WormBase Tree Display for Variation: WBVar02126671

WBVar02126671 Evidence: Paper_evidence: WBPaper00045317
  Name: Public_name: h4570
    Other_name: F32B5.7b.1:c.544-413G>A
      F32B5.7a.2:c.760-413G>A
      F32B5.7a.1:c.760-413G>A
    HGVSg: CHROMOSOME_I:g.2677161C>T
  Sequence_details: SMap: S_parent: Sequence: F32B5
    Flanking_sequences: TTTTGCCAGAAGTTCTCATTCCGGCAATTTGCCGACTTGC GATTTGCCGGAAATTTTGATTTTCGGCAAATTGCGGATTC
    Mapping_target: CHROMOSOME_I
    Source_location: 200 CHROMOSOME_I 2677162 2677162
    Type_of_mutation: Substitution: C T
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023661
    Laboratory: KR
    Analysis: WGS_Rose
    Status: Live
  Affects: Gene: WBGene00017980
    Transcript: F32B5.7a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F32B5.7a.1:c.760-413G>A
        Intron_number: 7/12
      F32B5.7a.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F32B5.7a.2:c.760-413G>A
        Intron_number: 7/13
      F32B5.7b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F32B5.7b.1:c.544-413G>A
        Intron_number: 5/9
  Reference: WBPaper00040589
    WBPaper00000975
    WBPaper00003985
    WBPaper00000699
    WBPaper00045317
  Method: WGS_Rose