{"context":{"query":">>hgnc>>clinvar","source_dataset":"hgnc","target_dataset":"clinvar"},"stats":{"queried":1,"total":46,"mapped":1},"pagination":{"has_next":false},"schema":"id|name|type|germline_classification|gene_symbol|review_status|chromosome","mappings":[{"input":"HGNC:7553","source":"HGNC:7553|MYC proto-oncogene, bHLH transcription factor","targets":["12574|NM_002467.6(MYC):c.214C>T (p.Pro72Ser)|single nucleotide variant|Pathogenic|MYC|no assertion criteria provided|8","12575|NM_002467.6(MYC):c.302A>C (p.Asn101Thr)|single nucleotide variant|Pathogenic|MYC|no assertion criteria provided|8","12576|NM_002467.6(MYC):c.162G>C (p.Glu54Asp)|single nucleotide variant|Pathogenic|MYC|no assertion criteria provided|8","12577|NM_002467.6(MYC):c.220C>G (p.Pro74Ala)|single nucleotide variant|other|MYC|criteria provided, single submitter|8","1340984|GRCh37/hg19 8q24.21(chr8:128717255-128918996)x3|copy number gain|Likely benign|MYC|no assertion criteria provided|8","1679939|NM_002467.6(MYC):c.77A>G (p.Asn26Ser)|single nucleotide variant|Uncertain significance|MYC|criteria provided, multiple submitters, no conflicts|8","2286886|NM_002467.6(MYC):c.409G>C (p.Glu137Gln)|single nucleotide variant|Uncertain significance|MYC|criteria provided, single submitter|8","2413166|NM_002467.6(MYC):c.223C>A (p.Pro75Thr)|single nucleotide variant|other|MYC|criteria provided, single submitter|8","2468497|NM_002467.6(MYC):c.909C>G (p.Ser303Arg)|single nucleotide variant|Uncertain significance|MYC|criteria provided, single submitter|8","2510151|NM_002467.6(MYC):c.671C>T (p.Ala224Val)|single nucleotide variant|Uncertain significance|MYC|criteria provided, single submitter|8","2658810|NM_002467.6(MYC):c.-263G>A|single nucleotide variant|Likely benign|MYC|criteria provided, single submitter|8","2658811|NM_002467.6(MYC):c.-96C>T|single nucleotide variant|Benign|MYC|criteria provided, single submitter|8","2658812|NM_002467.6(MYC):c.30+4A>T|single nucleotide variant|Uncertain significance|MYC|criteria provided, single submitter|8","2658813|NM_002467.6(MYC):c.30+600C>T|single nucleotide variant|Benign|MYC|criteria provided, single submitter|8","2658814|NM_002467.6(MYC):c.31-172G>A|single nucleotide variant|Benign|MYC|criteria provided, single submitter|8","2658815|NM_002467.6(MYC):c.217A>G (p.Thr73Ala)|single nucleotide variant|Pathogenic|MYC|criteria provided, single submitter|8","3057137|NM_002467.6(MYC):c.738G>A (p.Pro246=)|single nucleotide variant|Benign|MYC|no assertion criteria provided|8","3058659|NM_002467.6(MYC):c.438G>A (p.Gln146=)|single nucleotide variant|Likely benign|MYC|no assertion criteria provided|8","3154445|NM_002467.6(MYC):c.1228A>G (p.Ile410Val)|single nucleotide variant|Uncertain significance|MYC|criteria provided, single submitter|8","3154448|NM_002467.6(MYC):c.1297G>C (p.Asp433His)|single nucleotide variant|Uncertain significance|MYC|criteria provided, single submitter|8","3257924|NM_002467.6(MYC):c.1177C>T (p.Arg393Cys)|single nucleotide variant||MYC||8","3297249|NM_002467.6(MYC):c.544G>A (p.Gly182Ser)|single nucleotide variant|Uncertain significance|MYC|criteria provided, single submitter|8","3400454|NM_002467.6(MYC):c.814G>A (p.Glu272Lys)|single nucleotide variant|Uncertain significance|MYC|criteria provided, single submitter|8","3764865|NM_002467.6(MYC):c.211C>A (p.Leu71Met)|single nucleotide variant||MYC||8","3764866|NM_002467.6(MYC):c.218C>A (p.Thr73Asn)|single nucleotide variant||MYC||8","3764867|NM_002467.6(MYC):c.490C>G (p.Leu164Val)|single nucleotide variant||MYC||8","3915251|NM_002467.6(MYC):c.688G>T (p.Ala230Ser)|single nucleotide variant|Uncertain significance|MYC|criteria provided, single submitter|8","4343267|NM_002467.6(MYC):c.-342C>T|single nucleotide variant||MYC||8","4343268|NM_002467.6(MYC):c.14G>A (p.Arg5Gln)|single nucleotide variant||MYC||8","4343269|NM_002467.6(MYC):c.30G>C (p.Gln10His)|single nucleotide variant||MYC||8","4343270|NM_002467.6(MYC):c.30+1G>A|single nucleotide variant||MYC||8","4343271|NM_002467.6(MYC):c.30+1G>T|single nucleotide variant||MYC||8","4343272|NM_002467.6(MYC):c.30+3A>C|single nucleotide variant||MYC||8","4343273|NM_002467.6(MYC):c.31-11C>A|single nucleotide variant||MYC||8","4530452|NM_002467.6(MYC):c.217_261del (p.Thr73_Pro87del)|Deletion||MYC||8","4530453|NM_002467.6(MYC):c.221C>T (p.Pro74Leu)|single nucleotide variant||MYC||8","4530454|NM_002467.6(MYC):c.176C>T (p.Ala59Val)|single nucleotide variant||MYC||8","4539640|NM_002467.6(MYC):c.17T>C (p.Val6Ala)|single nucleotide variant||MYC||8","4539641|NM_002467.6(MYC):c.229T>C (p.Ser77Pro)|single nucleotide variant||MYC||8","4539642|NM_002467.6(MYC):c.482C>T (p.Ser161Leu)|single nucleotide variant||MYC||8","4539643|NM_002467.6(MYC):c.770A>G (p.Glu257Gly)|single nucleotide variant||MYC||8","719682|NM_002467.6(MYC):c.1085C>T (p.Ser362Phe)|single nucleotide variant|Benign/Likely benign|MYC|criteria provided, multiple submitters, no conflicts|8","722844|NM_002467.6(MYC):c.64T>C (p.Phe22Leu)|single nucleotide variant|Benign/Likely benign|MYC|criteria provided, multiple submitters, no conflicts|8","791168|NM_002467.6(MYC):c.144G>A (p.Gln48=)|single nucleotide variant|Benign|MYC|criteria provided, multiple submitters, no conflicts|8","810340|GRCh37/hg19 8q24.21(chr8:128750494-128753204)x3|copy number gain|Likely pathogenic|MYC|criteria provided, single submitter|8","929760|NM_002467.6(MYC):c.478G>A (p.Val160Ile)|single nucleotide variant|Uncertain significance|MYC|criteria provided, single submitter|8"]}]}