WormBase Tree Display for Variation: WBVar01463228

WBVar01463228 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01463228
    Other_name: C01G10.11f.1:c.288-38G>C
      C01G10.11a.1:c.288-38G>C
      C01G10.11c.1:c.15-38G>C
      C01G10.11b.1:c.288-38G>C
    HGVSg: CHROMOSOME_V:g.15074743G>C
  Sequence_details: SMap: S_parent: Sequence: C01G10
    Flanking_sequences: TTAGTAGTAAAACATAAAAAATTTGTTTTT AGTTTTTCCAAAAATTAAGAAATTTCTAAA
    Mapping_target: C01G10
    Type_of_mutation: Substitution: g c
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00031279 From_analysis: WGS_Andersen
      WBStrain00031284 From_analysis: WGS_Andersen
    Laboratory: QX
    Person: WBPerson1730
    Analysis: WGS_Andersen
    DB_info: Database: dbSNP_rs rs 193348884
        dbSNP_ss ss 295524803
    Status: Live
  Affects: Gene: WBGene00305248
      WBGene00006808
      WBGene00305285
      WBGene00305247
    Transcript: C01G10.21
      C01G10.11f.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C01G10.11f.1:c.288-38G>C
        Intron_number: 4/11
      C01G10.11b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C01G10.11b.1:c.288-38G>C
        Intron_number: 4/9
      C01G10.11a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C01G10.11a.1:c.288-38G>C
        Intron_number: 4/10
      C25D7.19
      C01G10.20
      C01G10.11c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C01G10.11c.1:c.15-38G>C
        Intron_number: 1/6
  Reference: WBPaper00040707
  Method: WGS_Andersen