### LOVD-version 3000-30b ### Full data download ### To import, do not remove or alter this header ### ## Filter: (gene_public = ERLIN1) # 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}}" "ERLIN1" "ER lipid raft associated 1" "10" "q21-q22" "unknown" "NC_000010.10" "UD_136017990518" "" "http://www.LOVD.nl/ERLIN1" "" "1" "16947" "10613" "611604" "1" "1" "1" "1" "Establishment of this gene variant database (LSDB) was supported by the Leiden University Medical Center (LUMC), Leiden, Nederland." "" "g" "http://databases.lovd.nl/shared/refseq/ERLIN1_codingDNA.html" "1" "" "" "-1" "" "-1" "00001" "2013-05-03 00:00:00" "00006" "2016-09-26 09:42:25" "00000" "2024-04-19 20:27:30" ## 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}}" "00007227" "ERLIN1" "ER lipid raft associated 1" "002" "NM_006459.3" "" "NP_006450.2" "" "" "" "-351" "3088" "1047" "101945734" "101909847" "" "0000-00-00 00:00:00" "" "" ## Diseases ## Do not remove or alter this header ## ## Count = 5 "{{id}}" "{{symbol}}" "{{name}}" "{{inheritance}}" "{{id_omim}}" "{{tissues}}" "{{features}}" "{{remarks}}" "{{created_by}}" "{{created_date}}" "{{edited_by}}" "{{edited_date}}" "00325" "SPG" "paraplegia, spastic (SPG)" "" "" "" "" "" "00006" "2014-02-15 22:29:17" "00006" "2016-11-28 13:01:43" "01972" "neuropathy (CCT5)" "neuropathy, sensory, with spastic paraplegia, hereditary, autosomal recessive" "AR" "256840" "" "" "" "00006" "2014-09-25 23:29:40" "00006" "2021-12-10 21:51:32" "02640" "IAHSP" "paralysis, spastic, hereditary, ascending, infantile-onset (IAHSP)" "AR" "607225" "" "" "" "00006" "2014-09-25 23:29:40" "00006" "2021-12-10 21:51:32" "04255" "ALS" "sclerosis, lateral, amyotrophic (ALS)" "" "" "" "" "" "00015" "2015-05-08 11:45:27" "00006" "2015-12-08 23:53:05" "05187" "SPG62" "paraplegia, spastic, type 62 (SPG-62)" "AR" "615681" "" "" "" "00006" "2016-10-05 08:33:45" "00006" "2021-12-10 21:51:32" ## Genes_To_Diseases ## Do not remove or alter this header ## ## Count = 1 "{{geneid}}" "{{diseaseid}}" "ERLIN1" "05187" ## Individuals ## Do not remove or alter this header ## ## Count = 10 "{{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}}" "00095122" "" "" "" "3" "" "00006" "{PMID:Novarino 2014:24482476}, {DOI:Novarino 2014:10.1126/science.1247363}" "5-generation family, 3 affected (2F, M), 3 unaffected siblings, unaffected heterozygous carrier parents, patient 786-V-3" "M" "yes" "" "" "0" "added by student Jente Houweling" "" "" "" "00095123" "" "" "" "2" "" "00006" "{PMID:Novarino 2014:24482476}, {DOI:Novarino 2014:10.1126/science.1247363}" "4-generation family, 2 affecteds, 2 unaffected siblings, 2 unaffected heterozygous carrier parents (consanguineous), 1098-IV-3" "M" "" "" "" "0" "added by student Merel van Kan" "" "" "" "00095124" "" "" "00095123" "1" "" "00006" "{PMID:Novarino 2014:24482476}, {DOI:Novarino 2014:10.1126/science.1247363}" "brother of 1098-IV-3" "M" "" "" "" "0" "added by student Merel van Kan" "" "" "" "00095125" "" "" "00095122" "1" "" "00006" "{PMID:Novarino 2014:24482476}, {DOI:Novarino 2014:10.1126/science.1247363}" "sister of 786-V-3" "F" "yes" "" "" "0" "added by student Jente Houweling" "" "" "" "00095126" "" "" "" "2" "" "00006" "{PMID:Novarino 2014:24482476}, {DOI:Novarino 2014:10.1126/science.1247363}" "5-generation family, 2 affected sisters, unaffected heterozygous carrier parents, Pat1598V2" "F" "" "" "" "0" "added by student Seline Keijzer" "" "" "" "00095127" "" "" "00095126" "1" "" "00006" "{PMID:Novarino 2014:24482476}, {DOI:Novarino 2014:10.1126/science.1247363}" "sister of 1598PatV4" "F" "" "" "" "0" "added by student Seline Keijzer" "" "" "" "00143683" "" "" "" "4" "" "02332" "" "6 generation family, 10 affected (DNA available from 1F, 3M), unaffected heterozygous carrier parents" "F" "yes" "Turkey" "" "0" "" "" "white" "ALS-518" "00143789" "" "" "00143683" "1" "" "02332" "" "" "M" "yes" "Turkey" "" "0" "" "" "" "ALS-856" "00143791" "" "" "00143683" "1" "" "02332" "" "" "M" "yes" "Turkey" "" "0" "" "" "" "ALS-869" "00143792" "" "" "00143683" "1" "" "02332" "" "" "M" "yes" "Turkey" "" "0" "" "" "" "ALS-1077" ## Individuals_To_Diseases ## Do not remove or alter this header ## ## Count = 10 "{{individualid}}" "{{diseaseid}}" "00095122" "00325" "00095123" "01972" "00095124" "01972" "00095125" "00325" "00095126" "02640" "00095127" "02640" "00143683" "04255" "00143789" "04255" "00143791" "04255" "00143792" "04255" ## Phenotypes ## Do not remove or alter this header ## ## Note: Only showing Phenotype columns active for Diseases 00325, 01972, 02640, 04255, 05187 ## Count = 10 "{{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}}" "0000073517" "01972" "00095123" "00006" "Familial, autosomal recessive" "" "tiptoe walking (HP0030051)spasticity of lower limbs (HP0002061)no dysarthria (-HP0001260)spastic gait (HP0002064)no cerebellar signs (-HP0001317)absent achilles reflex (HP0003438)no plantar tendon reflex (-HP:0003487)no babinski sign (-HP0003487)abnormal gait (HP0001288)no amyotrophy (-HP0003202)no fasciculations (-HP0002380)vibration sense at ankles (HP0006938)no sensory loss (-HP0010835)no skeletal deformities (-HP0000924)no sphincter deformities (-HP0002839)normal brain MRI (-HP0002500)N/A spinal MRI (-HP0002143)flexion contractures of knees (HP0006380)" "02y" "" "" "" "" "" "" "" "" "0000073518" "01972" "00095124" "00006" "Familial, autosomal recessive" "" "tiptoe walking (HP0030051)spasticity (HP0001257)no dysarthria (-HP0001260)spastic gait (HP0002064)no cerebellar signs (-HP0001317)increased deep tendon reflex in lower limbs (HP0002395)no babinski sign (-HP0003487)abnormal gait (HP0001288)no amyotrophy (-HP0003202)no fasciculations (-HP0002380)vibration sense at ankles (HP0006938)no sensory loss (-HP0010835)no skeletal deformities (-HP0000924)no sphincter deformities (-HP0002839)normal brain MRI (-HP0002500)N/A spinal MRI (-HP0002143)flexion contractures of knees (HP0006380)" "03y" "" "" "" "" "" "" "" "" "0000073519" "00325" "00095122" "00006" "Familial, autosomal recessive" "" "thoracic kyphosis (HP:0002942), cerebellar signs (HP:0001317), Pain in extremities (HP:0009763), hyperreflexia (HP:0001347), dysarthria (HP:0001260), borderline personality disorder (HP:0012076), Skeletal muscle atrophy (HP:0003202), Limb fasciculations (-HP:0007289), Impaired vibration sensation at ankles (-HP:0006938), urinary bladder sphincter dysfunction (-HP:0002839), babinski sign (-HP:0003487)" "03y" "" "" "" "" "" "" "" "" "0000073520" "02640" "00095126" "00006" "Familial" "" "tiptoewalking, spasticity of lower limbs, can walk alone with unsteady gait (postoperation), increased deep tendon reflexes and positive clonus, abnormal gait, plantar reflex" "01y05m" "" "" "" "" "" "" "" "" "0000073521" "02640" "00095127" "00006" "Isolated (sporadic)" "" "tiptoewalking, spasticity of lower limbs, can walk alone mild scissors gait, increased deep tendon reflexes and positive clonus, abnormal gait, plantar reflex" "01y08m" "" "" "" "" "" "" "" "" "0000073522" "00325" "00095125" "00006" "Familial, autosomal recessive" "" "thoracic kyphosis (HP:0002942), cerebellar signs (HP:0001317), hyperreflexia (HP:0001347), dysarthria (-HP:0001260), borderline personality disorder (HP:0012076), Skeletal muscle atrophy (HP:0003202), Limb fasciculations (-HP:0007289), Impaired vibration sensation at ankles (-HP:0006938), urinary bladder sphincter dysfunction (-HP:0002839), babinski sign (-HP:0003487), inability to walk (HP:0002540)" "13y" "" "" "" "" "" "" "" "" "0000116445" "04255" "00143683" "02332" "Familial, autosomal recessive" "25y" "increased deep tendon reflexes in the lower limbs (HP:0002395), hand interosseous muscle atrophy (HP:0007181), limb fasciculation (HP:0007289) and muscle fibrillation (HP:0010546)in right first interracial, biceps and both tibialis anterior muscles, tongue fasciculations (HP:0001308)" "15y-20y" "20y?" "Difficulty in walking (HP:0002355)" "" "" "" "" "" "" "0000116559" "04255" "00143789" "02332" "Familial, autosomal recessive" "37y" "" "32y" "37y" "" "" "" "" "" "" "" "0000116560" "04255" "00143791" "02332" "Familial, autosomal recessive" "53y" "" "49y" "53y" "" "" "" "" "" "" "" "0000116561" "04255" "00143792" "02332" "Familial, autosomal recessive" "15y" "" "15y?" "15y" "" "" "" "" "" "" "" ## Screenings ## Do not remove or alter this header ## ## Count = 10 "{{id}}" "{{individualid}}" "{{variants_found}}" "{{owned_by}}" "{{created_by}}" "{{created_date}}" "{{edited_by}}" "{{edited_date}}" "{{Screening/Technique}}" "{{Screening/Template}}" "{{Screening/Tissue}}" "{{Screening/Remarks}}" "0000095520" "00095123" "1" "00006" "00006" "2016-09-22 13:17:45" "" "" "arraySNP;SEQ-NG-I;SEQ-NG-R;PCR;RT-PCR;Western" "DNA" "blood" "" "0000095521" "00095124" "1" "00006" "00006" "2016-09-22 13:56:34" "" "" "arraySNP;SEQ-NG-I;SEQ-NG-R;PCR;RT-PCR;Western" "DNA" "blood" "" "0000095522" "00095126" "1" "00006" "00006" "2016-09-23 17:46:08" "" "" "arraySNP;SEQ" "RNA" "neural tissue" "" "0000095523" "00095127" "1" "00006" "00006" "2016-09-23 17:50:24" "" "" "arraySNP;SEQ" "RNA" "neural tissue" "" "0000095524" "00095122" "1" "00006" "00006" "2016-09-24 10:50:56" "00006" "2016-09-24 11:56:59" "SEQ-NG" "DNA" "" "" "0000095525" "00095125" "1" "00006" "00006" "2016-09-24 13:25:50" "" "" "SEQ-NG" "DNA" "" "" "0000144540" "00143683" "1" "02332" "02332" "2017-12-03 21:36:56" "" "" "SEQ-NG" "DNA" "Blood" "" "0000144648" "00143789" "1" "02332" "02332" "2017-12-06 10:27:52" "" "" "SEQ-NG" "DNA" "" "" "0000144650" "00143791" "1" "02332" "02332" "2017-12-06 10:44:23" "" "" "SEQ-NG" "DNA" "" "" "0000144651" "00143792" "1" "02332" "02332" "2017-12-06 10:52:48" "" "" "PCR" "DNA" "" "" ## Screenings_To_Genes ## Do not remove or alter this header ## ## Count = 18 "{{screeningid}}" "{{geneid}}" "0000095520" "ERLIN1" "0000095521" "ERLIN1" "0000095522" "ERLIN1" "0000095523" "ERLIN1" "0000095524" "ERLIN1" "0000095525" "ERLIN1" "0000144540" "ABCC2" "0000144540" "C9orf72" "0000144540" "ERLIN1" "0000144540" "FUS" "0000144540" "SOD1" "0000144540" "TARDBP" "0000144648" "ABCC2" "0000144648" "ERLIN1" "0000144650" "ABCC2" "0000144650" "ERLIN1" "0000144651" "ABCC2" "0000144651" "ERLIN1" ## Variants_On_Genome ## Do not remove or alter this header ## ## Please note that not necessarily all variants found in the given individuals are shown. This output is restricted to variants in the selected gene. ## Count = 16 "{{id}}" "{{allele}}" "{{effectid}}" "{{chromosome}}" "{{position_g_start}}" "{{position_g_end}}" "{{type}}" "{{average_frequency}}" "{{owned_by}}" "{{VariantOnGenome/DBID}}" "{{VariantOnGenome/DNA}}" "{{VariantOnGenome/Frequency}}" "{{VariantOnGenome/Reference}}" "{{VariantOnGenome/Restriction_site}}" "{{VariantOnGenome/Published_as}}" "{{VariantOnGenome/Remarks}}" "{{VariantOnGenome/Genetic_origin}}" "{{VariantOnGenome/Segregation}}" "{{VariantOnGenome/dbSNP}}" "{{VariantOnGenome/VIP}}" "{{VariantOnGenome/Methylation}}" "{{VariantOnGenome/ISCN}}" "{{VariantOnGenome/DNA/hg38}}" "{{VariantOnGenome/ClinVar}}" "{{VariantOnGenome/ClinicalClassification}}" "{{VariantOnGenome/ClinicalClassification/Method}}" "0000154090" "3" "90" "10" "101943559" "101943559" "subst" "0" "00006" "ERLIN1_000002" "g.101943559C>A" "" "{PMID:Novarino 2014:24482476}, {DOI:Novarino 2014:10.1126/science.1247363}" "" "" "" "Germline" "yes" "" "0" "" "" "g.100183802C>A" "" "pathogenic" "" "0000154091" "3" "90" "10" "101943559" "101943559" "subst" "0" "00006" "ERLIN1_000002" "g.101943559C>A" "" "{PMID:Novarino 2014:24482476}, {DOI:Novarino 2014:10.1126/science.1247363}" "" "" "" "Germline" "yes" "" "0" "" "" "g.100183802C>A" "" "pathogenic" "" "0000154092" "3" "90" "10" "101912070" "101912075" "del" "0" "00006" "ERLIN1_000001" "g.101912070_101912075del" "" "{PMID:Novarino 2014:24482476}, {DOI:Novarino 2014:10.1126/science.1247363}" "" "862_868delACCAGG (incorrect)" "" "Germline" "yes" "" "0" "" "" "g.100152313_100152318del" "" "pathogenic" "" "0000154093" "3" "90" "10" "101912070" "101912075" "del" "0" "00006" "ERLIN1_000001" "g.101912070_101912075del" "" "{PMID:Novarino 2014:24482476}, {DOI:Novarino 2014:10.1126/science.1247363}" "" "" "" "Germline" "yes" "" "0" "" "" "g.100152313_100152318del" "" "pathogenic" "" "0000154094" "3" "90" "10" "101914679" "101914679" "subst" "4.06197E-6" "00006" "ERLIN1_000003" "g.101914679G>A" "" "{PMID:Novarino 2014:24482476}, {DOI:Novarino 2014:10.1126/science.1247363}" "" "" "" "Germline" "yes" "" "0" "" "" "g.100154922G>A" "" "pathogenic" "" "0000154095" "3" "90" "10" "101914679" "101914679" "subst" "4.06197E-6" "00006" "ERLIN1_000003" "g.101914679G>A" "" "{PMID:Novarino 2014:24482476}, {DOI:Novarino 2014:10.1126/science.1247363}" "" "" "" "Germline" "yes" "" "0" "" "" "g.100154922G>A" "" "pathogenic" "" "0000235009" "3" "50" "10" "101937913" "101937913" "subst" "0" "02332" "ERLIN1_000004" "g.101937913A>G" "" "" "" "" "" "Germline" "yes" "" "0" "" "" "g.100178156A>G" "" "VUS" "" "0000235463" "3" "50" "10" "101937913" "101937913" "subst" "0" "02332" "ERLIN1_000004" "g.101937913A>G" "" "" "" "" "" "Germline" "yes" "" "0" "" "" "g.100178156A>G" "" "VUS" "" "0000235465" "3" "50" "10" "101937913" "101937913" "subst" "0" "02332" "ERLIN1_000004" "g.101937913A>G" "" "" "" "" "" "Germline" "yes" "" "0" "" "" "g.100178156A>G" "" "VUS" "" "0000235469" "3" "50" "10" "101937913" "101937913" "subst" "0" "02332" "ERLIN1_000004" "g.101937913A>G" "" "" "" "" "" "Germline" "yes" "" "0" "" "" "g.100178156A>G" "" "VUS" "" "0000321725" "0" "50" "10" "101914679" "101914679" "subst" "4.06197E-6" "01804" "ERLIN1_000003" "g.101914679G>A" "" "" "" "ERLIN1(NM_006459.3):c.763C>T (p.(Arg255Ter))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "0" "" "" "g.100154922G>A" "" "VUS" "" "0000690627" "0" "50" "10" "101950680" "101950680" "subst" "0" "01943" "CHUK_000007" "g.101950680G>A" "" "" "" "CHUK(NM_001320928.1):c.2137C>T (p.P713S)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "VUS" "" "0000722633" "0" "30" "10" "101914680" "101914680" "subst" "9.74817E-5" "01943" "ERLIN1_000005" "g.101914680G>T" "" "" "" "ERLIN1(NM_006459.3):c.762C>A (p.A254=)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely benign" "" "0000861787" "0" "30" "10" "101911919" "101911919" "subst" "4.06167E-6" "01943" "ERLIN1_000006" "g.101911919T>C" "" "" "" "ERLIN1(NM_006459.3):c.1016A>G (p.N339S)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely benign" "" "0000888960" "0" "30" "10" "101916013" "101916015" "del" "0" "02326" "ERLIN1_000007" "g.101916013_101916015del" "" "" "" "ERLIN1(NM_006459.4):c.656-20_656-18delCTT" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely benign" "" "0000978855" "0" "30" "10" "101950734" "101950734" "subst" "4.06157E-6" "01804" "CHUK_000014" "g.101950734T>C" "" "" "" "CHUK(NM_001278.5):c.2109-9A>G" "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 ERLIN1 ## Count = 16 "{{id}}" "{{transcriptid}}" "{{effectid}}" "{{position_c_start}}" "{{position_c_start_intron}}" "{{position_c_end}}" "{{position_c_end_intron}}" "{{VariantOnTranscript/DNA}}" "{{VariantOnTranscript/RNA}}" "{{VariantOnTranscript/Protein}}" "{{VariantOnTranscript/Exon}}" "0000154090" "00007227" "90" "149" "0" "149" "0" "c.149G>T" "r.(149g>u)" "p.(Gly50Val)" "2" "0000154091" "00007227" "90" "149" "0" "149" "0" "c.149G>T" "r.(147g>u)" "p.(Gly50Val)" "2" "0000154092" "00007227" "90" "862" "0" "867" "0" "c.862_867del" "r.(?)" "p.(Tyr288_Gln289del)" "11" "0000154093" "00007227" "90" "862" "0" "867" "0" "c.862_867del" "r.(?)" "p.(Tyr288_Gln289del)" "11" "0000154094" "00007227" "90" "763" "0" "763" "0" "c.763C>T" "r.(?)" "p.(Arg255*)" "10" "0000154095" "00007227" "90" "763" "0" "763" "0" "c.763C>T" "r.(?)" "p.(Arg255*)" "10" "0000235009" "00007227" "50" "281" "0" "281" "0" "c.281T>C" "r.(?)" "p.(Val94Ala)" "4" "0000235463" "00007227" "50" "281" "0" "281" "0" "c.281T>C" "r.(?)" "p.(Val94Ala)" "4" "0000235465" "00007227" "50" "281" "0" "281" "0" "c.281T>C" "r.(?)" "p.(Val94Ala)" "4" "0000235469" "00007227" "50" "281" "0" "281" "0" "c.281T>C" "r.(?)" "p.(Val94Ala)" "4" "0000321725" "00007227" "50" "763" "0" "763" "0" "c.763C>T" "r.(?)" "p.(Arg255Ter)" "" "0000690627" "00007227" "50" "-5297" "0" "-5297" "0" "c.-5297C>T" "r.(?)" "p.(=)" "" "0000722633" "00007227" "30" "762" "0" "762" "0" "c.762C>A" "r.(?)" "p.(Ala254=)" "" "0000861787" "00007227" "30" "1016" "0" "1016" "0" "c.1016A>G" "r.(?)" "p.(Asn339Ser)" "" "0000888960" "00007227" "30" "656" "-20" "656" "-18" "c.656-20_656-18del" "r.(=)" "p.(=)" "" "0000978855" "00007227" "30" "-5351" "0" "-5351" "0" "c.-5351A>G" "r.(?)" "p.(=)" "" ## Screenings_To_Variants ## Do not remove or alter this header ## ## Count = 10 "{{screeningid}}" "{{variantid}}" "0000095520" "0000154090" "0000095521" "0000154091" "0000095522" "0000154092" "0000095523" "0000154093" "0000095524" "0000154094" "0000095525" "0000154095" "0000144540" "0000235009" "0000144648" "0000235463" "0000144650" "0000235465" "0000144651" "0000235469"