WormBase Tree Display for Variation: WBVar02127476

WBVar02127476 Evidence: Paper_evidence: WBPaper00045317
  Name: Public_name: h3937
    Other_name: B0414.2.3:c.498+156G>A
      B0414.2.2:c.498+156G>A
      B0414.2.1:c.498+156G>A
    HGVSg: CHROMOSOME_I:g.5787424G>A
  Sequence_details: SMap: S_parent: Sequence: B0414
    Flanking_sequences: AGAAGTACAGTAGTCTCCTTTTTCTGAAATCGAGGCAAAT AAAACGCTCCGCCCCCTCATGTTGGGTCTCGTTAGGTATT
    Mapping_target: CHROMOSOME_I
    Source_location: 200 CHROMOSOME_I 5787427 5787427
    Type_of_mutation: Substitution: G A
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023775
    Laboratory: KR
    Analysis: WGS_Rose
    Status: Live
  Affects: Gene: WBGene00004393
    Transcript: B0414.2.3 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: B0414.2.3:c.498+156G>A
        Intron_number: 9/12
      B0414.2.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: B0414.2.2:c.498+156G>A
        Intron_number: 9/12
      B0414.2.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: B0414.2.1:c.498+156G>A
        Intron_number: 6/9
  Reference: WBPaper00040589
    WBPaper00000975
    WBPaper00003985
    WBPaper00000699
    WBPaper00045317
  Method: WGS_Rose