### LOVD-version 3000-30b ### Full data download ### To import, do not remove or alter this header ### ## Filter: (gene_public = KCNH5) # 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}}" "KCNH5" "potassium voltage-gated channel, subfamily H (eag-related), member 5" "14" "q23.1" "unknown" "NC_000014.8" "UD_132319795481" "" "https://www.LOVD.nl/KCNH5" "" "1" "6254" "27133" "605716" "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/KCNH5_codingDNA.html" "1" "" "" "-1" "" "-1" "00001" "2013-05-03 00:00:00" "00006" "2023-12-01 13:41:17" "00000" "2026-01-20 18:57:21" ## 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}}" "00025479" "KCNH5" "transcript variant 1" "002" "NM_139318.4" "" "NP_647479.2" "" "" "" "-52" "3902" "2967" "63511956" "63173291" "00006" "2019-11-29 12:33:38" "" "" ## Diseases ## Do not remove or alter this header ## ## Count = 6 "{{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" "00198" "?" "unclassified / mixed" "" "" "" "" "" "00006" "2013-09-13 14:21:47" "00006" "2024-11-23 09:38:12" "00344" "EE" "encephalopathy, epileptic (EE)" "" "" "" "" "" "00006" "2014-03-12 21:57:45" "00006" "2015-12-07 07:11:25" "05611" "NDD" "neurodevelopmental disorder (NDD)" "" "" "" "" "" "00006" "2019-06-19 12:27:20" "00006" "2024-12-13 11:12:21" "06906" "DEE" "encephalopathy, developmental and epileptic" "" "" "" "" "" "00006" "2022-04-07 09:24:23" "" "" "07046" "DEE112" "encephalopathy, developmental and epileptic, type 112" "AD" "620537" "" "" "" "00006" "2023-12-01 13:40:52" "" "" ## Genes_To_Diseases ## Do not remove or alter this header ## ## Count = 2 "{{geneid}}" "{{diseaseid}}" "KCNH5" "06906" "KCNH5" "07046" ## Individuals ## Do not remove or alter this header ## ## Count = 25 "{{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}}" "00207956" "" "" "" "1" "" "01164" "" "" "F" "" "Germany" "" "0" "" "" "" "" "00269489" "" "" "" "1" "" "03512" "{PMID:Minardi 2020:32725632}, {PMID:Happ 2023:36307226}" "1 affected, parents not available" "M" "" "Italy" "" "0" "" "" "" "patient;Pat10" "00291067" "" "" "" "1" "" "03575" "{PMID:Narang 2020:32906206}, {DOI:Narang 2020:10.1002/humu.24102}" "analysis 2794 individuals (India)" "" "" "India" "" "0" "" "" "" "" "00427815" "" "" "" "1" "" "00006" "{PMID:Veeramah 2013:23647072}, {PMID:Happ 2023:36307226}" "2-generation family, 1 affected, unaffected heterozygous carrier parents" "M" "" "United States" "" "0" "" "" "" "PatF;Pat2" "00428191" "" "" "" "1" "" "00006" "Wiel 2023, {DOI:Wiel 2023:10.1016/j.ajhg.2022.12.001}" "" "" "" "" "" "0" "" "" "" "" "00443772" "" "" "" "1" "" "00006" "{PMID:Hu 2022:35874597}" "" "M" "" "China" "" "0" "" "" "" "Pat1" "00443773" "" "" "" "1" "" "00006" "{PMID:Hu 2022:35874597}" "2-generation family, 1 affected, unaffected non-carrier parents" "F" "" "China" "" "0" "" "" "" "Pat2" "00443774" "" "" "" "1" "" "00006" "{PMID:Hu 2022:35874597}" "2-generation family, 1 affected, unaffected non-carrier parents" "M" "" "China" "" "0" "" "" "" "Pat3" "00443775" "" "" "" "1" "" "00006" "{PMID:Imafidon 2021:34136434}, {PMID:Happ 2023:36307226}" "2-generation family, 1 affected, unaffected non-carrier parents" "F" "" "Netherlands" "00y11m" "0" "" "" "" "Pat532;Pat15" "00443776" "" "" "" "1" "" "00006" "{PMID:Happ 2023:36307226}" "2-generation family, 1 affected, unaffected non-carrier parents" "M" "" "" "" "0" "" "" "" "Pat1" "00443777" "" "" "" "1" "" "00006" "{PMID:Happ 2023:36307226}" "2-generation family, 1 affected, unaffected non-carrier parents" "M" "" "" "" "0" "" "" "" "Pat3" "00443778" "" "" "" "1" "" "00006" "{PMID:Happ 2023:36307226}" "1 affected, parents not available" "F" "" "" "" "0" "" "" "" "Pat4" "00443779" "" "" "" "1" "" "00006" "{PMID:Happ 2023:36307226}" "2-generation family, 1 affected, unaffected non-carrier parents" "F" "" "" "" "0" "" "" "" "Pat5" "00443780" "" "" "" "1" "" "00006" "{PMID:Happ 2023:36307226}" "2-generation family, 1 affected, unaffected non-carrier parents" "F" "" "" "" "0" "" "" "" "Pat6" "00443781" "" "" "" "1" "" "00006" "{PMID:Happ 2023:36307226}" "2-generation family, 1 affected, unaffected non-carrier parents" "M" "" "" "" "0" "" "" "" "Pat7" "00443782" "" "" "" "1" "" "00006" "{PMID:Happ 2023:36307226}" "2-generation family, 1 affected, unaffected non-carrier parents" "F" "" "" "" "0" "" "" "" "Pat8" "00443783" "" "" "" "1" "" "00006" "{PMID:Happ 2023:36307226}" "2-generation family, 1 affected, unaffected non-carrier parents" "M" "" "" "" "0" "" "" "" "Pat9" "00443784" "" "" "" "1" "" "00006" "{PMID:Happ 2023:36307226}" "2-generation family, 1 affected, unaffected non-carrier parents" "F" "" "" "" "0" "" "" "" "Pat11" "00443785" "" "" "" "1" "" "00006" "{PMID:Happ 2023:36307226}" "2-generation family, 1 affected, unaffected non-carrier parents" "F" "" "" "" "0" "" "" "" "Pat12" "00443786" "" "" "" "1" "" "00006" "{PMID:Happ 2023:36307226}" "2-generation family, 1 affected, unaffected non-carrier parents" "F" "" "" "" "0" "" "" "" "Pat13" "00443787" "" "" "" "1" "" "00006" "{PMID:Happ 2023:36307226}" "2-generation family, affected mother/daughter, unaffected non-carrier parents" "F" "" "" "" "0" "" "" "" "Pat14" "00443788" "" "" "" "1" "" "00006" "{PMID:Happ 2023:36307226}" "2-generation family, 1 affected, unaffected non-carrier parents" "F" "" "" "9y" "0" "" "" "" "Pat16" "00443789" "" "" "" "1" "" "00006" "{PMID:Happ 2023:36307226}" "2-generation family, 1 affected, unaffected non-carrier parents" "F" "" "" "" "0" "" "" "" "Pat17" "00443790" "" "" "" "1" "" "00006" "{PMID:Happ 2023:36307226}" "2-generation family, 2 affected brothers, unaffected non-carrier parents" "M" "" "" "" "0" "" "" "" "Pat18" "00443791" "" "" "" "1" "" "00006" "{PMID:Happ 2023:36307226}" "" "M" "" "" "" "0" "" "" "" "Pat19" ## Individuals_To_Diseases ## Do not remove or alter this header ## ## Count = 24 "{{individualid}}" "{{diseaseid}}" "00269489" "00344" "00291067" "00198" "00427815" "00344" "00428191" "05611" "00443772" "06906" "00443773" "06906" "00443774" "06906" "00443775" "00198" "00443776" "00139" "00443777" "00139" "00443778" "00139" "00443779" "00139" "00443780" "00139" "00443781" "00139" "00443782" "00139" "00443783" "00139" "00443784" "00139" "00443785" "00139" "00443786" "00139" "00443787" "00139" "00443788" "00139" "00443789" "00139" "00443790" "00139" "00443791" "00139" ## Phenotypes ## Do not remove or alter this header ## ## Note: Only showing Phenotype columns active for Diseases 00139, 00198, 00344, 05611, 06906, 07046 ## Count = 23 "{{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}}" "0000155726" "00198" "00207956" "01164" "Unknown" "" "HP:0002133 (Status epilepticus); HP:0001250 (Seizures); HP:0012638 (Abnormality of nervous system physiology)" "" "" "" "" "" "" "" "" "" "" "" "0000207316" "00344" "00269489" "03512" "Unknown" "61y" "see paper; ...; developmental and epileptic encephalopathy; <1y-tonic-clonic seizure; 8y-seizure offset; global developmental delay, no regression; mild intellectual disability, sentences, ambulatory, self-feeds; MRIbrain 52y/53y-multiple nonenhancing white matter abnormalities, arachnoid cyst, mineral deposits in the orbit; epileptic encephalopathy (HP:0200134)" "" "" "" "" "" "" "" "" "DEE112" "" "" "0000318789" "00344" "00427815" "00006" "Isolated (sporadic)" "13y" "birth at term; seizures nonfebrile generalized tonic-clonic, generalized tonic-clonic or hemiclonic, prolonged and often in clusters with illness, relatively good control with valproate, occasional, brief clonic (facial), now partly controlled; EEG frequent multifocal spikes, almost continuous during sleep, even with good seiure control; epileptic encephalopathy, normal until 6m; mild motor delay, severe language delay; 3y-regression, reduced social interaction/attention; nonverbal with limited comprehension; autism; hypotonia" "00y06m" "" "" "" "" "" "" "" "" "epileptic encephalopathy" "" "0000333046" "06906" "00443772" "00006" "Isolated (sporadic)" "04y" "see paper; ..., 8m-seizures, non-febrile GTCS; EEG wide high 2–3 Hz periodic sharp wave complexes; craniocerebral MRI normal; ASD; language delay; bad behavior control" "00y08m" "" "" "" "" "" "" "" "DEE112" "" "" "0000333047" "06906" "00443773" "00006" "Isolated (sporadic)" "04y" "see paper; ..., 6m-seizures, non-febrile eclampsia nutation; EEG high-amplitude slow waves and spikes or sharp waves occurring irregularly; craniocerebral MRI normal; psychomotor development delayed" "" "" "" "" "" "" "" "" "DEE112" "developmental and epileptic encephalopathy" "" "0000333048" "06906" "00443774" "00006" "Isolated (sporadic)" "02y" "see paper; ..., 7m-seizures, non-febrile clonic seizures; EEG normal; craniocerebral MRI normal" "00y07m" "" "" "" "" "" "" "" "DEE112" "developmental and epileptic encephalopathy" "" "0000333049" "00198" "00443775" "00006" "Isolated (sporadic)" "00y11m" "see paper; ..., 11m-deceased; developmental and epileptic encephalopathy, early infantile developmental and epileptic encephalopathy; 3m:-tonic-clonic seizure; epileptic spasm, myoclonic seizure; 1d-hypotonia, global developmental delay, 4m-regression; profound developmental delay; MRI brain 9d-normal, 3-delayed myelination, mild cerebral atrophy" "" "" "" "" "" "" "" "" "DEE112" "hyperekplexia, dysmorphic features" "" "0000333050" "00139" "00443776" "00006" "Isolated (sporadic)" "4y" "see paper; ...; developmental and epileptic encephalopathy; 3m-focal motor seizure, hemiclonic; focal to bilateral tonic-clonic seizure, status epilepticus, tonic-clonic seizure; 18m-global developmental delay, no regression; severe intellectual disability (single words, ambulatory, and assisted feeds; ADHD; MRI brain 3m-normal" "" "" "" "" "" "" "" "" "DEE112" "intellectual disability" "" "0000333051" "00139" "00443777" "00006" "Isolated (sporadic)" "5y6m" "see paper; ...; developmental and epileptic encephalopathy, developmental and/or epileptic encephalopathy with spike-wave activation in sleep; 5m-focal impaired awareness seizure; focal to bilateral tonic-clonic seizure, focal motor seizure, hemiclonic; 3y-seizure offset; 2y6m-language delay, regression; mild-moderate intellectual disability (sentences and ambulatory); ADHD; MRI brain 6m/4y-normal" "" "" "" "" "" "" "" "" "DEE112" "intellectual disability" "" "0000333052" "00139" "00443778" "00006" "Unknown" "61y" "see paper; ...; epilepsy (unknown type); 6m-seizure (unknown type); generalised tonic-clonic seizure, absence seizure, focal aware motor seizure; no regression; learning difficulties at school; sentences, ambulatory, and self-feeds; MRI brain 55y-normal" "" "" "" "" "" "" "" "" "DEE112" "intellectual disability" "" "0000333053" "00139" "00443779" "00006" "Isolated (sporadic)" "5y" "see paper; ...; focal developmental and epileptic encephalopathy; 6m-febrile seizure; focal motor seizure, focal to bilateral tonic-clonic seizure; 16m-language delay, no regression; moderate intellectual disability (2-word sentences, ambulatory, and self-feeds); autistic trait;" "" "" "" "" "" "" "" "" "DEE112" "intellectual disability" "" "0000333054" "00139" "00443780" "00006" "Isolated (sporadic)" "10y" "see paper; ...; focal developmental and epileptic encephalopathy; 7m-focal impaired awareness seizure; focal to bilateral tonic-clonic seizure, focal motor seizure, hemiclonic; 3y6m-language delay. behavior delay, no regression; mild intellectual disability (sentences, ambulatory, and self-feeds); behavioral difficulties; MRI brain 1y/3y/5y-normal" "" "" "" "" "" "" "" "" "DEE112" "intellectual disability" "" "0000333055" "00139" "00443781" "00006" "Isolated (sporadic)" "9y" "see paper; ...; developmental and epileptic encephalopathy; 10m-focal impaired awareness seizure; myoclonic-atonic seizure, myoclonic seizure, tonic-clonic seizure; 6y-seizure offset; 15m-language delay, no regression; moderate intellectual disability, sentences, ambulatory, self-feeds; MRI brain 10m/4y-normal" "" "" "" "" "" "" "" "" "DEE112" "intellectual disability" "" "0000333056" "00139" "00443782" "00006" "Isolated (sporadic)" "3y10m" "see paper; ...; focal developmental and epileptic encephalopathy; 2m-focal motor seizure; focal to bilateral tonic-clonic seizure, focal impaired awareness seizure; 15m-language delay, no regression; severe intellectual disability; 2-word sentences, ambulatory, assisted feeds; autism spectrum disorder; MRI brain 11m/18m-normal" "" "" "" "" "" "" "" "" "DEE112" "intellectual disability" "" "0000333057" "00139" "00443783" "00006" "Isolated (sporadic)" "19m" "see paper; ...; combined focal and generalized epilepsy; 7m=generalised tonic-clonic seizure; focal to bilateral tonic-clonic seizure; 14m-seizure offset; 14m-language delay, no regression; language delay (single words), ambulatory, self-feeds; MRI brain 14m-normal" "" "" "" "" "" "" "" "" "DEE112" "intellectual disability" "" "0000333058" "00139" "00443784" "00006" "Isolated (sporadic)" "3y6m" "see paper; ...; focal epilepsy; 8m-focal impaired awareness seizure; focal to bilateral tonic-clonic seizure; 12m-seizure offset; no regression; behavioral difficulties, sentences, ambulatory, self-feeds; MRI brain 13m-normal" "" "" "" "" "" "" "" "" "DEE112" "intellectual disability" "" "0000333059" "00139" "00443785" "00006" "Isolated (sporadic)" "7y" "see paper; ...; epilepsy (unknown type); 9m-tonic-clonic seizure; 5y-seizure offset; 18m-language dealy, no regression; no intellectual disability, sentences, ambulatory, self-feeds; MRI brain 15m/7y-normal" "" "" "" "" "" "" "" "" "DEE112" "intellectual disability" "" "0000333060" "00139" "00443786" "00006" "Isolated (sporadic)" "10y" "see paper; ...; focal epilepsy; 10m-focal impaired awareness seizure; 1y-seizure offset; focal to bilateral tonic-clonic seizure; 18m-languagelay, gross motor delay, no regression; no intellectual disability; sentences, ambulatory, self-feeds; behavioral difficulties; MRI brain 4y/9y: frontal atrophy (not progressive), arachnoid cyst, Chiari I malformation" "" "" "" "" "" "" "" "" "DEE112" "intellectual disability" "" "0000333061" "00139" "00443787" "00006" "Familial, autosomal dominant" "1y4m" "see paper; ...; generalized epilepsy; 2m-myoclonic seizure; 3m-seizure offset; 4m-hypotonia, no regression; behavioral difficulties, single words, walks with support; MRI brain 4m-normal" "" "" "" "" "" "" "" "" "DEE112" "intellectual disability" "" "0000333062" "00139" "00443788" "00006" "Isolated (sporadic)" "9y" "see paper; ...; 9y-deceased (pneumonia); developmental and epileptic encephalopathy, early infantile developmental and epileptic encephalopathy; 1m-focal tonic seizure; epileptic spasm, tonic-clonic seizure, myoclonic seizure; 1d-hypotonia, global developmental delay, no regression; profound intellectual disability: no speech, nonambulatory; G-tube; MRI brain 3w-increased signal posterior fossa, CT scan 2y-cerebral atrophy" "" "" "" "" "" "" "" "" "DEE112" "intellectual disability" "" "0000333063" "00139" "00443789" "00006" "Isolated (sporadic)" "12y" "see paper; ...; evelopmental encephalopathy, focal epilepsy; 1y-tonic-clonic seizure; focal impaired awareness seizure; 5y-seizure offset; 9m-global developmental delay, no regression; moderate intellectual disability (sentences), ambulatory, self-feeds; MRI brain 1y/3y-normal" "" "" "" "" "" "" "" "" "DEE112" "intellectual disability" "" "0000333064" "00139" "00443790" "00006" "Unknown" "10y" "see paper; ..., 2y-mild fine motordelay, language delay; learning difficulties, autism spectrum disorder, oppositional defiant disorder,attention-deficit-hyperactivity disorder; MRI brain Chiari I malformation, spinal cord syrinx" "" "" "" "" "" "" "" "" "" "intellectual disability" "" "0000333065" "00139" "00443791" "00006" "Unknown" "4y" "see paper; ..., 18m-global developmental delay; 10y-limited language, autism spectrum disorder; EEG 9m-normal" "" "" "" "" "" "" "" "" "" "intellectual disability" "" ## Screenings ## Do not remove or alter this header ## ## Count = 25 "{{id}}" "{{individualid}}" "{{variants_found}}" "{{owned_by}}" "{{created_by}}" "{{created_date}}" "{{edited_by}}" "{{edited_date}}" "{{Screening/Technique}}" "{{Screening/Template}}" "{{Screening/Tissue}}" "{{Screening/Remarks}}" "0000209001" "00207956" "1" "01164" "01164" "2018-12-04 16:43:54" "" "" "SEQ-NG" "DNA" "" "" "0000270643" "00269489" "1" "03512" "03512" "2019-11-28 18:05:34" "" "" "SEQ-NG-I" "DNA" "" "" "0000292235" "00291067" "1" "03575" "00006" "2020-03-11 19:30:02" "" "" "arraySNP" "DNA" "" "Infinium Global Screening Array v1.0" "0000429138" "00427815" "1" "00006" "00006" "2022-12-13 13:34:17" "" "" "SEQ;SEQ-NG" "DNA" "" "trio WES" "0000429602" "00428191" "1" "00006" "00006" "2022-12-23 14:15:36" "" "" "SEQ;SEQ-NG" "DNA" "" "" "0000445268" "00443772" "1" "00006" "00006" "2023-12-01 13:48:27" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000445269" "00443773" "1" "00006" "00006" "2023-12-01 16:59:05" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000445270" "00443774" "1" "00006" "00006" "2023-12-01 17:04:49" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000445271" "00443775" "1" "00006" "00006" "2023-12-01 17:14:11" "" "" "SEQ;SEQ-NG" "DNA" "" "gene panel" "0000445272" "00443776" "1" "00006" "00006" "2023-12-02 16:06:35" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000445273" "00443777" "1" "00006" "00006" "2023-12-02 16:06:35" "" "" "MIP;SEQ;SEQ-NG" "DNA" "" "" "0000445274" "00443778" "1" "00006" "00006" "2023-12-02 16:06:35" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000445275" "00443779" "1" "00006" "00006" "2023-12-02 16:06:35" "" "" "SEQ;SEQ-NG" "DNA" "" "gene panel" "0000445276" "00443780" "1" "00006" "00006" "2023-12-02 16:06:35" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000445277" "00443781" "1" "00006" "00006" "2023-12-02 16:06:35" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000445278" "00443782" "1" "00006" "00006" "2023-12-02 16:06:35" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000445279" "00443783" "1" "00006" "00006" "2023-12-02 16:06:35" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000445280" "00443784" "1" "00006" "00006" "2023-12-02 16:06:35" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000445281" "00443785" "1" "00006" "00006" "2023-12-02 16:06:35" "" "" "SEQ;SEQ-NG" "DNA" "" "gene panel" "0000445282" "00443786" "1" "00006" "00006" "2023-12-02 16:06:35" "" "" "SEQ;SEQ-NG" "DNA" "" "WGS" "0000445283" "00443787" "1" "00006" "00006" "2023-12-02 16:06:35" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000445284" "00443788" "1" "00006" "00006" "2023-12-02 16:06:35" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000445285" "00443789" "1" "00006" "00006" "2023-12-02 16:06:35" "" "" "SEQ;SEQ-NG" "DNA" "" "WGS" "0000445286" "00443790" "1" "00006" "00006" "2023-12-02 16:06:35" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000445287" "00443791" "1" "00006" "00006" "2023-12-02 16:06:35" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" ## Screenings_To_Genes ## Do not remove or alter this header ## ## Count = 0 ## Variants_On_Genome ## Do not remove or alter this header ## ## Please note that not necessarily all variants found in the given individuals are shown. This output is restricted to variants in the selected gene. ## Count = 43 "{{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}}" "0000439073" "0" "50" "14" "63175004" "63175004" "subst" "0" "01164" "KCNH5_000001" "g.63175004T>A" "" "" "" "" "" "Germline" "" "" "0" "" "" "g.62708286T>A" "" "VUS" "ACMG" "0000552759" "0" "50" "14" "63174483" "63174483" "subst" "0" "01804" "KCNH5_000002" "g.63174483G>A" "" "" "" "KCNH5(NM_139318.3):c.2710C>T (p.(Gln904Ter))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "g.62707765G>A" "" "VUS" "" "0000604428" "0" "70" "14" "63417240" "63417240" "subst" "0" "03512" "KCNH5_000004" "g.63417240C>T" "" "{PMID:Minardi 2020:32725632}, {PMID:Happ 2023:36307226}" "" "" "ACMG PS2_Very strong, PS3_Moderate, PM2, PP2, PP3" "Germline/De novo (untested)" "" "" "0" "" "" "g.62950522C>T" "" "pathogenic (dominant)" "ACMG" "0000648924" "1" "10" "14" "63417122" "63417122" "subst" "0.00110329" "03575" "KCNH5_000005" "g.63417122T>C" "1/2795 individuals" "{PMID:Narang 2020:32906206}, {DOI:Narang 2020:10.1002/humu.24102}" "" "" "1 heterozygous, no homozygous; {DB:CLININrs146883958}" "Germline" "" "rs146883958" "0" "" "" "g.62950404T>C" "" "benign" "" "0000908563" "0" "90" "14" "63417240" "63417240" "subst" "0" "00006" "KCNH5_000004" "g.63417240C>T" "" "{PMID:Veeramah 2013:23647072}, {PMID:Happ 2023:36307226}" "" "G980A" "ACMG PS2_Very strong, PS3_Moderate, PM2, PP2, PP3" "De novo" "" "" "0" "" "" "" "" "pathogenic (dominant)" "ACMG" "0000909184" "0" "50" "14" "63417240" "63417240" "subst" "0" "00006" "KCNH5_000004" "g.63417240C>T" "" "Wiel 2023, {DOI:Wiel 2023:10.1016/j.ajhg.2022.12.001}" "" "" "gene predicted as candidate involved in neurodevelopmental dealy" "Germline/De novo (untested)" "" "" "0" "" "" "g.62950522C>T" "" "VUS (!)" "" "0000952171" "0" "90" "14" "63417240" "63417240" "subst" "0" "00006" "KCNH5_000004" "g.63417240C>T" "" "{PMID:Hu 2022:35874597}" "" "" "" "De novo" "" "" "0" "" "" "g.62950522C>T" "" "pathogenic (dominant)" "" "0000952173" "0" "70" "14" "63175177" "63175177" "subst" "0" "00006" "KCNH5_000006" "g.63175177T>C" "" "{PMID:Hu 2022:35874597}" "" "" "" "De novo" "" "" "0" "" "" "g.62708459T>C" "" "likely pathogenic (dominant)" "ACMG" "0000952175" "0" "70" "14" "63417258" "63417258" "subst" "0" "00006" "KCNH5_000007" "g.63417258C>T" "" "{PMID:Hu 2022:35874597}" "" "" "" "De novo" "" "" "0" "" "" "g.62950540C>T" "" "likely pathogenic (dominant)" "" "0000952176" "0" "70" "14" "63316552" "63316552" "subst" "0" "00006" "KCNH5_000008" "g.63316552A>G" "" "{PMID:Imafidon 2021:34136434}, {PMID:Happ 2023:36307226}" "" "" "ACMG PS2, PM2, PP2, PP3" "De novo" "" "" "0" "" "" "g.62849834A>G" "" "likely pathogenic (dominant)" "ACMG" "0000952180" "0" "70" "14" "63417250" "63417250" "subst" "0" "00006" "KCNH5_000013" "g.63417250T>C" "" "{PMID:Happ 2023:36307226}" "" "" "ACMG PS2_Moderate, PM2, PP2, PP3" "De novo" "" "" "0" "" "" "g.62950532T>C" "" "likely pathogenic (dominant)" "" "0000952181" "0" "90" "14" "63417240" "63417240" "subst" "0" "00006" "KCNH5_000004" "g.63417240C>T" "" "{PMID:Happ 2023:36307226}" "" "" "ACMG PS2_Very strong, PS3_Moderate, PM2, PP2, PP3" "De novo" "" "" "0" "" "" "g.62950522C>T" "" "pathogenic (dominant)" "" "0000952182" "0" "90" "14" "63417240" "63417240" "subst" "0" "00006" "KCNH5_000004" "g.63417240C>T" "" "{PMID:Happ 2023:36307226}" "" "" "ACMG PS2_Very strong, PS3_Moderate, PM2, PP2, PP3" "Germline/De novo (untested)" "" "" "0" "" "" "g.62950522C>T" "" "pathogenic (dominant)" "" "0000952183" "0" "90" "14" "63417240" "63417240" "subst" "0" "00006" "KCNH5_000004" "g.63417240C>T" "" "{PMID:Happ 2023:36307226}" "" "" "ACMG PS2_Very strong, PS3_Moderate, PM2, PP2, PP3" "De novo" "" "" "0" "" "" "g.62950522C>T" "" "pathogenic (dominant)" "" "0000952184" "0" "90" "14" "63417240" "63417240" "subst" "0" "00006" "KCNH5_000004" "g.63417240C>T" "" "{PMID:Happ 2023:36307226}" "" "" "ACMG PS2_Very strong, PS3_Moderate, PM2, PP2, PP3" "De novo" "" "" "0" "" "" "g.62950522C>T" "" "pathogenic (dominant)" "" "0000952185" "0" "90" "14" "63417240" "63417240" "subst" "0" "00006" "KCNH5_000004" "g.63417240C>T" "" "{PMID:Happ 2023:36307226}" "" "" "ACMG PS2_Very strong, PS3_Moderate, PM2, PP2, PP3" "De novo" "" "" "0" "" "" "g.62950522C>T" "" "pathogenic (dominant)" "" "0000952186" "0" "90" "14" "63417240" "63417240" "subst" "0" "00006" "KCNH5_000004" "g.63417240C>T" "" "{PMID:Happ 2023:36307226}" "" "" "ACMG PS2_Very strong, PS3_Moderate, PM2, PP2, PP3" "De novo" "" "" "0" "" "" "g.62950522C>T" "" "pathogenic (dominant)" "" "0000952187" "0" "90" "14" "63417240" "63417240" "subst" "0" "00006" "KCNH5_000004" "g.63417240C>T" "" "{PMID:Happ 2023:36307226}" "" "" "ACMG PS2_Very strong, PS3_Moderate, PM2, PP2, PP3" "De novo" "" "" "0" "" "" "g.62950522C>T" "" "pathogenic (dominant)" "" "0000952188" "0" "70" "14" "63417222" "63417222" "subst" "0" "00006" "KCNH5_000012" "g.63417222C>T" "" "{PMID:Happ 2023:36307226}" "" "" "ACMG PS2, PM2, PP2, PP3" "De novo" "" "" "0" "" "" "g.62950504C>T" "" "likely pathogenic (dominant)" "" "0000952189" "0" "70" "14" "63417222" "63417222" "subst" "0" "00006" "KCNH5_000012" "g.63417222C>T" "" "{PMID:Happ 2023:36307226}" "" "" "ACMG PS2, PM2, PP2, PP3" "De novo" "" "" "0" "" "" "g.62950504C>T" "" "likely pathogenic (dominant)" "" "0000952190" "0" "70" "14" "63417222" "63417222" "subst" "0" "00006" "KCNH5_000012" "g.63417222C>T" "" "{PMID:Happ 2023:36307226}" "" "" "ACMG PS2, PM2, PP2, PP3" "De novo" "" "" "0" "" "" "g.62950504C>T" "" "likely pathogenic (dominant)" "" "0000952191" "21" "70" "14" "63417222" "63417222" "subst" "0" "00006" "KCNH5_000012" "g.63417222C>T" "" "{PMID:Happ 2023:36307226}" "" "" "ACMG PS2, PM2, PP2, PP3" "Germline" "yes" "" "0" "" "" "g.62950504C>T" "" "likely pathogenic (dominant)" "" "0000952192" "0" "70" "14" "63316538" "63316538" "subst" "0" "00006" "KCNH5_000011" "g.63316538T>G" "" "{PMID:Happ 2023:36307226}" "" "" "ACMG PS2, PM2, PP2, PP3" "De novo" "" "" "0" "" "" "g.62849820T>G" "" "likely pathogenic (dominant)" "" "0000952193" "0" "70" "14" "63316528" "63316528" "subst" "0" "00006" "KCNH5_000010" "g.63316528A>G" "" "{PMID:Happ 2023:36307226}" "" "" "ACMG PS2, PM2, PP2, PP3" "De novo" "" "" "0" "" "" "g.62849810A>G" "" "likely pathogenic (dominant)" "" "0000952194" "0" "50" "14" "63453797" "63453797" "subst" "0" "00006" "KCNH5_000014" "g.63453797A>G" "" "{PMID:Happ 2023:36307226}" "" "" "does not seggregate" "De novo" "no" "" "0" "" "" "g.62987079A>G" "" "VUS" "" "0000952195" "0" "50" "14" "63269052" "63269052" "subst" "0" "00006" "KCNH5_000009" "g.63269052A>G" "" "{PMID:Happ 2023:36307226}" "" "" "carries a maternally inherited 16p12.2 microdeletion, associated with various neurodevelopmental disorders" "De novo" "" "" "0" "" "" "g.62802334A>G" "" "VUS" "" "0000952196" "21" "50" "14" "63417122" "63417122" "subst" "0.00110329" "00006" "KCNH5_000005" "g.63417122T>C" "" "{PMID:Happ 2023:36307226}" "" "" "" "Germline" "" "" "0" "" "" "g.62950404T>C" "" "VUS" "" "0000980949" "0" "30" "14" "63174828" "63174828" "subst" "9.33957E-5" "01804" "KCNH5_000015" "g.63174828C>A" "" "" "" "KCNH5(NM_139318.5):c.2365G>T (p.(Gly789Cys))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely benign" "" "0000980950" "0" "50" "14" "63416874" "63416874" "subst" "1.22096E-5" "01804" "KCNH5_000016" "g.63416874G>A" "" "" "" "KCNH5(NM_139318.5):c.1346C>T (p.(Ser449Leu))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "VUS" "" "0000980951" "0" "30" "14" "63416881" "63416881" "subst" "4.88245E-5" "01804" "KCNH5_000017" "g.63416881T>C" "" "" "" "KCNH5(NM_139318.5):c.1339A>G (p.(Met447Val))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely benign" "" "0000980952" "0" "50" "14" "63417130" "63417130" "subst" "4.07143E-6" "02327" "KCNH5_000018" "g.63417130C>T" "" "" "" "" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "VUS" "" "0000980953" "0" "30" "14" "63417301" "63417301" "dup" "0" "01804" "KCNH5_000019" "g.63417301dup" "" "" "" "KCNH5(NM_139318.5):c.943-9dup" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely benign" "" "0000980954" "0" "30" "14" "63447620" "63447620" "subst" "2.03588E-5" "01804" "KCNH5_000020" "g.63447620G>C" "" "" "" "KCNH5(NM_139318.5):c.912C>G (p.(Asp304Glu))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely benign" "" "0001001059" "0" "30" "14" "63174329" "63174329" "subst" "0" "01804" "KCNH5_000021" "g.63174329G>A" "" "" "" "KCNH5(NM_139318.4):c.2864C>T (p.(Ser955Phe))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely benign" "" "0001001060" "0" "30" "14" "63269244" "63269244" "subst" "8.14166E-6" "01804" "KCNH5_000022" "g.63269244C>T" "" "" "" "KCNH5(NM_139318.4):c.1625G>A (p.(Arg542Gln))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely benign" "" "0001001061" "0" "50" "14" "63316502" "63316502" "subst" "0" "01804" "KCNH5_000023" "g.63316502G>A" "" "" "" "KCNH5(NM_139318.4):c.1438C>T (p.(Arg480*))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "VUS" "" "0001001062" "0" "30" "14" "63447979" "63447979" "subst" "0" "01804" "KCNH5_000024" "g.63447979G>T" "" "" "" "KCNH5(NM_139318.4):c.553C>A (p.(Leu185Ile))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely benign" "" "0001001063" "0" "50" "14" "63468118" "63468118" "subst" "0" "01804" "KCNH5_000025" "g.63468118C>T" "" "" "" "KCNH5(NM_139318.4):c.364G>A (p.(Val122Ile))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "VUS" "" "0001040022" "0" "30" "14" "63174309" "63174309" "subst" "1.03407E-5" "01804" "KCNH5_000026" "g.63174309G>A" "" "" "" "KCNH5(NM_139318.5):c.2884C>T (p.(Pro962Ser))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely benign" "" "0001040023" "0" "50" "14" "63175011" "63175011" "subst" "0" "01804" "KCNH5_000027" "g.63175011C>T" "" "" "" "KCNH5(NM_139318.5):c.2182G>A (p.(Asp728Asn))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "VUS" "" "0001040024" "0" "50" "14" "63269287" "63269287" "subst" "0" "01804" "KCNH5_000028" "g.63269287A>T" "" "" "" "KCNH5(NM_139318.5):c.1582T>A (p.(Cys528Ser))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "VUS" "" "0001054855" "0" "50" "14" "63473120" "63473120" "subst" "0" "01804" "KCNH5_000029" "g.63473120A>G" "" "" "" "KCNH5(NM_139318.5):c.268T>C (p.(Ser90Pro))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "VUS" "" "0001066077" "0" "50" "14" "63246461" "63246461" "subst" "0" "02325" "KCNH5_000030" "g.63246461G>C" "" "" "" "" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "VUS" "" ## 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 KCNH5 ## Count = 43 "{{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}}" "0000439073" "00025479" "50" "2189" "0" "2189" "0" "c.2189A>T" "r.(?)" "p.Glu730Val" "" "0000552759" "00025479" "50" "2710" "0" "2710" "0" "c.2710C>T" "r.(?)" "p.(Gln904Ter)" "" "0000604428" "00025479" "70" "980" "0" "980" "0" "c.980G>A" "r.(?)" "p.(Arg327His)" "" "0000648924" "00025479" "10" "1098" "0" "1098" "0" "c.1098A>G" "r.(?)" "p.(Ile366Met)" "" "0000908563" "00025479" "90" "980" "0" "980" "0" "c.980G>A" "r.(?)" "p.(Arg327His)" "" "0000909184" "00025479" "50" "980" "0" "980" "0" "c.980G>A" "r.(?)" "p.(Arg327His)" "" "0000952171" "00025479" "90" "980" "0" "980" "0" "c.980G>A" "r.(?)" "p.(Arg327His)" "" "0000952173" "00025479" "70" "2020" "-4" "2020" "-4" "c.2020-4A>G" "r.spl" "p.?" "" "0000952175" "00025479" "70" "962" "0" "962" "0" "c.962G>A" "r.(?)" "p.(Ser321Asn)" "" "0000952176" "00025479" "70" "1388" "0" "1388" "0" "c.1388T>C" "r.(?)" "p.(Ile463Thr)" "" "0000952180" "00025479" "70" "970" "0" "970" "0" "c.970A>G" "r.(?)" "p.(Lys324Glu)" "" "0000952181" "00025479" "90" "980" "0" "980" "0" "c.980G>A" "r.(?)" "p.(Arg327His)" "" "0000952182" "00025479" "90" "980" "0" "980" "0" "c.980G>A" "r.(?)" "p.(Arg327His)" "" "0000952183" "00025479" "90" "980" "0" "980" "0" "c.980G>A" "r.(?)" "p.(Arg327His)" "" "0000952184" "00025479" "90" "980" "0" "980" "0" "c.980G>A" "r.(?)" "p.(Arg327His)" "" "0000952185" "00025479" "90" "980" "0" "980" "0" "c.980G>A" "r.(?)" "p.(Arg327His)" "" "0000952186" "00025479" "90" "980" "0" "980" "0" "c.980G>A" "r.(?)" "p.(Arg327His)" "" "0000952187" "00025479" "90" "980" "0" "980" "0" "c.980G>A" "r.(?)" "p.(Arg327His)" "" "0000952188" "00025479" "70" "998" "0" "998" "0" "c.998G>A" "r.(?)" "p.(Arg333His)" "" "0000952189" "00025479" "70" "998" "0" "998" "0" "c.998G>A" "r.(?)" "p.(Arg333His)" "" "0000952190" "00025479" "70" "998" "0" "998" "0" "c.998G>A" "r.(?)" "p.(Arg333His)" "" "0000952191" "00025479" "70" "998" "0" "998" "0" "c.998G>A" "r.(?)" "p.(Arg333His)" "" "0000952192" "00025479" "70" "1402" "0" "1402" "0" "c.1402A>C" "r.(?)" "p.(Thr468Pro)" "" "0000952193" "00025479" "70" "1412" "0" "1412" "0" "c.1412T>C" "r.(?)" "p.(Phe471Ser)" "" "0000952194" "00025479" "50" "542" "0" "542" "0" "c.542T>C" "r.(?)" "p.(Leu181Pro)" "" "0000952195" "00025479" "50" "1817" "0" "1817" "0" "c.1817T>C" "r.(?)" "p.(Ile606Thr)" "" "0000952196" "00025479" "50" "1098" "0" "1098" "0" "c.1098A>G" "r.(?)" "p.(Ile366Met)" "" "0000980949" "00025479" "30" "2365" "0" "2365" "0" "c.2365G>T" "r.(?)" "p.(Gly789Cys)" "" "0000980950" "00025479" "50" "1346" "0" "1346" "0" "c.1346C>T" "r.(?)" "p.(Ser449Leu)" "" "0000980951" "00025479" "30" "1339" "0" "1339" "0" "c.1339A>G" "r.(?)" "p.(Met447Val)" "" "0000980952" "00025479" "50" "1090" "0" "1090" "0" "c.1090G>A" "r.(?)" "p.(Ala364Thr)" "" "0000980953" "00025479" "30" "943" "-9" "943" "-9" "c.943-9dup" "r.(=)" "p.(=)" "" "0000980954" "00025479" "30" "912" "0" "912" "0" "c.912C>G" "r.(?)" "p.(Asp304Glu)" "" "0001001059" "00025479" "30" "2864" "0" "2864" "0" "c.2864C>T" "r.(?)" "p.(Ser955Phe)" "" "0001001060" "00025479" "30" "1625" "0" "1625" "0" "c.1625G>A" "r.(?)" "p.(Arg542Gln)" "" "0001001061" "00025479" "50" "1438" "0" "1438" "0" "c.1438C>T" "r.(?)" "p.(Arg480*)" "" "0001001062" "00025479" "30" "553" "0" "553" "0" "c.553C>A" "r.(?)" "p.(Leu185Ile)" "" "0001001063" "00025479" "50" "364" "0" "364" "0" "c.364G>A" "r.(?)" "p.(Val122Ile)" "" "0001040022" "00025479" "30" "2884" "0" "2884" "0" "c.2884C>T" "r.(?)" "p.(Pro962Ser)" "" "0001040023" "00025479" "50" "2182" "0" "2182" "0" "c.2182G>A" "r.(?)" "p.(Asp728Asn)" "" "0001040024" "00025479" "50" "1582" "0" "1582" "0" "c.1582T>A" "r.(?)" "p.(Cys528Ser)" "" "0001054855" "00025479" "50" "268" "0" "268" "0" "c.268T>C" "r.(?)" "p.(Ser90Pro)" "" "0001066077" "00025479" "50" "2004" "0" "2004" "0" "c.2004C>G" "r.(?)" "p.(Cys668Trp)" "" ## Screenings_To_Variants ## Do not remove or alter this header ## ## Count = 26 "{{screeningid}}" "{{variantid}}" "0000209001" "0000439073" "0000270643" "0000604428" "0000292235" "0000648924" "0000429138" "0000908563" "0000429602" "0000909184" "0000445268" "0000952171" "0000445269" "0000952173" "0000445270" "0000952175" "0000445271" "0000952176" "0000445272" "0000952180" "0000445273" "0000952181" "0000445274" "0000952182" "0000445275" "0000952183" "0000445276" "0000952184" "0000445277" "0000952185" "0000445278" "0000952186" "0000445279" "0000952187" "0000445280" "0000952188" "0000445281" "0000952189" "0000445282" "0000952190" "0000445283" "0000952191" "0000445284" "0000952192" "0000445285" "0000952193" "0000445286" "0000952194" "0000445286" "0000952196" "0000445287" "0000952195"