WormBase Tree Display for Variation: WBVar00323166

WBVar00323166 Evidence: Paper_evidence: WBPaper00031335
  Name: Public_name: nDf60
    Other_name: F25G6.2.1:c.3418-1678_3418-87del
    HGVSg: CHROMOSOME_V:g.8579529_8581120del
  Sequence_details: SMap: S_parent: Sequence: C10B5
    Flanking_sequences: TCGCACACGTCTTCTGTTTGACGATGATGG TCTTTTTGGGTTACTGTAGTTGCTCTTTGG
    Mapping_target: C10B5
    Type_of_mutation: Deletion
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00027503
      WBStrain00027580
    Laboratory: MT
    Status: Live
  Affects: Gene: WBGene00017796
      WBGene00023455
      WBGene00023454
      WBGene00017797
    Transcript: F25G6.11
      F25G6.1.4 VEP_consequence: 3_prime_UTR_variant
        VEP_impact: MODIFIER
        cDNA_position: 2598-?
        Exon_number: 18/18
      F25G6.1.3 VEP_consequence: 3_prime_UTR_variant
        VEP_impact: MODIFIER
        cDNA_position: 2601-?
        Exon_number: 18/18
      F25G6.1.2 VEP_consequence: 3_prime_UTR_variant
        VEP_impact: MODIFIER
        cDNA_position: 3580-?
        Exon_number: 18/18
      F25G6.1.1 VEP_consequence: 3_prime_UTR_variant
        VEP_impact: MODIFIER
        cDNA_position: 3591-?
        Exon_number: 19/19
      F25G6.1.5 VEP_consequence: 3_prime_UTR_variant
        VEP_impact: MODIFIER
        cDNA_position: 2641-?
        Exon_number: 17/17
      F25G6.10
      F25G6.2.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F25G6.2.1:c.3418-1678_3418-87del
        Intron_number: 5/7
  Genetics: Interpolated_map_position: V 1.47492
  Reference: WBPaper00031335
  Method: Deletion_allele