WormBase Tree Display for Variation: WBVar02127761

WBVar02127761 Evidence: Paper_evidence: WBPaper00045317
  Name: Public_name: h16849
    Other_name: W01A8.2a.3:c.*4+270G>A
      W01A8.2a.1:c.*274G>A
      W01A8.2a.2:c.*4+270G>A
    HGVSg: CHROMOSOME_I:g.7055339C>T
  Sequence_details: SMap: S_parent: Sequence: W01A8
    Flanking_sequences: TTTCGAAATTATGCGAGTTTTACTCCAAAAGTACAGTACC AGTCTCGCGACGACAAATTTTTGTTAAATACAAAAGCGTG
    Mapping_target: CHROMOSOME_I
    Source_location: 200 CHROMOSOME_I 7055338 7055338
    Type_of_mutation: Substitution: C T
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023779
    Laboratory: KR
    Analysis: WGS_Rose
    Status: Live
  Affects: Gene: WBGene00012164
    Transcript: W01A8.2a.3 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: W01A8.2a.3:c.*4+270G>A
        Intron_number: 5/6
      W01A8.2a.1 VEP_consequence: 3_prime_UTR_variant
        VEP_impact: MODIFIER
        HGVSc: W01A8.2a.1:c.*274G>A
        cDNA_position: 723
        Exon_number: 6/6
      W01A8.2a.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: W01A8.2a.2:c.*4+270G>A
        Intron_number: 5/5
  Reference: WBPaper00040589
    WBPaper00000975
    WBPaper00003985
    WBPaper00000699
    WBPaper00045317
  Method: WGS_Rose