### LOVD-version 3000-30b ### Full data download ### To import, do not remove or alter this header ### ## Filter: (gene_public = MEG3) # 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}}" "MEG3" "maternally expressed 3 (non-protein coding)" "14" "q32.2" "paternal" "NG_016853.2" "UD_136061442815" "" "https://www.LOVD.nl/MEG3" "" "1" "14575" "55384" "605636" "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" "2020-11-25 19:12:21" "00006" "2022-02-20 16:58:54" ## 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}}" "00011985" "MEG3" "transcript variant 1" "009" "NR_002766.2" "" "" "" "" "" "1" "1595" "1595" "101292445" "101327363" "" "0000-00-00 00:00:00" "" "" ## Diseases ## Do not remove or alter this header ## ## Count = 3 "{{id}}" "{{symbol}}" "{{name}}" "{{inheritance}}" "{{id_omim}}" "{{tissues}}" "{{features}}" "{{remarks}}" "{{created_by}}" "{{created_date}}" "{{edited_by}}" "{{edited_date}}" "00232" "SRS;RSS" "Silver-Russell syndrome (SRS, Russell-Silver syndrome (RSS))" "AD" "180860" "" "" "" "00006" "2013-10-09 19:30:21" "00006" "2021-12-10 21:51:32" "00233" "KOS14" "Kagami-Ogata syndrome (KOS14, upd(14)pat, Wang-Kagama-Ogata syndrome)" "" "608149" "" "" "" "00006" "2013-10-09 19:32:37" "00006" "2015-12-08 23:59:30" "00234" "TS14" "Temple syndrome (TS-14, upd(14)mat)" "" "" "" "" "" "00006" "2013-10-09 19:34:25" "00006" "2021-12-11 13:56:28" ## Genes_To_Diseases ## Do not remove or alter this header ## ## Count = 0 ## 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}}" "00011680" "" "" "" "2" "" "00663" "{PMID:Beygo 2014:24801763}" "2-generation family, PatII3" "M" "yes" "Turkey" "" "0" "" "" "" "" "00017596" "" "" "00011680" "1" "" "00663" "{PMID:Beygo 2014:24801763}" "2-generation family, patII4" "F" "yes" "Turkey" "" "0" "" "" "" "" "00017597" "" "" "" "1" "" "00006" "{PMID:Beygo 2014:24801763}" "2-generation family, 1 affected (pat1)" "M" "no" "" "" "0" "" "" "" "" "00027197" "" "" "" "1" "" "00006" "{PMID:Kagami 2014:25351781}" "" "M" "no" "Japan" "" "0" "" "" "" "" "00027198" "" "" "" "1" "" "00006" "{PMID:Kagami 2014:25351781}" "in vitro fertilization-embryo transfer" "F" "no" "Japan" "" "0" "" "7y-gonadotropin-releasing hormone analog (precocious puberty, breast development)" "" "" "00028649" "" "" "" "1" "" "01185" "{PMID:Kagami 2010:20585555}" "" "F" "no" "Ireland" "" "0" "" "" "" "" "00403690" "" "" "" "2" "" "00006" "{PMID:Sabria-Back 2022:33579810}," "2-generation family, affected mother/child" "F" "" "Spain" "" "0" "" "" "" "family" "00403691" "" "" "00403690" "1" "" "00006" "{PMID:Sabria-Back 2022:33579810}" "child" "" "" "Spain" "00y00m74d" "0" "" "" "" "family" ## Individuals_To_Diseases ## Do not remove or alter this header ## ## Count = 8 "{{individualid}}" "{{diseaseid}}" "00011680" "00233" "00017596" "00233" "00017597" "00233" "00027197" "00232" "00027198" "00232" "00028649" "00233" "00403690" "00234" "00403691" "00233" ## Phenotypes ## Do not remove or alter this header ## ## Note: Only showing Phenotype columns active for Diseases 00232, 00233, 00234 ## Count = 8 "{{id}}" "{{diseaseid}}" "{{individualid}}" "{{owned_by}}" "{{Phenotype/Inheritance}}" "{{Phenotype/Age}}" "{{Phenotype/Additional}}" "{{Phenotype/Age/Onset}}" "{{Phenotype/Head/Microcephaly}}" "{{Phenotype/Birth/Gestational_age_wk}}" "{{Phenotype/Feeding/Problems}}" "{{Phenotype/Age/Diagnosis}}" "{{Phenotype/Onset}}" "{{Phenotype/Protein}}" "{{Phenotype/Intrauterine_growth_retardation/HPO/0001511}}" "{{Phenotype/Prenatal}}" "{{Phenotype/Enzyme/CPK}}" "{{Phenotype/Heart/Myocardium}}" "{{Phenotype/Lung}}" "{{Phenotype/Growth/Retardation/Postnatal/HPO_0008897}}" "{{Phenotype/Asymmetry/Body}}" "{{Phenotype/Diagnosis/Definite}}" "{{Phenotype/Diagnosis/Initial}}" "0000010368" "00233" "00011680" "00663" "Isolated (sporadic)" "" "see paper; ..." "" "" "" "" "" "" "" "" "" "" "" "" "" "" "" "" "0000015955" "00233" "00017596" "00663" "Isolated (sporadic)" "" "see paper; ..." "" "" "" "" "" "" "" "" "" "" "" "" "" "" "" "" "0000015956" "00233" "00017597" "00663" "Isolated (sporadic)" "" "see paper; ..." "" "" "" "" "" "" "" "" "" "" "" "" "" "" "" "" "0000023270" "00232" "00027197" "00006" "Isolated (sporadic)" "09y06m" "karyotype 46XY, birth length 46.5cm (-2.1 SD), birth weight 2.2 kg (-2.7 SD), birth occipitofrontal circumference 32.5cm (-0.7 SD); present height 120.4cm (-2.3 SD), present weight 26.5kg (-0.7 SD), BMI 18.3 (+1.0 SD), present occipitofrontal circumference 51.5cm (-0.9 SD); speech delayed (HP:0000750); small hands (HP:0200055); single palmar crease (HP:0000954); brachydactyly (HP:000156); clinodactyly (HP:0030084); joint hypermobility (HP:0001382); ear abnormality (HP:0000598); irregular teeth (HP:0040079); no precocious puberty (-HP:0000826); no intellectual disability (-HP:0001249); muscular hypotonia (HP:0001252); dysmorphic face (HP:0001999); prominent forehead (HP:0011220)" "" "macrocephaly congenital" "41w" "nr" "" "" "" "small" "" "" "" "" "growth retardation (postnatal)" "asymmetric growth" "clinical SRS (Netchine Harbison-Score 5/6" "SRS-like" "0000023271" "00232" "00027198" "00006" "Isolated (sporadic)" "09y02m" "karyotpe 46XX, birth length 36.5cm (-6.0 SD), birth weight 1.2 kg (-4.6 SD), birth occipitofrontal circumference 30.0 cm (-2.0 SD); menarche 8y8m (normal 12.3y +/-1.3y); present height 125.5cm (-1.0 SD), present weight 22.3kg (-1.2 SD), BMI 14.2 (-1.1 SD), present occipitofrontal circumference 50.3cm (-1.5 SD); recurrent otitis media (HP:0000403); small hands (HP:0200055); no single palmar crease (-HP:0000954); no brachydactyly (-HP:000156); clinodactyly (HP:0030084); puberty, precocious (HP:0000826); no intellectual disability (-HP:0001249); no muscular hypotonia (-HP:0001252); dysmorphic face (HP:0001999); prominent forehead (HP:0011220)" "" "macrocephaly congenital" "37w" "nr" "" "" "" "small" "" "" "" "" "growth retardation (postnatal)" "asymmetric growth" "clinical SRS (Netchine Harbison-Score 5/6" "SRS-like" "0000024714" "00233" "00028649" "01185" "Isolated (sporadic)" "" "no polyhydramnios (-HP:0001561); no large placenta (-HP:0006267); birth 28w gestation, weight 1.32kg, length 34cm; prenatal overgrowth (HP:0003517); frontal bossing (HP:0002007); frontal hirsutism (HP:0011335); no blepharophimosis (-HP:0000581); small ears (HP:0008551); no anteverted nares (-HP:0000463); no full cheeks (-HP:0000293); normal lips; micrognathia (HP:0000347); webbed neck (HP:0000465); bell-shaped thorax (HP:0001591); coat hanger sign ribs (HP:0006665); abdominal wall defect (HP:0010866); normal; no contractures (-HP:0001371); no coxa valga (-HP:0002673); patent ductus arteriosus (HP:0001643); omphalocele (HP:0001539); no seizures (-HP:0001250); no flat nasal bridge (-HP:0005280); normal philtrum (-HP:0000288); no scoliosis (-HP:0002650)" "" "" "28" "n/a" "" "" "" "-" "" "" "" "" "" "" "" "" "0000296385" "00234" "00403690" "00006" "Unknown" "" "see paper; ..., short stature (adult height 152 cm);, 7y-precocious puberty (with Decapeptyl GNRH agonist therapy until 13 years), high fasting blood sugar levels consistent with diabetes" "" "" "" "" "" "" "" "" "" "" "" "" "" "" "" "" "0000296386" "00233" "00403691" "00006" "Familial, autosomal dominant" "00y00m74d" "see papr; ..., 74d-deceased respiratory and infectious complications; prenatal omphalocele, severe polyhydramnios; 26w gestation amniodrainage required to avoid premature delivery, uterine contractions, cervical shortening; placental abruption requiring emergency Caesarean section; birth weight 760g; after birth silo applied to contain omphalocele, 4d-surgical correction completed; 0d-macroglossia,large philtrum, hypersialorrhea, bell-shaped thorax, coat-hanger ribs" "" "" "" "" "" "" "" "" "" "" "" "" "" "" "KOS14" "Kagami-Ogata syndrome" ## 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}}" "0000011597" "00011680" "1" "00663" "00663" "2014-02-19 19:47:39" "" "" "SEQ" "DNA" "lymphocyte" "" "0000017579" "00017596" "1" "00006" "00006" "2014-06-20 22:53:51" "" "" "arraySNP;MLPA-ms;PCR" "DNA" "" "" "0000017580" "00017597" "1" "00006" "00006" "2014-06-20 23:03:24" "00006" "2014-06-20 23:17:39" "arraySNP;PCR;PCRms;SEQ" "DNA" "" "" "0000027203" "00027197" "1" "00006" "00006" "2014-12-28 22:03:48" "00006" "2014-12-29 15:05:42" "SEQp" "DNA" "leukocytes" "" "0000027206" "00027198" "1" "00006" "00006" "2014-12-28 22:03:48" "00006" "2014-12-29 17:04:47" "SEQp" "DNA" "leukocytes" "" "0000028660" "00028649" "1" "01185" "01185" "2015-01-02 04:21:19" "00006" "2015-01-03 13:10:13" "FISH;SEQ" "DNA" "blood" "" "0000404929" "00403690" "1" "00006" "00006" "2022-02-20 16:43:09" "" "" "arraySNP;MLPA-ms;PCR;SEQ" "DNA" "" "" "0000404930" "00403691" "1" "00006" "00006" "2022-02-20 16:55:39" "" "" "arraySNP;MLPA-ms;PCR;SEQ" "DNA" "" "" ## Screenings_To_Genes ## Do not remove or alter this header ## ## Count = 20 "{{screeningid}}" "{{geneid}}" "0000011597" "MEG3" "0000017579" "MEG3" "0000017580" "MEG3" "0000017580" "MEG8" "0000017580" "RTL1" "0000027203" "GNAS" "0000027203" "H19" "0000027203" "KCNQ1" "0000027203" "MEG3" "0000027203" "MEST" "0000027203" "PLAGL1" "0000027203" "SNRPN" "0000027206" "GNAS" "0000027206" "H19" "0000027206" "KCNQ1" "0000027206" "MEG3" "0000027206" "MEST" "0000027206" "PLAGL1" "0000027206" "SNRPN" "0000028660" "MEG3" ## 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 = 16 "{{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}}" "0000031254" "21" "90" "14" "101291322" "101297145" "del" "0" "00663" "MEG3_000001" "g.101291322_101297145del" "" "{PMID:Beygo 2014:24801763}" "" "" "5.8 kb deletion" "Germline" "yes" "" "0" "" "" "g.100824985_100830808del" "" "pathogenic" "" "0000037553" "21" "90" "14" "101291322" "101297145" "del" "0" "00663" "MEG3_000001" "g.101291322_101297145del" "" "{PMID:Beygo 2014:24801763}" "" "" "5.8 kb deletion" "Germline" "yes" "" "0" "" "" "g.100824985_100830808del" "" "pathogenic" "" "0000037554" "1" "90" "14" "101285914" "101451066" "delins" "0" "00006" "MEG3_000002" "g.101285914_101451066delinsTTCCCC" "" "{PMID:Beygo 2014:24801763}" "" "101285913_101451066delinsTTCCCC" "de novo 165 kb deletion maternal allele" "De novo" "yes" "" "0" "" "" "g.100819577_100984729delinsTTCCCC" "" "pathogenic" "" "0000050348" "10" "70" "14" "101292195" "101292195" "" "0" "00006" "MEG3_000003" "g.101292195|bsrC" "" "{PMID:Kagami 2014:25351781}" "" "MEG3-DMR CG1" "hypomethylation DLK1-MEG3 intergenic differentially methylated region" "Somatic" "" "" "0" "0.03 (controls 0.43-0.56)" "" "" "" "likely pathogenic" "" "0000050349" "10" "30" "14" "101292200" "101292200" "" "0" "00006" "MEG3_000004" "g.101292200|bsrC" "" "{PMID:Kagami 2014:25351781}" "" "MEG3-DMR CG2" "hypomethylation DLK1-MEG3 intergenic differentially methylated region" "Somatic" "" "" "0" "0.03 (controls 0.52-0.65)" "" "" "" "likely benign" "" "0000050350" "10" "70" "14" "101292208" "101292208" "" "0" "00006" "MEG3_000005" "g.101292208|bsrC" "" "{PMID:Kagami 2014:25351781}" "" "MEG3-DMR CG3" "hypomethylation DLK1-MEG3 intergenic differentially methylated region" "Somatic" "" "" "0" "0.04 (controls 0.32-0.55)" "" "" "" "likely pathogenic" "" "0000050351" "10" "70" "14" "101292225" "101292225" "" "0" "00006" "MEG3_000006" "g.101292225|bsrC" "" "{PMID:Kagami 2014:25351781}" "" "MEG3-DMR CG4" "hypomethylation DLK1-MEG3 intergenic differentially methylated region" "Somatic" "" "" "0" "0.06 (controls 0.40-0.74)" "" "" "" "likely pathogenic" "" "0000050352" "10" "70" "14" "101292227" "101292227" "" "0" "00006" "MEG3_000007" "g.101292227|bsrC" "" "{PMID:Kagami 2014:25351781}" "" "MEG3-DMR CG5" "hypomethylation DLK1-MEG3 intergenic differentially methylated region" "Somatic" "" "" "0" "0.02 (controls 0.26-0.47)" "" "" "" "likely pathogenic" "" "0000050360" "10" "70" "14" "101292195" "101292195" "" "0" "00006" "MEG3_000003" "g.101292195|bsrC" "" "{PMID:Kagami 2014:25351781}" "" "MEG3-DMR CG1" "hypomethylation DLK1-MEG3 intergenic differentially methylated region" "Somatic" "" "" "0" "0.25 (controls 0.43-0.56)" "" "" "" "likely pathogenic" "" "0000050361" "10" "70" "14" "101292200" "101292200" "" "0" "00006" "MEG3_000004" "g.101292200|bsrC" "" "{PMID:Kagami 2014:25351781}" "" "MEG3-DMR CG2" "hypomethylation DLK1-MEG3 intergenic differentially methylated region" "Somatic" "" "" "0" "0.25 (controls 0.52-0.65)" "" "" "" "likely pathogenic" "" "0000050362" "10" "70" "14" "101292208" "101292208" "" "0" "00006" "MEG3_000005" "g.101292208|bsrC" "" "{PMID:Kagami 2014:25351781}" "" "MEG3-DMR CG3" "hypomethylation DLK1-MEG3 intergenic differentially methylated region" "Somatic" "" "" "0" "0.26 (controls 0.32-0.55)" "" "" "" "likely pathogenic" "" "0000050363" "10" "70" "14" "101292225" "101292225" "" "0" "00006" "MEG3_000006" "g.101292225|bsrC" "" "{PMID:Kagami 2014:25351781}" "" "MEG3-DMR CG4" "hypomethylation DLK1-MEG3 intergenic differentially methylated region" "Somatic" "" "" "0" "0.28 (controls 0.40-0.74)" "" "" "" "likely pathogenic" "" "0000050364" "10" "70" "14" "101292227" "101292227" "" "0" "00006" "MEG3_000007" "g.101292227|bsrC" "" "{PMID:Kagami 2014:25351781}" "" "MEG3-DMR CG5" "hypomethylation DLK1-MEG3 intergenic differentially methylated region" "Somatic" "" "" "0" "0.22 (controls 0.26-0.47)" "" "" "" "likely pathogenic" "" "0000051924" "21" "90" "14" "101291225" "101295527" "delins" "0" "01185" "MEG3_000008" "g.101291225_101295527delins101299974_101300039" "" "{PMID:Kagami 2010:20585555}, {CV:SCV000190042}" "" "NT_026437:82290978–82295280del, 82299727–82299792dup" "4303 bp deletion with 66 bp duplicative insertion (from MEG3 intron 5)" "De novo" "yes" "" "0" "" "" "" "" "pathogenic" "" "0000840898" "11" "90" "14" "101190852" "101299551" "delins" "0" "00006" "DLK1_000004" "g.101190852_101299551delinsT" "" "{PMID:Sabria-Back 2022:33579810}" "" "" "" "Germline" "" "" "0" "extensive methylation analysis" "" "g.100724515_100833214delinsT" "" "pathogenic (dominant)" "" "0000840899" "21" "90" "14" "101190852" "101299551" "delins" "0" "00006" "DLK1_000004" "g.101190852_101299551delinsT" "" "{PMID:Sabria-Back 2022:33579810}" "" "" "" "Germline" "" "" "0" "extensive methylation analysis" "" "g.100724515_100833214delinsT" "" "pathogenic (dominant)" "" ## 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 MEG3 ## Count = 16 "{{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}}" "0000031254" "00011985" "90" "0" "" "0" "" "n.-1123_936-613del" "r.0?" "p.0?" "" "0000037553" "00011985" "90" "0" "" "0" "" "n.-1123_936-613del" "r.0?" "-" "_1_3i" "0000037554" "00011985" "90" "1" "0" "1845" "0" "n.1_1845del" "r.0" "-" "_1_9_" "0000050348" "00011985" "70" "0" "" "0" "" "n.-250bsrC" "r.=" "-" "_1" "0000050349" "00011985" "30" "0" "" "0" "" "n.-245bsrC" "r.=" "-" "_1" "0000050350" "00011985" "70" "0" "" "0" "" "n.-237bsrC" "r.=" "-" "_1" "0000050351" "00011985" "70" "0" "" "0" "" "n.-220bsrC" "r.=" "-" "_1" "0000050352" "00011985" "70" "0" "" "0" "" "n.-218bsrC" "r.=" "-" "_1" "0000050360" "00011985" "70" "0" "" "0" "" "n.-250bsrC" "r.=" "-" "_1" "0000050361" "00011985" "70" "0" "" "0" "" "n.-245bsrC" "r.=" "-" "_1" "0000050362" "00011985" "70" "0" "" "0" "" "n.-237bsrC" "r.=" "-" "_1" "0000050363" "00011985" "70" "0" "" "0" "" "n.-220bsrC" "r.=" "-" "_1" "0000050364" "00011985" "70" "0" "" "0" "" "n.-218bsrC" "r.=" "-" "_1" "0000051924" "00011985" "90" "0" "" "0" "" "n.-1220_376delins1049+2103_1049+2168" "r.?" "-" "4i" "0000840898" "00011985" "90" "0" "0" "0" "0" "n.-1_1049+1680{0}" "r.?" "-" "" "0000840899" "00011985" "90" "0" "0" "0" "0" "n.-1_1049+1680{0}" "r.0?" "-" "" ## Screenings_To_Variants ## Do not remove or alter this header ## ## Count = 16 "{{screeningid}}" "{{variantid}}" "0000011597" "0000031254" "0000017579" "0000037553" "0000017580" "0000037554" "0000027203" "0000050348" "0000027203" "0000050349" "0000027203" "0000050350" "0000027203" "0000050351" "0000027203" "0000050352" "0000027206" "0000050360" "0000027206" "0000050361" "0000027206" "0000050362" "0000027206" "0000050363" "0000027206" "0000050364" "0000028660" "0000051924" "0000404929" "0000840898" "0000404930" "0000840899"