### LOVD-version 3000-30b ### Full data download ### To import, do not remove or alter this header ### ## Filter: (gene_public = CAMK2A) # 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}}" "CAMK2A" "calcium/calmodulin-dependent protein kinase II alpha" "5" "q32" "unknown" "NG_047040.1" "UD_132612475112" "" "https://www.LOVD.nl/CAMKA2A" "" "1" "1460" "815" "114078" "1" "1" "1" "1" "Establishment of this gene variant database (LSDB) was supported by the Leiden University Medical Center (LUMC), Leiden, Nederland." "" "g" "https://databases.lovd.nl/shared/refseq/CAMK2A_codingDNA.html" "1" "" "" "-1" "" "-1" "00001" "2013-05-03 00:00:00" "00006" "2021-05-18 15:07:32" "00000" "2025-05-05 21:14:00" ## Transcripts ## Do not remove or alter this header ## ## Count = 1 "{{id}}" "{{geneid}}" "{{name}}" "{{id_mutalyzer}}" "{{id_ncbi}}" "{{id_ensembl}}" "{{id_protein_ncbi}}" "{{id_protein_ensembl}}" "{{id_protein_uniprot}}" "{{remarks}}" "{{position_c_mrna_start}}" "{{position_c_mrna_end}}" "{{position_c_cds_end}}" "{{position_g_mrna_start}}" "{{position_g_mrna_end}}" "{{created_by}}" "{{created_date}}" "{{edited_by}}" "{{edited_date}}" "00004305" "CAMK2A" "transcript variant 1" "002" "NM_015981.3" "" "NP_057065.2" "" "" "" "-215" "4689" "1470" "149669403" "149599054" "" "0000-00-00 00:00:00" "" "" ## Diseases ## Do not remove or alter this header ## ## Count = 9 "{{id}}" "{{symbol}}" "{{name}}" "{{inheritance}}" "{{id_omim}}" "{{tissues}}" "{{features}}" "{{remarks}}" "{{created_by}}" "{{created_date}}" "{{edited_by}}" "{{edited_date}}" "00000" "Healthy/Control" "Healthy individual / control" "" "" "" "" "" "00000" "2012-07-26 17:29:43" "" "" "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" "04270" "epilepsy" "epilepsy" "" "" "" "" "" "00006" "2015-05-14 16:00:06" "00006" "2017-09-07 14:25:59" "05532" "MRD" "mental retardation, autosomal dominant (MRD, intellectual disability (IDD))" "" "" "" "autosomal dominant" "" "00006" "2018-12-18 09:20:18" "00006" "2018-12-18 09:24:21" "05533" "MR;ID" "mental retardation (MR, intellectual disability (ID))" "" "" "" "" "" "00006" "2018-12-18 09:22:07" "" "" "05611" "NDD" "neurodevelopmental disorder (NDD)" "" "" "" "" "" "00006" "2019-06-19 12:27:20" "00006" "2024-12-13 11:12:21" "05938" "MRD53" "mental retardation, autosomal dominant, type 53 (MRD53)" "AD" "617798" "" "" "" "00006" "2021-05-18 15:07:08" "" "" "06670" "MRT63" "?Mental retardation, autosomal recessive 63" "AR" "618095" "" "" "" "00006" "2021-12-10 23:20:41" "" "" ## Genes_To_Diseases ## Do not remove or alter this header ## ## Count = 4 "{{geneid}}" "{{diseaseid}}" "CAMK2A" "05532" "CAMK2A" "05533" "CAMK2A" "05938" "CAMK2A" "06670" ## Individuals ## Do not remove or alter this header ## ## Count = 27 "{{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}}" "00106539" "" "" "" "1" "" "01197" "{PMID:Kury 2017:29100089}" "2-generation family, 1 affected, unaffected non-carrier parents" "M" "no" "United States" "" "0" "" "" "" "Pat1" "00106591" "" "" "" "1" "" "01197" "{PMID:Kury 2017:29100089}" "2-generation family, 1 affected, unaffected non-carrier parents" "F" "no" "France" "" "0" "" "" "" "Pat2" "00106592" "" "" "" "1" "" "01197" "{PMID:Kury 2017:29100089}" "2-generation family, 1 affected, unaffected non-carrier parents" "M" "no" "United Kingdom (Great Britain)" "" "0" "" "" "" "Pat3" "00106593" "" "" "" "1" "" "01197" "{PMID:Kury 2017:29100089}" "2-generation family, 1 affected, unaffected non-carrier parents" "M" "no" "United States" "" "0" "" "" "" "Pat5" "00106594" "" "" "" "1" "" "01197" "{PMID:Kury 2017:29100089}" "2-generation family, 1 affected, unaffected non-carrier parents" "M" "no" "United States" "" "0" "" "" "" "Pat6" "00106595" "" "" "" "1" "" "01197" "{PMID:Kury 2017:29100089}" "2-generation family, 1 affected, unaffected non-carrier parents" "M" "no" "France" "" "0" "" "" "" "Pat7" "00106596" "" "" "" "1" "" "01197" "{PMID:Kury 2017:29100089}" "2-generation family, 1 affected, unaffected non-carrier parents" "M" "no" "France" "" "0" "" "" "" "Pat8" "00106601" "" "" "" "1" "" "01197" "{PMID:Kury 2017:29100089}" "2-generation family, 1 affected, unaffected non-carrier parents" "F" "no" "Netherlands" "" "0" "" "" "" "Pat9(DECIPHER332886)" "00106640" "" "" "" "1" "" "01197" "{PMID:Kury 2017:29100089}" "2-generation family, 1 affected, unaffected non-carrier parents" "M" "" "United States" "" "0" "" "" "" "Pat10" "00106653" "" "" "" "1" "" "01197" "{PMID:Kury 2017:29100089}" "2-generation family, 1 affected, unaffected non-carrier parents" "M" "no" "Netherlands" "" "0" "" "" "" "Pat12" "00106654" "" "" "" "1" "" "01197" "{PMID:Kury 2017:29100089}" "2-generation family, 1 affected, unaffected non-carrier parents" "F" "no" "United States" "" "0" "" "" "" "Pat13" "00106656" "" "" "" "1" "" "01197" "{PMID:Kury 2017:29100089}" "2-generation family, 1 affected, unaffected non-carrier parents" "F" "" "United Kingdom (Great Britain)" "" "0" "" "" "" "Pat14" "00132017" "" "" "" "1" "" "01197" "{PMID:Kury 2017:29100089}" "2-generation family, 1 affected, unaffected non-carrier parents" "F" "no" "Germany" "" "0" "" "" "" "Pat4" "00132018" "" "" "" "1" "" "01197" "{PMID:Kury 2017:29100089}" "2-generation family, 1 affected, unaffected non-carrier parents" "F" "no" "Germany" "" "0" "" "" "" "Pat11" "00205862" "" "" "" "1" "" "03104" "" "" "F" "no" "China" "" "0" "" "" "" "patient2" "00207964" "" "" "" "1" "" "01807" "" "" "M" "" "" "" "0" "" "" "" "" "00231051" "" "" "" "1" "" "01807" "" "" "M" "" "" "" "0" "" "" "" "" "00373535" "" "" "" "1" "" "01864" "" "" "M" "no" "China" "" "0" "" "" "Chinese" "iw007" "00391786" "" "" "" "1" "" "02494" "" "" "F" "no" "Spain" "" "" "" "" "" "142P" "00404794" "" "" "" "1" "" "01164" "" "" "F" "?" "" "" "0" "" "" "" "192233" "00447957" "" "" "" "1" "" "00006" "{PMID:Akita 2018:29560374}" "2-generation family, 1 affected, unaffected non-carrier parents" "F" "" "Japan" "" "0" "" "" "" "Pat1" "00447958" "" "" "" "1" "" "00006" "{PMID:Akita 2018:29560374}" "2-generation family, 1 affected, unaffected non-carrier parents" "M" "" "Japan" "" "0" "" "" "" "Pat2" "00447959" "" "" "" "1" "" "00006" "{PMID:Akita 2018:29560374}" "2-generation family, 1 affected, unaffected non-carrier parents" "F" "" "Japan" "" "0" "" "" "" "Pat3" "00447962" "" "" "" "4" "" "00006" "{PMID:Chia 2018:29784083}" "2-generation family, 2 affected, unaffectedheteroczugous carrier parents/sibs" "M" "yes" "Jordan" "" "0" "" "" "" "FamPatII1" "00447963" "" "" "00447962" "1" "" "00006" "{PMID:Chia 2018:29784083}" "affected sister" "F" "yes" "Jordan" "" "0" "" "" "" "FamPatII4" "00447964" "" "" "00447962" "1" "" "00006" "{PMID:Chia 2018:29784083}" "brother" "M" "yes" "Jordan" "" "0" "" "" "" "FamPatII2" "00447965" "" "" "00447962" "1" "" "00006" "{PMID:Chia 2018:29784083}" "sister" "F" "yes" "Jordan" "" "0" "" "" "" "FamPatII5" ## Individuals_To_Diseases ## Do not remove or alter this header ## ## Count = 27 "{{individualid}}" "{{diseaseid}}" "00106539" "00139" "00106591" "00139" "00106592" "00139" "00106593" "00139" "00106594" "00139" "00106595" "00139" "00106596" "00139" "00106601" "00139" "00106640" "00139" "00106653" "00139" "00106654" "00139" "00106656" "00139" "00132017" "00139" "00132018" "00139" "00205862" "04270" "00207964" "00198" "00231051" "00198" "00373535" "00198" "00391786" "05938" "00404794" "05938" "00447957" "05611" "00447958" "05611" "00447959" "05611" "00447962" "05611" "00447963" "05611" "00447964" "00000" "00447965" "00000" ## Phenotypes ## Do not remove or alter this header ## ## Note: Only showing Phenotype columns active for Diseases 00000, 00139, 00198, 04270, 05532, 05533, 05611, 05938, 06670 ## Count = 24 "{{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}}" "0000084396" "00198" "00106539" "01197" "Isolated (sporadic)" "09y" "HP:0001263; HP:0001249; HP:0000750; HP:0002194; HP:0100851; HP:0000478; HP:0000271" "" "" "" "" "" "" "" "" "" "Intellectual disability" "" "0000084397" "00139" "00106591" "01197" "Isolated (sporadic)" "04y08m" "HP:0001263; HP:0001249; HP:0000750; HP:0002194; HP:0001252; HP:0100851; HP:0000478; HP:0000271; intellectual disability (HP:0001249); global developmental delay (HP:0001263); speech delay (HP:0000750)" "" "" "" "" "" "" "" "" "" "" "" "0000084398" "00139" "00106592" "01197" "Isolated (sporadic)" "05y03m" "HP:0001263; HP:0001249; HP:0000750; HP:0002194; HP:0001252; HP:0100851; HP:0001250; HP:0000271; intellectual disability (HP:0001249); global developmental delay (HP:0001263); speech delay (HP:0000750)" "" "" "" "" "" "" "" "" "" "" "" "0000084399" "00139" "00106593" "01197" "Isolated (sporadic)" "05y03m" "HP:0001263; HP:0001249; HP:0000750; HP:0002194; HP:0100851; intellectual disability (HP:0001249); global developmental delay (HP:0001263); speech delay (HP:0000750)" "" "" "" "" "" "" "" "" "" "" "" "0000084400" "00139" "00106594" "01197" "Isolated (sporadic)" "11y" "HP:0001263; HP:0001249; HP:0000750; HP:0002194; HP:0100851; intellectual disability (HP:0001249); global developmental delay (HP:0001263); speech delay (HP:0000750)" "" "" "" "" "" "" "" "" "" "" "" "0000084402" "00139" "00106595" "01197" "Isolated (sporadic)" "18y" "HP:0001263; HP:0001249; HP:0000750; HP:0002194; HP:0001252; HP:0001250; HP:0001507; HP:0000271; HP:0000256; intellectual disability (HP:0001249); global developmental delay (HP:0001263); speech delay (HP:0000750)" "" "" "" "" "" "" "" "" "" "" "" "0000084403" "00139" "00106596" "01197" "Isolated (sporadic)" "09y09m" "HP:0001263; HP:0001249; HP:0000750; HP:0002194; HP:0001252; HP:0100851; HP:0001250; HP:0000119; intellectual disability (HP:0001249); global developmental delay (HP:0001263); speech delay (HP:0000750)" "" "" "" "" "" "" "" "" "" "" "" "0000084408" "00139" "00106601" "01197" "Isolated (sporadic)" "04y" "HP:0001263; HP:0001249; HP:0000750; HP:0002194; HP:0100851; intellectual disability (HP:0001249); global developmental delay (HP:0001263); speech delay (HP:0000750)" "" "" "" "" "" "" "" "" "" "" "" "0000084453" "00139" "00106640" "01197" "Isolated (sporadic)" "03y" "HP:0001249; HP:0000750; HP:0100851; HP:0001507; HP:0000478; HP:0000271; intellectual disability (HP:0001249); speech delay (HP:0000750)" "" "" "" "" "" "" "" "" "" "" "" "0000084460" "00139" "00106653" "01197" "Isolated (sporadic)" "07y10m" "HP:0001263; HP:0001249; HP:0000750; HP:0002194; ; ; HP:0100851; HP:0000119; intellectual disability (HP:0001249); global developmental delay (HP:0001263); speech delay (HP:0000750)" "" "" "" "" "" "" "" "" "" "" "" "0000084461" "00139" "00106654" "01197" "Isolated (sporadic)" "01y05m" "HP:0001263; HP:0001249; HP:0000750; HP:0002194; HP:0001252; HP:0100022; intellectual disability (HP:0001249); global developmental delay (HP:0001263); speech delay (HP:0000750)" "" "" "" "" "" "" "" "" "" "" "" "0000084462" "00139" "00106656" "01197" "Isolated (sporadic)" "03y09m" "HP:0001249; HP:0100851; HP:0000478; HP:0000256; HP:0025031; HP:0001629; intellectual disability (HP:0001249); no speech delay (-HP:0000750)" "" "" "" "" "" "" "" "" "" "" "" "0000154007" "04270" "00205862" "03104" "Isolated (sporadic)" "" "" "" "" "" "" "" "" "" "" "" "" "" "0000155734" "00198" "00207964" "01807" "Unknown" "" "Moderate global developmental delay (HP:0011343); Delayed speech and language development (HP:0000750); Muscular hypotonia (HP:0001252)" "" "" "" "" "" "" "" "" "" "" "" "0000173494" "00198" "00231051" "01807" "Unknown" "" "Global developmental delay (HP:0001263); Hypospadias (HP:0000047); Short stature (HP:0004322)" "" "" "" "" "" "" "" "" "" "" "" "0000268809" "00198" "00373535" "01864" "Familial, autosomal dominant" "" "HP:0001263; HP:0000708; HP:0002360; HP:0003234; HP:0000574; HP:0012389; HP:0001288" "" "" "" "?" "" "" "" "" "MRD53" "mental retardation" "" "0000297360" "05938" "00404794" "01164" "Familial" "11y" "Neurodevelopmental delay, Severe global developmental delay; Developmental delay, mental retardation, brother dwarfism with growth hormone treatment, two sisters with developmental delay, several family members in the paternal family with mental retardation" "" "" "" "" "" "" "" "" "" "" "" "0000337147" "05611" "00447957" "00006" "Isolated (sporadic)" "13y" "see paper; ..., 3m-seizure; focal seizures with apnea or focal clonic seizures; EEG 7m-normal, 2y-multifocal spikes, 10y-fast rhythm; OFC 38.5 cm (+4.3 SD) at birth, 43.5 cm(−1.2 SD) at 9 month, 46.8 cm(−2.1 SD) at 3y 50.0 cm (−2.3 SD) at 13y; 3m-head control, 7m-rolling‐over, no sitting, no words; profound intelletucal disability, periodic irritability, hypotonia; stereotypic movements of extremities; no ataxia; MRI brain 2m/10m/2y-normal; 11y-microcephaly" "" "" "" "" "" "" "" "" "MRD53" "seizure" "" "0000337148" "05611" "00447958" "00006" "Isolated (sporadic)" "5y" "see paper; ..., 4m-seizure; 4m-epileptic spasms, 8m-focal seizure with apnea, 9m-epileptic spasms; EEG 4m-hypsarrhythmia, 8m-spike and sharp waves predominantly in occipital region, 1y1m-hypsarrhythmia; OFC 33.5 cm (+0.1 SD) at birth, 43.5 cm (+0.7 SD) at 5 month, 50.0 cm (+0.3 SD) at 3y; 4m-social smile, 5m-head control, 14-sitting, 1y8m-walking, no words; profound intelletucal disability, autistic and hyperkinetic behavior; no involuntary movement; no ataxia; MRI brain 4m/3y-normal; elder brother Duane syndrome" "" "" "" "" "" "" "" "" "MRD53" "seizure" "" "0000337149" "05611" "00447959" "00006" "Isolated (sporadic)" "16y" "see paper; ..., 3m-seizure; eye deviation to left, tonic opisthotonic posturing, upward gazing; EEG multifocal spikes in fp2, t4, t8, o1 and o2; OFC 33.5 cm (+0.4 SD) at birth, 45.6 cm (+0.8 SD) at 10 month, 49.9 cm (−0.2 SD) at 5y; bedridden; profound intelletucal disability, hypotonia, erratic myoclonus; erratic myoclonus; no ataxia; MRI brain 2y-normal; 9y-progressive cerebellar atrophy" "" "" "" "" "" "" "" "" "MRD53" "seizure" "" "0000337152" "05611" "00447962" "00006" "Familial, autosomal recessive" "" "see paper; ..., birth at term, weight 3.2kg, length 50cm, OFC 35cm; 11y-growth failure, height 149cm (<5th), weight 30kg (<5th), OFC 54.5cm; severe developmental dealy; never walked; no speech; seizures; convulsions; EEG abnormal; hypotonia, spastic; MRI brain 11y-normal; no behavioural anomalies" "" "" "" "" "" "" "" "" "MRT63" "intellectual disability" "" "0000337153" "05611" "00447963" "00006" "Familial, autosomal recessive" "" "see paper; ..., birth at term, weight 3.1kg, length 49cm, OFC 34cm; 4y-growth failure, height 108cm (15th), weight 16kg (5th), OFC 47.5cm; severe developmental dealy; never walked; no speech; seizures; convulsions; EEG abnormal; hypotonia, spastic; MRI brain 4y-normal; no behavioural anomalies" "" "" "" "" "" "" "" "" "MRT63" "intellectual disability" "" "0000337154" "00000" "00447964" "00006" "Unknown" "" "see paper; ..., birth at term, weight 2.9kg, length 49cm, OFC 35cm; normal growth; no developmental dealy; 11m-walk; normal speech; no seizures; no convulsions; no hypotonia; no behavioural anomalies" "" "" "" "" "" "" "" "" "" "healthy" "" "0000337155" "00000" "00447965" "00006" "Unknown" "" "see paper; ..., birth at term, weight 3.2kg, length 50cm, OFC 35cm; normal growth; no developmental dealy; 12m-walk; normal speech; no seizures; no convulsions; no hypotonia; MRI brain normal; no behavioural anomalies" "" "" "" "" "" "" "" "" "" "healthy" "" ## Screenings ## Do not remove or alter this header ## ## Count = 27 "{{id}}" "{{individualid}}" "{{variants_found}}" "{{owned_by}}" "{{created_by}}" "{{created_date}}" "{{edited_by}}" "{{edited_date}}" "{{Screening/Technique}}" "{{Screening/Template}}" "{{Screening/Tissue}}" "{{Screening/Remarks}}" "0000107009" "00106539" "1" "01197" "01197" "2017-07-05 10:03:30" "" "" "SEQ-NG" "DNA" "blood" "exome sequencing" "0000107061" "00106591" "1" "01197" "01197" "2017-07-06 17:11:29" "" "" "SEQ-NG" "DNA" "blood" "exome sequencing" "0000107062" "00106592" "1" "01197" "01197" "2017-07-06 17:26:36" "" "" "SEQ-NG" "DNA" "blood" "exome sequencing" "0000107063" "00106593" "1" "01197" "01197" "2017-07-06 17:35:18" "" "" "SEQ-NG" "DNA" "blood" "exome sequencing" "0000107064" "00106594" "1" "01197" "01197" "2017-07-06 17:43:11" "" "" "SEQ-NG" "DNA" "blood" "exome sequencing" "0000107066" "00106595" "1" "01197" "01197" "2017-07-07 09:31:07" "" "" "SEQ-NG" "DNA" "blood" "exome sequencing" "0000107067" "00106596" "1" "01197" "01197" "2017-07-07 10:02:24" "" "" "SEQ-NG" "DNA" "blood" "exome sequencing" "0000107072" "00106601" "1" "01197" "01197" "2017-07-07 10:34:40" "" "" "SEQ-NG" "DNA" "blood" "exome sequencing" "0000107117" "00106640" "1" "01197" "01197" "2017-07-07 11:00:07" "" "" "SEQ-NG" "DNA" "blood" "exome sequencing" "0000107124" "00106653" "1" "01197" "01197" "2017-07-07 11:05:56" "" "" "SEQ-NG" "DNA" "blood" "exome sequencing" "0000107125" "00106654" "1" "01197" "01197" "2017-07-07 11:30:48" "" "" "SEQ-NG" "DNA" "blood" "exome sequencing" "0000107127" "00106656" "1" "01197" "01197" "2017-07-07 11:40:21" "" "" "SEQ-NG" "DNA" "blood" "exome sequencing" "0000132856" "00132017" "1" "01197" "01197" "2017-10-09 09:36:21" "" "" "SEQ-NG" "DNA" "blood" "exome sequencing" "0000132858" "00132018" "1" "01197" "01197" "2017-10-09 09:54:56" "" "" "SEQ-NG" "DNA" "blood" "exome sequencing" "0000206892" "00205862" "1" "03104" "03104" "2018-11-12 11:26:51" "" "" "SEQ;SEQ-NG-I" "DNA" "Peripheral blood" "" "0000209009" "00207964" "1" "01807" "01807" "2018-12-04 16:44:02" "" "" "SEQ" "DNA" "" "" "0000232148" "00231051" "1" "01807" "01807" "2019-04-25 09:55:30" "" "" "SEQ" "DNA" "" "" "0000374885" "00373535" "1" "01864" "01864" "2021-05-17 17:49:22" "" "" "SEQ-NG" "DNA" "blood" "WGS" "0000393029" "00391786" "1" "02494" "02494" "2021-11-19 10:15:35" "" "" "SEQ-NG" "DNA" "" "WES" "0000406033" "00404794" "1" "01164" "01164" "2022-03-08 14:31:55" "" "" "SEQ-NG-I" "DNA" "" "" "0000449530" "00447957" "1" "00006" "00006" "2024-02-05 12:29:02" "" "" "SEQ;SEQ-NG" "DNA" "" "trio WES" "0000449531" "00447958" "1" "00006" "00006" "2024-02-05 12:29:02" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000449532" "00447959" "1" "00006" "00006" "2024-02-05 12:29:02" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000449535" "00447962" "1" "00006" "00006" "2024-02-05 12:59:22" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000449536" "00447963" "1" "00006" "00006" "2024-02-05 12:59:22" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000449537" "00447964" "1" "00006" "00006" "2024-02-05 12:59:22" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000449538" "00447965" "1" "00006" "00006" "2024-02-05 12:59:22" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" ## Screenings_To_Genes ## Do not remove or alter this header ## ## Count = 3 "{{screeningid}}" "{{geneid}}" "0000206892" "CAMK2A" "0000374885" "CAMK2A" "0000406033" "CAMK2A" ## 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 = 45 "{{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}}" "0000172749" "0" "70" "5" "149652723" "149652723" "del" "0" "01197" "CAMK2A_000001" "g.149652723del" "1/20000 trios with developmental disorder" "{PMID:Kury 2017:29100089}" "" "" "" "De novo" "" "" "0" "" "" "g.150273160del" "" "likely pathogenic (dominant)" "" "0000172803" "0" "90" "5" "149636374" "149636374" "subst" "0" "01197" "CAMK2A_000002" "g.149636374A>G" "1/20,000 trios with developmental disorders" "{PMID:Kury 2017:29100089}" "" "" "Pathogenicity assessed in vitro and in vivo" "De novo" "-" "" "0" "" "" "g.150256811A>G" "" "pathogenic (dominant)" "" "0000172804" "0" "90" "5" "149636340" "149636340" "subst" "0" "01197" "CAMK2A_000003" "g.149636340C>G" "" "{PMID:Kury 2017:29100089}" "" "" "" "De novo" "-" "" "0" "" "" "g.150256777C>G" "" "pathogenic (dominant)" "" "0000172805" "0" "90" "5" "149631595" "149631595" "subst" "0" "01197" "CAMK2A_000004" "g.149631595T>A" "1/20,000 trios with developmental disorders" "{PMID:Kury 2017:29100089}" "" "" "Pathogenicity assessed in vivo and in vitro" "De novo" "-" "" "0" "" "" "g.150252032T>A" "" "pathogenic (dominant)" "" "0000172806" "0" "70" "5" "149631543" "149631543" "dup" "0" "01197" "CAMK2A_000005" "g.149631543dup" "1/20,000 trios with developmental disorders" "{PMID:Kury 2017:29100089}" "" "" "" "De novo" "-" "" "0" "" "" "g.150251980dup" "" "likely pathogenic (dominant)" "" "0000172807" "0" "50" "5" "149631371" "149631371" "subst" "0" "01197" "CAMK2A_000006" "g.149631371G>A" "3/20,000 trios with developmental disorders" "{PMID:Kury 2017:29100089}" "" "" "" "De novo" "-" "" "0" "" "" "g.150251808G>A" "" "VUS" "" "0000172808" "0" "50" "5" "149631371" "149631371" "subst" "0" "01197" "CAMK2A_000006" "g.149631371G>A" "3/20,000 trios with developmental disorders" "{PMID:Kury 2017:29100089}" "" "" "" "De novo" "-" "" "0" "" "" "g.150251808G>A" "" "VUS" "" "0000172814" "0" "50" "5" "149631371" "149631371" "subst" "0" "01197" "CAMK2A_000006" "g.149631371G>A" "3/20,000 trios with developmental disorders" "{PMID:Kury 2017:29100089}" "" "" "" "De novo" "-" "" "0" "" "" "g.150251808G>A" "" "VUS" "" "0000172880" "0" "50" "5" "149630363" "149630363" "subst" "0" "01197" "CAMK2A_000008" "g.149630363G>A" "1/20,000 trios with developmental disorders" "{PMID:Kury 2017:29100089}" "" "" "" "De novo" "-" "" "0" "" "" "g.150250800G>A" "" "VUS" "" "0000172881" "0" "90" "5" "149629844" "149629844" "subst" "0" "01197" "CAMK2A_000009" "g.149629844T>C" "1/20,000 trios with developmental disorders" "{PMID:Kury 2017:29100089}" "" "" "" "De novo" "-" "" "0" "" "" "g.150250281T>C" "" "pathogenic (dominant)" "" "0000172882" "0" "90" "5" "149629833" "149629833" "subst" "0" "01197" "CAMK2A_000010" "g.149629833T>G" "1/20,000 trios with developmental disorders" "{PMID:Kury 2017:29100089}" "" "" "" "De novo" "-" "" "0" "" "" "g.150250270T>G" "" "pathogenic (dominant)" "" "0000172884" "0" "70" "5" "149607754" "149607754" "subst" "0" "01197" "CAMK2A_000007" "g.149607754C>T" "1/20,000 trios with developmental disorders" "{PMID:Kury 2017:29100089}" "" "" "" "De novo" "-" "" "0" "" "" "g.150228191C>T" "" "likely pathogenic (dominant)" "" "0000222042" "0" "70" "5" "149636332" "149636332" "subst" "0" "01197" "CAMK2A_000012" "g.149636332G>A" "1/20,000 trios with developmental disorders" "{PMID:Kury 2017:29100089}" "" "" "" "De novo" "" "" "0" "" "" "g.150256769G>A" "" "likely pathogenic (dominant)" "" "0000222044" "0" "70" "5" "149629873" "149629873" "subst" "0" "01197" "CAMK2A_000011" "g.149629873C>T" "1/20,000 trios with developmental disorders" "{PMID:Kury 2017:29100089}" "" "" "" "De novo" "" "" "0" "" "" "g.150250310C>T" "" "likely pathogenic (dominant)" "" "0000330675" "0" "50" "5" "149631371" "149631371" "subst" "0" "01804" "CAMK2A_000006" "g.149631371G>A" "" "" "" "CAMK2A(NM_015981.3):c.635C>T (p.(Pro212Leu))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "0" "" "" "g.150251808G>A" "" "VUS" "" "0000436541" "0" "90" "5" "149631371" "149631371" "subst" "0" "03104" "CAMK2A_000013" "g.149631371G>T" "" "" "" "" "" "De novo" "" "" "0" "" "" "g.150251808G>T" "" "pathogenic" "" "0000439087" "0" "70" "5" "149627376" "149627376" "subst" "0" "01807" "CAMK2A_000014" "g.149627376C>T" "" "" "" "" "" "Unknown" "" "" "0" "" "" "g.150247813C>T" "" "likely pathogenic" "" "0000474481" "0" "70" "5" "149610865" "149610865" "subst" "0" "01807" "CAMK2A_000015" "g.149610865C>A" "" "" "" "1109+3G>T" "" "Unknown" "" "" "0" "" "" "g.150231302C>A" "" "likely pathogenic" "" "0000524923" "0" "30" "5" "149619303" "149619303" "subst" "0" "01804" "CAMK2A_000016" "g.149619303G>C" "" "" "" "CAMK2A(NM_015981.3):c.985-4C>G (p.?)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "g.150239740G>C" "" "likely benign" "" "0000524924" "0" "90" "5" "149631371" "149631371" "subst" "0" "02327" "CAMK2A_000013" "g.149631371G>T" "" "" "" "" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "g.150251808G>T" "" "pathogenic" "" "0000524925" "0" "30" "5" "149631375" "149631375" "subst" "0" "02327" "CAMK2A_000017" "g.149631375G>A" "" "" "" "" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "g.150251812G>A" "" "likely benign" "" "0000524926" "0" "70" "5" "149631392" "149631392" "subst" "0" "02327" "CAMK2A_000018" "g.149631392A>T" "" "" "" "" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "g.150251829A>T" "" "likely pathogenic" "" "0000655336" "0" "50" "5" "149630292" "149630292" "subst" "0" "01943" "CAMK2A_000020" "g.149630292G>A" "" "" "" "CAMK2A(NM_001363989.1):c.775C>T (p.R259C)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "g.150250729G>A" "" "VUS" "" "0000785733" "0" "90" "5" "149629855" "149629880" "del" "0" "01864" "CAMK2A_000021" "g.149629855_149629880del" "" "" "" "" "" "De novo" "yes" "" "0" "" "" "g.150250292_150250317del" "" "pathogenic (dominant)" "" "0000801966" "0" "50" "5" "149630362" "149630362" "subst" "3.65735E-5" "01943" "CAMK2A_000022" "g.149630362C>T" "" "" "" "CAMK2A(NM_001363989.1):c.705G>A (p.P235=), CAMK2A(NM_015981.3):c.705G>A (p.P235=)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "VUS" "" "0000823615" "0" "50" "5" "149633110" "149633110" "subst" "0" "02494" "CAMK2A_000023" "g.149633110C>A" "" "" "" "" "" "De novo" "" "" "" "" "" "" "" "likely pathogenic" "" "0000842212" "0" "70" "5" "149652703" "149652703" "subst" "4.07057E-6" "01164" "CAMK2A_000024" "g.149652703G>A" "" "" "" "" "ACMG: PVS1, PM2_SUP; variant has AC=1 in gnomAD, read data imply mosaic constellation" "Germline" "?" "" "" "" "" "" "" "likely pathogenic (dominant)" "ACMG" "0000859834" "0" "30" "5" "149631542" "149631542" "subst" "0" "01943" "CAMK2A_000019" "g.149631542C>T" "" "" "" "CAMK2A(NM_001363989.1):c.598+3G>A" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely benign" "" "0000859835" "0" "50" "5" "149636387" "149636387" "subst" "0" "02327" "CAMK2A_000025" "g.149636387C>G" "" "" "" "" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "VUS" "" "0000886694" "0" "50" "5" "149602613" "149602613" "subst" "4.07169E-6" "02325" "CAMK2A_000026" "g.149602613G>A" "" "" "" "CAMK2A(NM_015981.4):c.1405C>T (p.R469W), CAMK2A(NM_171825.2):c.1372C>T (p.(Arg458Trp))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "VUS" "" "0000886696" "0" "50" "5" "149637163" "149637163" "subst" "4.43228E-5" "02325" "CAMK2A_000028" "g.149637163T>C" "" "" "" "CAMK2A(NM_015981.4):c.235A>G (p.I79V)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "VUS" "" "0000886697" "0" "70" "5" "149637178" "149637178" "subst" "0" "02327" "CAMK2A_000029" "g.149637178G>A" "" "" "" "" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely pathogenic" "" "0000912265" "0" "70" "5" "149652711" "149652711" "subst" "0" "02327" "CAMK2A_000030" "g.149652711G>A" "" "" "" "" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely pathogenic" "" "0000959752" "0" "90" "5" "149631371" "149631371" "subst" "0" "00006" "CAMK2A_000013" "g.149631371G>T" "" "{PMID:Akita 2018:29560374}" "" "" "" "De novo" "" "" "0" "" "" "g.150251808G>T" "" "pathogenic (dominant)" "ACMG" "0000959753" "0" "90" "5" "149630363" "149630363" "subst" "0" "00006" "CAMK2A_000008" "g.149630363G>A" "" "{PMID:Akita 2018:29560374}" "" "" "somatic mosaicism 0.4-0.8" "Somatic" "" "" "0" "" "" "g.150250800G>A" "" "pathogenic (dominant)" "ACMG" "0000959754" "0" "90" "5" "149629873" "149629873" "subst" "0" "00006" "CAMK2A_000011" "g.149629873C>T" "" "{PMID:Akita 2018:29560374}" "" "" "consequences on RNA predicted from mini-gene splicing assay" "De novo" "" "" "0" "" "" "g.150250310C>T" "" "pathogenic (dominant)" "ACMG" "0000959757" "3" "90" "5" "149602589" "149602589" "subst" "0" "00006" "CAMK2A_000031" "g.149602589G>A" "" "{PMID:Chia 2018:29784083}" "" "" "" "Germline" "yes" "" "0" "" "" "g.150223026G>A" "" "pathogenic (recessive)" "" "0000959758" "3" "90" "5" "149602589" "149602589" "subst" "0" "00006" "CAMK2A_000031" "g.149602589G>A" "" "{PMID:Chia 2018:29784083}" "" "" "" "Germline" "yes" "" "0" "" "" "g.150223026G>A" "" "pathogenic (recessive)" "" "0000959759" "1" "90" "5" "149602589" "149602589" "subst" "0" "00006" "CAMK2A_000031" "g.149602589G>A" "" "{PMID:Chia 2018:29784083}" "" "" "" "Germline" "" "" "0" "" "" "g.150223026G>A" "" "pathogenic (recessive)" "" "0000959760" "1" "90" "5" "149602589" "149602589" "subst" "0" "00006" "CAMK2A_000031" "g.149602589G>A" "" "{PMID:Chia 2018:29784083}" "" "" "" "Germline" "" "" "0" "" "" "g.150223026G>A" "" "pathogenic (recessive)" "" "0000959871" "3" "50" "5" "149602589" "149602589" "subst" "0" "00006" "CAMK2A_000031" "g.149602589G>A" "" "{PMID:Chia 2018:29784083}" "" "" "" "Germline" "" "" "0" "" "" "g.150223026G>A" "" "likely benign" "" "0000959944" "3" "50" "5" "149602589" "149602589" "subst" "0" "00006" "CAMK2A_000031" "g.149602589G>A" "" "{PMID:Chia 2018:29784083}" "" "" "" "Germline" "" "" "0" "" "" "g.150223026G>A" "" "likely benign" "" "0000976665" "0" "50" "5" "149637351" "149637351" "subst" "0" "01804" "CAMK2A_000032" "g.149637351T>C" "" "" "" "CAMK2A(NM_015981.4):c.218-171A>G" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "VUS" "" "0000994802" "0" "50" "5" "149602613" "149602613" "subst" "4.07169E-6" "01804" "CAMK2A_000026" "g.149602613G>A" "" "" "" "CAMK2A(NM_015981.4):c.1405C>T (p.R469W), CAMK2A(NM_171825.2):c.1372C>T (p.(Arg458Trp))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "VUS" "" "0000994803" "0" "50" "5" "149631347" "149631347" "subst" "0" "01804" "CAMK2A_000033" "g.149631347C>T" "" "" "" "CAMK2A(NM_015981.3):c.659G>A (p.(Arg220His))" "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 CAMK2A ## Count = 45 "{{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}}" "0000172749" "00004305" "70" "65" "0" "65" "0" "c.65del" "r.(?)" "p.(Gly22Glufs*10)" "2" "0000172803" "00004305" "90" "293" "0" "293" "0" "c.293T>C" "r.(?)" "p.(Phe98Ser)" "5" "0000172804" "00004305" "90" "327" "0" "327" "0" "c.327G>C" "r.(?)" "p.(Glu109Asp)" "5" "0000172805" "00004305" "90" "548" "0" "548" "0" "c.548A>T" "r.(?)" "p.(Glu183Val)" "8" "0000172806" "00004305" "70" "598" "2" "598" "2" "c.598+2dup" "r.spl?" "p.?" "8i" "0000172807" "00004305" "50" "635" "0" "635" "0" "c.635C>T" "r.(?)" "p.(Pro212Leu)" "" "0000172808" "00004305" "50" "635" "0" "635" "0" "c.635C>T" "r.(?)" "p.(Pro212Leu)" "" "0000172814" "00004305" "50" "635" "0" "635" "0" "c.635C>T" "r.(?)" "p.(Pro212Leu)" "" "0000172880" "00004305" "50" "704" "0" "704" "0" "c.704C>T" "r.(?)" "p.(Pro235Leu)" "" "0000172881" "00004305" "90" "845" "0" "845" "0" "c.845A>G" "r.(?)" "p.(His282Arg)" "" "0000172882" "00004305" "90" "856" "0" "856" "0" "c.856A>C" "r.(?)" "p.(Thr286Pro)" "" "0000172884" "00004305" "70" "1237" "1" "1237" "1" "c.1237+1G>A" "r.spl?" "p.?" "" "0000222042" "00004305" "70" "335" "0" "335" "0" "c.335C>T" "r.(?)" "p.(Ala112Val)" "" "0000222044" "00004305" "70" "817" "-1" "817" "-1" "c.817-1G>A" "r.spl?" "p.?" "" "0000330675" "00004305" "50" "635" "0" "635" "0" "c.635C>T" "r.(?)" "p.(Pro212Leu)" "" "0000436541" "00004305" "90" "635" "0" "635" "0" "c.635C>A" "r.(?)" "p.(Pro212Gln)" "" "0000439087" "00004305" "70" "902" "0" "902" "0" "c.902G>A" "r.(?)" "p.(Gly301Glu)" "" "0000474481" "00004305" "70" "1142" "3" "1142" "3" "c.1142+3G>T" "r.spl" "p.?" "" "0000524923" "00004305" "30" "985" "-4" "985" "-4" "c.985-4C>G" "r.spl?" "p.?" "" "0000524924" "00004305" "90" "635" "0" "635" "0" "c.635C>A" "r.(?)" "p.(Pro212Gln)" "" "0000524925" "00004305" "30" "631" "0" "631" "0" "c.631C>T" "r.(?)" "p.(Pro211Ser)" "" "0000524926" "00004305" "70" "614" "0" "614" "0" "c.614T>A" "r.(?)" "p.(Ile205Asn)" "" "0000655336" "00004305" "50" "775" "0" "775" "0" "c.775C>T" "r.(?)" "p.(Arg259Cys)" "" "0000785733" "00004305" "90" "817" "-4" "838" "0" "c.817-4_838del" "r.spl" "p.?" "9" "0000801966" "00004305" "50" "705" "0" "705" "0" "c.705G>A" "r.(?)" "p.(Pro235=)" "" "0000823615" "00004305" "50" "412" "-1" "412" "-1" "c.412-1G>T" "r.spl?" "p.?" "" "0000842212" "00004305" "70" "82" "0" "82" "0" "c.82C>T" "r.(?)" "p.(Arg28*)" "" "0000859834" "00004305" "30" "598" "3" "598" "3" "c.598+3G>A" "r.spl?" "p.?" "" "0000859835" "00004305" "50" "280" "0" "280" "0" "c.280G>C" "r.(?)" "p.(Gly94Arg)" "" "0000886694" "00004305" "50" "1405" "0" "1405" "0" "c.1405C>T" "r.(?)" "p.(Arg469Trp)" "" "0000886696" "00004305" "50" "235" "0" "235" "0" "c.235A>G" "r.(?)" "p.(Ile79Val)" "" "0000886697" "00004305" "70" "220" "0" "220" "0" "c.220C>T" "r.(?)" "p.(Arg74*)" "" "0000912265" "00004305" "70" "74" "0" "74" "0" "c.74C>T" "r.(?)" "p.(Ser25Leu)" "" "0000959752" "00004305" "90" "635" "0" "635" "0" "c.635C>A" "r.(?)" "p.(Pro212Gln)" "" "0000959753" "00004305" "90" "704" "0" "704" "0" "c.704C>T" "r.(?)" "p.(Pro235Leu)" "" "0000959754" "00004305" "90" "817" "-1" "817" "-1" "c.817-1G>A" "r.[(817_900del,816_817ins[816+1_817-2;a],?)]" "p.[(His273_Lys300del,His273ThrfsTer69,His273ValfsTer17)]" "" "0000959757" "00004305" "90" "1429" "0" "1429" "0" "c.1429C>T" "r.(?)" "p.(His477Tyr)" "" "0000959758" "00004305" "90" "1429" "0" "1429" "0" "c.1429C>T" "r.(?)" "p.(His477Tyr)" "" "0000959759" "00004305" "90" "1429" "0" "1429" "0" "c.1429C>T" "r.(?)" "p.(His477Tyr)" "" "0000959760" "00004305" "90" "1429" "0" "1429" "0" "c.1429C>T" "r.(?)" "p.(His477Tyr)" "" "0000959871" "00004305" "50" "1429" "0" "1429" "0" "c.1429C>T" "r.(?)" "p.(His477Tyr)" "" "0000959944" "00004305" "50" "1429" "0" "1429" "0" "c.1429C>T" "r.(?)" "p.(His477Tyr)" "" "0000976665" "00004305" "50" "218" "-171" "218" "-171" "c.218-171A>G" "r.(=)" "p.(=)" "" "0000994802" "00004305" "50" "1405" "0" "1405" "0" "c.1405C>T" "r.(?)" "p.(Arg469Trp)" "" "0000994803" "00004305" "50" "659" "0" "659" "0" "c.659G>A" "r.(?)" "p.(Arg220His)" "" ## Screenings_To_Variants ## Do not remove or alter this header ## ## Count = 29 "{{screeningid}}" "{{variantid}}" "0000107009" "0000172749" "0000107061" "0000172803" "0000107062" "0000172804" "0000107063" "0000172805" "0000107064" "0000172806" "0000107066" "0000172807" "0000107067" "0000172808" "0000107072" "0000172814" "0000107117" "0000172880" "0000107124" "0000172881" "0000107125" "0000172882" "0000107127" "0000172884" "0000132856" "0000222042" "0000132858" "0000222044" "0000206892" "0000436541" "0000209009" "0000439087" "0000232148" "0000474481" "0000374885" "0000785733" "0000393029" "0000823615" "0000406033" "0000842212" "0000449530" "0000959752" "0000449531" "0000959753" "0000449532" "0000959754" "0000449535" "0000959757" "0000449535" "0000959871" "0000449536" "0000959758" "0000449536" "0000959944" "0000449537" "0000959759" "0000449538" "0000959760"