--- 
- 
  allele_string: ACCTAGGAGATAACACAGGCCCAAGATGAGGCCAGTGCGCCTTGGGGAGACCTGTGGCAAGCAGGGGAGGCCTTTTTTTTTTTTTTTTGAGATGGAATCTCGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCGTGATCTCAGCTCACTGCAAGCTCCACCGCCCAGGTTCACGCCATTCTCCTTCCTCAGCCTCCCGAGTAGCTGGGACTACAGGTGCCCAGCACCACGCCCGGCTAATTTTTTTTTGTATTTTTCAGTAGAGACGGGGTTTCACCGTTAGCCAGGATGGTCTCGATCTCCCAACCTCGTGATCCGCCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGCGCCCAGCCAAGCAGGGGAGGCCCTTAGCCTCTGTAAGCTTCAGTTTTTTCAACTGTGCAATAGTTAAACCCATTTACTTTGCACATCTCATGGGGTTATAGGGAGGTCAAATAAGCAGCAGGAGAAAGCCCCCCTACTGCTCACCTGGAGGGCCACTGACAACCACCCTTAACCCCTCCTCCCAGAGACCCCAGTTGCAAACCAG/-
  assembly_name: GRCh37
  end: 7578174
  id: 17:g.7577607_7578174del
  input: 17:g.7577607_7578174del
  most_severe_consequence: splice_acceptor_variant
  seq_region_name: 17
  start: 7577607
  strand: 1
  transcript_consequences: 
    - 
      biotype: protein_coding
      cdna_end: 864
      cds_end: 674
      consequence_terms: 
        - splice_acceptor_variant
        - splice_donor_5th_base_variant
        - coding_sequence_variant
        - intron_variant
      gene_id: ENSG00000141510
      gene_symbol: TP53
      gene_symbol_source: HGNC
      hgnc_id: 11998
      impact: HIGH
      protein_end: 225
      strand: -1
      transcript_id: ENST00000269305
      variant_allele: "-"
    - 
      biotype: protein_coding
      cdna_end: 674
      cds_end: 674
      consequence_terms: 
        - splice_acceptor_variant
        - splice_donor_5th_base_variant
        - coding_sequence_variant
        - intron_variant
      gene_id: ENSG00000141510
      gene_symbol: TP53
      gene_symbol_source: HGNC
      hgnc_id: 11998
      impact: HIGH
      protein_end: 225
      strand: -1
      transcript_id: ENST00000359597
      variant_allele: "-"
    - 
      biotype: protein_coding
      cdna_end: 674
      cds_end: 674
      consequence_terms: 
        - splice_acceptor_variant
        - splice_donor_5th_base_variant
        - coding_sequence_variant
        - intron_variant
      gene_id: ENSG00000141510
      gene_symbol: TP53
      gene_symbol_source: HGNC
      hgnc_id: 11998
      impact: HIGH
      protein_end: 225
      strand: -1
      transcript_id: ENST00000413465
      variant_allele: "-"
    - 
      biotype: protein_coding
      cdna_end: 807
      cds_end: 674
      consequence_terms: 
        - splice_acceptor_variant
        - splice_donor_5th_base_variant
        - coding_sequence_variant
        - intron_variant
      gene_id: ENSG00000141510
      gene_symbol: TP53
      gene_symbol_source: HGNC
      hgnc_id: 11998
      impact: HIGH
      protein_end: 225
      strand: -1
      transcript_id: ENST00000420246
      variant_allele: "-"
    - 
      biotype: protein_coding
      cdna_end: 810
      cds_end: 674
      consequence_terms: 
        - splice_acceptor_variant
        - splice_donor_5th_base_variant
        - coding_sequence_variant
        - intron_variant
      gene_id: ENSG00000141510
      gene_symbol: TP53
      gene_symbol_source: HGNC
      hgnc_id: 11998
      impact: HIGH
      protein_end: 225
      strand: -1
      transcript_id: ENST00000445888
      variant_allele: "-"
    - 
      biotype: protein_coding
      cdna_end: 807
      cds_end: 674
      consequence_terms: 
        - splice_acceptor_variant
        - splice_donor_5th_base_variant
        - coding_sequence_variant
        - intron_variant
      gene_id: ENSG00000141510
      gene_symbol: TP53
      gene_symbol_source: HGNC
      hgnc_id: 11998
      impact: HIGH
      protein_end: 225
      strand: -1
      transcript_id: ENST00000455263
      variant_allele: "-"
    - 
      biotype: protein_coding
      consequence_terms: 
        - downstream_gene_variant
      distance: 373
      flags: 
        - cds_end_NF
      gene_id: ENSG00000141510
      gene_symbol: TP53
      gene_symbol_source: HGNC
      hgnc_id: 11998
      impact: MODIFIER
      strand: -1
      transcript_id: ENST00000503591
      variant_allele: "-"
    - 
      biotype: retained_intron
      cdna_end: 556
      consequence_terms: 
        - splice_acceptor_variant
        - splice_donor_5th_base_variant
        - non_coding_transcript_exon_variant
        - intron_variant
      gene_id: ENSG00000141510
      gene_symbol: TP53
      gene_symbol_source: HGNC
      hgnc_id: 11998
      impact: HIGH
      strand: -1
      transcript_id: ENST00000504290
      variant_allele: "-"
    - 
      biotype: retained_intron
      cdna_end: 556
      consequence_terms: 
        - splice_acceptor_variant
        - splice_donor_5th_base_variant
        - non_coding_transcript_exon_variant
        - intron_variant
      gene_id: ENSG00000141510
      gene_symbol: TP53
      gene_symbol_source: HGNC
      hgnc_id: 11998
      impact: HIGH
      strand: -1
      transcript_id: ENST00000504937
      variant_allele: "-"
    - 
      biotype: retained_intron
      cdna_end: 931
      cdna_start: 931
      consequence_terms: 
        - non_coding_transcript_exon_variant
      gene_id: ENSG00000141510
      gene_symbol: TP53
      gene_symbol_source: HGNC
      hgnc_id: 11998
      impact: MODIFIER
      strand: -1
      transcript_id: ENST00000505014
      variant_allele: "-"
    - 
      biotype: protein_coding
      consequence_terms: 
        - downstream_gene_variant
      distance: 260
      flags: 
        - cds_end_NF
      gene_id: ENSG00000141510
      gene_symbol: TP53
      gene_symbol_source: HGNC
      hgnc_id: 11998
      impact: MODIFIER
      strand: -1
      transcript_id: ENST00000508793
      variant_allele: "-"
    - 
      biotype: protein_coding
      cdna_end: 410
      cds_end: 278
      consequence_terms: 
        - splice_acceptor_variant
        - splice_donor_5th_base_variant
        - coding_sequence_variant
        - intron_variant
      flags: 
        - cds_end_NF
      gene_id: ENSG00000141510
      gene_symbol: TP53
      gene_symbol_source: HGNC
      hgnc_id: 11998
      impact: HIGH
      protein_end: 93
      strand: -1
      transcript_id: ENST00000509690
      variant_allele: "-"
    - 
      biotype: retained_intron
      cdna_end: 556
      consequence_terms: 
        - splice_acceptor_variant
        - splice_donor_5th_base_variant
        - non_coding_transcript_exon_variant
        - intron_variant
      gene_id: ENSG00000141510
      gene_symbol: TP53
      gene_symbol_source: HGNC
      hgnc_id: 11998
      impact: HIGH
      strand: -1
      transcript_id: ENST00000510385
      variant_allele: "-"
    - 
      biotype: protein_coding
      cdna_end: 474
      cds_end: 395
      consequence_terms: 
        - splice_acceptor_variant
        - splice_donor_5th_base_variant
        - coding_sequence_variant
        - intron_variant
      flags: 
        - cds_end_NF
      gene_id: ENSG00000141510
      gene_symbol: TP53
      gene_symbol_source: HGNC
      hgnc_id: 11998
      impact: HIGH
      protein_end: 132
      strand: -1
      transcript_id: ENST00000514944
      variant_allele: "-"
    - 
      biotype: processed_transcript
      cdna_end: 69
      consequence_terms: 
        - splice_acceptor_variant
        - non_coding_transcript_exon_variant
        - intron_variant
      gene_id: ENSG00000141510
      gene_symbol: TP53
      gene_symbol_source: HGNC
      hgnc_id: 11998
      impact: HIGH
      strand: -1
      transcript_id: ENST00000574684
      variant_allele: "-"
    - 
      biotype: protein_coding
      consequence_terms: 
        - upstream_gene_variant
      distance: 702
      flags: 
        - cds_start_NF
      gene_id: ENSG00000141510
      gene_symbol: TP53
      gene_symbol_source: HGNC
      hgnc_id: 11998
      impact: MODIFIER
      strand: -1
      transcript_id: ENST00000576024
      variant_allele: "-"
    - 
      biotype: protein_coding
      consequence_terms: 
        - downstream_gene_variant
      distance: 306
      flags: 
        - cds_end_NF
      gene_id: ENSG00000141510
      gene_symbol: TP53
      gene_symbol_source: HGNC
      hgnc_id: 11998
      impact: MODIFIER
      strand: -1
      transcript_id: ENST00000604348
      variant_allele: "-"