### LOVD-version 3000-30b ### Full data download ### To import, do not remove or alter this header ### ## Filter: (gene_public = UBR7) # 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}}" "UBR7" "ubiquitin protein ligase E3 component n-recognin 7 (putative)" "14" "q32.12" "unknown" "NG_051089.1" "UD_132319827250" "" "https://www.LOVD.nl/UBR7" "" "1" "20344" "55148" "613816" "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/UBR7_codingDNA.html" "1" "" "" "-1" "" "-1" "00001" "2013-05-03 00:00:00" "00006" "2020-12-22 18:44:26" "00000" "2025-05-05 21:14:00" ## 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}}" "00022296" "UBR7" "transcript variant 2" "001" "NM_175748.3" "" "NP_786924.2" "" "" "" "-236" "3458" "1278" "93673401" "93695561" "" "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" "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" ## Genes_To_Diseases ## Do not remove or alter this header ## ## Count = 1 "{{geneid}}" "{{diseaseid}}" "UBR7" "00139" ## 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}}" "00324677" "" "" "" "1" "" "00006" "{PMID:Li 2021:33340455}, {DOI:Li 2021:10.1016/j.ajhg.2020.11.018 }" "2-generation family, 1 affected, unaffected heterozygous carrier parents" "M" "" "" "" "0" "" "" "" "Pat1" "00324678" "" "" "" "1" "" "00006" "{PMID:Li 2021:33340455}, {DOI:Li 2021:10.1016/j.ajhg.2020.11.018 }" "2-generation family, 1 affected, unaffected heterozygous carrier parents" "M" "" "United States" "" "0" "" "" "" "Pat2" "00324679" "" "" "" "1" "" "00006" "{PMID:Li 2021:33340455}, {DOI:Li 2021:10.1016/j.ajhg.2020.11.018 }" "2-generation family, 1 affected, unaffected heterozygous carrier parents" "M" "" "Germany" "" "0" "" "" "" "Pat3" "00324680" "" "" "" "1" "" "00006" "{PMID:Li 2021:33340455}, {DOI:Li 2021:10.1016/j.ajhg.2020.11.018 }" "2-generation family, 1 affected, unaffected heterozygous carrier parents" "M" "yes" "Saudi Arabia" "" "0" "" "" "" "Pat4" "00324681" "" "" "" "1" "" "00006" "{PMID:Li 2021:33340455}, {DOI:Li 2021:10.1016/j.ajhg.2020.11.018 }" "2-generation family, 1 affected, unaffected heterozygous carrier parents" "M" "yes" "Saudi Arabia" "" "0" "" "" "" "Pat5" "00324682" "" "" "" "2" "" "00006" "{PMID:Li 2021:33340455}, {DOI:Li 2021:10.1016/j.ajhg.2020.11.018 }" "2-generation family, affected brother/sister, unaffected heterozygous carrier parents" "M" "yes" "" "" "0" "" "" "" "Pat6" "00324683" "" "" "00324682" "1" "" "00006" "{PMID:Li 2021:33340455}, {DOI:Li 2021:10.1016/j.ajhg.2020.11.018 }" "sister" "F" "yes" "" "2y" "0" "" "" "" "Pat7" "00380298" "" "" "" "4" "" "00000" "{PMID:Abu-Safieh-2013:23105016}" "" "" "" "Saudi Arabia" "" "0" "" "" "" "" "00435497" "" "" "" "1" "" "00006" "{PMID:Rots 2023:37196654}" "2-generation family, unaffected non-carrier parents" "M" "" "" "" "0" "" "" "" "Pat15" ## Individuals_To_Diseases ## Do not remove or alter this header ## ## Count = 9 "{{individualid}}" "{{diseaseid}}" "00324677" "05611" "00324678" "05611" "00324679" "05611" "00324680" "05611" "00324681" "05611" "00324682" "05611" "00324683" "05611" "00380298" "04214" "00435497" "05611" ## Phenotypes ## Do not remove or alter this header ## ## Note: Only showing Phenotype columns active for Diseases 00139, 04214, 05611 ## Count = 9 "{{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}}" "0000243177" "05611" "00324677" "00006" "Familial, autosomal recessive" "9y" "short stature; developmental delay/intellectual disability; no epilepsy; no hypotonia; ptosis; hypothyroidism; small penis; patent ductus arteriosus" "" "" "" "" "" "" "" "" "intellectual disability" "0000243178" "05611" "00324678" "00006" "Familial, autosomal recessive" "17y" "short stature; developmental delay/intellectual disability; epilepsy; hypotonia; no ptosis; no hypothyroidism; cryptorchidism; ventricular septal defect" "" "" "" "" "" "" "" "" "intellectual disability" "0000243179" "05611" "00324679" "00006" "Familial, autosomal recessive" "3y9m" "short stature; developmental delay/intellectual disability; epilepsy; hypotonia; no ptosis; hypothyroidism; cryptorchidism; patent ductus arteriosus, patent foramen ovale" "" "" "" "" "" "" "" "" "intellectual disability" "0000243180" "05611" "00324680" "00006" "Familial, autosomal recessive" "7y" "no short stature; developmental delay/intellectual disability; epilepsy; hypotonia; ptosis; hypothyroidism; cryptorchidism; no cardiac anomalies" "" "" "" "" "" "" "" "" "intellectual disability" "0000243181" "05611" "00324681" "00006" "Familial, autosomal recessive" "3y7m" "no short stature; developmental delay/intellectual disability; epilepsy; hypotonia; ptosis; hypothyroidism; cryptorchidism; no cardiac anomalies" "" "" "" "" "" "" "" "" "intellectual disability" "0000243182" "05611" "00324682" "00006" "Familial, autosomal recessive" "5y" "short stature; developmental delay/intellectual disability; epilepsy; hypotonia; ptosis; no hypothyroidism; cryptorchidism; atrial septal defect" "" "" "" "" "" "" "" "" "intellectual disability" "0000243183" "05611" "00324683" "00006" "Familial, autosomal recessive" "1y10m" "2y-deceased; short stature; developmental delay/intellectual disability; epilepsy; hypotonia; ptosis; no hypothyroidism; no genital anomalies; ventricular septal defect" "" "" "" "" "" "" "" "" "intellectual disability" "0000274149" "04214" "00380298" "00000" "Familial, autosomal recessive" "" "" "" "" "" "" "" "" "" "" "retinitis pigmentosa (RP)" "0000325684" "05611" "00435497" "00006" "Isolated (sporadic)" "5y" "see paper; ..., pregnancy small for gestational age, C-section; birth 38w+0d; no language/speech delay, 19.5, but inconsistent use of words; consistent use of words 29m; motor delay, 25m-first steps; moderate intellectual disability; autism spectrum disorder; ADHD, aggression, problems in social interaction; no psychosis/schizophrenia; no use psychiatric drugs; sleep apnea; absence seizures and GTC; hypotonia; no dystonia; no spasticity; MRI brain normal; joint hypermobility; no syndactyly; no vertebral abnormalities; no abnormalities hand/foot/finger; no pectus excavatum; hypertelorism, synorphys, fine upper lip hair, deep set elanguage/speech delay, prominent upper nasal bridge with downturned nasal tip, short filtrum, prognathism, cheeks full (steroids), hypodontia, microdontia, wide hands, minimal hypermobility elbows, cryptorchidism; no lip/cleft palate; no hypermetropia/myopia; strabismus (exotropia); normal hearing; no recurrent ear infections; congenital heart disease (PDA); neonatal feeding difficulties, admitted to NICU for 8d for feeding difficulties; gastroesophageal reflux; constipation; on ketogenic diet; no skin hyperlaxity; no genitourinary abnormalities; cryptorchidism; admitted for pneumonia and was given dose of antibiotics which showed a \"transformative improvement \" in cognition/behavior after antibiotic administration. Dad describes change as using more words, longer attention span. Only temporary. He then received a steroid transfusion which again showed huge improvement which gradually wears off. He is now on oral prednisone, he gets crushed prednisone every 3 days, shown to have huge improvements to cognition and then he regresses back to his baseline. NYU plan is to bring him back in and do a few rounds of steroid pulse therapy." "" "" "" "" "" "" "" "NEDCFSA" "neurodevelopmental delay" ## 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}}" "0000325885" "00324677" "1" "00006" "00006" "2020-12-22 19:17:48" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000325886" "00324678" "1" "00006" "00006" "2020-12-22 19:17:48" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000325887" "00324679" "1" "00006" "00006" "2020-12-22 19:17:48" "" "" "RT-PCR;SEQ;SEQ-NG" "DNA;RNA" "" "WES" "0000325888" "00324680" "1" "00006" "00006" "2020-12-22 19:17:48" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000325889" "00324681" "1" "00006" "00006" "2020-12-22 19:17:48" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000325890" "00324682" "1" "00006" "00006" "2020-12-22 19:17:48" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000325891" "00324683" "1" "00006" "00006" "2020-12-22 19:17:48" "" "" "SEQ;SEQ-NG" "DNA" "" "WES" "0000381512" "00380298" "1" "00000" "00008" "2021-08-13 14:56:11" "" "" "SEQ-NG" "DNA" "blood" "autozygome-guided sequencing" "0000436976" "00435497" "1" "00006" "00006" "2023-08-03 13:47:25" "" "" "SEQ;SEQ-NG" "DNA" "" "" ## Screenings_To_Genes ## Do not remove or alter this header ## ## Count = 8 "{{screeningid}}" "{{geneid}}" "0000325885" "UBR7" "0000325886" "UBR7" "0000325887" "UBR7" "0000325888" "UBR7" "0000325889" "UBR7" "0000325890" "UBR7" "0000325891" "UBR7" "0000381512" "UBR7" ## 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}}" "0000312935" "0" "10" "14" "93693422" "93693422" "subst" "0.278674" "02325" "UBR7_000002" "g.93693422C>T" "" "" "" "UBR7(NR_038150.2):n.1221C>T" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "0" "" "" "g.93227076C>T" "" "benign" "" "0000312936" "0" "10" "14" "93686585" "93686586" "del" "0" "02325" "UBR7_000001" "g.93686585_93686586del" "" "" "" "UBR7(NM_175748.4):c.961-10_961-9delTT" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "0" "" "" "g.93220239_93220240del" "" "benign" "" "0000351442" "0" "50" "14" "93676305" "93676305" "subst" "0" "02327" "UBR7_000003" "g.93676305T>C" "" "" "" "" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "0" "" "" "g.93209959T>C" "" "VUS" "" "0000553427" "0" "50" "14" "93673776" "93673776" "subst" "0" "01943" "C14orf142_000001" "g.93673776C>A" "" "" "" "UBR7(NM_175748.3):c.140C>A (p.S47Y)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "g.93207431C>A" "" "VUS" "" "0000553428" "0" "30" "14" "93686588" "93686588" "subst" "0" "01804" "C14orf142_000002" "g.93686588C>T" "" "" "" "UBR7(NM_175748.3):c.961-7C>T (p.(=))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "g.93220242C>T" "" "likely benign" "" "0000553429" "0" "30" "14" "93686589" "93686589" "subst" "0" "01804" "C14orf142_000003" "g.93686589C>T" "" "" "" "UBR7(NM_175748.3):c.961-6C>T (p.(=))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "g.93220243C>T" "" "likely benign" "" "0000709029" "11" "90" "14" "93673673" "93673673" "subst" "0" "00006" "UBR7_000005" "g.93673673G>T" "" "{PMID:Li 2021:33340455}, {DOI:Li 2021:10.1016/j.ajhg.2020.11.018 }" "" "" "" "Germline" "" "" "0" "" "" "g.93207328G>T" "" "pathogenic (recessive)" "" "0000709030" "3" "90" "14" "93685661" "93685661" "subst" "0" "00006" "UBR7_000009" "g.93685661G>C" "" "{PMID:Li 2021:33340455}, {DOI:Li 2021:10.1016/j.ajhg.2020.11.018 }" "" "" "" "Germline" "" "" "0" "" "" "g.93219315G>C" "" "pathogenic (recessive)" "" "0000709031" "11" "90" "14" "93681520" "93681520" "subst" "0" "00006" "UBR7_000006" "g.93681520A>G" "" "{PMID:Li 2021:33340455}, {DOI:Li 2021:10.1016/j.ajhg.2020.11.018 }" "" "" "" "Germline" "" "" "0" "" "" "g.93215174A>G" "" "pathogenic (recessive)" "" "0000709032" "3" "90" "14" "93684889" "93684889" "del" "0" "00006" "UBR7_000008" "g.93684889del" "" "{PMID:Li 2021:33340455}, {DOI:Li 2021:10.1016/j.ajhg.2020.11.018 }" "" "618delT" "" "Germline" "" "" "0" "" "" "g.93218543del" "" "pathogenic (recessive)" "" "0000709033" "3" "90" "14" "93684889" "93684889" "del" "0" "00006" "UBR7_000008" "g.93684889del" "" "{PMID:Li 2021:33340455}, {DOI:Li 2021:10.1016/j.ajhg.2020.11.018 }" "" "619delT" "" "Germline" "" "" "0" "" "" "g.93218543del" "" "pathogenic (recessive)" "" "0000709034" "3" "90" "14" "93693288" "93693288" "subst" "0" "00006" "UBR7_000010" "g.93693288G>C" "" "{PMID:Li 2021:33340455}, {DOI:Li 2021:10.1016/j.ajhg.2020.11.018 }" "" "" "" "Germline" "" "" "0" "" "" "g.93226942G>C" "" "pathogenic (recessive)" "" "0000709035" "3" "90" "14" "93693288" "93693288" "subst" "0" "00006" "UBR7_000010" "g.93693288G>C" "" "{PMID:Li 2021:33340455}, {DOI:Li 2021:10.1016/j.ajhg.2020.11.018 }" "" "" "" "Germline" "" "" "0" "" "" "g.93226942G>C" "" "pathogenic (recessive)" "" "0000709036" "21" "90" "14" "93681590" "93681591" "dup" "0" "00006" "UBR7_000007" "g.93681590_93681591dup" "" "{PMID:Li 2021:33340455}, {DOI:Li 2021:10.1016/j.ajhg.2020.11.018 }" "" "" "" "Germline" "" "" "0" "" "" "g.93215244_93215245dup" "" "pathogenic (recessive)" "" "0000709037" "21" "90" "14" "93673401" "93688721" "del" "0" "00006" "UBR7_000004" "g.(?_93673401)_(93688721_93693288)del" "" "{PMID:Li 2021:33340455}, {DOI:Li 2021:10.1016/j.ajhg.2020.11.018 }" "" "deletion ex1-10" "" "Germline" "" "" "0" "" "" "g.(?_93207056)_(93222375_93226942)del" "" "pathogenic (recessive)" "" "0000794973" "3" "50" "14" "93681299" "93681299" "subst" "0.000215624" "00000" "UBR7_000011" "g.93681299G>A" "" "{PMID:Abu-Safieh-2013:23105016}" "" "NM_001100417:c.G238A (p.Val80Ile)" "" "Germline" "" "" "0" "" "" "" "" "VUS" "" "0000931796" "3" "50" "14" "93688720" "93688720" "subst" "8.12203E-6" "00006" "UBR7_000012" "g.93688720G>A" "" "{PMID:Rots 2023:37196654}" "" "" "" "Germline" "" "" "0" "" "" "g.93222374G>A" "" "VUS" "" "0001040170" "0" "50" "14" "93681613" "93681613" "subst" "0" "01804" "C14orf142_000004" "g.93681613C>T" "" "" "" "UBR7(NM_175748.4):c.587C>T (p.(Ala196Val))" "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 UBR7 ## 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}}" "0000312935" "00022296" "10" "1319" "0" "1319" "0" "c.*41C>T" "r.(=)" "p.(=)" "" "0000312936" "00022296" "10" "961" "-10" "961" "-9" "c.961-10_961-9del" "r.(=)" "p.(=)" "" "0000351442" "00022296" "50" "284" "2" "284" "2" "c.284+2T>C" "r.spl?" "p.?" "" "0000553427" "00022296" "50" "140" "0" "140" "0" "c.140C>A" "r.(?)" "p.(Ser47Tyr)" "" "0000553428" "00022296" "30" "961" "-7" "961" "-7" "c.961-7C>T" "r.(=)" "p.(=)" "" "0000553429" "00022296" "30" "961" "-6" "961" "-6" "c.961-6C>T" "r.(=)" "p.(=)" "" "0000709029" "00022296" "90" "37" "0" "37" "0" "c.37G>T" "r.(?)" "p.(Glu13*)" "" "0000709030" "00022296" "90" "914" "0" "914" "0" "c.914G>C" "r.(?)" "p.(Trp305Ser)" "" "0000709031" "00022296" "90" "496" "-2" "496" "-2" "c.496-2A>G" "r.496_601del" "p.His166*" "5i" "0000709032" "00022296" "90" "618" "0" "618" "0" "c.618del" "r.(?)" "p.(Glu207Argfs*12)" "" "0000709033" "00022296" "90" "618" "0" "618" "0" "c.618del" "r.(?)" "p.(Glu207Argfs*12)" "" "0000709034" "00022296" "90" "1186" "-1" "1186" "-1" "c.1186-1G>C" "r.spl" "p.?" "" "0000709035" "00022296" "90" "1186" "-1" "1186" "-1" "c.1186-1G>C" "r.spl" "p.?" "" "0000709036" "00022296" "90" "564" "0" "565" "0" "c.564_565dup" "r.(?)" "p.(Cys189Phefs*14)" "" "0000709037" "00022296" "90" "0" "0" "0" "0" "c.-236_(c.1185+1_1186-1){0}" "r.0?" "p.0?" "_1_10i" "0000794973" "00022296" "50" "466" "0" "466" "0" "c.466G>A" "r.(?)" "p.(Val156Ile)" "5" "0000931796" "00022296" "50" "1185" "0" "1185" "0" "c.1185G>A" "r.spl?" "p.(?)" "" "0001040170" "00022296" "50" "587" "0" "587" "0" "c.587C>T" "r.(?)" "p.(Ala196Val)" "" ## Screenings_To_Variants ## Do not remove or alter this header ## ## Count = 11 "{{screeningid}}" "{{variantid}}" "0000325885" "0000709029" "0000325885" "0000709036" "0000325886" "0000709030" "0000325887" "0000709031" "0000325887" "0000709037" "0000325888" "0000709032" "0000325889" "0000709033" "0000325890" "0000709034" "0000325891" "0000709035" "0000381512" "0000794973" "0000436976" "0000931796"