### LOVD-version 3000-30b ### Full data download ### To import, do not remove or alter this header ### ## Filter: (gene_public = SF3B4) # 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}}" "SF3B4" "splicing factor 3b, subunit 4, 49kDa" "1" "q21.2" "unknown" "NG_032777.1" "UD_132319158802" "" "http://www.LOVD.nl//SF3B4" "" "1" "10771" "10262" "605593" "1" "1" "1" "1" "Establishment of this gene variant database (LSDB) was supported by the European Community\'s Seventh Framework Programme (FP7/2007-2013) under grant agreement No 200754 - the GEN2PHEN project." "" "g" "http://databases.lovd.nl/shared/refseq/SF3B4_codingDNA.html" "1" "" "" "-1" "" "-1" "00001" "2012-06-04 00:00:00" "00006" "2016-07-20 16:43:47" "00006" "2025-10-14 09:22:11" ## 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}}" "00018769" "SF3B4" "splicing factor 3b, subunit 4, 49kDa" "001" "NM_005850.4" "" "NP_005841.1" "" "" "" "-493" "1500" "1275" "149900144" "149895209" "" "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}}" "00194" "AFD1" "dysostosis, acrofacial, type 1, (AFD-1, Nager type)" "AD" "154400" "" "" "" "00001" "2013-09-09 16:24:18" "00006" "2021-12-10 21:51:32" "00198" "?" "unclassified / mixed" "" "" "" "" "" "00006" "2013-09-13 14:21:47" "00006" "2024-11-23 09:38:12" "04254" "CLP" "cleft lip, cleft palate (CLP)" "" "" "" "" "" "00006" "2015-05-08 09:59:28" "00006" "2015-05-08 10:00:15" "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}}" "SF3B4" "00194" ## Individuals ## Do not remove or alter this header ## ## Count = 29 "{{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}}" "00078550" "" "" "" "1" "" "00006" "{PMID:Bernier 2012:22541558}" "" "F" "" "" ">5y" "0" "" "" "" "" "00078551" "" "" "" "1" "" "00006" "{PMID:Bernier 2012:22541558}" "father of F-2" "M" "" "" ">38y" "0" "" "" "" "" "00078552" "" "" "" "1" "" "00006" "{PMID:Bernier 2012:22541558}" "daughter of F-1" "F" "" "" ">1y" "0" "" "" "" "" "00078553" "" "" "" "1" "" "00006" "{PMID:Bernier 2012:22541558}" "" "F" "" "" ">13y" "0" "" "" "" "" "00078554" "" "" "" "1" "" "00006" "{PMID:Bernier 2012:22541558}" "Clinical features not determined" "F" "" "" ">15y" "0" "" "" "" "" "00078555" "" "" "" "1" "" "00006" "{PMID:Bernier 2012:22541558}" "" "F" "" "" ">1y" "0" "" "" "" "" "00078556" "" "" "" "1" "" "00006" "{PMID:Bernier 2012:22541558}" "" "M" "" "" ">2y" "0" "" "" "" "" "00078557" "" "" "" "1" "" "00006" "{PMID:Bernier 2012:22541558}" "son of J-2" "M" "" "" ">17y" "0" "" "" "" "" "00078558" "" "" "" "1" "" "00006" "{PMID:Bernier 2012:22541558}" "mother of J-1" "F" "" "" ">56y" "0" "" "" "" "" "00078559" "" "" "" "1" "" "00006" "{PMID:Bernier 2012:22541558}" "" "M" "" "" ">2y" "0" "" "" "" "" "00078560" "" "" "" "1" "" "00006" "{PMID:Bernier 2012:22541558}" "" "F" "" "" ">4y" "0" "" "" "" "" "00078561" "" "" "" "1" "" "00006" "{PMID:Bernier 2012:22541558}" "" "F" "" "" ">12y" "0" "" "" "" "" "00078562" "" "" "" "1" "" "00006" "{PMID:Bernier 2012:22541558}" "" "F" "" "" ">4y" "0" "" "" "" "" "00078563" "" "" "" "1" "" "00006" "{PMID:Bernier 2012:22541558}" "" "F" "" "" ">4y" "0" "" "" "" "" "00078564" "" "" "" "1" "" "00006" "{PMID:Bernier 2012:22541558}" "" "F" "" "" ">24y" "0" "" "" "" "" "00078565" "" "" "" "1" "" "00006" "{PMID:Bernier 2012:22541558}" "" "F" "" "" ">28y" "0" "" "" "" "" "00078566" "" "" "" "1" "" "00006" "{PMID:Bernier 2012:22541558}" "" "M" "" "" ">2y" "0" "" "" "" "" "00078567" "" "" "" "1" "" "00006" "{PMID:Bernier 2012:22541558}" "son of O-2" "M" "" "" ">1y" "0" "" "" "" "" "00078568" "" "" "" "1" "" "00006" "{PMID:Bernier 2012:22541558}" "mother of O-1" "F" "" "" ">28y" "0" "" "" "" "" "00078569" "" "" "" "1" "" "00006" "{PMID:Bernier 2012:22541558}" "" "F" "" "" ">23y" "0" "" "" "" "" "00078570" "" "" "" "1" "" "00006" "{PMID:Bernier 2012:22541558}" "mother (in publication: father) of M-2, M-3" "F" "" "" ">49y" "0" "" "" "" "" "00078571" "" "" "" "1" "" "00006" "{PMID:Bernier 2012:22541558}" "son of M-1" "M" "" "" ">20y" "0" "" "" "" "" "00078572" "" "" "" "1" "" "00006" "{PMID:Bernier 2012:22541558}" "son of M-1" "M" "" "" ">17y" "0" "" "" "" "" "00078573" "" "" "" "1" "" "00006" "{PMID:Bernier 2012:22541558}" "" "F" "" "" ">5y" "0" "" "" "" "" "00078574" "" "" "" "1" "" "00006" "{PMID:Bernier 2012:22541558}" "" "F" "" "" ">7y" "0" "" "" "" "" "00078575" "" "" "" "1" "" "00235" "" "" "M" "no" "Italy" "" "0" "" "" "" "" "00289517" "" "" "" "1" "" "03575" "{PMID:Narang 2020:32906206}, {DOI:Narang 2020:10.1002/humu.24102}" "analysis 2794 individuals (India)" "" "" "India" "" "0" "" "" "" "" "00449542" "" "" "" "1" "" "00006" "{PMID:Pan 2024:38479391}, {DOI:Pan 2024:10.1016/j.ajhg.2024.02.007}" "2-generation family, 1 affected, unaffected non-carrier parents" "F" "" "" "" "0" "" "" "" "Pat2" "00467266" "" "" "" "1" "cc_by-nc-nd_4.0;1" "04760" "CLP-1247-3" "" "F" "no" "" "" "" "" "" "" "CLP-1247-3" ## Individuals_To_Diseases ## Do not remove or alter this header ## ## Count = 29 "{{individualid}}" "{{diseaseid}}" "00078550" "00194" "00078551" "00194" "00078552" "00194" "00078553" "00194" "00078554" "00194" "00078555" "00194" "00078556" "00194" "00078557" "00194" "00078558" "00194" "00078559" "00194" "00078560" "00194" "00078561" "00194" "00078562" "00194" "00078563" "00194" "00078564" "00194" "00078565" "00194" "00078566" "00194" "00078567" "00194" "00078568" "00194" "00078569" "00194" "00078570" "00194" "00078571" "00194" "00078572" "00194" "00078573" "00194" "00078574" "00194" "00078575" "00194" "00289517" "00198" "00449542" "05611" "00467266" "04254" ## Phenotypes ## Do not remove or alter this header ## ## Note: Only showing Phenotype columns active for Diseases 00194, 00198, 04254, 05611 ## Count = 28 "{{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/Lung}}" "{{Phenotype/Diagnosis/Definite}}" "{{Phenotype/Diagnosis/Initial}}" "{{Phenotype/Diagnosis/Criteria}}" "0000058321" "00194" "00078550" "00006" "Isolated (sporadic)" "5y" "Nager syndrome; Downslanted palpebral fissures; absent lower eyelashes (sparse); midface retrusion; micrognathia; cleft soft palate; abnormal ears; hearing loss; abnormal thumbs (stiff bilateral); radioulnar synostosis (bilateral)" "" "" "" "" "" "" "" "" "" "" "" "0000058322" "00194" "00078551" "00006" "Isolated (sporadic)" "38y" "Nager syndrome; Downslanted palpebral fissures; micrognathia; radioulnar synostosis; valgus laxity of knees and ankles" "" "" "" "" "" "" "" "" "" "" "" "0000058323" "00194" "00078552" "00006" "Familial, autosomal dominant" "1y" "Nager syndrome; Micrognathia; cleft palate; tracheotomy; hearing loss; radioulnar synostosis; subglottic stenosis" "" "" "" "" "" "" "" "" "" "" "" "0000058324" "00194" "00078553" "00006" "Isolated (sporadic)" "13y" "Nager syndrome; Downslanted palpebral fissures; absent lower eyelashes; midface retrusion; micrognathia; ankylosis of temporomandibular joint; high arched, cleft soft palate; tracheotomy; abnormal ears; hearing loss; absent right thumb and small and stiff left thumb; radioulnar synostosis; delayed development; limited range of movement in elbows and shoulders, camptodactyly, left clubfoot, renal abnormalities, ventriculoseptal defect and dacryostenosis" "" "" "" "" "" "" "" "" "" "" "" "0000058325" "00194" "00078554" "00006" "Isolated (sporadic)" "15y" "Nager syndrome" "" "" "" "" "" "" "" "" "" "" "" "0000058326" "00194" "00078555" "00006" "Isolated (sporadic)" "1y" "Nager syndrome; Absent lower eyelashes (minimal); midface retrusion; micrognathia; abnormal soft palate; abnormal ears; hearing loss; radial ray abnormality; absent thumbs (bilateral); hair extension on cheek, strabismus, mitral valve prolapse, and limited range of movement in elbows" "" "" "" "" "" "" "" "" "" "" "" "0000058327" "00194" "00078556" "00006" "Isolated (sporadic)" "2y" "Nager syndrome; Downslanted palpebral fissures; midface retrusion; micrognathia; abnormal palate; abnormal ears; hearing loss; radial ray abnormality; abnormal thumbs; radioulnar synostosis; intellectual disability" "" "" "" "" "" "" "" "" "" "" "" "0000058328" "00194" "00078557" "00006" "Familial, autosomal dominant" "17y" "Nager syndrome; Downslanted palpebral fissures; absent lower eyelashes; midface retrusion; micrognathia; tracheotomy; abnormal ears; hearing loss; abnormal thumbs" "" "" "" "" "" "" "" "" "" "" "" "0000058329" "00194" "00078558" "00006" "Isolated (sporadic)" "56y" "Nager syndrome; Downslanted palpebral fissures; micrognathia" "" "" "" "" "" "" "" "" "" "" "" "0000058330" "00194" "00078559" "00006" "Isolated (sporadic)" "2y" "Nager syndrome; Downslanted palpebral fissures; absent lower eyelashes (decreased); midface retrusion; micrognathia; abnormal soft palate; abnormal ears; hearing loss; radial ray abnormality; abnormal thumbs (proximally placed and stiff); radioulnar synostosis (right)" "" "" "" "" "" "" "" "" "" "" "" "0000058331" "00194" "00078560" "00006" "Isolated (sporadic)" "4y" "Nager syndrome; Downslanted palpebral fissures; midface retrusion; micrognathia; high arched palate; tracheotomy; abnormal ears; radial ray abnormality; abnormal thumbs; short stature and bilateral syndactyly of the 4th and 5th toes" "" "" "" "" "" "" "" "" "" "" "" "0000058332" "00194" "00078561" "00006" "Isolated (sporadic)" "12y" "Nager syndrome; Micrognathia; ankylosis of temporomandibular joint; cleft palate; tracheotomy; hearing loss; radial ray abnormality; abnormal thumbs (absent bilateral); radioulnar synostosis" "" "" "" "" "" "" "" "" "" "" "" "0000058333" "00194" "00078562" "00006" "Isolated (sporadic)" "4y" "Nager syndrome; Downslanted palpebral fissures; absent lower eyelashes; micrognathia; hearing loss; radial ray abnormality; absent left thumb and fused right distal interphalangeal joint; radioulnar synostosis; limited range of motion in all extremities at birth, arachnodactyly, and small 5th fingers" "" "" "" "" "" "" "" "" "" "" "" "0000058334" "00194" "00078563" "00006" "Isolated (sporadic)" "4y" "Nager syndrome; Downslanted palpebral fissures; midface retrusion; micrognathia; tracheotomy; abnormal ears; radial ray abnormality; abnormal thumbs; radioulnar synostosis; ventriculoseptal defect and diaphragmatic hernia" "" "" "" "" "" "" "" "" "" "" "" "0000058335" "00194" "00078564" "00006" "Isolated (sporadic)" "24y" "Nager syndrome; Downslanted palpebral fissures; absent lower eyelashes; midface retrusion; micrognathia; tracheotomy; abnormal ears; hearing loss; small right thumb and slender left thumb; radioulnar synostosis (unilateral); abnormal teeth, partial absence of left fingers 3-5, slencer haluces, and hallux valgus" "" "" "" "" "" "" "" "" "" "" "" "0000058336" "00194" "00078565" "00006" "Isolated (sporadic)" "28y" "Nager syndrome; Downslanted palpebral fissures; absent lower eyelashes (sparse); midface retrusion; micrognathia; abnormal ears; hearing loss; small abnormal thumbs" "" "" "" "" "" "" "" "" "" "" "" "0000058337" "00194" "00078566" "00006" "Isolated (sporadic)" "2y" "Nager syndrome; Downslanted palpebral fissures; midface retrusion; micrognathia; cleft palate; tracheotomy; abnormal ears; radial ray abnormality (absent bilateral); abnormal thumbs (absent bilateral); delayed development; fused 1st and 2nd right metacarpals and bilateral foot deformities" "" "" "" "" "" "" "" "" "" "" "" "0000058338" "00194" "00078567" "00006" "Familial, autosomal dominant" "1y" "Nager syndrome; Downslanted palpebral fissures; micrognathia; abnormal soft palate; abnormal ears; hearing loss; absent right thumb and small left thumb" "" "" "" "" "" "" "" "" "" "" "" "0000058339" "00194" "00078568" "00006" "Isolated (sporadic)" "28y" "Nager syndrome; Downslanted palpebral fissures; micrognathia; abnormal soft palate; abnormal ears; hearing loss; small abnormal thumbs; radioulnar synostosis (bilateral)" "" "" "" "" "" "" "" "" "" "" "" "0000058340" "00194" "00078569" "00006" "Isolated (sporadic)" "23y" "Nager syndrome; Downslanted palpebral fissures; midface retrusion; micrognathia; abnormal ears (mild); hearing loss; abnormal thumbs (hypoplasia); radioulnar synostosis (bilateral); speech delay; asymmetric face, velopharyngeal insufficiency; and cervical ribs" "" "" "" "" "" "" "" "" "" "" "" "0000058341" "00194" "00078570" "00006" "Isolated (sporadic)" "49y" "Nager syndrome; Downslanted palpebral fissures; midface retrusion; cleft palate; abnormal ears (cupped); hearing loss; abnormal thumbs (small)" "" "" "" "" "" "" "" "" "" "" "" "0000058342" "00194" "00078571" "00006" "Familial, autosomal dominant" "20y" "Nager syndrome; Downslanted palpebral fissures; absent lower eyelashes (sparse); midface retrusion; micrognathia; tracheotomy; abnormal ears (cupped, narrow canals); hearing loss; absent right thumb and small left thumb; radioulnar synostosis (right > left); delayed speech and fine motor; short stature (3-5%), dacryostenosis, and small first toes and first metatarsals" "" "" "" "" "" "" "" "" "" "" "" "0000058343" "00194" "00078572" "00006" "Familial, autosomal dominant" "17y" "Nager syndrome; Downslanted palpebral fissures; absent lower eyelashes; midface retrusion; micrognathia; abnormal palate; abnormal ears (cupped, narrow canals); hearing loss; small right thumb compared to left; radioulnar synostosis (left); delayed development; dacryostenosis, short first metatarsals, and sandal gap" "" "" "" "" "" "" "" "" "" "" "" "0000058344" "00194" "00078573" "00006" "Isolated (sporadic)" "5y" "Nager syndrome; Absent lower eyelashes; micrognathia; cleft palate; hearing loss; radial ray abnormality; abnormal thumbs" "" "" "" "" "" "" "" "" "" "" "" "0000058345" "00194" "00078574" "00006" "Familial, autosomal dominant" "7y" "Nager syndrome; Downslanted palpebral fissures; midface retrusion; micrognathia; abnormal palate; abnormal ears; hearing loss; radial ray abnormality (short); abnormal thumbs (stiff bilateral)" "" "" "" "" "" "" "" "" "" "" "" "0000058346" "00194" "00078575" "00235" "Familial, autosomal dominant" "" "Nager syndrome" "" "" "" "" "" "" "" "" "" "" "" "0000338716" "05611" "00449542" "00006" "Isolated (sporadic)" "19y" "see paper; ..., premature placental abruption; developmental delay and/or intellectual disability; delayed speech, delayed language; no autism; dissociative motor disorder, borderline personality disorder, recurrent depressive disorders, eating disorder; hypotonia; no seizure; brain MRI/CT normal; patent ductus arteriosus, patent foramen ovale, pulmonary artery stenosis; urinary incontinence; no gastrointestinal anomalies; long face, down-slanted palpebral fissures, retrognathy, low-set ears (can be attributed to SF3B4 variant); hearing impairment; median cleft palate; dental crowding (can be attributed to SF3B4 variant)" "" "" "" "" "" "" "" "" "" "developmental delay, intellectual disability, dysmorphic features" "" "0000352473" "04254" "00467266" "04760" "Isolated (sporadic)" "06y" "posterior cleft palate" "" "" "" "" "" "" "" "" "" "" "" ## Screenings ## Do not remove or alter this header ## ## Count = 29 "{{id}}" "{{individualid}}" "{{variants_found}}" "{{owned_by}}" "{{created_by}}" "{{created_date}}" "{{edited_by}}" "{{edited_date}}" "{{Screening/Technique}}" "{{Screening/Template}}" "{{Screening/Tissue}}" "{{Screening/Remarks}}" "0000078731" "00078550" "1" "00006" "00002" "2012-06-06 09:16:40" "" "" "SEQ-NG-I" "DNA" "" "" "0000078732" "00078551" "1" "00006" "00002" "2012-06-06 09:16:40" "" "" "SEQ-NG-I" "DNA" "" "" "0000078733" "00078552" "1" "00006" "00002" "2012-06-06 09:16:40" "" "" "SEQ-NG-I" "DNA" "" "" "0000078734" "00078553" "1" "00006" "00002" "2012-06-06 09:16:40" "" "" "SEQ-NG-I" "DNA" "" "" "0000078735" "00078554" "1" "00006" "00002" "2012-06-06 09:16:40" "" "" "SEQ-NG-I" "DNA" "" "" "0000078736" "00078555" "1" "00006" "00002" "2012-06-06 09:16:40" "" "" "SEQ-NG-I" "DNA" "" "" "0000078737" "00078556" "1" "00006" "00002" "2012-06-06 09:16:40" "" "" "SEQ-NG-I" "DNA" "" "" "0000078738" "00078557" "1" "00006" "00002" "2012-06-06 09:16:40" "" "" "SEQ-NG-I" "DNA" "" "" "0000078739" "00078558" "1" "00006" "00002" "2012-06-06 09:16:40" "" "" "SEQ-NG-I" "DNA" "" "" "0000078740" "00078559" "1" "00006" "00002" "2012-06-06 09:16:40" "" "" "SEQ-NG-I" "DNA" "" "" "0000078741" "00078560" "1" "00006" "00002" "2012-06-06 09:16:40" "" "" "SEQ-NG-I" "DNA" "" "" "0000078742" "00078561" "1" "00006" "00002" "2012-06-06 09:16:40" "" "" "SEQ-NG-I" "DNA" "" "" "0000078743" "00078562" "1" "00006" "00002" "2012-06-06 09:16:40" "" "" "SEQ-NG-I" "DNA" "" "" "0000078744" "00078563" "1" "00006" "00002" "2012-06-06 09:16:40" "" "" "SEQ-NG-I" "DNA" "" "" "0000078745" "00078564" "1" "00006" "00002" "2012-06-06 09:16:40" "" "" "SEQ-NG-I" "DNA" "" "" "0000078746" "00078565" "1" "00006" "00002" "2012-06-06 09:16:40" "" "" "SEQ-NG-I" "DNA" "" "" "0000078747" "00078566" "1" "00006" "00002" "2012-06-06 09:16:40" "" "" "SEQ-NG-I" "DNA" "" "" "0000078748" "00078567" "1" "00006" "00002" "2012-06-06 09:16:40" "" "" "SEQ-NG-I" "DNA" "" "" "0000078749" "00078568" "1" "00006" "00002" "2012-06-06 09:16:40" "" "" "SEQ-NG-I" "DNA" "" "" "0000078750" "00078569" "1" "00006" "00002" "2012-06-06 09:16:40" "" "" "SEQ-NG-I" "DNA" "" "" "0000078751" "00078570" "1" "00006" "00002" "2012-06-06 09:16:40" "" "" "SEQ-NG-I" "DNA" "" "" "0000078752" "00078571" "1" "00006" "00002" "2012-06-06 09:16:40" "" "" "SEQ-NG-I" "DNA" "" "" "0000078753" "00078572" "1" "00006" "00002" "2012-06-06 09:16:40" "" "" "SEQ-NG-I" "DNA" "" "" "0000078754" "00078573" "1" "00006" "00002" "2012-06-06 09:16:40" "" "" "SEQ-NG-I" "DNA" "" "" "0000078755" "00078574" "1" "00006" "00002" "2012-06-06 09:16:40" "" "" "SEQ-NG-I" "DNA" "" "" "0000078756" "00078575" "1" "00235" "00235" "2016-07-20 10:46:03" "" "" "SEQ" "DNA" "" "" "0000290685" "00289517" "1" "03575" "00006" "2020-03-11 19:30:02" "" "" "arraySNP" "DNA" "" "Infinium Global Screening Array v1.0" "0000451132" "00449542" "1" "00006" "00006" "2024-04-22 10:35:23" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000468929" "00467266" "1" "04760" "04760" "2025-10-09 15:43:53" "" "" "SEQ-NG" "DNA" "" "WES (whole exome sequencing)" ## Screenings_To_Genes ## Do not remove or alter this header ## ## Count = 26 "{{screeningid}}" "{{geneid}}" "0000078731" "SF3B4" "0000078732" "SF3B4" "0000078733" "SF3B4" "0000078734" "SF3B4" "0000078735" "SF3B4" "0000078736" "SF3B4" "0000078737" "SF3B4" "0000078738" "SF3B4" "0000078739" "SF3B4" "0000078740" "SF3B4" "0000078741" "SF3B4" "0000078742" "SF3B4" "0000078743" "SF3B4" "0000078744" "SF3B4" "0000078745" "SF3B4" "0000078746" "SF3B4" "0000078747" "SF3B4" "0000078748" "SF3B4" "0000078749" "SF3B4" "0000078750" "SF3B4" "0000078751" "SF3B4" "0000078752" "SF3B4" "0000078753" "SF3B4" "0000078754" "SF3B4" "0000078755" "SF3B4" "0000078756" "SF3B4" ## 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 = 44 "{{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}}" "0000125833" "0" "70" "1" "149899651" "149899651" "subst" "0" "00006" "SF3B4_000001" "g.149899651T>C" "" "{PMID:Bernier 2012:22541558}" "BceAI+;NcoI-" "p.Met1?" "" "De novo" "" "" "0" "" "" "g.149927759T>C" "" "likely pathogenic" "" "0000125834" "0" "70" "1" "149899651" "149899651" "subst" "0" "00006" "SF3B4_000001" "g.149899651T>C" "" "{PMID:Bernier 2012:22541558}" "BceAI+;NcoI-" "p.Met1?" "" "Germline" "" "" "0" "" "" "g.149927759T>C" "" "likely pathogenic" "" "0000125835" "0" "70" "1" "149899651" "149899651" "subst" "0" "00006" "SF3B4_000001" "g.149899651T>C" "" "{PMID:Bernier 2012:22541558}" "BceAI+;NcoI-" "p.Met1?" "" "Germline" "" "" "0" "" "" "g.149927759T>C" "" "likely pathogenic" "" "0000125836" "0" "70" "1" "149899133" "149899133" "del" "0" "00006" "SF3B4_000002" "g.149899133del" "" "{PMID:Bernier 2012:22541558}" "BslI+" "88delT" "" "Germline" "" "" "0" "" "" "g.149927241del" "" "likely pathogenic" "" "0000125837" "0" "70" "1" "149898522" "149898522" "subst" "0" "00006" "SF3B4_000003" "g.149898522G>T" "" "{PMID:Bernier 2012:22541558}" "MseI+" "" "" "Germline" "" "" "0" "" "" "g.149926630G>T" "" "likely pathogenic" "" "0000125838" "0" "70" "1" "149898349" "149898349" "subst" "0" "00006" "SF3B4_000004" "g.149898349G>A" "" "{PMID:Bernier 2012:22541558}" "PvuII-" "" "" "Germline" "" "" "0" "" "" "g.149926457G>A" "" "likely pathogenic" "" "0000125839" "0" "70" "1" "149898310" "149898313" "dup" "0" "00006" "SF3B4_000005" "g.149898310_149898313dup" "" "{PMID:Bernier 2012:22541558}" "" "661_664dupCCCA" "" "Germline" "" "" "0" "" "" "g.149926418_149926421dup" "" "likely pathogenic" "" "0000125840" "0" "70" "1" "149899651" "149899651" "subst" "0" "00006" "SF3B4_000001" "g.149899651T>C" "" "{PMID:Bernier 2012:22541558}" "BceAI+;NcoI-" "p.Met1?" "" "Germline" "" "" "0" "" "" "g.149927759T>C" "" "likely pathogenic" "" "0000125841" "0" "70" "1" "149899651" "149899651" "subst" "0" "00006" "SF3B4_000001" "g.149899651T>C" "" "{PMID:Bernier 2012:22541558}" "BceAI+;NcoI-" "p.Met1?" "" "Germline" "" "" "0" "" "" "g.149927759T>C" "" "likely pathogenic" "" "0000125842" "0" "70" "1" "149897872" "149897872" "del" "0" "00006" "SF3B4_000006" "g.149897872del" "" "{PMID:Bernier 2012:22541558}" "BanI+;BciVI-" "769delA" "" "Germline" "" "" "0" "" "" "g.149925980del" "" "likely pathogenic" "" "0000125843" "0" "70" "1" "149897845" "149897845" "dup" "0" "00006" "SF3B4_000007" "g.149897845dup" "" "{PMID:Bernier 2012:22541558}" "" "796dupA" "" "Germline" "" "" "0" "" "" "g.149925953dup" "" "likely pathogenic" "" "0000125844" "0" "70" "1" "149897819" "149897819" "dup" "0" "00006" "SF3B4_000008" "g.149897819dup" "" "{PMID:Bernier 2012:22541558}" "" "827dupC" "" "Germline" "" "" "0" "" "" "g.149925927dup" "" "likely pathogenic" "" "0000125845" "0" "70" "1" "149897805" "149897806" "ins" "0" "00006" "SF3B4_000009" "g.149897805_149897806insATACCCC" "" "{PMID:Bernier 2012:22541558}" "NlaIV-" "" "" "De novo" "" "" "0" "" "" "g.149925913_149925914insATACCCC" "" "likely pathogenic" "" "0000125846" "0" "70" "1" "149897777" "149897777" "del" "0" "00006" "SF3B4_000010" "g.149897777del" "" "{PMID:Bernier 2012:22541558}" "Hpy188III+FatI-" "864delT" "" "De novo" "" "" "0" "" "" "g.149925885del" "" "likely pathogenic" "" "0000125847" "0" "70" "1" "149897727" "149897727" "subst" "0" "00006" "SF3B4_000011" "g.149897727C>T" "" "{PMID:Bernier 2012:22541558}" "Hpy188III+BslI-" "" "" "Germline" "" "" "0" "" "" "g.149925835C>T" "" "likely pathogenic" "" "0000125848" "0" "70" "1" "149895766" "149895766" "dup" "0" "00006" "SF3B4_000012" "g.149895766dup" "" "{PMID:Bernier 2012:22541558}" "" "1060dupC" "" "De novo" "" "" "0" "" "" "g.149923874dup" "" "likely pathogenic" "" "0000125849" "0" "70" "1" "149895568" "149895568" "del" "0" "00006" "SF3B4_000013" "g.149895568del" "" "{PMID:Bernier 2012:22541558}" "BslI-" "1147delC" "" "De novo" "" "" "0" "" "" "g.149923676del" "" "likely pathogenic" "" "0000125850" "0" "70" "1" "149895568" "149895568" "dup" "0" "00006" "SF3B4_000014" "g.149895568dup" "" "{PMID:Bernier 2012:22541558}" "" "1147dupC" "" "Germline" "" "" "0" "" "" "g.149923676dup" "" "likely pathogenic" "" "0000125851" "0" "70" "1" "149895568" "149895568" "dup" "0" "00006" "SF3B4_000014" "g.149895568dup" "" "{PMID:Bernier 2012:22541558}" "" "1147dupC" "" "Germline" "" "" "0" "" "" "g.149923676dup" "" "likely pathogenic" "" "0000125852" "0" "70" "1" "149895561" "149895561" "dup" "0" "00006" "SF3B4_000015" "g.149895561dup" "" "{PMID:Bernier 2012:22541558}" "BtgI-" "1148dupA" "" "Germline" "" "" "0" "" "" "g.149923669dup" "" "likely pathogenic" "" "0000125853" "0" "70" "1" "149895511" "149895511" "del" "0" "00006" "SF3B4_000016" "g.149895511del" "" "{PMID:Bernier 2012:22541558}" "BanII+;MnlI-" "1199delC" "" "Germline" "" "" "0" "" "" "g.149923619del" "" "likely pathogenic" "" "0000125854" "0" "70" "1" "149895511" "149895511" "del" "0" "00006" "SF3B4_000016" "g.149895511del" "" "{PMID:Bernier 2012:22541558}" "BanII+;MnlI-" "1199delC" "" "Germline" "" "" "0" "" "" "g.149923619del" "" "likely pathogenic" "" "0000125855" "0" "70" "1" "149895511" "149895511" "del" "0" "00006" "SF3B4_000016" "g.149895511del" "" "{PMID:Bernier 2012:22541558}" "BanII+;MnlI-" "1199delC" "" "Germline" "" "" "0" "" "" "g.149923619del" "" "likely pathogenic" "" "0000125856" "0" "70" "1" "149895478" "149895478" "del" "0" "00006" "SF3B4_000017" "g.149895478del" "" "{PMID:Bernier 2012:22541558}" "HpyCH4III+BsrI-" "1232delC" "" "Germline" "" "" "0" "" "" "g.149923586del" "" "likely pathogenic" "" "0000125857" "0" "70" "1" "149895451" "149895457" "del" "0" "00006" "SF3B4_000018" "g.149895451_149895457del" "" "" "BseYI+;MnlI-" "1252_1258delCTTCGAG" "" "Germline" "" "" "0" "" "" "g.149923559_149923565del" "" "likely pathogenic" "" "0000125858" "21" "90" "1" "149898557" "149898557" "subst" "0" "00235" "SF3B4_000019" "g.149898557G>A" "" "" "" "" "The deleterious effect of the synonymous variant on splcing was proven by a hybrid minigene assay on HEK293 cells" "Germline" "yes" "" "0" "" "" "g.149926665G>A" "" "pathogenic" "" "0000320965" "0" "30" "1" "149903313" "149903313" "subst" "3.03764E-5" "01804" "MTMR11_000002" "g.149903313C>T" "" "" "" "MTMR11(NM_001145862.1):c.1129G>A (p.(Gly377Ser))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "0" "" "" "g.149931421C>T" "" "likely benign" "" "0000503058" "0" "30" "1" "149895819" "149895819" "subst" "0" "01804" "MTMR11_000003" "g.149895819G>A" "" "" "" "SF3B4(NM_005850.4):c.1001C>T (p.(Pro334Leu))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "g.149923927G>A" "" "likely benign" "" "0000503059" "0" "70" "1" "149895907" "149895907" "subst" "0" "02327" "MTMR11_000004" "g.149895907C>G" "" "" "" "" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "g.149924015C>G" "" "likely pathogenic" "" "0000503060" "0" "30" "1" "149895911" "149895911" "subst" "0" "01804" "MTMR11_000005" "g.149895911G>C" "" "" "" "SF3B4(NM_005850.4):c.914-5C>G (p.?)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "g.149924019G>C" "" "likely benign" "" "0000503061" "0" "50" "1" "149898400" "149898400" "subst" "0" "02325" "MTMR11_000006" "g.149898400C>T" "" "" "" "SF3B4(NM_005850.5):c.574G>A (p.E192K)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "g.149926508C>T" "" "VUS" "" "0000647374" "1" "70" "1" "149898811" "149898811" "subst" "0" "03575" "SF3B4_000020" "g.149898811C>T" "1/2795 individuals" "{PMID:Narang 2020:32906206}, {DOI:Narang 2020:10.1002/humu.24102}" "" "" "1 heterozygous, no homozygous; {DB:CLININrs797044869}" "Germline" "" "rs797044869" "0" "" "" "g.149926919C>T" "" "likely pathogenic" "" "0000798761" "0" "90" "1" "149895865" "149895865" "dup" "0" "01943" "MTMR11_000010" "g.149895865dup" "" "" "" "SF3B4(NM_005850.4):c.956dupT (p.L319Ffs*167)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "pathogenic" "" "0000882756" "0" "90" "1" "149898365" "149898365" "del" "0" "02327" "MTMR11_000011" "g.149898365del" "" "" "" "" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "pathogenic" "" "0000922942" "0" "50" "1" "149895738" "149895738" "subst" "4.49507E-6" "02325" "MTMR11_000012" "g.149895738G>T" "" "" "" "SF3B4(NM_005850.5):c.1082C>A (p.P361H)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "VUS" "" "0000946974" "0" "30" "1" "149897906" "149897906" "subst" "0.00327463" "02326" "MTMR11_000013" "g.149897906G>A" "" "" "" "SF3B4(NM_005850.5):c.735C>T (p.P245=)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely benign" "" "0000984912" "0" "90" "1" "149898557" "149898557" "subst" "0" "00006" "SF3B4_000019" "g.149898557G>A" "" "{PMID:Pan 2024:38479391}, {DOI:Pan 2024:10.1016/j.ajhg.2024.02.007}" "" "" "ACMG PVS1, PS2_M, PS3, PS4_S, PM2_S; variant associated with acrofacial dysostosis 1, Nager type" "De novo" "" "" "0" "" "" "g.149926665G>A" "" "pathogenic (dominant)" "" "0000990254" "0" "50" "1" "149895728" "149895728" "subst" "9.31932E-6" "01804" "MTMR11_000014" "g.149895728C>T" "" "" "" "SF3B4(NM_005850.4):c.1087+5G>A (p.?)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "VUS" "" "0000990255" "0" "30" "1" "149895850" "149895850" "subst" "0" "01804" "MTMR11_000015" "g.149895850C>T" "" "" "" "SF3B4(NM_005850.4):c.970G>A (p.(Ala324Thr))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely benign" "" "0000990256" "0" "50" "1" "149897723" "149897723" "subst" "8.14511E-6" "01804" "MTMR11_000016" "g.149897723C>A" "" "" "" "SF3B4(NM_005850.4):c.913+5G>T (p.?)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "VUS" "" "0000990257" "0" "50" "1" "149897737" "149897737" "subst" "4.07289E-6" "01804" "MTMR11_000017" "g.149897737G>A" "" "" "" "SF3B4(NM_005850.4):c.904C>T (p.(Pro302Ser))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "VUS" "" "0000990258" "0" "30" "1" "149897942" "149897942" "subst" "0.000141857" "01804" "MTMR11_000018" "g.149897942G>A" "" "" "" "SF3B4(NM_005850.4):c.707-8C>T (p.?)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely benign" "" "0001031236" "0" "10" "1" "149898292" "149898292" "subst" "0.0176041" "01804" "MTMR11_000019" "g.149898292A>G" "" "" "" "SF3B4(NM_005850.5):c.682T>C (p.(Leu228=))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "benign" "" "0001048966" "11" "70" "1" "149898663" "149898663" "subst" "1.21817E-5" "04760" "SF3B4_000021" "g.149898663A>G" "" "" "" "" "" "Germline" "no" "" "" "" "" "g.149926771A>G" "" "likely pathogenic" "ACMG" ## 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 SF3B4 ## Count = 44 "{{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}}" "0000125833" "00018769" "70" "1" "0" "1" "0" "c.1A>G" "r.(?)" "p.0?" "1" "0000125834" "00018769" "70" "1" "0" "1" "0" "c.1A>G" "r.(?)" "p.0?" "1" "0000125835" "00018769" "70" "1" "0" "1" "0" "c.1A>G" "r.(?)" "p.0?" "1" "0000125836" "00018769" "70" "88" "0" "88" "0" "c.88del" "r.(?)" "p.(Trp30Glyfs*10)" "2" "0000125837" "00018769" "70" "452" "0" "452" "0" "c.452C>A" "r.(?)" "p.(Ser151*)" "3" "0000125838" "00018769" "70" "625" "0" "625" "0" "c.625C>T" "r.(?)" "p.(Gln209*)" "3" "0000125839" "00018769" "70" "661" "0" "664" "0" "c.661_664dup" "r.(?)" "p.(Asn222Thrfs*265)" "3" "0000125840" "00018769" "70" "1" "0" "1" "0" "c.1A>G" "r.(?)" "p.0?" "1" "0000125841" "00018769" "70" "1" "0" "1" "0" "c.1A>G" "r.(?)" "p.0?" "1" "0000125842" "00018769" "70" "769" "0" "769" "0" "c.769del" "r.(?)" "p.(Ile257Tyrfs*63)" "4" "0000125843" "00018769" "70" "796" "0" "796" "0" "c.796dup" "r.(?)" "p.(Met266Asnfs*220)" "4" "0000125844" "00018769" "70" "827" "0" "827" "0" "c.827dup" "r.(?)" "p.(Ser277Ilefs*209)" "4" "0000125845" "00018769" "70" "836" "0" "837" "0" "c.836_837insGGGTATG" "r.(?)" "p.(Thr280Glyfs*208)" "4" "0000125846" "00018769" "70" "864" "0" "864" "0" "c.864del" "r.(?)" "p.(His288Glnfs*32)" "4" "0000125847" "00018769" "70" "913" "1" "913" "1" "c.913+1G>A" "r.(?)" "p.(=)" "4i" "0000125848" "00018769" "70" "1060" "0" "1060" "0" "c.1060dup" "r.(?)" "p.(Arg354Profs*132)" "5" "0000125849" "00018769" "70" "1147" "0" "1147" "0" "c.1147del" "r.(?)" "p.(His383Metfs*75)" "6" "0000125850" "00018769" "70" "1147" "0" "1147" "0" "c.1147dup" "r.(?)" "p.(His383Profs*103)" "6" "0000125851" "00018769" "70" "1147" "0" "1147" "0" "c.1147dup" "r.(?)" "p.(His383Profs*103)" "6" "0000125852" "00018769" "70" "1148" "0" "1148" "0" "c.1148dup" "r.(?)" "p.(His383Glnfs*103)" "6" "0000125853" "00018769" "70" "1199" "0" "1199" "0" "c.1199del" "r.(?)" "p.(Pro400Leufs*58)" "6" "0000125854" "00018769" "70" "1199" "0" "1199" "0" "c.1199del" "r.(?)" "p.(Pro400Leufs*58)" "6" "0000125855" "00018769" "70" "1199" "0" "1199" "0" "c.1199del" "r.(?)" "p.(Pro400Leufs*58)" "6" "0000125856" "00018769" "70" "1232" "0" "1232" "0" "c.1232del" "r.(?)" "p.(Pro411Glnfs*47)" "6" "0000125857" "00018769" "70" "1252" "0" "1258" "0" "c.1252_1258del" "r.(?)" "p.(Leu418Alafs*38)" "6" "0000125858" "00018769" "90" "417" "0" "417" "0" "c.417C>T" "r.[=, 416_537del, 416_540del]" "p.[=, p.Gly139Glufs*6, p.Asn140Leufs*4]" "3" "0000320965" "00018769" "30" "-3662" "0" "-3662" "0" "c.-3662G>A" "r.(?)" "p.(=)" "" "0000503058" "00018769" "30" "1001" "0" "1001" "0" "c.1001C>T" "r.(?)" "p.(Pro334Leu)" "" "0000503059" "00018769" "70" "914" "-1" "914" "-1" "c.914-1G>C" "r.spl?" "p.?" "" "0000503060" "00018769" "30" "914" "-5" "914" "-5" "c.914-5C>G" "r.spl?" "p.?" "" "0000503061" "00018769" "50" "574" "0" "574" "0" "c.574G>A" "r.(?)" "p.(Glu192Lys)" "" "0000647374" "00018769" "70" "164" "-1" "164" "-1" "c.164-1G>A" "r.spl?" "p.?" "" "0000798761" "00018769" "90" "956" "0" "956" "0" "c.956dup" "r.(?)" "p.(Leu319Phefs*167)" "" "0000882756" "00018769" "90" "610" "0" "610" "0" "c.610del" "r.(?)" "p.(Ala204Leufs*116)" "" "0000922942" "00018769" "50" "1082" "0" "1082" "0" "c.1082C>A" "r.(?)" "p.(Pro361His)" "" "0000946974" "00018769" "30" "735" "0" "735" "0" "c.735C>T" "r.(?)" "p.(=)" "" "0000984912" "00018769" "90" "417" "0" "417" "0" "c.417C>T" "r.spl" "p.(Asp140LeufsTer3)" "" "0000990254" "00018769" "50" "1087" "5" "1087" "5" "c.1087+5G>A" "r.spl?" "p.?" "" "0000990255" "00018769" "30" "970" "0" "970" "0" "c.970G>A" "r.(?)" "p.(Ala324Thr)" "" "0000990256" "00018769" "50" "913" "5" "913" "5" "c.913+5G>T" "r.spl?" "p.?" "" "0000990257" "00018769" "50" "904" "0" "904" "0" "c.904C>T" "r.(?)" "p.(Pro302Ser)" "" "0000990258" "00018769" "30" "707" "-8" "707" "-8" "c.707-8C>T" "r.(=)" "p.(=)" "" "0001031236" "00018769" "10" "682" "0" "682" "0" "c.682T>C" "r.(?)" "p.(=)" "" "0001048966" "00018769" "70" "311" "0" "311" "0" "c.311T>C" "r.(?)" "p.(Ile104Thr)" "3" ## Screenings_To_Variants ## Do not remove or alter this header ## ## Count = 29 "{{screeningid}}" "{{variantid}}" "0000078731" "0000125833" "0000078732" "0000125834" "0000078733" "0000125835" "0000078734" "0000125836" "0000078735" "0000125837" "0000078736" "0000125838" "0000078737" "0000125839" "0000078738" "0000125840" "0000078739" "0000125841" "0000078740" "0000125842" "0000078741" "0000125843" "0000078742" "0000125844" "0000078743" "0000125845" "0000078744" "0000125846" "0000078745" "0000125847" "0000078746" "0000125848" "0000078747" "0000125849" "0000078748" "0000125850" "0000078749" "0000125851" "0000078750" "0000125852" "0000078751" "0000125853" "0000078752" "0000125854" "0000078753" "0000125855" "0000078754" "0000125856" "0000078755" "0000125857" "0000078756" "0000125858" "0000290685" "0000647374" "0000451132" "0000984912" "0000468929" "0001048966"