{"context":{"query":">>hgnc>>clinvar[germline_classification==\"Likely pathogenic\"]","source_dataset":"hgnc","target_dataset":"clinvar"},"stats":{"queried":1,"total":6,"mapped":1},"pagination":{"has_next":false},"schema":"id|name|type|germline_classification|gene_symbol|review_status|chromosome","mappings":[{"input":"HGNC:4851","source":"HGNC:4851|huntingtin","targets":["1357041|NM_001388492.1(HTT):c.8110-1G>A|single nucleotide variant|Likely pathogenic|HTT|criteria provided, single submitter|4","1375718|NM_001388492.1(HTT):c.1403-1G>C|single nucleotide variant|Likely pathogenic|HTT|criteria provided, single submitter|4","1687507|NM_001388492.1(HTT):c.54GCA[40] (p.Gln18_Gln38dup)|Microsatellite|Likely pathogenic|HTT|criteria provided, single submitter|4","3779747|NM_001388492.1(HTT):c.107del (p.Gln36fs)|Deletion|Likely pathogenic|HTT|criteria provided, single submitter|4","3779749|NM_001388492.1(HTT):c.99del (p.Gln33fs)|Deletion|Likely pathogenic|HTT|criteria provided, single submitter|4","3897713|NM_001388492.1:c.52CAG[55_59]|Microsatellite|Likely pathogenic|HTT|criteria provided, single submitter|"]}]}