WormBase Tree Display for Variation: WBVar01274156

WBVar01274156 Evidence: Paper_evidence: WBPaper00037807
  Name: Public_name: WBVar01274156
    Other_name: cewivar00029953
      F45G2.2b.3:c.1063-128G>T
      F45G2.2a.1:c.3598-128G>T
      F45G2.2b.1:c.1063-128G>T
      F45G2.2b.2:c.1063-128G>T
    HGVSg: CHROMOSOME_III:g.13423102G>T
  Sequence_details: SMap: S_parent: Sequence: F45G2
    Flanking_sequences: AGCAAAAAAGAGATAATATGCGTCGAAATTGATGAAAACTGGAAAAATAG CGGGGCTTAGGAACATGGTAACTCAAATCAAGAAATCAGCAAGATGTGAA
    Mapping_target: F45G2
    Type_of_mutation: Substitution: g T Paper_evidence: WBPaper00037807
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain (93)
    Laboratory: AX
    Analysis: WGS_De_Bono
      Million_mutation_project_reanalysis
      WGS_Andersen
    DB_info: Database: dbSNP_ss ss 539108684
    History: Acquires_merge: WBVar01449874
    Status: Live
  Affects: Gene: WBGene00009730
    Transcript: F45G2.2b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F45G2.2b.1:c.1063-128G>T
        Intron_number: 7/8
      F45G2.2b.3 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F45G2.2b.3:c.1063-128G>T
        Intron_number: 8/9
      F45G2.2b.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F45G2.2b.2:c.1063-128G>T
        Intron_number: 20/21
      F45G2.2a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F45G2.2a.1:c.3598-128G>T
        Intron_number: 23/24
  Reference: WBPaper00037807
  Method: WGS_De_Bono