WormBase Tree Display for Variation: WBVar01445796

WBVar01445796 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01445796
    Other_name: F09F7.7a.1:c.590+67A>G
    HGVSg: CHROMOSOME_III:g.5554097T>C
  Sequence_details: SMap: S_parent: Sequence: F09F7
    Flanking_sequences: ATATTCGCGTTTTTTTTGCAAAAATAAAAA TTTTTGTCGAATTTCTGCCGAAAATAATAT
    Mapping_target: F09F7
    Type_of_mutation: Substitution: t c
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00022928 From_analysis: WGS_Andersen
      WBStrain00022930 From_analysis: WGS_Andersen
          Million_mutation_project_reanalysis
      WBStrain00023150 From_analysis: WGS_Andersen
      WBStrain00023180 From_analysis: WGS_Andersen
      WBStrain00023211 From_analysis: WGS_Andersen
      WBStrain00023279 From_analysis: WGS_Andersen
    Laboratory: QX
    Person: WBPerson1730
    Analysis: WGS_Andersen
    DB_info: Database: dbSNP_rs rs 193332779
        dbSNP_ss ss 295508698
    Status: Live
  Affects: Gene: WBGene00017304
    Transcript: F09F7.7a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F09F7.7a.1:c.590+67A>G
        Intron_number: 5/6
  Reference: WBPaper00040707
  Method: WGS_Andersen