Thank you for your quick response but I am getting the same error:
It was done as you suggested and the response is coming correctly because is logging as expected but the error keeps going on.
My data model is like the following:
175 dataModel: {
176 location: "remote",
177 cache: true,
178 url: urlResult,
179 getData: function (response) {
180 console.log('logging response.data' + JSON.stringify(response.data))
181 return { data: JSON.stringify(response.data) };
182 }
183 },
Any suggestion? Please help
I have no idea to save the problem!!
My remote response:
{
data: [
{
1: "20472",
Yale New Genes: "",
Gene Ontology: "
http://genecards.org/cgi-bin/carddisp.pl?gene=IDH1&go_proc=1000&rf=/home/genecards/current/website/carddisp.pl#go_proc",
RefgeneExonLocation: "",
snp135_MultAl: "",
hg19_esp6500siv2_aa: "",
EnsgeneExonFunction: "",
snp135_Frequency: "",
Parents: "",
KnownGeneExonFunction: "",
snp137_common_no_known_medical_impact: "",
Approved Symbol: "IDH1",
Gerp++elem_Pvalue: "",
Interactions: "",
Afalt_1000g2015aug_afr: "",
Hopkins Samples (SNV): "",
OMIM: "
https://omim.org/entry/147700",
QualityRMS: "",
ValidForAnnovar: "1",
Hopkins Samples (Indel): "",
RefgeneGeneLocation: "intronic",
ExAC03: "",
ExAC03_EAS: "",
CADD Score: "",
tfbsConsSites: "",
segdup: "",
band: "2q34",
ExAC_r03_pLI: "Name=0.001453708",
Score_Ljb_lrt: "",
CCDS Intolerance Percentile: "55.44939844",
Score_Ljb_mt: "",
OMIM Inheritance: "",
snp137_common: "",
ExAC03_NFE: "",
500 Genes: "",
Score_Ljb_phylop: "",
Mouse Model: "Electrophoretic variation has been shown in tissues of liver, kidney, spleen and muscle. Strains C57BL/6, C3H/He carry the a allele; DBA/2 carries the b allele; M.m. castaneus and M.m. molossinus carry the c allele; the d allele is found at low frequencyin M. m. molossinus in Japan.",
snp132: "",
UW New Genes: "",
AFalt_hg19_cg69: "",
snp137_all: "",
Genotype: "hom",
CCDS Intolerance Score: "0.018483465",
Afalt_1000g2015aug_amr: "",
evofold: "",
KnownGeneGeneName: "IDH1",
ClinVar: "",
VEST_Score: "",
ExAC03_SAS: "",
Status / Expressed Allele: "",
OMIM Phenotypes: "{Glioma, susceptibility to, somatic}",
ExAC03_AMR: "",
snp135_ClinAssoID: "",
Score_Ljb_All: "",
Interaction: "AADAT, ABCF2, ACACB, ACO1, ACO2, ADSL, ALDH5A1, AMD1, ASL, ASS1, CEP57L1, DDA1, DDO, ELAVL1, FH, GLUD1, GLUD2, GMPPB, GOT1, GOT2, HAAO, HSPA5, IDH1, IDH2, IDH3A, IDH3B, IDH3G, IL4I1, MDH2, MTG1, MTHFR, NAGS, NIT2, OGDHL, OTC, PABPC1, PC, PIK3C2A, PKLR, PKM, PRKAG2, PSAT1, PSMD14, RIOK2, RPL10A, RPL4, RPS3A, RPS8, SRR, SUMO4, TARS, TP53I3, TRAPPC3, UBA5, UBA52, UBC, USP7, VAMP7, YWHAZ, ZHX1",
ExAC03_Global: "",
Afalt_1000g2015aug_all: "",
KnownGeneGeneLocation: "intronic",
PubMed: "
https://www.ncbi.nlm.nih.gov/pubmed?term=IDH1",
ExAC03_FIN: "",
snp135_Allele: "",
omimgene: "Name=147700",
cosmic68wgs: "",
Score_Ljb_pp2hdiv: "",
Afalt_1000g2015aug_eas: "",
wgEncodeRegTfbsClusteredV3_Score: "",
Gerp++gt2: "",
SiftScore: "",
AFalt_hg19_cg46: "",
hg19_esp6500siv2_all: "",
StartPosition: "209101907",
RefgeneGeneName: "IDH1",
ExAC03_AFR: "",
EnsgeneGeneLocation: "intronic",
snp135_Common: "",
CADDgt20: "",
EndPosition: "209101907",
mce46way: "",
Score_Ljb_pp2hvar: "",
gnomAD_genome_freq: "",
HGMD_2017.2: "",
mirna: "",
wgEncodeRegDnaseClusteredV3_Score: "",
TotalDepth: "50",
UniProt: "
http://www.uniprot.org/uniprot/O75874",
Score_Ljb_gerp++: "",
AlternativeAllele: "-",
Expression: "Adipose tissue / Adrenal / Bone marrow / Brain / Breast / Cartilage / Cervix / Colon / Eye / Gi tract / Head n neck / Kidney / Liver / Lung / Nervous / Ovary / Pancreas / Peripheral nerv / Pituitary gland / Placenta / Prostate / Retina / Skin / Spleen / Stomach / Testis / Uterus / Vascular",
gwascatalog: "",
Mammalian Phenotype: "
http://www.informatics.jax.org/batch/summary?ids=IDH1&association=MP",
cosmic70: "",
snp129: "",
snp126: "",
OMIM Matching Phenotypes: "",
Afalt_1000g2015aug_sas: "",
fathmm_score: "",
RefgeneExonFunction: "",
EnsgeneExonLocation: "",
Kaviar_AF: "",
Hopkins Total Allele Count (Indel): "46_4598_6",
wgEncodeBroadHmmGm12878HMM_ChromatinStateSegmentation: "Name=10_Txn_Elongation",
GWAS Catalog: "",
ExAC_r03_mis_z: "Name=0.100659045",
gme_AF: "",
Gerp++elem_RSscore: "",
ExAC03_OTH: "",
revel_score: "",
CIDRVar50Mb: "",
ClinVar Variant Classification: "",
vistaEnhancer_ID: "",
miRdSNP: "
http://mirdsnp.ccr.buffalo.edu/search.php?filter_gene_name=IDH1",
snp138: "",
EnsgeneGeneName: "ENSG00000138413",
snp135: "",
snp137: "",
snp131: "",
ReferenceAllele: "A",
Hopkins Total Allele Count (SNV): "",
VariantType: "Indel",
KnownGeneExonLocation: "",
dgv: "Name=nsv834517,nsv584297,nsv525747",
WG_GWAVA_score: "",
gnomAD_exome_freq: "",
Afalt_1000g2015aug_eur: "",
snp135_ClinAssoSubmit: "",
VISTA Enhancer: "",
ExAC_r03_gene: "Name=IDH1",
CIDRVar51Mb: "",
WG_EIGEN_score: "",
TraP: "",
hg19_esp6500siv2_ea: "",
simpleRepeat: "",
Quality: "2247559.94",
Chromosome: "2"
},
]
}
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