### LOVD-version 3000-30b ### Full data download ### To import, do not remove or alter this header ### ## Filter: (gene_public = PSMD12) # 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}}" "PSMD12" "proteasome (prosome, macropain) 26S subunit, non-ATPase, 12" "17" "q24.3" "unknown" "NC_000017.10" "UD_132378649560" "" "http://www.LOVD.nl/PSMD12" "" "1" "9557" "5718" "604450" "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/PSMD12_codingDNA.html" "1" "" "" "-1" "" "-1" "00001" "2013-05-03 00:00:00" "00006" "2016-10-14 10:44:39" "00000" "2025-11-01 13:22:20" ## 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}}" "00017052" "PSMD12" "transcript variant 1" "002" "NM_002816.3" "" "NP_002807.1" "" "" "" "-86" "1711" "1371" "65362721" "65336619" "" "0000-00-00 00:00:00" "" "" ## Diseases ## Do not remove or alter this header ## ## Count = 3 "{{id}}" "{{symbol}}" "{{name}}" "{{inheritance}}" "{{id_omim}}" "{{tissues}}" "{{features}}" "{{remarks}}" "{{created_by}}" "{{created_date}}" "{{edited_by}}" "{{edited_date}}" "00139" "ID" "intellectual disability (ID)" "" "" "" "" "" "00084" "2013-06-04 18:18:07" "00006" "2015-02-09 10:02:49" "05422" "MRFACD" "mental retardation, distinctive facial features with/without cardiac defects" "AD" "616789" "" "autosomal dominant" "" "00006" "2018-05-04 13:48:09" "00006" "2021-12-10 21:51:32" "06341" "STISS" "Stankiewicz-Isidor syndrome" "AD" "617516" "" "" "" "00006" "2021-12-10 23:20:41" "" "" ## Genes_To_Diseases ## Do not remove or alter this header ## ## Count = 1 "{{geneid}}" "{{diseaseid}}" "PSMD12" "06341" ## Individuals ## Do not remove or alter this header ## ## Count = 5 "{{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}}" "00081460" "" "" "" "1" "" "01197" "" "" "M" "no" "France" "" "0" "" "" "white" "" "00081461" "" "" "" "1" "" "01197" "" "" "M" "no" "(United States)" "" "0" "" "" "white" "" "00081462" "" "" "" "1" "" "01197" "" "" "M" "no" "(United States)" "" "0" "" "" "white" "" "00081463" "" "" "" "1" "" "01197" "" "" "M" "no" "(United States)" "" "0" "" "" "white" "" "00234320" "" "" "" "1" "" "03288" "" "" "M" "no" "Italy" "19y" "0" "" "" "" "" ## Individuals_To_Diseases ## Do not remove or alter this header ## ## Count = 5 "{{individualid}}" "{{diseaseid}}" "00081460" "00139" "00081461" "00139" "00081462" "00139" "00081463" "00139" "00234320" "05422" ## Phenotypes ## Do not remove or alter this header ## ## Note: Only showing Phenotype columns active for Diseases 00139, 05422, 06341 ## Count = 5 "{{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}}" "0000061046" "00139" "00081460" "01197" "Isolated (sporadic)" "08y04m" "Abnormality of the cardiovascular system (HP:0001626); truncus arteriosus (HP:0001660); Ventricular septal defect (HP:0001652); atrial septal defect (HP:0001631); Hypoplastic aortic arch (HP:0012304); Patent ductus arteriosus (HP:0001643); Abnormality of the kidney (HP:0000077); Crossed fused renal ectopia (HP:0004736); Abnormality of male external genitalia (HP:0000032); Hypospadias (HP:0000047); Abnormality of the upper limb (HP:0002817); Aplasia/Hypoplasia of the thumb (HP:0009601); Intellectual disability (HP:0001249); Motor delay (HP:0001270); Delayed speech and language development (HP:0000750); Muscular hypotonia (HP:0001252); Behavioral abnormality (HP:0000708); Hearing impairment (HP:0000365); Feeding difficulties (HP:0011968); Abnormality of the eye (HP:0000478); Strabismus (HP:0000486); Abnormality of the outer ear (HP:0000356); Low-set ears (HP:0000369); Posteriorly rotated ears (HP:0000358); Microretrognathia (HP:0000308); Abnormality of the mandible (HP:0000277); Recurrent pneumonia (HP:0006532); severe intellectual disability (HP:0010864); severe global developmental delay (HP:0011344); speech delay (HP:0000750)" "" "" "1d" "" "" "" "" "" "" "0000061047" "00139" "00081461" "01197" "Isolated (sporadic)" "10y07m" "Birth length less than 3rd percentile (HP:0003561); Abnormality of the cardiovascular system (HP:0001626); Patent ductus arteriosus (HP:0001643); Abnormality of the kidney (HP:0000077); Fetal pyelectasis (HP:0010945); Abnormality of the ureter (HP:0000069); Urinary retention (HP:0000016); Abnormality of male external genitalia (HP:0000032); Micropenis (HP:0000054); Abnormality of the upper limb (HP:0002817); Aplasia/Hypoplasia of the thumb (HP:0009601); Sacral dimple (HP:0000960); Tracheomalacia (HP:0002779); Laryngeal cleft (HP:0008751); Intellectual disability (HP:0001249); Motor delay (HP:0001270); Delayed speech and language development (HP:0000750); Behavioral abnormality (HP:0000708); Autistic behavior (HP:0000729); Seizures (HP:0001250); Hearing impairment (HP:0000365); Feeding difficulties (HP:0011968); Abnormality of the eye (HP:0000478); Cortical visual impairment (HP:0100704); Abnormality of the optic nerve (HP:0000587); Abnormality of the outer ear (HP:0000356); Low-set ears (HP:0000369); intellectual disability (HP:0001249); global developmental delay (HP:0001263); speech delay (HP:0000750)" "" "" "" "" "" "" "" "" "" "0000061048" "00139" "00081462" "01197" "Isolated (sporadic)" "14y08m" "Abnormality of the cardiovascular system (HP:0001626); Heart murmur (HP:0030148); Abnormality of male external genitalia (HP:0000032); Intellectual disability (HP:0001249); Delayed speech and language development (HP:0000750); Behavioral abnormality (HP:0000708); Autistic behavior (HP:0000729); intellectual disability (HP:0001249); no motor delay (-HP:0001270), delayed social development (HP:0012434); speech delay (HP:0000750)" "" "" "" "" "" "" "" "" "" "0000061049" "00139" "00081463" "01197" "Isolated (sporadic)" "14y10m" "Abnormality of male external genitalia (HP:0000032); Cryptorchidism (HP:0000028); Micropenis (HP:0000054); Shawl scrotum (HP:0000049); Intellectual disability (HP:0001249); Muscular hypotonia (HP:0001252); Behavioral abnormality (HP:0000708); Autistic behavior (HP:0000729); Seizures (HP:0001250); Abnormality of the eye (HP:0000478); Impaired smooth pursuit (HP:0007772); Pineal cyst (HP:0012683); Abnormality of the outer ear (HP:0000356); Low-set ears (HP:0000369); Posteriorly rotated ears (HP:0000358); Abnormality of the face (HP:0000271); Facial asymmetry (HP:0000324); Hypertelorism (HP:0000316); Prominent nose (HP:0000448); Cutis marmorata (HP:0000965); Lymphangioma (HP:0100764); intellectual disability (HP:0001249); no motor delay (-HP:0001270); no speech delay (-HP:0000750)" "" "" "" "" "" "" "" "" "" "0000174739" "05422" "00234320" "03288" "Familial, autosomal dominant" "19y" "" "" "" "" "" "" "" "" "" "" ## Screenings ## Do not remove or alter this header ## ## Count = 6 "{{id}}" "{{individualid}}" "{{variants_found}}" "{{owned_by}}" "{{created_by}}" "{{created_date}}" "{{edited_by}}" "{{edited_date}}" "{{Screening/Technique}}" "{{Screening/Template}}" "{{Screening/Tissue}}" "{{Screening/Remarks}}" "0000081591" "00081460" "1" "01197" "01197" "2016-10-14 09:51:35" "" "" "SEQ;SEQ-NG-I" "DNA" "Blood" "" "0000081592" "00081461" "1" "01197" "01197" "2016-10-14 10:28:03" "" "" "SEQ;SEQ-NG-I" "DNA" "Blood" "" "0000081593" "00081462" "1" "01197" "01197" "2016-10-14 10:36:02" "" "" "SEQ;SEQ-NG-I" "DNA" "Blood" "" "0000081594" "00081463" "1" "01197" "01197" "2016-10-14 10:42:08" "" "" "SEQ;SEQ-NG-I" "DNA" "Blood" "" "0000235424" "00234320" "1" "03288" "03288" "2019-05-07 14:53:19" "" "" "SEQ-NG" "DNA" "" "" "0000235425" "00234320" "1" "03288" "03288" "2019-05-07 15:06:44" "" "" "SEQ-NG" "DNA" "" "" ## Screenings_To_Genes ## Do not remove or alter this header ## ## Count = 14 "{{screeningid}}" "{{geneid}}" "0000235424" "NLGN3" "0000235424" "NLGN4X" "0000235424" "NRXN1" "0000235424" "PSMD12" "0000235424" "YWHAE" "0000235424" "YY1" "0000235424" "ZDHHC15" "0000235424" "ZEB2" "0000235425" "PSMD12" "0000235425" "TBR1" "0000235425" "YWHAE" "0000235425" "YY1" "0000235425" "ZDHHC15" "0000235425" "ZEB2" ## 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 = 23 "{{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}}" "0000132255" "0" "90" "17" "65346383" "65346383" "subst" "0" "01197" "PSMD12_000001" "g.65346383G>A" "1/100,000 chromosomes" "" "" "" "" "De novo" "yes" "" "0" "" "" "g.67350267G>A" "" "pathogenic" "" "0000132256" "0" "70" "17" "65337056" "65337056" "subst" "0" "01197" "PSMD12_000002" "g.65337056A>C" "1/100,000 chromosomes" "" "" "" "" "De novo" "yes" "" "0" "" "" "g.67340940A>C" "" "likely pathogenic" "" "0000132257" "0" "70" "17" "65343511" "65343511" "subst" "0" "01197" "PSMD12_000003" "g.65343511G>A" "1/100,000 chromosomes" "" "" "" "" "De novo" "" "" "0" "" "" "g.67347395G>A" "" "likely pathogenic" "" "0000132258" "0" "70" "17" "65340898" "65340898" "subst" "0" "01197" "PSMD12_000004" "g.65340898T>C" "1/100,000 chromosomes" "" "" "" "" "De novo" "" "" "0" "" "" "g.67344782T>C" "" "likely pathogenic" "" "0000306561" "0" "50" "17" "65346365" "65346365" "subst" "0" "01943" "PSMD12_000005" "g.65346365G>A" "" "" "" "PSMD12(NM_002816.5):c.385C>T (p.R129*)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "0" "" "" "g.67350249G>A" "" "VUS" "" "0000478178" "11" "70" "17" "65341903" "65341903" "subst" "4.06091E-6" "03288" "PSMD12_000006" "g.65341903C>G" "" "" "" "" "dominant, reduced risk" "Germline" "" "" "0" "" "" "g.67345787C>G" "" "pathogenic (!)" "" "0000562833" "0" "50" "17" "65343496" "65343496" "subst" "0" "02325" "PSMD12_000007" "g.65343496T>C" "" "" "" "PSMD12(NM_001316341.2):c.439A>G (p.S147G)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "g.67347380T>C" "" "VUS" "" "0000562834" "0" "90" "17" "65344730" "65344730" "subst" "0" "02327" "PSMD12_000008" "g.65344730A>T" "" "" "" "" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "g.67348614A>T" "" "pathogenic" "" "0000562835" "0" "50" "17" "65344748" "65344748" "subst" "0" "01804" "PSMD12_000009" "g.65344748G>A" "" "" "" "PSMD12(NM_002816.3):c.428C>T (p.(Ala143Val))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "g.67348632G>A" "" "VUS" "" "0000562836" "0" "50" "17" "65353645" "65353645" "del" "0" "02329" "PSMD12_000010" "g.65353645del" "" "" "" "PSMD12(NM_002816.5):c.158delA (p.Q53Rfs*15)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "g.67357529del" "" "VUS" "" "0000894213" "0" "50" "17" "65341900" "65341900" "subst" "0" "02327" "PSMD12_000011" "g.65341900A>T" "" "" "" "" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "VUS" "" "0000894214" "0" "70" "17" "65353659" "65353662" "del" "0" "02327" "PSMD12_000012" "g.65353659_65353662del" "" "" "" "" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely pathogenic" "" "0000914958" "0" "70" "17" "65346418" "65346418" "dup" "0" "02329" "PSMD12_000013" "g.65346418dup" "" "" "" "PSMD12(NM_001316341.2):c.155dupA (p.Y52*)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely pathogenic" "" "0000982732" "0" "50" "17" "65353639" "65353639" "subst" "4.06491E-6" "01804" "PSMD12_000014" "g.65353639C>T" "" "" "" "PSMD12(NM_002816.5):c.164G>A (p.(Arg55His))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "VUS" "" "0001003591" "0" "30" "17" "65341910" "65341910" "subst" "0" "01804" "PSMD12_000015" "g.65341910C>T" "" "" "" "PSMD12(NM_002816.3):c.859G>A (p.(Val287Ile))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely benign" "" "0001003592" "0" "50" "17" "65343333" "65343333" "subst" "0" "01804" "PSMD12_000016" "g.65343333G>A" "" "" "" "PSMD12(NM_002816.3):c.694C>T (p.(Gln232*))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "VUS" "" "0001003593" "0" "30" "17" "65343510" "65343510" "subst" "8.13041E-6" "01804" "PSMD12_000017" "g.65343510C>T" "" "" "" "PSMD12(NM_002816.3):c.602G>A (p.(Arg201Gln))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely benign" "" "0001027044" "0" "90" "17" "65341877" "65341877" "subst" "0" "02329" "PSMD12_000018" "g.65341877C>A" "" "" "" "PSMD12(NM_002816.5):c.892G>T (p.E298*)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "pathogenic" "" "0001027045" "0" "90" "17" "65344746" "65344746" "subst" "0" "02329" "PSMD12_000019" "g.65344746G>A" "" "" "" "PSMD12(NM_002816.5):c.430C>T (p.R144*)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "pathogenic" "" "0001042110" "0" "30" "17" "65340813" "65340813" "subst" "2.03082E-5" "01804" "PSMD12_000020" "g.65340813C>A" "" "" "" "PSMD12(NM_002816.5):c.992G>T (p.(Gly331Val))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely benign" "" "0001042111" "0" "50" "17" "65344679" "65344679" "subst" "0" "01804" "PSMD12_000021" "g.65344679A>G" "" "" "" "PSMD12(NM_002816.5):c.497T>C (p.(Leu166Ser))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "VUS" "" "0001056147" "0" "30" "17" "65337736" "65337738" "dup" "0" "01804" "PSMD12_000022" "g.65337736_65337738dup" "" "" "" "PSMD12(NM_002816.5):c.1161+567_1162-565dup" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely benign" "" "0001056148" "0" "50" "17" "65338348" "65338348" "subst" "8.14346E-6" "01804" "PSMD12_000023" "g.65338348C>T" "" "" "" "PSMD12(NM_002816.5):c.1115G>A (p.(Arg372Gln))" "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 PSMD12 ## Count = 23 "{{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}}" "0000132255" "00017052" "90" "367" "0" "367" "0" "c.367C>T" "r.(?)" "p.(Arg123*)" "4" "0000132256" "00017052" "70" "1274" "0" "1274" "0" "c.1274T>G" "r.(?)" "p.(Leu425*)" "11" "0000132257" "00017052" "70" "601" "0" "601" "0" "c.601C>T" "r.(?)" "p.(Arg201*)" "6" "0000132258" "00017052" "70" "909" "-2" "909" "-2" "c.909-2A>G" "r.spl" "p.?" "8i" "0000306561" "00017052" "50" "385" "0" "385" "0" "c.385C>T" "r.(?)" "p.(Arg129Ter)" "" "0000478178" "00017052" "70" "866" "0" "866" "0" "c.866G>C" "r.(?)" "p.(Arg289Pro)" "8" "0000562833" "00017052" "50" "616" "0" "616" "0" "c.616A>G" "r.(?)" "p.(Ser206Gly)" "" "0000562834" "00017052" "90" "446" "0" "446" "0" "c.446T>A" "r.(?)" "p.(Leu149Ter)" "" "0000562835" "00017052" "50" "428" "0" "428" "0" "c.428C>T" "r.(?)" "p.(Ala143Val)" "" "0000562836" "00017052" "50" "158" "0" "158" "0" "c.158del" "r.(?)" "p.(Gln53ArgfsTer15)" "" "0000894213" "00017052" "50" "869" "0" "869" "0" "c.869T>A" "r.(?)" "p.(Ile290Lys)" "" "0000894214" "00017052" "70" "146" "0" "149" "0" "c.146_149del" "r.(?)" "p.(Ser49Trpfs*18)" "" "0000914958" "00017052" "70" "332" "0" "332" "0" "c.332dup" "r.(?)" "p.(Tyr111*)" "" "0000982732" "00017052" "50" "164" "0" "164" "0" "c.164G>A" "r.(?)" "p.(Arg55His)" "" "0001003591" "00017052" "30" "859" "0" "859" "0" "c.859G>A" "r.(?)" "p.(Val287Ile)" "" "0001003592" "00017052" "50" "694" "0" "694" "0" "c.694C>T" "r.(?)" "p.(Gln232*)" "" "0001003593" "00017052" "30" "602" "0" "602" "0" "c.602G>A" "r.(?)" "p.(Arg201Gln)" "" "0001027044" "00017052" "90" "892" "0" "892" "0" "c.892G>T" "r.(?)" "p.(Glu298*)" "" "0001027045" "00017052" "90" "430" "0" "430" "0" "c.430C>T" "r.(?)" "p.(Arg144*)" "" "0001042110" "00017052" "30" "992" "0" "992" "0" "c.992G>T" "r.(?)" "p.(Gly331Val)" "" "0001042111" "00017052" "50" "497" "0" "497" "0" "c.497T>C" "r.(?)" "p.(Leu166Ser)" "" "0001056147" "00017052" "30" "1161" "567" "1162" "-565" "c.1161+567_1162-565dup" "r.(?)" "p.(=)" "" "0001056148" "00017052" "50" "1115" "0" "1115" "0" "c.1115G>A" "r.(?)" "p.(Arg372Gln)" "" ## Screenings_To_Variants ## Do not remove or alter this header ## ## Count = 6 "{{screeningid}}" "{{variantid}}" "0000081591" "0000132255" "0000081592" "0000132256" "0000081593" "0000132257" "0000081594" "0000132258" "0000235424" "0000478178" "0000235425" "0000478178"