{"context":{"query":">>hgnc>>gencc","source_dataset":"hgnc","target_dataset":"gencc"},"stats":{"queried":1,"total":15,"mapped":1},"pagination":{"has_next":false},"schema":"id|gene_symbol|disease_title|classification_title|moi_title|submitter_title","mappings":[{"input":"HGNC:1097","source":"HGNC:1097|B-Raf proto-oncogene, serine/threonine kinase","targets":["GENCC_000101-HGNC_1097-MONDO_0016684-HP_0000006-GENCC_100004|BRAF|anaplastic astrocytoma|Limited|Autosomal dominant|Ambry Genetics","GENCC_000101-HGNC_1097-OMIM_115150-HP_0000006-GENCC_100001|BRAF|cardiofaciocutaneous syndrome 1|Definitive|Autosomal dominant|Ambry Genetics","GENCC_000101-HGNC_1097-OMIM_613706-HP_0000006-GENCC_100003|BRAF|Noonan syndrome 7|Moderate|Autosomal dominant|Ambry Genetics","GENCC_000101-HGNC_1097-OMIM_613707-HP_0000006-GENCC_100004|BRAF|LEOPARD syndrome 3|Limited|Autosomal dominant|Ambry Genetics","GENCC_000104-HGNC_1097-OMIM_115150-HP_0000006-GENCC_100002|BRAF|cardiofaciocutaneous syndrome 1|Strong|Autosomal dominant|Genomics England PanelApp","GENCC_000104-HGNC_1097-OMIM_613706-HP_0000006-GENCC_100002|BRAF|Noonan syndrome 7|Strong|Autosomal dominant|Genomics England PanelApp","GENCC_000104-HGNC_1097-OMIM_613707-HP_0000006-GENCC_100002|BRAF|LEOPARD syndrome 3|Strong|Autosomal dominant|Genomics England PanelApp","GENCC_000106-HGNC_1097-OMIM_115150-HP_0000006-GENCC_100002|BRAF|cardiofaciocutaneous syndrome 1|Strong|Autosomal dominant|Labcorp Genetics (formerly Invitae)","GENCC_000106-HGNC_1097-OMIM_613706-HP_0000006-GENCC_100002|BRAF|Noonan syndrome 7|Strong|Autosomal dominant|Labcorp Genetics (formerly Invitae)","GENCC_000106-HGNC_1097-OMIM_613707-HP_0000006-GENCC_100002|BRAF|LEOPARD syndrome 3|Strong|Autosomal dominant|Labcorp Genetics (formerly Invitae)","GENCC_000110-HGNC_1097-ORPHANET_1340-HP_0000006-GENCC_100009|BRAF|cardiofaciocutaneous syndrome|Supportive|Autosomal dominant|Orphanet","GENCC_000110-HGNC_1097-ORPHANET_500-HP_0000006-GENCC_100009|BRAF|Noonan syndrome with multiple lentigines|Supportive|Autosomal dominant|Orphanet","GENCC_000112-HGNC_1097-OMIM_115150-HP_0000006-GENCC_100001|BRAF|cardiofaciocutaneous syndrome 1|Definitive|Autosomal dominant|G2P","GENCC_000112-HGNC_1097-OMIM_613706-HP_0000006-GENCC_100001|BRAF|Noonan syndrome 7|Definitive|Autosomal dominant|G2P","GENCC_000112-HGNC_1097-OMIM_613707-HP_0000006-GENCC_100001|BRAF|LEOPARD syndrome 3|Definitive|Autosomal dominant|G2P"]}]}