WormBase Tree Display for Variation: WBVar02136291

WBVar02136291 Evidence: Paper_evidence: WBPaper00045317
  Name: Public_name: h3639
    Other_name: T19H12.5.1:c.839-187C>T
    HGVSg: CHROMOSOME_V:g.4869696C>T
  Sequence_details: SMap: S_parent: Sequence: T19H12
    Flanking_sequences: TTTATATAAGGTAACCTCAACTACAATCTAGGTTGCTCAT TTTTCCGTGCACCACCAACACATTTATTCTAGTTTCCATA
    Mapping_target: CHROMOSOME_V
    Source_location: 200 CHROMOSOME_V 4869682 4869682
    Type_of_mutation: Substitution: C T
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023882
    Laboratory: KR
    Analysis: WGS_Rose
    Status: Live
  Affects: Gene: WBGene00005110
    Transcript: T19H12.5.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T19H12.5.1:c.839-187C>T
        Intron_number: 6/7
  Reference: WBPaper00040589
    WBPaper00000975
    WBPaper00003985
    WBPaper00000699
    WBPaper00045317
  Method: WGS_Rose