WormBase Tree Display for Variation: WBVar01431598

WBVar01431598 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01431598
    Other_name: F55A12.9c.1:c.49-382A>T
      F55A12.9a.1:c.64-382A>T
      F55A12.9b.1:c.25-382A>T
    HGVSg: CHROMOSOME_I:g.5376723T>A
  Sequence_details: SMap: S_parent: Sequence: F55A12
    Flanking_sequences: GTTGGCCCCCCCCCCCCTTTGCCATTTGAA CTACAGAATTCTTGCCGTGCCAACCTCTCT
    Mapping_target: F55A12
    Type_of_mutation: Substitution: t a
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00005835 From_analysis: WGS_Andersen
    Laboratory: QX
    Person: WBPerson1730
    Analysis: WGS_Andersen
    DB_info: Database: dbSNP_rs rs 193319661
        dbSNP_ss ss 295495578
    Status: Live
  Affects: Gene: WBGene00004131
    Transcript: F55A12.9a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F55A12.9a.1:c.64-382A>T
        Intron_number: 2/8
      F55A12.9c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F55A12.9c.1:c.49-382A>T
        Intron_number: 2/8
      F55A12.9b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F55A12.9b.1:c.25-382A>T
        Intron_number: 2/8
  Reference: WBPaper00040707
  Method: WGS_Andersen