### LOVD-version 3000-30b ### Full data download ### To import, do not remove or alter this header ### ## Filter: (gene_public = EED) # 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}}" "EED" "embryonic ectoderm development" "11" "q14.2-q22.3" "unknown" "NG_029595.1" "UD_136080178119" "" "https://www.LOVD.nl/EED" "" "1" "3188" "8726" "605984" "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/EED_codingDNA.html" "1" "" "" "-1" "" "-1" "00001" "2013-05-03 00:00:00" "00006" "2017-11-27 16:35:32" "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}}" "00006877" "EED" "transcript variant 1" "002" "NM_003797.3" "" "NP_003788.2" "" "" "" "-466" "1544" "1326" "85955806" "85989785" "" "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" "05717" "COGIS" "Cohen-Gibson syndrome (COGIS)" "AD" "617561" "" "" "" "00006" "2020-04-06 13:49:36" "00006" "2021-12-10 21:51:32" ## Genes_To_Diseases ## Do not remove or alter this header ## ## Count = 1 "{{geneid}}" "{{diseaseid}}" "EED" "05717" ## Individuals ## Do not remove or alter this header ## ## Count = 9 "{{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}}" "00081829" "" "" "" "1" "" "01794" "{PMID:Imagawa 2017:28229514}" "2-generation family, 1 affected, unaffected heterozygous carrier parents" "M" "no" "Japan" "" "0" "" "" "Japanese" "Fam2PatII1/EX0065" "00134093" "" "" "" "1" "" "02182" "" "" "F" "-" "United States" "?" "0" "yes" "none" "White" "Patient 1" "00134094" "" "" "" "1" "" "02182" "" "" "F" "-" "United States" "" "0" "yes" "none" "" "Patient 2" "00164661" "" "" "" "1" "" "02182" "" "" "M" "?" "" "" "0" "" "" "" "Patient 3" "00296443" "" "" "" "1" "" "00006" "{PMID:Cohen 2016:27193220}" "" "M" "" "" "" "0" "" "" "white" "A1544B" "00296444" "" "" "" "1" "" "00006" "{PMID:Cohen 2015:25787343}" "2-generation family, 1 affected, unaffected heterozygous carrier parents" "M" "" "Turkey" "" "0" "" "" "" "A1477" "00296445" "" "" "" "1" "" "00006" "{PMID:Cooney 2017:27868325}" "2-generation family, 1 affected, unaffected heterozygous carrier parents" "F" "" "United States" "" "0" "" "" "Hispanic" "patient" "00450291" "" "" "" "1" "" "00006" "{PMID:Tatton-Brown 2017:28475857}" "patient" "" "" "United States" "" "0" "" "" "" "COG0877" "00450292" "" "" "" "1" "" "00006" "{PMID:Tatton-Brown 2017:28475857}" "patient" "" "" "United States" "" "0" "" "" "" "COG1738" ## Individuals_To_Diseases ## Do not remove or alter this header ## ## Count = 7 "{{individualid}}" "{{diseaseid}}" "00081829" "00198" "00134093" "00198" "00296443" "00198" "00296444" "00198" "00296445" "00198" "00450291" "00198" "00450292" "00198" ## Phenotypes ## Do not remove or alter this header ## ## Note: Only showing Phenotype columns active for Diseases 00198, 05717 ## Count = 7 "{{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}}" "0000115935" "00198" "00134093" "02182" "Unknown" "" "clinically diagnosed with a Weaver-like overgrowth syndrome" "" "" "" "" "" "" "" "" "" "overgrowth" "" "0000223855" "00198" "00296443" "00006" "Isolated (sporadic)" "30y" "see paper; ..." "" "" "" "" "" "" "" "" "COGIS" "Weaver syndrome" "" "0000223856" "00198" "00296444" "00006" "Isolated (sporadic)" "27y" "see paper; ..." "" "" "" "" "" "" "" "" "COGIS" "overgrowth" "" "0000223857" "00198" "00296445" "00006" "Isolated (sporadic)" "16y" "see paper; ..." "" "" "" "" "" "" "" "" "COGIS" "Weaver syndrome" "" "0000223866" "00198" "00081829" "00006" "Isolated (sporadic)" "05y" "see paper; ..." "" "" "" "" "" "" "" "" "COGIS" "Weaver syndrome" "" "0000339351" "00198" "00450291" "00006" "Isolated (sporadic)" "25y" "overgrowth; moderate intellectual disability;" "" "" "" "" "" "" "" "" "" "overgrowth" "" "0000339352" "00198" "00450292" "00006" "Isolated (sporadic)" "20y" "overgrowth head, overgrowth height; severe intellectual disability;" "" "" "" "" "" "" "" "" "" "overgrowth" "" ## Screenings ## Do not remove or alter this header ## ## Count = 9 "{{id}}" "{{individualid}}" "{{variants_found}}" "{{owned_by}}" "{{created_by}}" "{{created_date}}" "{{edited_by}}" "{{edited_date}}" "{{Screening/Technique}}" "{{Screening/Template}}" "{{Screening/Tissue}}" "{{Screening/Remarks}}" "0000081961" "00081829" "1" "01794" "01794" "2016-10-26 03:58:28" "" "" "SEQ-NG-I" "DNA" "peripheral blood" "" "0000134933" "00134093" "1" "02182" "02182" "2017-11-24 20:39:11" "" "" "SEQ-NG-I" "DNA" "blood" "WES" "0000134934" "00134094" "1" "02182" "02182" "2017-11-24 20:52:14" "" "" "SEQ-NG-I" "DNA" "blood" "WES" "0000165527" "00164661" "1" "02182" "02182" "2018-06-04 19:20:03" "" "" "SEQ-NG" "DNA" "blood" "" "0000297553" "00296443" "1" "00006" "00006" "2020-04-06 14:06:31" "" "" "SEQ" "DNA" "" "" "0000297554" "00296444" "1" "00006" "00006" "2020-04-06 14:06:31" "" "" "SEQ" "DNA" "" "" "0000297555" "00296445" "1" "00006" "00006" "2020-04-06 14:06:31" "" "" "SEQ" "DNA" "" "" "0000451887" "00450291" "1" "00006" "00006" "2024-05-24 16:57:38" "" "" "SEQ;SEQ-NG" "DNA" "" "" "0000451888" "00450292" "1" "00006" "00006" "2024-05-24 16:57:38" "" "" "SEQ;SEQ-NG" "DNA" "" "" ## Screenings_To_Genes ## Do not remove or alter this header ## ## Count = 3 "{{screeningid}}" "{{geneid}}" "0000297553" "EED" "0000297554" "EED" "0000297555" "EED" ## 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 = 27 "{{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}}" "0000134733" "0" "50" "11" "85975286" "85975286" "subst" "0" "01794" "EED_000001" "g.85975286G>C" "" "{PMID:Imagawa 2017:28229514}, {PMID:Choufani 2020:32243864}" "" "" "" "De novo" "" "" "0" "EZH2 methylation signature" "" "g.86264244G>C" "" "pathogenic (dominant)" "" "0000225128" "0" "50" "11" "85977171" "85977171" "subst" "0" "02182" "EED_000002" "g.85977171A>T" "" "" "" "" "" "Germline/De novo (untested)" "" "" "0" "" "" "g.86266129A>T" "" "VUS" "" "0000225129" "0" "50" "11" "85968585" "85968585" "subst" "0" "02182" "EED_000003" "g.85968585A>G" "" "" "" "" "" "Germline/De novo (untested)" "" "" "0" "" "" "g.86257543A>G" "" "VUS" "" "0000369245" "0" "50" "11" "85977170" "85977170" "subst" "0" "02182" "EED_000004" "g.85977170C>T" "" "" "" "" "" "Unknown" "" "" "0" "" "" "g.86266128C>T" "" "VUS" "" "0000546002" "0" "70" "11" "85968585" "85968585" "subst" "0" "01804" "EED_000003" "g.85968585A>G" "" "" "" "EED(NM_003797.3):c.581A>G (p.(Asn194Ser))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "g.86257543A>G" "" "likely pathogenic" "" "0000660155" "0" "90" "11" "85977170" "85977170" "subst" "0" "00006" "EED_000004" "g.85977170C>T" "" "{PMID:Cohen 2016:27193220}, {PMID:Choufani 2020:32243864}" "" "" "" "De novo" "" "" "0" "EZH2 methylation signature" "" "g.86266128C>T" "" "pathogenic (dominant)" "" "0000660156" "0" "90" "11" "85979543" "85979543" "subst" "0" "00006" "EED_000005" "g.85979543A>C" "" "{PMID:Cohen 2015:25787343}, {PMID:Choufani 2020:32243864}" "" "" "" "De novo" "" "" "0" "EZH2 methylation signature" "" "g.86268501A>C" "" "pathogenic (dominant)" "" "0000660157" "0" "90" "11" "85979541" "85979541" "subst" "0" "00006" "EED_000006" "g.85979541A>G" "" "{PMID:Cooney 2017:27868325}" "" "" "father not available" "Germline/De novo (untested)" "" "" "0" "" "" "g.86268499A>G" "" "pathogenic (dominant)" "" "0000723752" "0" "30" "11" "85956307" "85956324" "dup" "0" "01943" "EED_000007" "g.85956307_85956324dup" "" "" "" "EED(NM_001308007.1):c.36_53dupAACAGACATGCCTGCGGC (p.T13_A18dup), EED(NM_003797.3):c.36_53dupAACAGACATGCCTGCGGC (p.(Ala18_Lys19insThrAspMetProAlaAla))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely benign" "" "0000723753" "0" "30" "11" "85961371" "85961371" "subst" "0.000317319" "02325" "EED_000008" "g.85961371A>C" "" "" "" "EED(NM_003797.3):c.148A>C (p.(Thr50Pro)), EED(NM_003797.5):c.148A>C (p.T50P)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely benign" "" "0000723754" "0" "50" "11" "85989548" "85989548" "subst" "0" "02325" "EED_000009" "g.85989548G>T" "" "" "" "EED(NM_003797.5):c.1307G>T (p.R436L)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "VUS" "" "0000795579" "0" "50" "11" "85961395" "85961395" "subst" "0" "03779" "EED_000010" "g.85961395A>G" "" "" "" "" "" "CLASSIFICATION record" "" "rs890695718" "0" "" "" "" "" "VUS" "" "0000949812" "0" "50" "11" "85988034" "85988034" "subst" "0" "02325" "EED_000012" "g.85988034G>T" "" "" "" "EED(NM_003797.5):c.979G>T (p.A327S)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "VUS" "" "0000985804" "0" "90" "11" "85968585" "85968585" "subst" "0" "00006" "EED_000003" "g.85968585A>G" "" "{PMID:Tatton-Brown 2017:28475857}" "" "" "" "De novo" "" "" "0" "" "" "g.86257543A>G" "" "pathogenic (dominant)" "" "0000985805" "0" "90" "11" "85975285" "85975285" "subst" "0" "00006" "EED_000013" "g.85975285A>G" "" "{PMID:Tatton-Brown 2017:28475857}" "" "" "" "De novo" "" "" "0" "" "" "g.86264243A>G" "" "pathogenic (dominant)" "" "0000999528" "0" "50" "11" "85956307" "85956324" "dup" "0" "01804" "EED_000007" "g.85956307_85956324dup" "" "" "" "EED(NM_001308007.1):c.36_53dupAACAGACATGCCTGCGGC (p.T13_A18dup), EED(NM_003797.3):c.36_53dupAACAGACATGCCTGCGGC (p.(Ala18_Lys19insThrAspMetProAlaAla))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "VUS" "" "0000999529" "0" "30" "11" "85961371" "85961371" "subst" "0.000317319" "01804" "EED_000008" "g.85961371A>C" "" "" "" "EED(NM_003797.3):c.148A>C (p.(Thr50Pro)), EED(NM_003797.5):c.148A>C (p.T50P)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely benign" "" "0000999530" "0" "50" "11" "85968614" "85968614" "subst" "0" "01804" "EED_000014" "g.85968614A>C" "" "" "" "EED(NM_003797.3):c.610A>C (p.(Asn204His))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "VUS" "" "0000999531" "0" "50" "11" "85979547" "85979547" "subst" "0" "01804" "EED_000015" "g.85979547A>G" "" "" "" "EED(NM_003797.3):c.910A>G (p.(Ile304Val))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "VUS" "" "0001038823" "0" "50" "11" "85956110" "85956110" "subst" "0" "01804" "EED_000016" "g.85956110C>T" "" "" "" "EED(NM_003797.5):c.-162C>T" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "VUS" "" "0001038824" "0" "30" "11" "85956389" "85956389" "subst" "6.76253E-5" "01804" "EED_000017" "g.85956389A>C" "" "" "" "EED(NM_003797.5):c.114+4A>C" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely benign" "" "0001038825" "0" "50" "11" "85961363" "85961363" "subst" "1.3101E-5" "01804" "EED_000018" "g.85961363G>T" "" "" "" "EED(NM_003797.5):c.140G>T (p.(Gly47Val))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "VUS" "" "0001038826" "0" "50" "11" "85966274" "85966274" "subst" "0" "01804" "EED_000019" "g.85966274A>T" "" "" "" "EED(NM_003797.5):c.371A>T (p.(Tyr124Phe))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "VUS" "" "0001038827" "0" "30" "11" "85975305" "85975305" "subst" "2.44037E-5" "01804" "EED_000020" "g.85975305T>C" "" "" "" "EED(NM_003797.5):c.726T>C (p.(Ala242=))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely benign" "" "0001054027" "0" "50" "11" "85967472" "85967472" "subst" "0" "01804" "EED_000021" "g.85967472A>G" "" "" "" "EED(NM_003797.5):c.470A>G (p.(Asn157Ser))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "VUS" "" "0001054028" "0" "30" "11" "85977119" "85977119" "subst" "9.14093E-6" "01804" "EED_000022" "g.85977119A>C" "" "" "" "EED(NM_003797.5):c.727-6A>C" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely benign" "" "0001054029" "0" "30" "11" "85979491" "85979491" "subst" "0" "01804" "EED_000023" "g.85979491C>T" "" "" "" "EED(NM_003797.5):c.861-7C>T" "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 EED ## Count = 27 "{{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}}" "0000134733" "00006877" "50" "707" "0" "707" "0" "c.707G>C" "r.(?)" "p.(Arg236Thr)" "7" "0000225128" "00006877" "50" "773" "0" "773" "0" "c.773A>T" "r.(?)" "p.(His258Leu)" "8" "0000225129" "00006877" "50" "581" "0" "581" "0" "c.581A>G" "r.(?)" "p.(Asn194Ser)" "6" "0000369245" "00006877" "50" "772" "0" "772" "0" "c.772C>T" "r.(?)" "p.(His258Tyr)" "" "0000546002" "00006877" "70" "581" "0" "581" "0" "c.581A>G" "r.(?)" "p.(Asn194Ser)" "" "0000660155" "00006877" "90" "772" "0" "772" "0" "c.772C>T" "r.(?)" "p.(His258Tyr)" "" "0000660156" "00006877" "90" "906" "0" "906" "0" "c.906A>C" "r.(?)" "p.(Arg302Ser)" "" "0000660157" "00006877" "90" "904" "0" "904" "0" "c.904A>G" "r.(?)" "p.(Arg302Gly)" "" "0000723752" "00006877" "30" "36" "0" "53" "0" "c.36_53dup" "r.(?)" "p.(Thr13_Ala18dup)" "" "0000723753" "00006877" "30" "148" "0" "148" "0" "c.148A>C" "r.(?)" "p.(Thr50Pro)" "" "0000723754" "00006877" "50" "1307" "0" "1307" "0" "c.1307G>T" "r.(?)" "p.(Arg436Leu)" "" "0000795579" "00006877" "50" "172" "0" "172" "0" "c.172A>G" "r.(?)" "p.(Asn58Asp)" "" "0000949812" "00006877" "50" "979" "0" "979" "0" "c.979G>T" "r.(?)" "p.(Ala327Ser)" "" "0000985804" "00006877" "90" "581" "0" "581" "0" "c.581A>G" "r.(?)" "p.(Asn194Ser)" "" "0000985805" "00006877" "90" "706" "0" "706" "0" "c.706A>G" "r.(?)" "p.(Arg236Gly)" "" "0000999528" "00006877" "50" "36" "0" "53" "0" "c.36_53dup" "r.(?)" "p.(Thr13_Ala18dup)" "" "0000999529" "00006877" "30" "148" "0" "148" "0" "c.148A>C" "r.(?)" "p.(Thr50Pro)" "" "0000999530" "00006877" "50" "610" "0" "610" "0" "c.610A>C" "r.(?)" "p.(Asn204His)" "" "0000999531" "00006877" "50" "910" "0" "910" "0" "c.910A>G" "r.(?)" "p.(Ile304Val)" "" "0001038823" "00006877" "50" "-162" "0" "-162" "0" "c.-162C>T" "r.(?)" "p.(=)" "" "0001038824" "00006877" "30" "114" "4" "114" "4" "c.114+4A>C" "r.spl?" "p.?" "" "0001038825" "00006877" "50" "140" "0" "140" "0" "c.140G>T" "r.(?)" "p.(Gly47Val)" "" "0001038826" "00006877" "50" "371" "0" "371" "0" "c.371A>T" "r.(?)" "p.(Tyr124Phe)" "" "0001038827" "00006877" "30" "726" "0" "726" "0" "c.726T>C" "r.(?)" "p.(=)" "" "0001054027" "00006877" "50" "470" "0" "470" "0" "c.470A>G" "r.(?)" "p.(Asn157Ser)" "" "0001054028" "00006877" "30" "727" "-6" "727" "-6" "c.727-6A>C" "r.(=)" "p.(=)" "" "0001054029" "00006877" "30" "861" "-7" "861" "-7" "c.861-7C>T" "r.(=)" "p.(=)" "" ## Screenings_To_Variants ## Do not remove or alter this header ## ## Count = 9 "{{screeningid}}" "{{variantid}}" "0000081961" "0000134733" "0000134933" "0000225128" "0000134934" "0000225129" "0000165527" "0000369245" "0000297553" "0000660155" "0000297554" "0000660156" "0000297555" "0000660157" "0000451887" "0000985804" "0000451888" "0000985805"