### LOVD-version 3000-30b ### Full data download ### To import, do not remove or alter this header ### ## Filter: (gene_public = SPOP) # 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}}" "SPOP" "speckle-type POZ protein" "17" "q21.33" "unknown" "NG_041815.1" "UD_136092190799" "" "https://www.LOVD.nl/SPOP" "" "1" "11254" "8405" "602650" "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/SPOP_codingDNA.html" "1" "" "" "-1" "" "-1" "00001" "2013-05-03 00:00:00" "00006" "2020-03-08 16:46:09" "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}}" "00025499" "SPOP" "transcript variant 1" "006" "NM_001007226.1" "" "NP_001007227.1" "" "" "" "-471" "2619" "1125" "47755525" "47676246" "00006" "2020-03-08 16:38:39" "" "" ## Diseases ## Do not remove or alter this header ## ## Count = 4 "{{id}}" "{{symbol}}" "{{name}}" "{{inheritance}}" "{{id_omim}}" "{{tissues}}" "{{features}}" "{{remarks}}" "{{created_by}}" "{{created_date}}" "{{edited_by}}" "{{edited_date}}" "04214" "-" "retinal disease" "" "" "" "" "" "00006" "2015-02-27 19:48:07" "00001" "2023-03-09 14:26:26" "05611" "NDD" "neurodevelopmental disorder (NDD)" "" "" "" "" "" "00006" "2019-06-19 12:27:20" "00006" "2024-12-13 11:12:21" "06392" "NSDVS1" "Nabais Sa-de Vries syndrome, type 1" "AD" "618828" "" "" "" "00006" "2021-12-10 23:20:41" "" "" "06393" "NSDVS2" "Nabais Sa-de Vries syndrome, type 2" "AD" "618829" "" "" "" "00006" "2021-12-10 23:20:41" "" "" ## Genes_To_Diseases ## Do not remove or alter this header ## ## Count = 2 "{{geneid}}" "{{diseaseid}}" "SPOP" "06392" "SPOP" "06393" ## Individuals ## Do not remove or alter this header ## ## Count = 8 "{{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}}" "00289405" "" "" "" "1" "" "00006" "{PMID:Nabais 2020:32109420}" "" "F" "" "" "" "0" "" "" "" "Pat1" "00289406" "" "" "" "1" "" "00006" "{PMID:Nabais 2020:32109420}" "" "M" "" "" "" "0" "" "" "" "Pat2" "00289407" "" "" "" "1" "" "00006" "{PMID:Nabais 2020:32109420}" "" "F" "" "" "" "0" "" "" "" "Pat3" "00289408" "" "" "" "1" "" "00006" "{PMID:Nabais 2020:32109420}" "" "M" "" "" "" "0" "" "" "" "Pat4" "00289409" "" "" "" "1" "" "00006" "{PMID:Nabais 2020:32109420}" "" "M" "" "Netherlands" "" "0" "" "" "" "Pat5" "00289410" "" "" "" "1" "" "00006" "{PMID:Nabais 2020:32109420}" "" "F" "" "Netherlands" "" "0" "" "" "" "Pat6" "00289411" "" "" "" "1" "" "00006" "{PMID:Nabais 2020:32109420}" "" "F" "" "" "" "0" "" "" "" "Pat7" "00334710" "" "" "" "6" "" "00000" "{PMID:Maranhao 2015:26352687}" "analysis 25 Pedigrees" "" "" "Pakistan" "" "0" "" "" "" "" ## Individuals_To_Diseases ## Do not remove or alter this header ## ## Count = 8 "{{individualid}}" "{{diseaseid}}" "00289405" "05611" "00289406" "05611" "00289407" "05611" "00289408" "05611" "00289409" "05611" "00289410" "05611" "00289411" "05611" "00334710" "04214" ## Phenotypes ## Do not remove or alter this header ## ## Note: Only showing Phenotype columns active for Diseases 04214, 05611, 06392, 06393 ## Count = 7 "{{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}}" "0000223017" "05611" "00289405" "00006" "Isolated (sporadic)" "4y7m" "birth 40w3d, length 47cm (10th-25th), weight 3.033kg (10th-25th), head 32cm (-3SD) at 16d NA (microcephaly); height 104.5cm (~50th), weight 15.3kg (10th-25th), head 44cm (-4SD); prenatal long bones (<-3 SD); congenital microcephaly; jaundice requiring phototherapy; motor delay; walk-19m; speech delay; 2y10m-60 words; no epilepsy; hypertonia; MRI brain 5y-simplified gyri; decreased stranger anxiety; brachycephaly, prominent glabella; dysplastic simple ears with thickened helix; highly arched eyebrows, underdeveloped supraorbital ridges, downslanted narrow palpebral fissures, deeply set eyes; prominent nasal bridge,; flat philtrum; pointed chin; clinodactyly 5th digits bilaterally; normal feet; sensorineural hearing loss; no ophthalmologic abnormality; no cardiovascular abnormality; no respiratory abnormality; no gastrointestinal abnormality; no urogenital abnormality; no skin abnormality; no endocrine abnormality; no sleep disturbance; sacral dimple" "" "4y7m" "" "" "" "" "" "" "" "0000223018" "05611" "00289406" "00006" "Isolated (sporadic)" "10y" "birth 39w, weight 2.409kg (3rd), head 33.5cm (10th-25th); height 77cm (10th-25th), weight 8.8kg (-2.3SD), head 40.5cm (-5SD); no prenatal anomalies; congenital microcephaly; jaundice that selfresolved, respiratory difficulties requiring tracheostomy; motor delay; walk-~36m; speech delay; 6y-vocalising; severe intellectual disability; autoagression; narrow forehead, low anterior hairline; normal ears; highly arched eyebrows, synophrys, long eyelashes, epicanthus, telecanthus, narrow palpebral fissures; wide and bulbous nasal tip, underdeveloped nasal alae; flat philtrum; pointed chin; normal hands; normal feet; bilateral hearing loss; bilateral optic nerve hypoplasia; no cardiovascular abnormality; 3m-tracheostomy; 3m-gastrostomy; bilateral vesicoureteric reflux; no skin abnormality; no endocrine abnormality" "" "16m" "" "" "" "" "" "" "" "0000223019" "05611" "00289407" "00006" "Isolated (sporadic)" "10m" "birth 33w5d, length 46.4cm (3rd-10th), weight 2.575kg (3rd-10th), head 35cm (25th-50th); height 65.1cm (-2.5SD), weight 5.6kg (-4SD), head 49cm (+3.5SD); prenatal polyhydramnios, breech presentation; congenital heart disease; hypotonia, swallowing dysfunction, feeding difficulties; motor delay; speech delay; no epilepsy; central hypotonia; MRI brain 4m-enlargement all ventricles, prominent subarachnoid spaces, bifrontal extra-axial fluid spaces, 17m-mildly increased ventriculomegaly, symmetrically dysmorphic hippocampi; frontal bossing, triangular face; low-set small ears; hypertelorism, deep set eyes; low and wide nasal bridge, wide and bulbous nasal tip, short nose; wide gums; micrognathia; normal hands; normal feet; no hearing impairment; small optic discs; small ventricular septal defect;, pulmonary stenosis and supravalvular pulmonary stenosis, mild right ventricular outflow obstruction; no respiratory abnormality; choking episodes, gastroesophageal reflux disease, Sandifer syndrome, 6m-gastrostomy; no urogenital abnormality; no skin abnormality; no endocrine abnormality; no sleep disturbance; failure to thrive" "" "10m" "" "" "" "" "" "" "" "0000223020" "05611" "00289408" "00006" "Isolated (sporadic)" "17y11m" "birth 39w, length 47cm (10th-25th), weight 2.700kg (3rd-10th); height 151.8cm (-3.1SD), weight 49.7kg (3rd), head (25th); prenatal hypoplastic left heart; congenital heart disease; bradycardia, dysrhytmia, thrombocytopenia; motor delay; walk-36m; speech delay; first words 4y; intellectual disability (IQ46); epilepsy; left hemiparesis, intractable migraines, dystonia, chorea; MRI brain 16y-borderline enlarged ventricles, slightly small corpus callosum splenium; overfriendliness, attention deficit hyperactivity disorder, agitation; normal cranium/normal forehead; low-set small ears; hypertelorism; short, low nasal bridge, upturned nares; high-arched palate; pointed chin; normal hands; normal feet; no hearing impairment; abnormality refraction; variant of hypoplastic left heart syndrome (atrial septal defect, small left ventricule, mitral valve and aorta) with left ventricular outflow tract obstruction (subaortic membrane, bicuspid aortic valve, coartation descending aorta); episode of hemoptysis; no astrointestinal abnormality; (hypogonadism; no skin abnormality; testosterone treatment; sleep apnea; failure to thrive in infancy, bleeding disorder with platelet dysfunction, chronic jaundice, mild scoliosis, osteoporosis, vitamin D deficiency" "" "17y11m" "" "" "" "" "" "" "" "0000223021" "05611" "00289409" "00006" "Isolated (sporadic)" "17y9m" "birth 38w, weight 3.070kg (10th-25th); height 178.5cm (50th-75th), weight 73kg (50th-75th), head 56.4cm (75th-90th); no prenatal anomalies; motor delay; walk-17m; speech delay; intellectual disability (IQ45); epilepsy; MRI brain 5y normal; autism; large forehead; protruding ears; hypertelorism, long palpebral fissures, sparse and thin eyebrows; normal nose; normal mouth; pointed chin; no hearing impairment; no ophthalmologic abnormality; urogenital abnormality; hypothyroidism; sleep disturbance;" "" "17y9m" "" "" "" "" "" "" "" "0000223022" "05611" "00289410" "00006" "Isolated (sporadic)" "20y" "birth 37w, length 47cm (10th-25th), weight 3.000kg (10th-25th); height 172cm (90th-97th), weight 89kg (97th), head 57cm (+2.5SD); no prenatal anomalies; congenital heart disease, bilateral cleft lip/palate; motor delay; walk-24m; speech delay; first words~5y; intellectual disability (IQ53); severe temper tantrums; large forehead; low-set posteriorly rotated ears; hypertelorism, sparse and thin eyebrows; prominent nasal bridge, bulbous nasal tip; bilateral cleft lip/palate; normal chin; distally tapered, long fingers; clinodactyly 5th fingers; short wide feet, pes cavus, short broad halluces; no hearing impairment; strabismus; atrial septal defect; no respiratory abnormality; no astrointestinal abnormality; no skin abnormality; sleep apnea;" "" "20y" "" "" "" "" "" "" "" "0000223023" "05611" "00289411" "00006" "Isolated (sporadic)" "15y" "birth 40w, length 54.6cm (97th), weight 3.800 kg (75th-90th), (macrocephalic); height 158.8cm (25th-50th), weight 90.7kg (+2.5SD), head 5y-56cm (+4SD); multicystic kidney dysplasia; hypotonia, respiratory and feeding difficulties; motor delay; walk-24m; speech delay; mild intellectual disability; no epilepsy; MRI brain normal; anxiety; large forehead; normal ears; asymmetric palpebral fissures; prominent and wide nasal bridge, wide and bulbous nasal tip; thin lips; norma chin; normal hands; normal feet; no hearing impairment; abnormality refraction; patent ductus arteriosus, small ventricular septal defect; no respiratory abnormality; chronic constipation, gastroesophageal reflux disease; left multicystic kidney; eczema; hypothyroidism; sleep apnea; unusual fat distribution" "" "15y" "" "" "" "" "" "" "" ## Screenings ## Do not remove or alter this header ## ## Count = 8 "{{id}}" "{{individualid}}" "{{variants_found}}" "{{owned_by}}" "{{created_by}}" "{{created_date}}" "{{edited_by}}" "{{edited_date}}" "{{Screening/Technique}}" "{{Screening/Template}}" "{{Screening/Tissue}}" "{{Screening/Remarks}}" "0000290575" "00289405" "1" "00006" "00006" "2020-03-08 16:45:25" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000290576" "00289406" "1" "00006" "00006" "2020-03-08 16:45:25" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000290577" "00289407" "1" "00006" "00006" "2020-03-08 16:45:25" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000290578" "00289408" "1" "00006" "00006" "2020-03-08 16:45:25" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000290579" "00289409" "1" "00006" "00006" "2020-03-08 16:45:25" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000290580" "00289410" "1" "00006" "00006" "2020-03-08 16:45:25" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000290581" "00289411" "1" "00006" "00006" "2020-03-08 16:45:25" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000335939" "00334710" "1" "00000" "00006" "2021-03-01 16:58:55" "" "" "SEQ-NG" "DNA" "" "WES" ## Screenings_To_Genes ## Do not remove or alter this header ## ## Count = 7 "{{screeningid}}" "{{geneid}}" "0000290575" "SPOP" "0000290576" "SPOP" "0000290577" "SPOP" "0000290578" "SPOP" "0000290579" "SPOP" "0000290580" "SPOP" "0000290581" "SPOP" ## 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 = 15 "{{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}}" "0000313885" "0" "50" "17" "47696411" "47696411" "subst" "0" "02326" "SPOP_000002" "g.47696411G>A" "" "" "" "SPOP(NM_001007226.1):c.412C>T (p.R138C)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "0" "" "" "g.49619049G>A" "" "VUS" "" "0000341892" "0" "50" "17" "47696411" "47696411" "subst" "0" "02327" "SPOP_000002" "g.47696411G>A" "" "" "" "SPOP(NM_001007226.1):c.412C>T (p.R138C)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "0" "" "" "g.49619049G>A" "" "VUS" "" "0000562112" "0" "50" "17" "47696703" "47696703" "subst" "0" "01943" "SPOP_000003" "g.47696703T>C" "" "" "" "SPOP(NM_001007226.1):c.245A>G (p.D82G)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "0" "" "" "g.49619341T>C" "" "VUS" "" "0000647260" "0" "90" "17" "47696461" "47696461" "subst" "0" "00006" "SPOP_000006" "g.47696461C>T" "" "{PMID:Nabais 2020:32109420}" "" "" "" "De novo" "" "" "0" "" "" "g.49619099C>T" "" "pathogenic (dominant)" "" "0000647261" "0" "90" "17" "47696393" "47696393" "subst" "0" "00006" "SPOP_000004" "g.47696393C>T" "" "{PMID:Nabais 2020:32109420}" "" "" "" "De novo" "" "" "0" "" "" "g.49619031C>T" "" "pathogenic (dominant)" "" "0000647262" "0" "90" "17" "47696428" "47696428" "subst" "0" "00006" "SPOP_000005" "g.47696428C>A" "" "{PMID:Nabais 2020:32109420}" "" "" "" "De novo" "" "" "0" "" "" "g.49619066C>A" "" "pathogenic (dominant)" "" "0000647263" "0" "90" "17" "47700100" "47700100" "subst" "0" "00006" "SPOP_000008" "g.47700100T>C" "" "{PMID:Nabais 2020:32109420}" "" "" "" "De novo" "" "" "0" "" "" "g.49622738T>C" "" "pathogenic (dominant)" "" "0000647264" "0" "90" "17" "47696411" "47696411" "subst" "0" "00006" "SPOP_000002" "g.47696411G>A" "" "{PMID:Nabais 2020:32109420}" "" "" "" "De novo" "" "" "0" "" "" "g.49619049G>A" "" "pathogenic (dominant)" "" "0000647265" "0" "90" "17" "47696411" "47696411" "subst" "0" "00006" "SPOP_000002" "g.47696411G>A" "" "{PMID:Nabais 2020:32109420}" "" "" "" "De novo" "" "" "0" "" "" "g.49619049G>A" "" "pathogenic (dominant)" "" "0000647266" "0" "90" "17" "47696700" "47696700" "subst" "0" "00006" "SPOP_000007" "g.47696700T>C" "" "{PMID:Nabais 2020:32109420}" "" "" "" "De novo" "" "" "0" "" "" "g.49619338T>C" "" "pathogenic (dominant)" "" "0000734851" "0" "30" "17" "47755248" "47755248" "subst" "0" "00000" "SPOP_000009" "g.47755248A>C" "6/25 families" "{PMID:Maranhao 2015:26352687}" "" "SPOP:c.-189+47T>G" "" "Germline" "" "" "0" "" "" "" "" "likely benign" "" "0000982586" "0" "70" "17" "47699431" "47699431" "subst" "0" "01804" "SPOP_000010" "g.47699431T>G" "" "" "" "SPOP(NM_001007228.2):c.79-2A>C (p.?)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely pathogenic" "" "0000982587" "0" "30" "17" "47753390" "47753391" "del" "0" "01804" "SPOP_000011" "g.47753390_47753391del" "" "" "" "SPOP(NM_001007226.1):c.-240-5_-240-4del" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely benign" "" "0001041942" "0" "30" "17" "47732772" "47732773" "ins" "0" "01804" "SPOP_000012" "g.47732772_47732773insA" "" "" "" "SPOP(NM_001007228.2):c.-67+22522_-67+22523insT" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely benign" "" "0001066802" "0" "50" "17" "47696638" "47696638" "subst" "0" "02325" "SPOP_000013" "g.47696638A>G" "" "" "" "" "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 SPOP ## Count = 15 "{{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}}" "0000313885" "00025499" "50" "412" "0" "412" "0" "c.412C>T" "r.(?)" "p.(Arg138Cys)" "" "0000341892" "00025499" "50" "412" "0" "412" "0" "c.412C>T" "r.(?)" "p.(Arg138Cys)" "" "0000562112" "00025499" "50" "245" "0" "245" "0" "c.245A>G" "r.(?)" "p.(Asp82Gly)" "" "0000647260" "00025499" "90" "362" "0" "362" "0" "c.362G>A" "r.(?)" "p.(Arg121Gln)" "" "0000647261" "00025499" "90" "430" "0" "430" "0" "c.430G>A" "r.(?)" "p.(Asp144Asn)" "" "0000647262" "00025499" "90" "395" "0" "395" "0" "c.395G>T" "r.(?)" "p.(Gly132Val)" "" "0000647263" "00025499" "90" "73" "0" "73" "0" "c.73A>G" "r.(?)" "p.(Thr25Ala)" "" "0000647264" "00025499" "90" "412" "0" "412" "0" "c.412C>T" "r.(?)" "p.(Arg138Cys)" "" "0000647265" "00025499" "90" "412" "0" "412" "0" "c.412C>T" "r.(?)" "p.(Arg138Cys)" "" "0000647266" "00025499" "90" "248" "0" "248" "0" "c.248A>G" "r.(?)" "p.(Tyr83Cys)" "" "0000734851" "00025499" "30" "-241" "47" "-241" "47" "c.-241+47T>G" "r.(=)" "p.(=)" "" "0000982586" "00025499" "70" "79" "-2" "79" "-2" "c.79-2A>C" "r.spl?" "p.?" "" "0000982587" "00025499" "30" "-240" "-5" "-240" "-4" "c.-240-5_-240-4del" "r.spl?" "p.?" "" "0001041942" "00025499" "30" "-67" "12616" "-67" "12617" "c.-67+12616_-67+12617insT" "r.(=)" "p.(=)" "" "0001066802" "00025499" "50" "310" "0" "310" "0" "c.310T>C" "r.(?)" "p.(Phe104Leu)" "" ## Screenings_To_Variants ## Do not remove or alter this header ## ## Count = 8 "{{screeningid}}" "{{variantid}}" "0000290575" "0000647260" "0000290576" "0000647261" "0000290577" "0000647262" "0000290578" "0000647263" "0000290579" "0000647264" "0000290580" "0000647265" "0000290581" "0000647266" "0000335939" "0000734851"