### LOVD-version 3000-30b ### Full data download ### To import, do not remove or alter this header ### ## Filter: (gene_public = ZNRF3) # 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}}" "ZNRF3" "zinc and ring finger 3" "22" "q12.1" "unknown" "NC_000022.10" "UD_132439546388" "" "" "" "1" "18126" "84133" "612062" "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/ZNRF3_codingDNA.html" "1" "" "" "-1" "" "-1" "00001" "2013-05-03 00:00:00" "00006" "2024-09-10 17:36:35" "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}}" "00023761" "ZNRF3" "transcript variant 1" "001" "NM_001206998.1" "" "NP_001193927.1" "" "" "" "1" "6677" "2811" "29279755" "29453476" "" "0000-00-00 00:00:00" "" "" ## Diseases ## Do not remove or alter this header ## ## Count = 1 "{{id}}" "{{symbol}}" "{{name}}" "{{inheritance}}" "{{id_omim}}" "{{tissues}}" "{{features}}" "{{remarks}}" "{{created_by}}" "{{created_date}}" "{{edited_by}}" "{{edited_date}}" "05611" "NDD" "neurodevelopmental disorder (NDD)" "" "" "" "" "" "00006" "2019-06-19 12:27:20" "00006" "2024-12-13 11:12:21" ## Genes_To_Diseases ## Do not remove or alter this header ## ## Count = 1 "{{geneid}}" "{{diseaseid}}" "ZNRF3" "05611" ## Individuals ## Do not remove or alter this header ## ## Count = 12 "{{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}}" "00453561" "" "" "" "1" "" "00006" "{PMID:Boonsawat 2024:39168120}" "2-generation family, 1 affected, unaffected non carrier parents" "F" "" "" "" "0" "" "" "" "Pat1" "00453562" "" "" "" "1" "" "00006" "{PMID:Boonsawat 2024:39168120}" "2-generation family, 1 affected, unaffected non carrier parents" "F" "" "" "" "0" "" "" "" "Pat2" "00453563" "" "" "" "1" "" "00006" "{PMID:Boonsawat 2024:39168120}" "2-generation family, 1 affected, unaffected non carrier parents" "M" "" "" "" "0" "" "" "" "Pat3" "00453564" "" "" "" "1" "" "00006" "{PMID:Boonsawat 2024:39168120}" "2-generation family, 1 affected, unaffected non carrier parents" "M" "" "" "" "0" "" "" "" "Pat4" "00453565" "" "" "" "1" "" "00006" "{PMID:Boonsawat 2024:39168120}" "2-generation family, 1 affected, unaffected non carrier parents" "M" "" "" "" "0" "" "" "" "Pat5" "00453566" "" "" "" "1" "" "00006" "{PMID:Boonsawat 2024:39168120}" "2-generation family, 1 affected, unaffected non carrier parents" "F" "" "" "" "0" "" "" "" "Pat6" "00453567" "" "" "" "1" "" "00006" "{PMID:Boonsawat 2024:39168120}" "2-generation family, 1 affected, unaffected non carrier parents" "F" "" "" "" "0" "" "" "" "Pat7" "00453568" "" "" "" "1" "" "00006" "{PMID:Boonsawat 2024:39168120}" "2-generation family, 1 affected, unaffected non carrier parents" "M" "" "" "" "0" "" "" "" "Pat8" "00453569" "" "" "" "1" "" "00006" "{PMID:Boonsawat 2024:39168120}" "2-generation family, 1 affected, unaffected non carrier parents" "F" "" "" "" "0" "" "" "" "Pat9" "00453570" "" "" "" "2" "" "00006" "{PMID:Boonsawat 2024:39168120}" "2-generation family, affected father/son" "M" "" "" "" "0" "" "" "" "FamPat10" "00453571" "" "" "00453570" "1" "" "00006" "{PMID:Boonsawat 2024:39168120}" "son" "M" "" "" "" "0" "" "" "" "FamPat11" "00453572" "" "" "" "1" "" "00006" "{PMID:Boonsawat 2024:39168120}" "2-generation family, 1 affected, unaffected non carrier parents" "M" "" "" "" "0" "" "" "" "Pat12" ## Individuals_To_Diseases ## Do not remove or alter this header ## ## Count = 12 "{{individualid}}" "{{diseaseid}}" "00453561" "05611" "00453562" "05611" "00453563" "05611" "00453564" "05611" "00453565" "05611" "00453566" "05611" "00453567" "05611" "00453568" "05611" "00453569" "05611" "00453570" "05611" "00453571" "05611" "00453572" "05611" ## Phenotypes ## Do not remove or alter this header ## ## Note: Only showing Phenotype columns active for Diseases 05611 ## Count = 12 "{{id}}" "{{diseaseid}}" "{{individualid}}" "{{owned_by}}" "{{Phenotype/Inheritance}}" "{{Phenotype/Age}}" "{{Phenotype/Additional}}" "{{Phenotype/Age/Onset}}" "{{Phenotype/Age/Diagnosis}}" "{{Phenotype/Onset}}" "{{Phenotype/Enzyme/CPK}}" "{{Phenotype/Heart/Myocardium}}" "{{Phenotype/Lung}}" "{{Phenotype/Diagnosis/Definite}}" "{{Phenotype/Diagnosis/Initial}}" "0000342219" "05611" "00453561" "00006" "Isolated (sporadic)" "5y" "see paper; ..., microcephaly; no intellectual disability; mild speech delay; no hypotonia; no seizures; no motor problems; coarctation of the aorta, hypoplastic aortic arch, bicuspid aortic valve,ventricular septal defect, atrial septal defect, persistent left superior vena cava; ectodermal dysplasia (nail hypoplasia, lacrimal duct obstruction, oligodontia), hyperopia" "" "" "" "" "" "" "" "neurodevelopmental disorder" "0000342220" "05611" "00453562" "00006" "Isolated (sporadic)" "13y1m" "see paper; ..., macrocephaly; moderate intellectual disability; speech delay; no hypotonia; no seizures; no motor problems; no heart problems" "" "" "" "" "" "" "" "neurodevelopmental disorder" "0000342221" "05611" "00453563" "00006" "Isolated (sporadic)" "13y10m" "see paper; ..., macrocephaly; no intellectual disability; speech delay; no hypotonia; no seizures; no motor problems; no heart problems; sandal gap" "" "" "" "" "" "" "" "neurodevelopmental disorder" "0000342222" "05611" "00453564" "00006" "Isolated (sporadic)" "19y" "see paper; ..., macrocephaly with megalencephaly, periventricular heterotopia and polymicrogyria in MRI; no intellectual disability; speech delay, 3y-first words; no hypotonia; focal epilepsy; no motor problems; no heart defect, ECG RBBB; cafe-au-lait spot, anxiety, sensorineural (left) hearing impairment" "" "" "" "" "" "" "" "neurodevelopmental disorder" "0000342223" "05611" "00453565" "00006" "Isolated (sporadic)" "1y5m" "see paper; ..., macrocephaly, ventriculomegaly; motor delay; hypotonia; paroxysmal movements" "" "" "" "" "" "" "" "neurodevelopmental disorder" "0000342224" "05611" "00453566" "00006" "Isolated (sporadic)" "7y5m" "see paper; ..., extreme macrocephaly; Chiari malformation with hydrocephalus (underwent a intradural Chiari decompression); learning difficulty; speech delay; no hypotonia; no seizures; no motor problems; ventricular septal defect that closed; choanal atresia" "" "" "" "" "" "" "" "neurodevelopmental disorder" "0000342225" "05611" "00453567" "00006" "Isolated (sporadic)" "12y" "see paper; ..., borderline macrocephaly; moderate intellectual disability; unable to speak; hypotonia; Lennox-Gastaut syndrome; gait disturbance, unable to walk; no heart problems reported; kyphosis, abnormal behaviors, sleep disturbances, strabismus, recurrent infections" "" "" "" "" "" "" "" "neurodevelopmental disorder" "0000342226" "05611" "00453568" "00006" "Isolated (sporadic)" "3y" "see paper; ..., microcephaly assumably caused by prenatal teratogens; profound developmental delay, speech delay; hypoglycemia seizures in early infancy; toe walk; mother heavy recreational drug user during early pregnancy: heroin, cannabis, cocaine, once realised she was pregnant, reduced drug use and only smoked cannabis, minimal alcohol ingestion" "" "" "" "" "" "" "" "neurodevelopmental disorder" "0000342227" "05611" "00453569" "00006" "Isolated (sporadic)" "3m" "see paper; ..., intraventricular hemorrhage; hypotonia; no seizures; no motor problems; atrial ventricular defect, patent ductus arteriosus that has closed with ibuprofen; in ICU since birth, bilateral choanal atresia, severe intraventricular hemorrhage, fungal infection" "" "" "" "" "" "" "" "neurodevelopmental disorder" "0000342228" "05611" "00453570" "00006" "Unknown" "35y" "see paper; ..., no brain phneotype; no intellectual disability; no developmental delay; no hypotonia; no seizures; no motor problems; 5m-5y-slight cardiac ectasia; adrenal insufficiency; no neurodevelopmental findings, recurrent infections, low serum-carnitine that normalized spontaneously at 5y" "" "" "" "" "" "" "" "neurodevelopmental disorder" "0000342229" "05611" "00453571" "00006" "Familial, autosomal dominant" "2y9m" "see paper; ..., no brain phneotype; no intellectual disability; no developmental delay; no hypotonia; no seizures; no motor problems; atrial septal defect; adrenal insufficiency, no neurodevelopmental findings, hypertension at birth" "" "" "" "" "" "" "" "neurodevelopmental disorder" "0000342230" "05611" "00453572" "00006" "Isolated (sporadic)" "1y" "see paper; ..., no brain phneotype; no intellectual disability; no developmental delay; no hypotonia; no seizures; no motor problems; no heart problems; nephrotic syndrome, recurrent infections" "" "" "" "" "" "" "" "neurodevelopmental disorder" ## Screenings ## Do not remove or alter this header ## ## Count = 12 "{{id}}" "{{individualid}}" "{{variants_found}}" "{{owned_by}}" "{{created_by}}" "{{created_date}}" "{{edited_by}}" "{{edited_date}}" "{{Screening/Technique}}" "{{Screening/Template}}" "{{Screening/Tissue}}" "{{Screening/Remarks}}" "0000455175" "00453561" "1" "00006" "00006" "2024-09-10 17:46:49" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000455176" "00453562" "1" "00006" "00006" "2024-09-10 17:46:49" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000455177" "00453563" "1" "00006" "00006" "2024-09-10 17:46:49" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000455178" "00453564" "1" "00006" "00006" "2024-09-10 17:46:49" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000455179" "00453565" "1" "00006" "00006" "2024-09-10 17:46:49" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000455180" "00453566" "1" "00006" "00006" "2024-09-10 17:46:49" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000455181" "00453567" "1" "00006" "00006" "2024-09-10 17:46:49" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000455182" "00453568" "1" "00006" "00006" "2024-09-10 17:46:49" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000455183" "00453569" "1" "00006" "00006" "2024-09-10 17:46:49" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000455184" "00453570" "1" "00006" "00006" "2024-09-10 17:46:49" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000455185" "00453571" "1" "00006" "00006" "2024-09-10 17:46:49" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000455186" "00453572" "1" "00006" "00006" "2024-09-10 17:46:49" "" "" "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 = 18 "{{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}}" "0000624281" "0" "50" "22" "29445615" "29445615" "subst" "0.00116326" "01943" "ZNRF3_000002" "g.29445615G>C" "" "" "" "ZNRF3(NM_001206998.1):c.1446G>C (p.Q482H)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "g.29049627G>C" "" "VUS" "" "0000658920" "0" "50" "22" "29454756" "29454756" "subst" "0" "01943" "C22orf31_000001" "g.29454756A>G" "" "" "" "C22orf31(NM_015370.1):c.847T>C (p.W283R)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "g.29058768A>G" "" "VUS" "" "0000856127" "0" "30" "22" "29445222" "29445222" "subst" "1.23817E-5" "01943" "ZNRF3_000003" "g.29445222C>T" "" "" "" "ZNRF3(NM_001206998.1):c.1053C>T (p.T351=)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely benign" "" "0001007195" "0" "70" "22" "29383074" "29383074" "subst" "0" "00006" "ZNRF3_000006" "g.29383074T>C" "" "{PMID:Boonsawat 2024:39168120}" "" "" "" "De novo" "" "" "0" "" "" "g.28987086T>C" "SCV005050154" "likely pathogenic (dominant)" "" "0001007196" "0" "70" "22" "29439321" "29439321" "subst" "0" "00006" "ZNRF3_000007" "g.29439321C>T" "" "{PMID:Boonsawat 2024:39168120}" "" "" "" "De novo" "" "" "0" "" "" "g.29043333C>T" "SCV005050155" "likely pathogenic (dominant)" "" "0001007197" "0" "70" "22" "29442837" "29442837" "subst" "0" "00006" "ZNRF3_000008" "g.29442837G>A" "" "{PMID:Boonsawat 2024:39168120}" "" "" "" "De novo" "" "" "0" "" "" "g.29046849G>A" "SCV005050156" "likely pathogenic (dominant)" "" "0001007198" "0" "70" "22" "29442846" "29442846" "subst" "0" "00006" "ZNRF3_000009" "g.29442846G>A" "" "{PMID:Boonsawat 2024:39168120}" "" "" "" "De novo" "" "" "0" "" "" "g.29046858G>A" "SCV005050157" "likely pathogenic (dominant)" "" "0001007199" "0" "70" "22" "29444384" "29444384" "subst" "0" "00006" "ZNRF3_000010" "g.29444384G>A" "" "{PMID:Boonsawat 2024:39168120}" "" "" "" "De novo" "" "" "0" "" "" "g.29048396G>A" "SCV005050158" "likely pathogenic (dominant)" "" "0001007200" "0" "70" "22" "29444420" "29444420" "subst" "0" "00006" "ZNRF3_000011" "g.29444420G>A" "" "{PMID:Boonsawat 2024:39168120}" "" "" "" "De novo" "" "" "0" "" "" "g.29048432G>A" "SCV005050159" "likely pathogenic (dominant)" "" "0001007201" "0" "70" "22" "29444429" "29444429" "subst" "0" "00006" "ZNRF3_000012" "g.29444429C>G" "" "{PMID:Boonsawat 2024:39168120}" "" "" "" "De novo" "" "" "0" "" "" "g.29048441C>G" "SCV005050160" "likely pathogenic (dominant)" "" "0001007202" "0" "70" "22" "29444464" "29444464" "subst" "0" "00006" "ZNRF3_000013" "g.29444464C>T" "" "{PMID:Boonsawat 2024:39168120}" "" "" "" "De novo" "" "" "0" "" "" "g.29048476C>T" "SCV005050161" "likely pathogenic (dominant)" "" "0001007203" "0" "70" "22" "29279944" "29279944" "del" "0" "00006" "ZNRF3_000004" "g.29279944del" "" "{PMID:Boonsawat 2024:39168120}" "" "" "" "De novo" "" "" "0" "" "" "g.28883956del" "SCV005050162" "likely pathogenic (dominant)" "" "0001007204" "0" "70" "22" "29372237" "29394246" "del" "0" "00006" "ZNRF3_000005" "g.29372237_29394246del" "" "{PMID:Boonsawat 2024:39168120}" "" "" "22 Kb deletion incl. ex2" "Unknown" "" "" "0" "" "" "g.28976249_28998258del" "SCV005050163" "likely pathogenic (dominant)" "" "0001007205" "11" "70" "22" "29372237" "29394246" "del" "0" "00006" "ZNRF3_000005" "g.29372237_29394246del" "" "{PMID:Boonsawat 2024:39168120}" "" "" "22 Kb deletion incl. ex2" "Germline" "yes" "" "0" "" "" "g.28976249_28998258del" "SCV005050163" "likely pathogenic (dominant)" "" "0001007206" "0" "70" "22" "29445200" "29445200" "del" "0" "00006" "ZNRF3_000014" "g.29445200del" "" "{PMID:Boonsawat 2024:39168120}" "" "" "" "De novo" "" "" "0" "" "" "g.29049212del" "SCV005050164" "likely pathogenic (dominant)" "" "0001043806" "0" "50" "22" "29446695" "29446695" "subst" "0.0222286" "01804" "ZNRF3_000015" "g.29446695G>A" "" "" "" "ZNRF3(NM_001206998.2):c.2526G>A (p.(Leu842=))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "VUS" "" "0001067492" "0" "70" "22" "29444396" "29444396" "subst" "0" "02325" "ZNRF3_000016" "g.29444396G>A" "" "" "" "" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely pathogenic" "" "0001067493" "0" "50" "22" "29446427" "29446427" "subst" "0" "02325" "ZNRF3_000017" "g.29446427G>A" "" "" "" "" "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 ZNRF3 ## Count = 18 "{{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}}" "0000624281" "00023761" "50" "1446" "0" "1446" "0" "c.1446G>C" "r.(?)" "p.(Gln482His)" "" "0000658920" "00023761" "50" "7957" "0" "7957" "0" "c.*5146A>G" "r.(=)" "p.(=)" "" "0000856127" "00023761" "30" "1053" "0" "1053" "0" "c.1053C>T" "r.(?)" "p.(Thr351=)" "" "0001007195" "00023761" "70" "311" "0" "311" "0" "c.311T>C" "r.(?)" "p.(Leu104Pro)" "" "0001007196" "00023761" "70" "536" "0" "536" "0" "c.536C>T" "r.(?)" "p.(Pro179Leu)" "" "0001007197" "00023761" "70" "878" "0" "878" "0" "c.878G>A" "r.(?)" "p.(Cys293Tyr)" "" "0001007198" "00023761" "70" "887" "0" "887" "0" "c.887G>A" "r.(?)" "p.(Cys296Tyr)" "" "0001007199" "00023761" "70" "920" "0" "920" "0" "c.920G>A" "r.(?)" "p.(Arg307Gln)" "" "0001007200" "00023761" "70" "956" "0" "956" "0" "c.956G>A" "r.(?)" "p.(Cys319Tyr)" "" "0001007201" "00023761" "70" "965" "0" "965" "0" "c.965C>G" "r.(?)" "p.(Pro322Arg)" "" "0001007202" "00023761" "70" "1000" "0" "1000" "0" "c.1000C>T" "r.(?)" "p.(Arg334Trp)" "" "0001007203" "00023761" "70" "190" "0" "190" "0" "c.190del" "r.(?)" "p.(Val64CysfsTer58)" "" "0001007204" "00023761" "70" "301" "-10827" "426" "11057" "c.301-10827_426+11057del" "r.(?)" "p.(Met101_Lys142del)" "" "0001007205" "00023761" "70" "301" "-10827" "426" "11057" "c.301-10827_426+11057del" "r.(?)" "p.(Met101_Lys142del)" "" "0001007206" "00023761" "70" "1031" "0" "1031" "0" "c.1031del" "r.(?)" "p.(Pro344GlnfsTer19)" "" "0001043806" "00023761" "50" "2526" "0" "2526" "0" "c.2526G>A" "r.(?)" "p.(=)" "" "0001067492" "00023761" "70" "932" "0" "932" "0" "c.932G>A" "r.(?)" "p.(Cys311Tyr)" "" "0001067493" "00023761" "50" "2258" "0" "2258" "0" "c.2258G>A" "r.(?)" "p.(Gly753Glu)" "" ## Screenings_To_Variants ## Do not remove or alter this header ## ## Count = 12 "{{screeningid}}" "{{variantid}}" "0000455175" "0001007195" "0000455176" "0001007196" "0000455177" "0001007197" "0000455178" "0001007198" "0000455179" "0001007199" "0000455180" "0001007200" "0000455181" "0001007201" "0000455182" "0001007202" "0000455183" "0001007203" "0000455184" "0001007204" "0000455185" "0001007205" "0000455186" "0001007206"