### LOVD-version 3000-30b ### Full data download ### To import, do not remove or alter this header ### ## Filter: (gene_public = P4HTM) # 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}}" "P4HTM" "prolyl 4-hydroxylase, transmembrane (endoplasmic reticulum)" "3" "p21.31" "unknown" "NC_000003.11" "UD_136089948393" "" "https://www.LOVD.nl/P4HTM" "" "1" "28858" "54681" "614584" "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/P4HTM_codingDNA.html" "1" "" "" "-1" "" "-1" "00001" "2013-05-03 00:00:00" "00006" "2019-02-01 11:19:42" "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}}" "00015569" "P4HTM" "transcript variant 3" "001" "NM_177938.2" "" "NP_808807.2" "" "" "" "-349" "1934" "1692" "49027341" "49044582" "" "0000-00-00 00:00:00" "" "" ## Diseases ## Do not remove or alter this header ## ## Count = 2 "{{id}}" "{{symbol}}" "{{name}}" "{{inheritance}}" "{{id_omim}}" "{{tissues}}" "{{features}}" "{{remarks}}" "{{created_by}}" "{{created_date}}" "{{edited_by}}" "{{edited_date}}" "00198" "?" "unclassified / mixed" "" "" "" "" "" "00006" "2013-09-13 14:21:47" "00006" "2024-11-23 09:38:12" "06590" "HIDEA" "Hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities" "AR" "618493" "" "" "" "00006" "2021-12-10 23:20:41" "" "" ## Genes_To_Diseases ## Do not remove or alter this header ## ## Count = 1 "{{geneid}}" "{{diseaseid}}" "P4HTM" "06590" ## Individuals ## Do not remove or alter this header ## ## Count = 11 "{{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}}" "00218659" "" "" "" "1" "" "03194" "" "" "F" "no" "Finland" "" "0" "" "" "" "Patient 1" "00218660" "" "" "" "6" "" "03194" "{PMID:Kaasinen 2014:25078763}" "12-generation family, 6 affected (3F, 3M), unaffected heterozygous carrier parents/relatives" "F;M" "yes" "Finland" "" "0" "" "" "" "" "00218661" "" "" "" "2" "" "03194" "{PMID:Rahikkala 2019:30940925}" "2-generation family, 2 affected brothers, unaffected heterozygous carrier parents" "M" "no" "United States" "" "0" "" "" "" "Fam2PatII1/3" "00218662" "" "" "" "3" "" "03194" "{PMID:Rahikkala 2019:30940925}" "2-generation family, 3 affected brothers, unaffected heterozygous carrier parents" "M" "yes" "" "" "0" "" "" "" "Fam3PatII1/2/4" "00377067" "" "" "" "1" "" "00006" "{PMID:Rahikkala 2019:30940925}" "2-generation family, 1 affected, unaffected heterozygous carrier parents" "M" "" "Finland" "" "0" "" "" "" "Fam4PatII2" "00411161" "" "" "" "1" "" "03194" "" "" "M" "yes" "Finland" "" "" "" "" "" "" "00411162" "" "" "" "1" "" "03194" "" "" "M" "yes" "Iran" "" "" "" "" "" "" "00411163" "" "" "" "1" "" "03194" "" "" "F" "no" "Finland" "" "" "" "" "" "" "00411164" "" "" "" "1" "" "03194" "" "" "F" "no" "Finland" "" "" "" "" "" "" "00411165" "" "" "" "1" "" "03194" "" "" "M" "yes" "France" "" "" "" "" "" "" "00411166" "" "" "" "1" "" "03194" "" "" "F" "yes" "Iran" "" "" "" "" "" "" ## Individuals_To_Diseases ## Do not remove or alter this header ## ## Count = 11 "{{individualid}}" "{{diseaseid}}" "00218659" "00198" "00218660" "00198" "00218661" "00198" "00218662" "00198" "00377067" "00198" "00411161" "06590" "00411162" "06590" "00411163" "06590" "00411164" "06590" "00411165" "06590" "00411166" "06590" ## Phenotypes ## Do not remove or alter this header ## ## Note: Only showing Phenotype columns active for Diseases 00198, 06590 ## Count = 4 "{{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}}" "0000167198" "00198" "00218661" "03194" "Familial, autosomal recessive" "" "see paper; ..." "" "" "" "" "" "" "" "" "" "" "" "0000167471" "00198" "00218660" "03194" "Familial, autosomal recessive" "" "" "" "" "" "" "" "" "" "" "" "" "" "0000272255" "00198" "00218662" "00006" "Familial, autosomal recessive" "" "see paper; ..." "" "" "" "" "" "" "" "" "" "" "" "0000272256" "00198" "00377067" "00006" "Familial, autosomal recessive" "" "see paper; ..." "" "" "" "" "" "" "" "" "" "" "" ## Screenings ## Do not remove or alter this header ## ## Count = 11 "{{id}}" "{{individualid}}" "{{variants_found}}" "{{owned_by}}" "{{created_by}}" "{{created_date}}" "{{edited_by}}" "{{edited_date}}" "{{Screening/Technique}}" "{{Screening/Template}}" "{{Screening/Tissue}}" "{{Screening/Remarks}}" "0000219730" "00218660" "1" "03194" "03194" "2019-01-31 14:21:00" "00006" "2019-02-01 14:34:41" "RT-PCR;SEQ" "DNA;RNA" "" "" "0000219731" "00218661" "1" "03194" "03194" "2019-01-31 14:55:57" "" "" "SEQ;SEQ-NG" "DNA" "" "" "0000219732" "00218662" "1" "03194" "03194" "2019-01-31 15:25:07" "" "" "SEQ;SEQ-NG" "DNA" "" "" "0000219733" "00218659" "1" "03194" "03194" "2019-01-31 15:40:04" "" "" "SEQ;SEQ-NG" "DNA" "" "" "0000378273" "00377067" "1" "00006" "00006" "2021-06-30 13:40:44" "" "" "SEQ;SEQ-NG" "DNA" "" "trio WES" "0000412426" "00411161" "1" "03194" "03194" "2022-06-04 15:59:12" "" "" "SEQ-NG" "DNA" "" "" "0000412427" "00411162" "1" "03194" "03194" "2022-06-04 16:14:04" "" "" "SEQ-NG" "DNA" "" "" "0000412428" "00411163" "1" "03194" "03194" "2022-06-04 16:18:20" "" "" "SEQ-NG" "DNA" "" "" "0000412429" "00411164" "1" "03194" "03194" "2022-06-04 16:22:53" "" "" "SEQ-NG" "DNA" "" "" "0000412430" "00411165" "1" "03194" "03194" "2022-06-04 16:28:10" "" "" "SEQ-NG" "DNA" "" "" "0000412431" "00411166" "1" "03194" "03194" "2022-06-04 16:38:24" "" "" "SEQ-NG" "DNA" "" "" ## 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 = 28 "{{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}}" "0000329400" "0" "50" "3" "49055133" "49055133" "subst" "0" "01804" "DALRD3_000001" "g.49055133C>T" "" "" "" "DALRD3(NM_001009996.2):c.631G>A (p.(Gly211Ser))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "0" "" "" "g.49017700C>T" "" "VUS" "" "0000329401" "0" "50" "3" "49055837" "49055837" "subst" "6.04763E-6" "01804" "DALRD3_000002" "g.49055837C>G" "" "" "" "DALRD3(NM_001009996.2):c.161G>C (p.(Gly54Ala))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "0" "" "" "g.49018404C>G" "" "VUS" "" "0000454604" "3" "90" "3" "49042479" "49042479" "subst" "9.7515E-5" "03194" "P4HTM_000004" "g.49042479G>A" "" "{PMID:Kaasinen 2014:25078763}" "" "" "reported r.888_1073del (Arg296Ser;Val297_Arg358del) not visible in Fig3B" "Germline" "yes" "rs182812551" "0" "" "" "g.49005046G>A" "" "pathogenic (recessive)" "" "0000454605" "21" "90" "3" "49038916" "49038916" "subst" "0" "03194" "P4HTM_000003" "g.49038916A>C" "" "{PMID:Rahikkala 2019:30940925}" "" "" "" "Germline" "yes" "" "0" "" "" "g.49001483A>C" "" "pathogenic (recessive)" "" "0000454606" "11" "70" "3" "49027975" "49027975" "dup" "0" "03194" "P4HTM_000002" "g.49027975dup" "" "{PMID:Rahikkala 2019:30940925}" "" "286dupC" "" "Germline" "" "" "0" "" "" "g.48990542dup" "" "likely pathogenic (recessive)" "" "0000454607" "3" "90" "3" "49044242" "49044242" "subst" "0" "03194" "P4HTM_000005" "g.49044242C>T" "" "{PMID:Rahikkala 2019:30940925}" "" "" "" "Germline" "yes" "" "0" "" "" "g.49006809C>T" "" "pathogenic (recessive)" "" "0000454608" "3" "90" "3" "49042479" "49042479" "subst" "9.7515E-5" "03194" "P4HTM_000004" "g.49042479G>A" "" "" "" "" "" "Germline" "yes" "rs182812551" "0" "" "" "g.49005046G>A" "" "pathogenic (recessive)" "" "0000520153" "0" "50" "3" "49051200" "49051200" "subst" "4.46878E-5" "01943" "P4HTM_000006" "g.49051200A>G" "" "" "" "WDR6(NM_001320546.2):c.2155A>G (p.T719A)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "g.49013767A>G" "" "VUS" "" "0000719489" "0" "50" "3" "49041570" "49041570" "subst" "0" "02325" "P4HTM_000007" "g.49041570G>A" "" "" "" "P4HTM(NM_177938.2):c.764G>A (p.R255Q)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "VUS" "" "0000719490" "0" "50" "3" "49042355" "49042355" "del" "0" "02329" "P4HTM_000001" "g.49042355del" "" "" "" "P4HTM(NM_177938.2):c.949delG (p.V317Ffs*30)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "VUS" "" "0000719491" "0" "70" "3" "49053104" "49053104" "subst" "2.43706E-5" "02325" "DALRD3_000003" "g.49053104G>A" "" "" "" "DALRD3(NM_001009996.3):c.1549C>T (p.R517C)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "0" "" "" "" "" "likely pathogenic" "" "0000790983" "3" "90" "3" "49042355" "49042355" "del" "0" "00006" "P4HTM_000001" "g.49042355del" "" "{PMID:Rahikkala 2019:30940925}" "" "949delG" "" "Germline" "" "" "0" "" "" "g.49004922del" "" "pathogenic (recessive)" "" "0000869756" "3" "90" "3" "49043570" "49043570" "subst" "6.11795E-5" "03194" "P4HTM_000010" "g.49043570C>T" "" "" "" "" "" "Germline" "yes" "" "0" "" "" "g.49006137C>T" "" "pathogenic (recessive)" "ACMG" "0000869757" "3" "70" "3" "49044202" "49044202" "subst" "0" "03194" "P4HTM_000011" "g.49044202G>A" "" "" "" "" "" "Germline" "yes" "" "0" "" "" "g.49006769G>A" "" "pathogenic (recessive)" "ACMG" "0000869758" "3" "90" "3" "49042479" "49042479" "subst" "9.7515E-5" "03194" "P4HTM_000004" "g.49042479G>A" "" "" "" "" "" "Germline" "yes" "rs182812551" "0" "" "" "g.49005046G>A" "" "pathogenic (recessive)" "ACMG" "0000869759" "11" "90" "3" "49042479" "49042479" "subst" "9.7515E-5" "03194" "P4HTM_000004" "g.49042479G>A" "" "" "" "" "" "Germline" "yes" "rs182812551" "0" "" "" "g.49005046G>A" "" "pathogenic (recessive)" "ACMG" "0000869760" "21" "90" "3" "49043570" "49043570" "subst" "6.11795E-5" "03194" "P4HTM_000010" "g.49043570C>T" "" "" "" "" "" "Germline" "yes" "rs757914897" "0" "" "" "g.49006137C>T" "" "pathogenic (recessive)" "ACMG" "0000869761" "0" "70" "3" "49043218" "49043218" "subst" "0" "03194" "P4HTM_000009" "g.49043218C>T" "" "" "" "" "" "Germline" "yes" "" "0" "" "" "g.49005785C>T" "" "pathogenic" "ACMG" "0000869762" "3" "90" "3" "49042340" "49042340" "subst" "0" "03194" "P4HTM_000008" "g.49042340G>A" "" "" "" "" "" "Germline" "yes" "" "0" "" "" "g.49004907G>A" "" "pathogenic (recessive)" "ACMG" "0000962817" "0" "30" "3" "49028355" "49028355" "subst" "0.00111909" "02330" "ARIH2_000002" "g.49028355C>T" "" "" "" "P4HTM(NM_177938.2):c.436+8C>T" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely benign" "" "0000962818" "0" "30" "3" "49042318" "49042318" "subst" "0.000115747" "02330" "P4HTM_000012" "g.49042318G>A" "" "" "" "P4HTM(NM_177938.2):c.912G>A (p.S304=)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely benign" "" "0000962819" "0" "30" "3" "49043492" "49043492" "subst" "4.0779E-6" "02330" "P4HTM_000013" "g.49043492C>T" "" "" "" "P4HTM(NM_177938.2):c.1348-5C>T" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely benign" "" "0000975885" "0" "50" "3" "49027853" "49027853" "subst" "0" "01804" "ARIH2_000003" "g.49027853T>A" "" "" "" "P4HTM(NM_177939.3):c.164T>A (p.(Ile55Asn))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "VUS" "" "0000993768" "0" "30" "3" "49042515" "49042515" "subst" "0.000443223" "02330" "P4HTM_000014" "g.49042515T>G" "" "" "" "P4HTM(NM_177938.2):c.1109T>G (p.L370R)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely benign" "" "0001034029" "0" "50" "3" "49050553" "49050553" "subst" "0" "01804" "P4HTM_000015" "g.49050553G>A" "" "" "" "WDR6(NM_018031.6):c.1586G>A (p.(Gly529Glu))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "VUS" "" "0001034030" "0" "50" "3" "49054042" "49054042" "subst" "0.000108968" "01804" "NDUFAF3_000001" "g.49054042C>T" "" "" "" "DALRD3(NM_001009996.3):c.1063+3G>A" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "VUS" "" "0001063966" "0" "30" "3" "49053230" "49053230" "subst" "0" "01804" "NDUFAF3_000004" "g.49053230T>C" "" "" "" "DALRD3(NM_001009996.3):c.1512+7A>G" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely benign" "" "0001063967" "0" "50" "3" "49054045" "49054045" "subst" "0" "01804" "NDUFAF3_000005" "g.49054045C>T" "" "" "" "DALRD3(NM_001009996.3):c.1063G>A (p.(Asp355Asn))" "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 P4HTM ## Count = 28 "{{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}}" "0000329400" "00015569" "50" "12485" "0" "12485" "0" "c.*10793C>T" "r.(=)" "p.(=)" "" "0000329401" "00015569" "50" "13189" "0" "13189" "0" "c.*11497C>G" "r.(=)" "p.(=)" "" "0000454604" "00015569" "90" "1073" "0" "1073" "0" "c.1073G>A" "r.888_1256del" "p.Arg296_Tyr418del" "6" "0000454605" "00015569" "90" "482" "0" "482" "0" "c.482A>C" "r.(?)" "p.(His161Pro)" "3" "0000454606" "00015569" "70" "286" "0" "286" "0" "c.286dup" "r.(?)" "p.(Gln96Profs*29)" "1" "0000454607" "00015569" "90" "1594" "0" "1594" "0" "c.1594C>T" "r.(?)" "p.(Gln532*)" "9" "0000454608" "00015569" "90" "1073" "0" "1073" "0" "c.1073G>A" "r.(?)" "p.(Arg358Gln)" "6" "0000520153" "00015569" "50" "8552" "0" "8552" "0" "c.*6860A>G" "r.(=)" "p.(=)" "" "0000719489" "00015569" "50" "764" "0" "764" "0" "c.764G>A" "r.(?)" "p.(Arg255Gln)" "" "0000719490" "00015569" "50" "949" "0" "949" "0" "c.949del" "r.(?)" "p.(Val317PhefsTer30)" "" "0000719491" "00015569" "70" "10456" "0" "10456" "0" "c.*8764G>A" "r.(=)" "p.(=)" "" "0000790983" "00015569" "90" "949" "0" "949" "0" "c.949del" "r.(?)" "p.(Val317Phefs*30)" "9" "0000869756" "00015569" "90" "1421" "0" "1421" "0" "c.1421C>T" "r.(?)" "p.(Pro474Leu)" "" "0000869757" "00015569" "70" "1554" "0" "1554" "0" "c.1554G>A" "r.(?)" "p.(Trp518*)" "" "0000869758" "00015569" "90" "1073" "0" "1073" "0" "c.1073G>A" "r.(?)" "p.(Arg358Gln)" "" "0000869759" "00015569" "90" "1073" "0" "1073" "0" "c.1073G>A" "r.(?)" "p.(Arg358Gln)" "" "0000869760" "00015569" "90" "1421" "0" "1421" "0" "c.1421C>T" "r.(?)" "p.(Pro474Leu)" "" "0000869761" "00015569" "70" "1265" "0" "1265" "0" "c.1265C>T" "r.(?)" "p.(Thr422Ile)" "" "0000869762" "00015569" "90" "934" "0" "934" "0" "c.934G>A" "r.(?)" "p.(Glu312Lys)" "" "0000962817" "00015569" "30" "436" "8" "436" "8" "c.436+8C>T" "r.(=)" "p.(=)" "" "0000962818" "00015569" "30" "912" "0" "912" "0" "c.912G>A" "r.(?)" "p.(Ser304=)" "" "0000962819" "00015569" "30" "1348" "-5" "1348" "-5" "c.1348-5C>T" "r.spl?" "p.?" "" "0000975885" "00015569" "50" "164" "0" "164" "0" "c.164T>A" "r.(?)" "p.(Ile55Asn)" "" "0000993768" "00015569" "30" "1109" "0" "1109" "0" "c.1109T>G" "r.(?)" "p.(Leu370Arg)" "" "0001034029" "00015569" "50" "7905" "0" "7905" "0" "c.*6213G>A" "r.(=)" "p.(=)" "" "0001034030" "00015569" "50" "11394" "0" "11394" "0" "c.*9702C>T" "r.(=)" "p.(=)" "" "0001063966" "00015569" "30" "10582" "0" "10582" "0" "c.*8890T>C" "r.(=)" "p.(=)" "" "0001063967" "00015569" "50" "11397" "0" "11397" "0" "c.*9705C>T" "r.(=)" "p.(=)" "" ## Screenings_To_Variants ## Do not remove or alter this header ## ## Count = 13 "{{screeningid}}" "{{variantid}}" "0000219730" "0000454604" "0000219731" "0000454605" "0000219731" "0000454606" "0000219732" "0000454607" "0000219733" "0000454608" "0000378273" "0000790983" "0000412426" "0000869756" "0000412427" "0000869757" "0000412428" "0000869758" "0000412429" "0000869759" "0000412429" "0000869760" "0000412430" "0000869761" "0000412431" "0000869762"