{"ambiguity":"R","ancestral_allele":"G","name":"rs116035550","var_class":"SNP","most_severe_consequence":"missense_variant","synonyms":["NM_021932.5:c.1018G>C","NP_001273063.1:p.Glu340Lys","NM_001286134.1:c.1018G>C","NP_001273063.1:p.Glu340Gln","NM_001286134.1:c.1018G>A","NP_068751.4:p.Glu340Lys","NM_021932.5:c.1018G>A","NP_068751.4:p.Glu340Gln"],"MAF":null,"source":"Variants (including SNPs and indels) imported from dbSNP","mappings":[{"location":"11:212464-212464","seq_region_name":"11","start":212464,"strand":1,"end":212464,"assembly_name":"GRCh37","coord_system":"chromosome","allele_string":"G/A"}],"genotypes":[],"evidence":["Frequency","1000Genomes","ESP","ExAC","TOPMed","gnomAD"],"minor_allele":null}