WormBase Tree Display for Variation: WBVar01289358

WBVar01289358 Evidence: Paper_evidence: WBPaper00037807
  Name: Public_name: WBVar01289358
    Other_name: cewivar00325895
      C37A5.9.1:c.105+122T>G
    HGVSg: CHROMOSOME_I:g.14179130A>C
  Sequence_details: SMap: S_parent: Sequence: C37A5
    Flanking_sequences: AAAATTTCAAATATTGGAACTTTGGGTCCCGCAGCAAAAGAAAATCTAAA ATTTTGCGCCAAAACCTAAAAATTTTCAAAATCATCGTAAAAATGTCATG
    Mapping_target: C37A5
    Type_of_mutation: Substitution: a C Paper_evidence: WBPaper00037807
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00006629 From_analysis: Million_mutation_project_reanalysis
      WBStrain00006642 From_analysis: WGS_De_Bono
      WBStrain00006643 From_analysis: Million_mutation_project_reanalysis
      WBStrain00006645 From_analysis: Million_mutation_project_reanalysis
      WBStrain00022850 From_analysis: WGS_De_Bono
          Million_mutation_project_reanalysis
      WBStrain00023018 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023191 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023665 From_analysis: Million_mutation_project_reanalysis
      WBStrain00027652 From_analysis: Million_mutation_project_reanalysis
    Laboratory: AX
    Analysis: WGS_De_Bono
      Million_mutation_project_reanalysis
    DB_info: Database: dbSNP_ss ss 539148703
    History: Acquires_merge: WBVar01428140
    Status: Live
  Affects: Gene: WBGene00004202
    Transcript: C37A5.9.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C37A5.9.1:c.105+122T>G
        Intron_number: 2/13
  Reference: WBPaper00037807
  Method: WGS_De_Bono