WormBase Tree Display for Variation: WBVar01451642

WBVar01451642 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01451642
    Other_name: T26C12.1.1:c.1635-90C>T
    HGVSg: CHROMOSOME_IV:g.3262010C>T
  Sequence_details: SMap: S_parent: Sequence: T26C12
    Flanking_sequences: GTGGTGGGCGGAGTTTGAAGTCGTTTATTG TCGGAGCTCTTATTTTGGTAGGAATTCGCG
    Mapping_target: T26C12
    Type_of_mutation: Substitution: c t
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00005305 From_analysis: WGS_Andersen
      WBStrain00005315 From_analysis: WGS_Andersen
      WBStrain00031279 From_analysis: WGS_Andersen
      WBStrain00031284 From_analysis: WGS_Andersen
    Laboratory: QX
    Person: WBPerson1730
    Analysis: WGS_Andersen
    DB_info: Database: dbSNP_rs rs 193337299
        dbSNP_ss ss 295513218
    Status: Live
  Affects: Gene: WBGene00020831
    Transcript: T26C12.1.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T26C12.1.1:c.1635-90C>T
        Intron_number: 4/6
  Reference: WBPaper00040707
  Method: WGS_Andersen