--- 
- 
  allele_string: -/CTG
  assembly_name: GRCh37
  colocated_variants: 
    - 
      allele_string: COSMIC_MUTATION
      end: 124887095
      id: COSV105907233
      phenotype_or_disease: 1
      seq_region_name: 12
      somatic: 1
      start: 124887096
      strand: 1
      var_synonyms: 
        COSMIC: 
          - COSM9961721
    - 
      allele_string: COSMIC_MUTATION
      end: 124887095
      id: COSV105907316
      phenotype_or_disease: 1
      seq_region_name: 12
      somatic: 1
      start: 124887096
      strand: 1
      var_synonyms: 
        COSMIC: 
          - COSM10008089
    - 
      allele_string: COSMIC_MUTATION
      end: 124887095
      id: COSV62292713
      phenotype_or_disease: 1
      seq_region_name: 12
      somatic: 1
      start: 124887096
      strand: 1
      var_synonyms: 
        COSMIC: 
          - COSM1476307
    - 
      allele_string: COSMIC_MUTATION
      end: 124887095
      id: COSV62292935
      phenotype_or_disease: 1
      seq_region_name: 12
      somatic: 1
      start: 124887096
      strand: 1
      var_synonyms: 
        COSMIC: 
          - COSM2227124
    - 
      allele_string: COSMIC_MUTATION
      end: 124887095
      id: COSV62300054
      phenotype_or_disease: 1
      seq_region_name: 12
      somatic: 1
      start: 124887096
      strand: 1
      var_synonyms: 
        COSMIC: 
          - COSM5970587
    - 
      allele_string: COSMIC_MUTATION
      end: 124887095
      id: COSV62304776
      phenotype_or_disease: 1
      seq_region_name: 12
      somatic: 1
      start: 124887096
      strand: 1
      var_synonyms: 
        COSMIC: 
          - COSM2227132
  end: 124887095
  id: 12:g124887095_124887096insCTG
  input: 12:g124887095_124887096insCTG
  most_severe_consequence: inframe_insertion
  regulatory_feature_consequences: 
    - 
      biotype: enhancer
      consequence_terms: 
        - regulatory_region_variant
      impact: MODIFIER
      regulatory_feature_id: ENSR00001046314
      variant_allele: CTG
  seq_region_name: 12
  start: 124887096
  strand: 1
  transcript_consequences: 
    - 
      amino_acids: -/Q
      biotype: protein_coding
      cdna_end: 1961
      cdna_start: 1960
      cds_end: 1492
      cds_start: 1491
      codons: -/CAG
      consequence_terms: 
        - inframe_insertion
      gene_id: 9612
      gene_symbol: NCOR2
      gene_symbol_source: EntrezGene
      given_ref: "-"
      hgvs_offset: -37
      hgvsc: NM_001077261.4:c.1526_1528dup
      hgvsp: NP_001070729.2:p.Pro510_Met511insAla
      impact: MODERATE
      protein_end: 498
      protein_start: 497
      strand: -1
      transcript_id: NM_001077261.4
      used_ref: "-"
      variant_allele: CTG
    - 
      amino_acids: -/Q
      biotype: protein_coding
      cdna_end: 1961
      cdna_start: 1960
      cds_end: 1492
      cds_start: 1491
      codons: -/CAG
      consequence_terms: 
        - inframe_insertion
      gene_id: 9612
      gene_symbol: NCOR2
      gene_symbol_source: EntrezGene
      given_ref: "-"
      hgvs_offset: -37
      hgvsc: NM_001206654.2:c.1526_1528dup
      hgvsp: NP_001193583.1:p.Pro510_Met511insAla
      impact: MODERATE
      protein_end: 498
      protein_start: 497
      strand: -1
      transcript_id: NM_001206654.2
      used_ref: "-"
      variant_allele: CTG
    - 
      amino_acids: -/Q
      biotype: protein_coding
      cdna_end: 1964
      cdna_start: 1963
      cds_end: 1495
      cds_start: 1494
      codons: -/CAG
      consequence_terms: 
        - inframe_insertion
      gene_id: 9612
      gene_symbol: NCOR2
      gene_symbol_source: EntrezGene
      given_ref: "-"
      hgvs_offset: -37
      hgvsc: NM_006312.6:c.1529_1531dup
      hgvsp: NP_006303.4:p.Pro511_Met512insAla
      impact: MODERATE
      protein_end: 499
      protein_start: 498
      strand: -1
      transcript_id: NM_006312.6
      used_ref: "-"
      variant_allele: CTG