0000064839" "00005909" "77" "37" "0" "37" "0" "c.37G>C" "r.37g>c" "p.Asp13His" "2" "0000064840" "00005909" "90" "946" "0" "946" "0" "c.946A>T" "r.946a>u" "p.Lys316*" "10" "0000065285" "00005909" "90" "964" "1" "964" "1" "c.964+1G>A" "r.850_964del" "p.Glu284Leufs*61" "9i" "0000321727" "00005909" "50" "656" "0" "656" "0" "c.656A>G" "r.(?)" "p.(His219Arg)" "" "0000538867" "00005909" "30" "1255" "-7" "1255" "-7" "c.1255-7C>A" "r.(=)" "p.(=)" "" "0000538868" "00005909" "30" "1164" "0" "1164" "0" "c.1164T>C" "r.(?)" "p.(Tyr388=)" "" "0000538869" "00005909" "30" "417" "0" "417" "0" "c.417G>A" "r.(?)" "p.(Met139Ile)" "" "0000538870" "00005909" "70" "35" "0" "35" "0" "c.35G>A" "r.(?)" "p.(Gly12Glu)" "" "0000630945" "00005909" "90" "949" "0" "949" "0" "c.949C>T" "r.[(949c>u),spl]" "p.[(Gln317*),?]" "" "0000630946" "00005909" "90" "949" "0" "949" "0" "c.949C>T" "r.[(949c>u),spl]" "p.[(Gln317*),?]" "" "0000656401" "00005909" "50" "437" "0" "437" "0" "c.437T>A" "r.(?)" "p.(Phe146Tyr)" "" "0000690628" "00005909" "30" "488" "0" "488" "0" "c.488A>G" "r.(?)" "p.(Asn163Ser)" "" "0000722636" "00005909" "30" "1419" "0" "1419" "0" "c.1419A>C" "r.(?)" "p.(Thr473=)" "" "0000763822" "00005909" "50" "1283" "0" "1283" "0" "c.1283C>T" "r.(?)" "p.(Thr428Ile)" "" "0000804260" "00005909" "50" "850" "-6" "850" "-6" "c.850-6T>G" "r.(=)" "p.(=)" "" "0000804261" "00005909" "70" "289" "5" "289" "5" "c.289+5G>A" "r.spl?" "p.?" "" "0000871647" "00005909" "90" "605" "0" "605" "0" "c.605dup" "r.(?)" "p.(Tyr202*)" "6" "0000874672" "00005909" "70" "605" "0" "605" "0" "c.605dup" "r.(?)" "p.(Tyr202*)" "" "0000925097" "00005909" "30" "5429" "0" "5429" "0" "c.*3812G>A" "r.(=)" "p.(=)" "" "0000949330" "00005909" "30" "5428" "0" "5428" "0" "c.*3811C>T" "r.(=)" "p.(=)" "" "0000998043" "00005909" "90" "964" "1" "964" "1" "c.964+1G>A" "r.spl?" "p.?" "" "0001025699" "00005909" "50" "217" "0" "217" "0" "c.217A>G" "r.(?)" "p.(Asn73Asp)" "" "0001037672" "00005909" "90" "964" "1" "964" "1" "c.964+1G>A" "r.spl?" "p.?" "" ## Screenings_To_Variants ## Do not remove or alter this header ## ## Count = 8 "{{screeningid}}" "{{variantid}}" "0000037685" "0000064839" "0000037685" "0000064840" "0000037975" "0000065285" "0000276806" "0000630945" "0000276807" "0000630946" "0000363256" "0000763822" "0000414057" "0000871647" "0000416544" "0000874672"