WormBase Tree Display for Variation: WBVar01394171

WBVar01394171 Evidence: Paper_evidence: WBPaper00037807
  Name: Public_name: WBVar01394171
    Other_name: C05D12.3a.1:c.2621-110del
      C05D12.3c.2:c.2621-110del
      C05D12.3c.3:c.2621-110del
      C05D12.3c.1:c.2621-110del
    HGVSg: CHROMOSOME_II:g.11429616del
  Sequence_details: SMap: S_parent: Sequence: C05D12
    Flanking_sequences: GATCACGCCTGTAGGCAGGCCAGCATGCATTTCGGCGCCTACAGCCATCA GGGGGGGGGGGTCTGGAGGCAACTTCCTGATGATAGGAAGCTGCTTCTAA
    Mapping_target: C05D12
    Type_of_mutation: Deletion: G Paper_evidence: WBPaper00037807
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00006642 From_analysis: WGS_De_Bono
    Laboratory: AX
    Analysis: WGS_De_Bono
    DB_info: Database: dbSNP_ss ss 539113549
    Status: Live
  Affects: Gene: WBGene00014666
    Transcript: C05D12.3a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C05D12.3a.1:c.2621-110del
        Intron_number: 13/15
      C05D12.3c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C05D12.3c.1:c.2621-110del
        Intron_number: 13/17
      C05D12.3c.3 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C05D12.3c.3:c.2621-110del
        Intron_number: 12/17
      C05D12.3c.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C05D12.3c.2:c.2621-110del
        Intron_number: 13/16
  Reference: WBPaper00037807
  Method: WGS_De_Bono