{"allele_string": "T/G", "transcript_consequences": [{"strand": 1, "amino_acids": "T", "codons": "acT/acG", "transcript_id": "ENST00000380152", "gene_id": "ENSG00000139618", "consequence_terms": ["synonymous_variant"], "gene_symbol_source": "HGNC", "biotype": "protein_coding", "cds_end": 2601, "cadd_phred": 1.39, "protein_end": 867, "gene_symbol": "BRCA2", "cdna_start": 2834, "cdna_end": 2834, "variant_allele": "G", "cadd_raw": -0.101183, "impact": "LOW", "protein_start": 867, "cds_start": 2601, "hgnc_id": 1101}, {"strand": 1, "cadd_raw": -0.101183, "variant_allele": "G", "transcript_id": "ENST00000530893", "gene_id": "ENSG00000139618", "consequence_terms": ["downstream_gene_variant"], "distance": 3665, "biotype": "protein_coding", "impact": "MODIFIER", "gene_symbol_source": "HGNC", "gene_symbol": "BRCA2", "cadd_phred": 1.39, "flags": ["cds_end_NF"], "hgnc_id": 1101}, {"hgnc_id": 1101, "cds_start": 2601, "impact": "LOW", "protein_start": 867, "variant_allele": "G", "cadd_raw": -0.101183, "cdna_end": 2828, "cdna_start": 2828, "canonical": 1, "cds_end": 2601, "cadd_phred": 1.39, "gene_symbol": "BRCA2", "protein_end": 867, "gene_symbol_source": "HGNC", "biotype": "protein_coding", "consequence_terms": ["synonymous_variant"], "gene_id": "ENSG00000139618", "transcript_id": "ENST00000544455", "amino_acids": "T", "codons": "acT/acG", "strand": 1}], "input": "13:g.32911093T>G", "strand": 1, "colocated_variants": [{"id": "rs730881589", "strand": 1, "frequencies": {"G": {"gnomad_eas": 0, "gnomad_sas": 4.065e-05, "gnomad_amr": 3.894e-05, "gnomad": 9.029e-06, "gnomad_afr": 0, "gnomad_nfe": 0, "gnomad_fin": 0, "gnomad_asj": 0, "gnomad_oth": 0}}, "clin_sig": ["likely_benign"], "start": 32911093, "allele_string": "T/G", "phenotype_or_disease": 1, "end": 32911093, "clin_sig_allele": "G:benign/likely_benign;G:likely_benign", "seq_region_name": "13"}], "id": "13:g.32911093T>G", "most_severe_consequence": "synonymous_variant", "assembly_name": "GRCh37", "start": 32911093, "end": 32911093, "seq_region_name": "13"}