### LOVD-version 3000-30b ### Full data download ### To import, do not remove or alter this header ### ## Filter: (gene_public = NCKAP1) # 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}}" "NCKAP1" "NCK-associated protein 1" "2" "q32" "unknown" "NC_000002.11" "UD_133490700645" "" "https://www.LOVD.nl/NCKAP1" "" "1" "7666" "10787" "604891" "1" "1" "1" "1" "Establishment of this gene variant database (LSDB) was performed by Johan den Dunnen, supported by Global Variome." "" "g" "https://databases.lovd.nl/shared/refseq/NCKAP1_codingDNA.html" "1" "" "" "-1" "" "-1" "00001" "2013-05-03 00:00:00" "00006" "2020-11-24 13:07:59" "00000" "2025-11-01 13:22:20" ## 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}}" "00025582" "NCKAP1" "transcript variant 2" "002" "NM_205842.2" "" "NP_995314.1" "" "" "" "-759" "4256" "3405" "183903586" "183789579" "00006" "2020-11-23 21:54:14" "" "" ## 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}}" "00139" "ID" "intellectual disability (ID)" "" "" "" "" "" "00084" "2013-06-04 18:18:07" "00006" "2015-02-09 10:02:49" "03381" "cancer, gastric" "cancer, gastric (Neoplasm of stomach)" "" "613659" "" "" "" "00006" "2014-09-25 23:29:40" "00006" "2017-07-14 15:28:09" "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}}" "NCKAP1" "05611" ## Individuals ## Do not remove or alter this header ## ## Count = 23 "{{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}}" "00104013" "" "" "" "1" "" "00587" "{PMID:Vogelaar 2017:28875981}, {DOI:Vogelaar 2017:10.1038/ejhg.2017.138}" "54 patients from 53 families with genetically unexplained diffuse-type and intestinal-type gastric cancer" "" "" "" "" "0" "" "" "" "Vogelaar-513A" "00104037" "" "" "" "1" "" "00587" "{PMID:Vogelaar 2017:28875981}, {DOI:Vogelaar 2017:10.1038/ejhg.2017.138}" "54 patients from 53 families with genetically unexplained diffuse-type and intestinal-type gastric cancer" "" "" "" "" "0" "" "" "" "Vogelaar-760A" "00307923" "" "" "" "1" "" "00006" "{PMID:Anazi 2017:28940097}" "family" "F" "" "" "" "0" "" "" "" "12DG1370" "00320179" "" "" "" "1" "" "00006" "{PMID:Iossifov 2014:25363768}, {PMID:Guo 2020:33157009}, {DOI:Guo 2020:10.1016/j.ajhg.2020.10.002}" "2-generation family, 1 affected, unaffected non-carrier parents" "M" "" "United States" "" "0" "" "" "" "?/Pat1" "00320180" "" "" "" "1" "" "00006" "{PMID:Guo 2020:33157009}, {DOI:Guo 2020:10.1016/j.ajhg.2020.10.002}" "2-generation family, 1 affected, unaffected non-carrier parents" "M" "" "United States" "" "0" "" "" "" "Pat2" "00320181" "" "" "" "1" "" "00006" "{PMID:Guo 2020:33157009}, {DOI:Guo 2020:10.1016/j.ajhg.2020.10.002}" "2-generation family, 1 affected, unaffected non-carrier parents" "M" "" "United States" "" "0" "" "" "" "Pat3" "00320182" "" "" "" "1" "" "00006" "{PMID:Guo 2020:33157009}, {DOI:Guo 2020:10.1016/j.ajhg.2020.10.002}" "2-generation family, 1 affected, unaffected non-carrier parents" "M" "" "Saudi Arabia" "" "0" "" "" "" "Pat4" "00320183" "" "" "" "1" "" "00006" "{PMID:Guo 2020:33157009}, {DOI:Guo 2020:10.1016/j.ajhg.2020.10.002}" "" "M" "" "France" "" "0" "" "" "" "Pat5" "00320184" "" "" "" "1" "" "00006" "{PMID:Guo 2020:33157009}, {DOI:Guo 2020:10.1016/j.ajhg.2020.10.002}" "" "M" "" "United States" "" "0" "" "" "" "Pat6" "00320185" "" "" "" "1" "" "00006" "{PMID:Guo 2020:33157009}, {DOI:Guo 2020:10.1016/j.ajhg.2020.10.002}" "4-generation family, 5 affected (F, 4M)" "M" "" "United States" "" "0" "" "" "" "Pat7(IV1)" "00320186" "" "" "" "1" "" "00006" "{PMID:Guo 2020:33157009}, {DOI:Guo 2020:10.1016/j.ajhg.2020.10.002}" "2-generation family, affected mather/son" "M" "" "" "" "0" "" "" "" "Pat8(II1)" "00320187" "" "" "" "2" "" "00006" "{PMID:Guo 2020:33157009}, {DOI:Guo 2020:10.1016/j.ajhg.2020.10.002}" "2-generation family, 2 affected brothers, unaffected heterozygous carrier mother" "M" "" "France" "" "0" "" "" "" "Fam9Pat9(II1)" "00320188" "" "" "00320187" "1" "" "00006" "{PMID:Guo 2020:33157009}, {DOI:Guo 2020:10.1016/j.ajhg.2020.10.002}" "brother" "M" "" "Switzerland" "" "0" "" "" "" "Fam9Pat10(II2)" "00320189" "" "" "" "2" "" "00006" "{PMID:Guo 2020:33157009}, {DOI:Guo 2020:10.1016/j.ajhg.2020.10.002}" "2-generation family, affected mother/son" "M" "" "United States" "" "0" "" "" "" "Pat11(II1)" "00320190" "" "" "" "1" "" "00006" "{PMID:Guo 2020:33157009}, {DOI:Guo 2020:10.1016/j.ajhg.2020.10.002}" "2-generation family, 1 affected, unaffected non-carrier parents" "M" "" "China" "" "0" "" "" "" "Pat12" "00320191" "" "" "" "1" "" "00006" "{PMID:Guo 2020:33157009}, {DOI:Guo 2020:10.1016/j.ajhg.2020.10.002}" "2-generation family, 1 affected, unaffected non-carrier parents" "M" "" "France" "" "0" "" "" "" "Pat13" "00320192" "" "" "" "1" "" "00006" "{PMID:Iossifov 2014:25363768}, {PMID:Guo 2020:33157009}, {DOI:Guo 2020:10.1016/j.ajhg.2020.10.002}" "2-generation family, 1 affected, unaffected non-carrier parents" "F" "" "United States" "" "0" "" "" "" "?/Pat14" "00320193" "" "" "" "1" "" "00006" "{PMID:Guo 2020:33157009}, {DOI:Guo 2020:10.1016/j.ajhg.2020.10.002}" "2-generation family, affected father/daughter" "F" "" "Saudi Arabia" "" "0" "" "" "" "Pat15(II1)" "00320194" "" "" "" "1" "" "00006" "{PMID:Guo 2020:33157009}, {DOI:Guo 2020:10.1016/j.ajhg.2020.10.002}" "2-generation family, 1 affected, unaffected non-carrier parents" "F" "" "Denmark" "" "0" "" "" "" "Pat16" "00320195" "" "" "" "1" "" "00006" "{PMID:Guo 2020:33157009}, {DOI:Guo 2020:10.1016/j.ajhg.2020.10.002}" "2-generation family, 1 affected, unaffected non-carrier parents" "M" "" "United States" "" "0" "" "" "" "Pat17" "00320196" "" "" "" "1" "" "00006" "{PMID:Guo 2020:33157009}, {DOI:Guo 2020:10.1016/j.ajhg.2020.10.002}" "" "" "" "United States" "" "0" "" "" "" "Pat18" "00320197" "" "" "" "1" "" "00006" "{PMID:Guo 2020:33157009}, {DOI:Guo 2020:10.1016/j.ajhg.2020.10.002}" "" "" "" "United States" "" "0" "" "" "" "Pat19" "00320198" "" "" "" "1" "" "00006" "{PMID:Guo 2020:33157009}, {DOI:Guo 2020:10.1016/j.ajhg.2020.10.002}" "" "" "" "United States" "" "0" "" "" "" "Pat20" ## Individuals_To_Diseases ## Do not remove or alter this header ## ## Count = 23 "{{individualid}}" "{{diseaseid}}" "00104013" "03381" "00104037" "03381" "00307923" "00139" "00320179" "05611" "00320180" "05611" "00320181" "05611" "00320182" "05611" "00320183" "05611" "00320184" "05611" "00320185" "05611" "00320186" "05611" "00320187" "05611" "00320188" "05611" "00320189" "05611" "00320190" "05611" "00320191" "05611" "00320192" "05611" "00320193" "05611" "00320194" "05611" "00320195" "05611" "00320196" "05611" "00320197" "05611" "00320198" "05611" ## Phenotypes ## Do not remove or alter this header ## ## Note: Only showing Phenotype columns active for Diseases 00139, 03381, 05611 ## Count = 23 "{{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}}" "{{Phenotype/Diagnosis/Criteria}}" "0000081947" "03381" "00104013" "00587" "Unknown" "" "diffuse-type or intestinal-type gastric cancer" "" "" "" "" "" "" "" "" "" "" "0000081971" "03381" "00104037" "00587" "Unknown" "" "diffuse-type or intestinal-type gastric cancer" "" "" "" "" "" "" "" "" "" "" "0000233346" "00139" "00307923" "00006" "Unknown" "6y" "see paper; ..., tip-toe gait; intellectual disability; speech delay and language development; attention deficit hyperactivity disorder; hypertelorism; macrocephaly; tall stature" "" "" "" "" "" "" "" "" "intellectual diability" "" "0000242225" "05611" "00320179" "00006" "Isolated (sporadic)" "15y" "autism spectrum disorder; no speech-language problems; no motor delay; no intellectual disability; repetitive behavior; aggressive behavior; depression; sleep disturbances; seizures; MRI brain normal; EEG brain normal; no macrocephaly; no microcephaly; not tall; no overweight; no gastrointestinal disturbance; no hearing impairment; no congenital heart defects" "" "" "" "" "" "" "" "" "neurodevelopmental disorder" "" "0000242226" "05611" "00320180" "00006" "Isolated (sporadic)" "16y" "autism spectrum disorder; no speech-language problems; no motor delay; no intellectual disability; repetitive behavior; no aggressive behavior; attention-deficit hyperactivity disorder; depression; no self-injury behavior; sleep disturbances; no seizures; no epilepsy; MRI brain normal; EEG brain normal; no macrocephaly; no microcephaly; not tall; no overweight; no gastrointestinal disturbance; no hearing impairment; no congenital heart defects" "" "" "" "" "" "" "" "" "neurodevelopmental disorder" "" "0000242227" "05611" "00320181" "00006" "Isolated (sporadic)" "10y" "autism spectrum disorder; speech-language problems; no motor delay; attention-deficit hyperactivity disorder; no depression; no self-injury behavior; no seizures; MRI brain normal; EEG brain normal; no macrocephaly; no microcephaly; not tall; no overweight; gastrointestinal disturbance; skeletal alterations; no visual impairment; no hearing impairment; no congenital heart defects" "" "" "" "" "" "" "" "" "neurodevelopmental disorder" "" "0000242228" "05611" "00320182" "00006" "Isolated (sporadic)" "10y" "no autism; speech-language problems; motor delay; intellectual disability; repetitive behavior; aggressive behavior; attention-deficit hyperactivity disorder; no anxiety; no depression; obsessive behavior; no self-injury behavior; sleep disturbances; no seizures; no epilepsy; MRI brain normal; EEG brain normal; no macrocephaly; no microcephaly; not tall; no overweight; no gastrointestinal disturbance; no skeletal alterations; visual impairment; no hearing impairment; no congenital heart defects" "" "" "" "" "" "" "" "" "neurodevelopmental disorder" "" "0000242229" "05611" "00320183" "00006" "Isolated (sporadic)" "7y" "autism spectrum disorder; speech-language problems; motor delay; intellectual disability; repetitive behavior; aggressive behavior; obsessive behavior; no self-injury behavior; no sleep disturbances; seizures; epilepsy; MRI brain normal; EEG brain normal; no macrocephaly; no microcephaly; tall; no overweight; no gastrointestinal disturbance; no skeletal alterations; no visual impairment; no hearing impairment; no congenital heart defects" "" "" "" "" "" "" "" "" "neurodevelopmental disorder" "" "0000242230" "05611" "00320184" "00006" "Unknown" "23y" "autism spectrum disorder; speech-language problems; motor delay; learning disability; repetitive behavior; no aggressive behavior; no attention-deficit hyperactivity disorder; anxiety; no depression; no obsessive behavior; no self-injury behavior; no sleep disturbances; seizures; epilepsy; MRI brain abnormal; EEG brain abnormal; macrocephaly; no microcephaly; tall; obesity; gastrointestinal disturbance; skeletal alterations; visual impairment; hearing impairment; no congenital heart defects" "" "" "" "" "" "" "" "" "neurodevelopmental disorder" "" "0000242231" "05611" "00320185" "00006" "Familial, autosomal dominant" "20y" "autism spectrum disorder; speech-language problems; motor delay; no intellectual disability; repetitive behavior; no aggressive behavior; no attention-deficit hyperactivity disorder; no anxiety; no depression; no obsessive behavior; no self-injury behavior; no sleep disturbances; no seizures; no epilepsy; MRI brain normal; EEG brain normal; no macrocephaly; no microcephaly; not tall; no overweight; no gastrointestinal disturbance; no skeletal alterations; no visual impairment; no hearing impairment; no congenital heart defects" "" "" "" "" "" "" "" "" "neurodevelopmental disorder" "" "0000242232" "05611" "00320186" "00006" "Familial, autosomal dominant" "22y" "no autism; speech-language problems; no motor delay; intellectual disability; no repetitive behavior; aggressive behavior; anxiety; no depression; no obsessive behavior; no self-injury behavior; no sleep disturbances; seizures; no epilepsy; MRI brain normal; EEG brain normal; no microcephaly; tall; overweight; no gastrointestinal disturbance; skeletal alterations; no visual impairment; no hearing impairment; no congenital heart defects" "" "" "" "" "" "" "" "" "neurodevelopmental disorder" "" "0000242233" "05611" "00320187" "00006" "Unknown" "21y" "speech-language problems; intellectual disability; aggressive behavior; anxiety; self-injury behavior; no seizures; no epilepsy; no macrocephaly; tall; no overweight; no gastrointestinal disturbance; no skeletal alterations; no visual impairment; no hearing impairment; no congenital heart defects" "" "" "" "" "" "" "" "" "neurodevelopmental disorder" "" "0000242234" "05611" "00320188" "00006" "Unknown" "11y" "no autism; speech-language problems; motor delay; intellectual disability; no repetitive behavior; aggressive behavior; no attention-deficit hyperactivity disorder; no anxiety; no depression; no obsessive behavior; no self-injury behavior; sleep disturbances; no seizures; no epilepsy; MRI brain normal; EEG brain normal; no macrocephaly; no macrocephaly; not tall; obesity; no gastrointestinal disturbance; no skeletal alterations; no visual impairment; hearing impairment; no congenital heart defects" "" "" "" "" "" "" "" "" "neurodevelopmental disorder" "" "0000242235" "05611" "00320189" "00006" "Familial, autosomal dominant" "9y" "autism spectrum disorder; speech-language problems; motor delay; intellectual disability; repetitive behavior; aggressive behavior; attention-deficit hyperactivity disorder; no depression; obsessive behavior; no self-injury behavior; sleep disturbances; seizures; MRI brain abnormal; EEG brain normal; no microcephaly; tall; obesity; no gastrointestinal disturbance; no skeletal alterations; no visual impairment; no hearing impairment; no congenital heart defects" "" "" "" "" "" "" "" "" "neurodevelopmental disorder" "" "0000242236" "05611" "00320190" "00006" "Isolated (sporadic)" "8y" "autism spectrum disorder; no speech-language problems; motor delay; intellectual disability; repetitive behavior; no aggressive behavior; attention-deficit hyperactivity disorder; no anxiety; no obsessive behavior; no sleep disturbances; no seizures; no epilepsy; MRI brain normal; EEG brain normal; no macrocephaly; no microcephaly; gastrointestinal disturbance" "" "" "" "" "" "" "" "" "neurodevelopmental disorder" "" "0000242237" "05611" "00320191" "00006" "Isolated (sporadic)" "7y" "autism spectrum disorder; speech-language problems; motor delay; repetitive behavior; no aggressive behavior; no attention-deficit hyperactivity disorder; no anxiety; no depression; no obsessive behavior; no self-injury behavior; sleep disturbances; no seizures; no epilepsy; MRI brain normal; EEG brain normal; no macrocephaly; no microcephaly; tall; no overweight; gastrointestinal disturbance; skeletal alterations; no visual impairment; no hearing impairment; no congenital heart defects" "" "" "" "" "" "" "" "" "neurodevelopmental disorder" "" "0000242238" "05611" "00320192" "00006" "Isolated (sporadic)" "22y" "autism spectrum disorder; no speech-language problems; no intellectual disability; attention-deficit hyperactivity disorder; depression; sleep disturbances; no seizures; no epilepsy; MRI brain normal; EEG brain normal; no macrocephaly; no microcephaly; not tall; no overweight; no gastrointestinal disturbance; no hearing impairment; no congenital heart defects" "" "" "" "" "" "" "" "" "neurodevelopmental disorder" "" "0000242239" "05611" "00320193" "00006" "Familial, autosomal dominant" "9y" "speech-language problems; motor delay; intellectual disability; attention-deficit hyperactivity disorder; sleep disturbances; seizures; MRI brain normal; EEG brain normal; macrocephaly; no microcephaly; not tall; no overweight" "" "" "" "" "" "" "" "" "neurodevelopmental disorder" "" "0000242240" "05611" "00320194" "00006" "Isolated (sporadic)" "15y" "autistic features; no speech-language problems; motor delay; learning disability; no repetitive behavior; no aggressive behavior; no attention-deficit hyperactivity disorder; no anxiety; no depression; no obsessive behavior; no self-injury behavior; no sleep disturbances; seizures; MRI brain normal; EEG brain normal; not tall; no overweight; no gastrointestinal disturbance; no skeletal alterations; no visual impairment; no hearing impairment; no congenital heart defects" "" "" "" "" "" "" "" "" "neurodevelopmental disorder" "" "0000242241" "05611" "00320195" "00006" "Isolated (sporadic)" "9y" "no autism; speech-language problems; motor delay; intellectual disability; no repetitive behavior; aggressive behavior; no attention-deficit hyperactivity disorder; anxiety; no depression; no obsessive behavior; no self-injury behavior; sleep disturbances; no seizures; no epilepsy; MRI brain normal; no macrocephaly; no microcephaly; not tall; no overweight; no gastrointestinal disturbance; no skeletal alterations; visual impairment; no hearing impairment; congenital heart defects" "" "" "" "" "" "" "" "" "neurodevelopmental disorder" "" "0000242242" "05611" "00320196" "00006" "Unknown" "" "" "" "" "" "" "" "" "" "" "neurodevelopmental disorder" "" "0000242243" "05611" "00320197" "00006" "Unknown" "" "" "" "" "" "" "" "" "" "" "neurodevelopmental disorder" "" "0000242244" "05611" "00320198" "00006" "Unknown" "" "" "" "" "" "" "" "" "" "" "neurodevelopmental disorder" "" ## Screenings ## Do not remove or alter this header ## ## Count = 23 "{{id}}" "{{individualid}}" "{{variants_found}}" "{{owned_by}}" "{{created_by}}" "{{created_date}}" "{{edited_by}}" "{{edited_date}}" "{{Screening/Technique}}" "{{Screening/Template}}" "{{Screening/Tissue}}" "{{Screening/Remarks}}" "0000104484" "00104013" "1" "00587" "00006" "2017-04-28 08:15:46" "" "" "SEQ-NG" "DNA" "" "" "0000104508" "00104037" "1" "00587" "00006" "2017-04-28 08:15:46" "" "" "SEQ-NG" "DNA" "" "" "0000309067" "00307923" "1" "00006" "00006" "2020-08-23 12:07:39" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000321364" "00320179" "1" "00006" "00006" "2020-11-23 22:10:59" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000321365" "00320180" "1" "00006" "00006" "2020-11-23 22:10:59" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000321366" "00320181" "1" "00006" "00006" "2020-11-23 22:10:59" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000321367" "00320182" "1" "00006" "00006" "2020-11-23 22:10:59" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000321368" "00320183" "1" "00006" "00006" "2020-11-23 22:10:59" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000321369" "00320184" "1" "00006" "00006" "2020-11-23 22:10:59" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000321370" "00320185" "1" "00006" "00006" "2020-11-23 22:10:59" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000321371" "00320186" "1" "00006" "00006" "2020-11-23 22:10:59" "" "" "SEQ;SEQ-NG" "DNA" "" "targeted gene panel" "0000321372" "00320187" "1" "00006" "00006" "2020-11-23 22:10:59" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000321373" "00320188" "1" "00006" "00006" "2020-11-23 22:10:59" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000321374" "00320189" "1" "00006" "00006" "2020-11-23 22:10:59" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000321375" "00320190" "1" "00006" "00006" "2020-11-23 22:10:59" "" "" "SEQ;SEQ-NG" "DNA" "" "targeted gene panel" "0000321376" "00320191" "1" "00006" "00006" "2020-11-23 22:10:59" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000321377" "00320192" "1" "00006" "00006" "2020-11-23 22:10:59" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000321378" "00320193" "1" "00006" "00006" "2020-11-23 22:10:59" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000321379" "00320194" "1" "00006" "00006" "2020-11-23 22:10:59" "" "" "arrayCGH" "DNA" "" "aCGH" "0000321380" "00320195" "1" "00006" "00006" "2020-11-23 22:10:59" "" "" "SEQ;SEQ-NG" "DNA" "" "mate pair sequencing of inversion" "0000321381" "00320196" "1" "00006" "00006" "2020-11-23 22:10:59" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000321382" "00320197" "1" "00006" "00006" "2020-11-23 22:10:59" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000321383" "00320198" "1" "00006" "00006" "2020-11-23 22:10:59" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" ## Screenings_To_Genes ## Do not remove or alter this header ## ## Count = 21 "{{screeningid}}" "{{geneid}}" "0000309067" "NCKAP1" "0000321364" "NCKAP1" "0000321365" "NCKAP1" "0000321366" "NCKAP1" "0000321367" "NCKAP1" "0000321368" "NCKAP1" "0000321369" "NCKAP1" "0000321370" "NCKAP1" "0000321371" "NCKAP1" "0000321372" "NCKAP1" "0000321373" "NCKAP1" "0000321374" "NCKAP1" "0000321375" "NCKAP1" "0000321376" "NCKAP1" "0000321377" "NCKAP1" "0000321378" "NCKAP1" "0000321379" "NCKAP1" "0000321380" "NCKAP1" "0000321381" "NCKAP1" "0000321382" "NCKAP1" "0000321383" "NCKAP1" ## 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 = 38 "{{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}}" "0000169341" "0" "70" "2" "183866948" "183866948" "subst" "1.23052E-5" "00587" "NCKAP1_000002" "g.183866948T>C" "" "{PMID:Vogelaar 2017:28875981}, {DOI:Vogelaar 2017:10.1038/ejhg.2017.138}" "" "NM_205842.2(NCKAP1):c.437A>G p.(Tyr146Cys)" "variant could not be associated with disease phenotype" "Germline" "" "" "0" "" "" "g.183002220T>C" "" "likely pathogenic" "" "0000169431" "0" "70" "2" "183853798" "183853798" "subst" "6.10884E-5" "00587" "NCKAP1_000001" "g.183853798T>G" "" "{PMID:Vogelaar 2017:28875981}, {DOI:Vogelaar 2017:10.1038/ejhg.2017.138}" "" "NM_205842.2(NCKAP1):c.925A>C p.(Ile309Leu)" "variant could not be associated with disease phenotype" "Germline" "" "" "0" "" "" "g.182989070T>G" "" "likely pathogenic" "" "0000683529" "1" "70" "2" "183790537" "183790537" "subst" "0" "00006" "NCKAP1_000003" "g.183790537C>A" "" "{PMID:Anazi 2017:28940097}" "" "" "" "Germline" "yes" "" "0" "" "" "g.182925809C>A" "" "likely pathogenic (dominant)" "" "0000704193" "0" "90" "2" "183866861" "183866862" "ins" "0" "00006" "NCKAP1_000004" "g.183866861_183866862insTG" "" "{PMID:Iossifov 2014:25363768}, {PMID:Guo 2020:33157009}, {DOI:Guo 2020:10.1016/j.ajhg.2020.10.002}" "" "" "" "De novo" "" "" "0" "" "" "g.183002133_183002134insTG" "" "pathogenic (dominant)" "" "0000704194" "0" "90" "2" "183866852" "183866852" "subst" "0" "00006" "NCKAP1_000006" "g.183866852T>C" "" "{PMID:Guo 2020:33157009}, {DOI:Guo 2020:10.1016/j.ajhg.2020.10.002}" "" "" "RNA effect predicted from in vitro mini-gene splicing assay" "De novo" "" "" "0" "" "" "g.183002124T>C" "" "pathogenic (dominant)" "" "0000704195" "0" "90" "2" "183860532" "183860532" "dup" "0" "00006" "NCKAP1_000021" "g.183860532dup" "" "{PMID:Guo 2020:33157009}, {DOI:Guo 2020:10.1016/j.ajhg.2020.10.002}" "" "656_657insT" "" "De novo" "" "" "0" "" "" "g.182995804dup" "" "pathogenic (dominant)" "" "0000704196" "0" "50" "2" "183859618" "183859618" "subst" "0" "00006" "NCKAP1_000008" "g.183859618T>G" "" "{PMID:Guo 2020:33157009}, {DOI:Guo 2020:10.1016/j.ajhg.2020.10.002}" "" "" "RNA effect predicted from in vitro mini-gene splicing assay" "De novo" "" "" "0" "" "" "" "" "VUS" "" "0000704197" "0" "90" "2" "183859579" "183859579" "subst" "0" "00006" "NCKAP1_000020" "g.183859579T>A" "" "{PMID:Guo 2020:33157009}, {DOI:Guo 2020:10.1016/j.ajhg.2020.10.002}" "" "" "" "De novo" "" "" "0" "" "" "g.182994851T>A" "" "pathogenic (dominant)" "" "0000704198" "0" "70" "2" "183826886" "183826886" "subst" "0" "00006" "NCKAP1_000019" "g.183826886C>T" "" "{PMID:Guo 2020:33157009}, {DOI:Guo 2020:10.1016/j.ajhg.2020.10.002}" "" "" "" "Germline/De novo (untested)" "" "" "0" "" "" "g.182962158C>T" "" "likely pathogenic (dominant)" "" "0000704199" "11" "90" "2" "183821230" "183821230" "subst" "0" "00006" "NCKAP1_000018" "g.183821230G>A" "" "{PMID:Guo 2020:33157009}, {DOI:Guo 2020:10.1016/j.ajhg.2020.10.002}" "" "" "" "Germline" "" "" "0" "" "" "g.182956502G>A" "" "pathogenic (dominant)" "" "0000704200" "21" "70" "2" "183817939" "183817939" "del" "0" "00006" "NCKAP1_000017" "g.183817939del" "" "{PMID:Guo 2020:33157009}, {DOI:Guo 2020:10.1016/j.ajhg.2020.10.002}" "" "" "" "Germline" "" "" "0" "" "" "g.182953211del" "" "likely pathogenic (dominant)" "" "0000704201" "0" "70" "2" "183817632" "183817632" "subst" "0" "00006" "NCKAP1_000016" "g.183817632G>A" "" "{PMID:Guo 2020:33157009}, {DOI:Guo 2020:10.1016/j.ajhg.2020.10.002}" "" "" "variant not maternal" "Germline/De novo (untested)" "" "" "0" "" "" "g.182952904G>A" "" "likely pathogenic (dominant)" "" "0000704202" "0" "70" "2" "183817632" "183817632" "subst" "0" "00006" "NCKAP1_000016" "g.183817632G>A" "" "{PMID:Guo 2020:33157009}, {DOI:Guo 2020:10.1016/j.ajhg.2020.10.002}" "" "" "variant not maternal" "Germline/De novo (untested)" "" "" "0" "" "" "g.182952904G>A" "" "likely pathogenic (dominant)" "" "0000704203" "21" "70" "2" "183817233" "183817233" "subst" "0" "00006" "NCKAP1_000009" "g.183817233G>C" "" "{PMID:Guo 2020:33157009}, {DOI:Guo 2020:10.1016/j.ajhg.2020.10.002}" "" "" "RNA effect predicted from in vitro mini-gene splicing assay" "Germline" "" "" "0" "" "" "" "" "likely pathogenic (dominant)" "" "0000704204" "0" "90" "2" "183792844" "183792844" "subst" "0" "00006" "NCKAP1_000015" "g.183792844C>T" "" "{PMID:Guo 2020:33157009}, {DOI:Guo 2020:10.1016/j.ajhg.2020.10.002}" "" "" "" "De novo" "" "" "0" "" "" "g.182928116C>T" "" "pathogenic (dominant)" "" "0000704205" "0" "90" "2" "183791592" "183791593" "dup" "0" "00006" "NCKAP1_000014" "g.183791592_183791593dup" "" "{PMID:Guo 2020:33157009}, {DOI:Guo 2020:10.1016/j.ajhg.2020.10.002}" "" "" "" "De novo" "" "" "0" "" "" "g.182926864_182926865dup" "" "pathogenic (dominant)" "" "0000704206" "0" "90" "2" "183791570" "183791570" "subst" "0" "00006" "NCKAP1_000005" "g.183791570C>A" "" "{PMID:Iossifov 2014:25363768}, {PMID:Guo 2020:33157009}, {DOI:Guo 2020:10.1016/j.ajhg.2020.10.002}" "" "" "" "De novo" "" "" "0" "" "" "g.182926842C>A" "" "pathogenic (dominant)" "" "0000704207" "11" "90" "2" "183790537" "183790537" "subst" "0" "00006" "NCKAP1_000003" "g.183790537C>A" "" "{PMID:Guo 2020:33157009}, {DOI:Guo 2020:10.1016/j.ajhg.2020.10.002}" "" "" "" "Germline" "" "" "0" "" "" "g.182925809C>A" "" "pathogenic (dominant)" "" "0000704208" "0" "90" "2" "183762482" "184182761" "del" "0" "00006" "NCKAP1_000007" "g.(?_183762482)_(184182761_?)del" "" "{PMID:Guo 2020:33157009}, {DOI:Guo 2020:10.1016/j.ajhg.2020.10.002}" "" "240 kb deletion" "240 kb deletion incl. DUSP19 and NUP35" "De novo" "" "" "0" "" "" "" "" "pathogenic (dominant)" "" "0000704209" "0" "90" "2" "30340928" "183896661" "" "0" "00006" "NCKAP1_000013" "g.(30340928_183896661)inv" "" "{PMID:Guo 2020:33157009}, {DOI:Guo 2020:10.1016/j.ajhg.2020.10.002}" "" "inv(2)(2pter-p23.1(30340928)::(183896661)-(30340928)::(183896662)2q32.1-2qter)" "inv(2)(2pter-p23.1(30340928)::(183896661)-(30340928)::(183896662)2q32.1-2qter)" "De novo" "" "" "0" "" "46,XX,inv(2)(p23q37.3)" "" "" "pathogenic (dominant)" "" "0000704210" "0" "50" "2" "183902823" "183902823" "subst" "0" "00006" "NCKAP1_000010" "g.183902823G>C" "" "{PMID:Guo 2020:33157009}, {DOI:Guo 2020:10.1016/j.ajhg.2020.10.002}" "" "" "patient has likely pathogenic variant in SCN5A" "De novo" "" "" "0" "" "" "g.183038095G>C" "" "VUS" "" "0000704211" "0" "50" "2" "183832053" "183832053" "subst" "0" "00006" "NCKAP1_000011" "g.183832053C>T" "" "{PMID:Guo 2020:33157009}, {DOI:Guo 2020:10.1016/j.ajhg.2020.10.002}" "" "" "patient has 375.67 kb 7q21.3 duplication" "De novo" "" "" "0" "" "" "g.182967325C>T" "" "VUS" "" "0000704212" "0" "50" "2" "183790473" "183790473" "subst" "0" "00006" "NCKAP1_000012" "g.183790473G>A" "" "{PMID:Guo 2020:33157009}, {DOI:Guo 2020:10.1016/j.ajhg.2020.10.002}" "" "" "patient has likely pathogenic variant in NLGN4X" "De novo" "" "" "0" "" "" "g.182925745G>A" "" "VUS" "" "0000911483" "0" "70" "2" "183821276" "183821276" "del" "0" "02327" "NCKAP1_000023" "g.183821276del" "" "" "" "" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely pathogenic" "" "0000947643" "0" "50" "2" "183850924" "183850924" "subst" "2.84789E-5" "02325" "NCKAP1_000024" "g.183850924A>G" "" "" "" "NCKAP1(NM_205842.3):c.997T>C (p.C333R)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "VUS" "" "0000947644" "0" "50" "2" "183850933" "183850933" "subst" "1.2206E-5" "02329" "NCKAP1_000025" "g.183850933T>C" "" "" "" "NCKAP1(NM_205842.3):c.988A>G (p.I330V)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "VUS" "" "0000961748" "0" "50" "2" "183790479" "183790479" "subst" "0" "02329" "NCKAP1_000026" "g.183790479C>T" "" "" "" "NCKAP1(NM_205842.3):c.3356G>A (p.R1119K)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "VUS" "" "0000992286" "0" "50" "2" "183806866" "183806866" "subst" "0" "01804" "NCKAP1_000027" "g.183806866A>G" "" "" "" "NCKAP1(NM_013436.4):c.2627T>C (p.(Val876Ala))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "VUS" "" "0000992287" "0" "30" "2" "183867725" "183867725" "subst" "3.67299E-5" "01804" "NCKAP1_000028" "g.183867725C>T" "" "" "" "NCKAP1(NM_205842.2):c.364G>A (p.(Val122Ile))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely benign" "" "0000992288" "0" "50" "2" "183902772" "183902772" "subst" "0" "01804" "NCKAP1_000029" "g.183902772A>T" "" "" "" "NCKAP1(NM_013436.4):c.56T>A (p.(Ile19Asn))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "VUS" "" "0000992289" "0" "30" "2" "183902798" "183902798" "subst" "0" "01804" "NCKAP1_000030" "g.183902798C>G" "" "" "" "NCKAP1(NM_013436.4):c.30G>C (p.(Gln10His))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely benign" "" "0001024441" "0" "70" "2" "183817902" "183817902" "dup" "0" "02327" "NCKAP1_000031" "g.183817902dup" "" "" "" "" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely pathogenic" "" "0001032842" "0" "30" "2" "183806903" "183806903" "dup" "0" "01804" "NCKAP1_000032" "g.183806903dup" "" "" "" "NCKAP1(NM_013436.5):c.2602-3dup" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely benign" "" "0001032843" "0" "30" "2" "183817659" "183817659" "subst" "2.53107E-5" "01804" "NCKAP1_000033" "g.183817659G>A" "" "" "" "NCKAP1(NM_013436.5):c.2373-8C>T" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely benign" "" "0001032844" "0" "30" "2" "183826879" "183826879" "subst" "1.75542E-5" "01804" "NCKAP1_000034" "g.183826879A>G" "" "" "" "NCKAP1(NM_013436.5):c.1881+8T>C" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely benign" "" "0001050984" "0" "50" "2" "183821299" "183821299" "subst" "0" "01804" "NCKAP1_000035" "g.183821299G>A" "" "" "" "NCKAP1(NM_013436.5):c.2044C>T (p.(Leu682Phe))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "VUS" "" "0001050985" "0" "50" "2" "183866758" "183866758" "subst" "7.72421E-5" "01804" "NCKAP1_000036" "g.183866758G>C" "" "" "" "NCKAP1(NM_013436.5):c.526C>G (p.(Pro176Ala))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "VUS" "" "0001050986" "0" "30" "2" "183866906" "183866906" "subst" "2.44121E-5" "01804" "NCKAP1_000037" "g.183866906T>C" "" "" "" "NCKAP1(NM_013436.5):c.461A>G (p.(Lys154Arg))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely benign" "" ## 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 NCKAP1 ## Count = 38 "{{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}}" "0000169341" "00025582" "70" "437" "0" "437" "0" "c.437A>G" "r.(?)" "p.(Tyr146Cys)" "" "0000169431" "00025582" "70" "925" "0" "925" "0" "c.925A>C" "r.(?)" "p.(Ile309Leu)" "" "0000683529" "00025582" "70" "3298" "0" "3298" "0" "c.3298G>T" "r.(?)" "p.(Glu1100*)" "" "0000704193" "00025582" "90" "523" "0" "524" "0" "c.523_524insCA" "r.(?)" "p.(Gly175Alafs*14)" "" "0000704194" "00025582" "90" "530" "3" "530" "3" "c.530+3A>G" "r.(388_530del)" "p.(Thr130*)" "" "0000704195" "00025582" "90" "656" "0" "656" "0" "c.656dup" "r.(?)" "p.(Tyr220Ilefs*9)" "" "0000704196" "00025582" "50" "760" "-3" "760" "-3" "c.760-3A>C" "r.(759_760=)" "p.(Thr253_Met254=)" "" "0000704197" "00025582" "90" "796" "0" "796" "0" "c.796A>T" "r.(?)" "p.(Lys266*)" "" "0000704198" "00025582" "70" "1899" "1" "1899" "1" "c.1899+1G>A" "r.spl" "p.?" "" "0000704199" "00025582" "90" "2131" "0" "2131" "0" "c.2131C>T" "r.(?)" "p.(Arg711*)" "" "0000704200" "00025582" "70" "2292" "0" "2292" "0" "c.2292del" "r.(?)" "p.(Ile765Leufs*18)" "" "0000704201" "00025582" "70" "2410" "0" "2410" "0" "c.2410C>T" "r.(?)" "p.(Arg804*)" "" "0000704202" "00025582" "70" "2410" "0" "2410" "0" "c.2410C>T" "r.(?)" "p.(Arg804*)" "" "0000704203" "00025582" "70" "2522" "-3" "2522" "-3" "c.2522-3C>G" "r.(2522_2619del)" "p.(Met842Thrfs*7)" "" "0000704204" "00025582" "90" "3198" "1" "3198" "1" "c.3198+1G>A" "r.spl" "p.?" "" "0000704205" "00025582" "90" "3240" "0" "3241" "0" "c.3240_3241dup" "r.(?)" "p.(Lys1081Ilefs*15)" "" "0000704206" "00025582" "90" "3262" "0" "3262" "0" "c.3262G>T" "r.(?)" "p.(Glu1088*)" "" "0000704207" "00025582" "90" "3298" "0" "3298" "0" "c.3298G>T" "r.(?)" "p.(Glu1100*)" "" "0000704208" "00025582" "90" "0" "0" "0" "0" "c.-721_*851{0}" "r.0" "p.0" "" "0000704209" "00025582" "90" "0" "0" "0" "0" "c.-759_108+6058{inv}" "r.?" "p.?" "_1_1i" "0000704210" "00025582" "50" "5" "0" "5" "0" "c.5C>G" "r.(?)" "p.(Ser2Trp)" "" "0000704211" "00025582" "50" "1537" "0" "1537" "0" "c.1537G>A" "r.(?)" "p.(Ala513Thr)" "" "0000704212" "00025582" "50" "3362" "0" "3362" "0" "c.3362C>T" "r.(?)" "p.(Ala1121Val)" "" "0000911483" "00025582" "70" "2087" "0" "2087" "0" "c.2087del" "r.(?)" "p.(Asn696Ilefs*19)" "" "0000947643" "00025582" "50" "997" "0" "997" "0" "c.997T>C" "r.(?)" "p.(Cys333Arg)" "" "0000947644" "00025582" "50" "988" "0" "988" "0" "c.988A>G" "r.(?)" "p.(Ile330Val)" "" "0000961748" "00025582" "50" "3356" "0" "3356" "0" "c.3356G>A" "r.(?)" "p.(Arg1119Lys)" "" "0000992286" "00025582" "50" "2645" "0" "2645" "0" "c.2645T>C" "r.(?)" "p.(Val882Ala)" "" "0000992287" "00025582" "30" "364" "0" "364" "0" "c.364G>A" "r.(?)" "p.(Val122Ile)" "" "0000992288" "00025582" "50" "56" "0" "56" "0" "c.56T>A" "r.(?)" "p.(Ile19Asn)" "" "0000992289" "00025582" "30" "30" "0" "30" "0" "c.30G>C" "r.(?)" "p.(Gln10His)" "" "0001024441" "00025582" "70" "2329" "0" "2329" "0" "c.2329dup" "r.(?)" "p.(Gln777Profs*52)" "" "0001032842" "00025582" "30" "2620" "-3" "2620" "-3" "c.2620-3dup" "r.spl?" "p.?" "" "0001032843" "00025582" "30" "2391" "-8" "2391" "-8" "c.2391-8C>T" "r.(=)" "p.(=)" "" "0001032844" "00025582" "30" "1899" "8" "1899" "8" "c.1899+8T>C" "r.(=)" "p.(=)" "" "0001050984" "00025582" "50" "2062" "0" "2062" "0" "c.2062C>T" "r.(?)" "p.(Leu688Phe)" "" "0001050985" "00025582" "50" "544" "0" "544" "0" "c.544C>G" "r.(?)" "p.(Pro182Ala)" "" "0001050986" "00025582" "30" "479" "0" "479" "0" "c.479A>G" "r.(?)" "p.(Lys160Arg)" "" ## Screenings_To_Variants ## Do not remove or alter this header ## ## Count = 23 "{{screeningid}}" "{{variantid}}" "0000104484" "0000169341" "0000104508" "0000169431" "0000309067" "0000683529" "0000321364" "0000704193" "0000321365" "0000704194" "0000321366" "0000704195" "0000321367" "0000704196" "0000321368" "0000704197" "0000321369" "0000704198" "0000321370" "0000704199" "0000321371" "0000704200" "0000321372" "0000704201" "0000321373" "0000704202" "0000321374" "0000704203" "0000321375" "0000704204" "0000321376" "0000704205" "0000321377" "0000704206" "0000321378" "0000704207" "0000321379" "0000704208" "0000321380" "0000704209" "0000321381" "0000704210" "0000321382" "0000704211" "0000321383" "0000704212"