WormBase Tree Display for Variation: WBVar00275066

WBVar00275066 Evidence: Paper_evidence: WBPaper00004281
  Name: Public_name: vs22
    Other_name: F16H9.1d.1:c.267+124_268-7del
      F16H9.1b.1:c.309+124_310-7del
      F16H9.2a.1:c.-23-20026_-23-19574del
      F16H9.1c.1:c.252+124_253-7del
      F16H9.2b.1:c.35-20026_35-19574del
      F16H9.1a.1:c.273+124_274-7del
    HGVSg: CHROMOSOME_X:g.12726877_12727329del
  Sequence_details: SMap: S_parent: Sequence: CHROMOSOME_X
    Flanking_sequences: tatatatatatatatatatatctcattact tttcaggctcgcattatctacgaagatttc
    Mapping_target: CHROMOSOME_X
    Type_of_mutation: Deletion
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Laboratory: LX
    Status: Live
  Affects: Gene: WBGene00008901
      WBGene00004345
    Transcript: F16H9.1a.1 VEP_consequence: splice_region_variant,intron_variant
        VEP_impact: LOW
        HGVSc: F16H9.1a.1:c.273+124_274-7del
        Intron_number: 5/6
      F16H9.2b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F16H9.2b.1:c.35-20026_35-19574del
        Intron_number: 1/3
      F16H9.1d.1 VEP_consequence: splice_region_variant,intron_variant
        VEP_impact: LOW
        HGVSc: F16H9.1d.1:c.267+124_268-7del
        Intron_number: 5/6
      F16H9.1c.1 VEP_consequence: splice_region_variant,intron_variant
        VEP_impact: LOW
        HGVSc: F16H9.1c.1:c.252+124_253-7del
        Intron_number: 5/6
      F16H9.2a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F16H9.2a.1:c.-23-20026_-23-19574del
        Intron_number: 1/4
      F16H9.1b.1 VEP_consequence: splice_region_variant,intron_variant
        VEP_impact: LOW
        HGVSc: F16H9.1b.1:c.309+124_310-7del
        Intron_number: 5/6
  Genetics: Interpolated_map_position: X 8.13237
  Reference: WBPaper00004281
  Method: Deletion_allele