WormBase Tree Display for Variation: WBVar02126015

WBVar02126015 Evidence: Paper_evidence: WBPaper00045317
  Name: Public_name: h8633
    Other_name: Y18H1A.3a.1:c.1438-96G>A
      Y18H1A.3e.1:c.1792-96G>A
      Y18H1A.3c.1:c.118-96G>A
      Y18H1A.3d.1:c.775-96G>A
    HGVSg: CHROMOSOME_I:g.704646C>T
  Sequence_details: SMap: S_parent: Sequence: Y18H1A
    Flanking_sequences: CAACAACAGAAAAAAATGCTGAAAAGGCATTTTTCAGGGT TATTTTCACAATGAGTTTGGGTATAAATTGGAGAGTTTTC
    Mapping_target: CHROMOSOME_I
    Source_location: 200 CHROMOSOME_I 704649 704649
    Type_of_mutation: Substitution: C T
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023676
    Laboratory: KR
    Analysis: WGS_Rose
    Status: Live
  Affects: Gene: WBGene00021209
    Transcript: Y18H1A.3c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y18H1A.3c.1:c.118-96G>A
        Intron_number: 1/4
      Y18H1A.3a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y18H1A.3a.1:c.1438-96G>A
        Intron_number: 8/12
      Y18H1A.3d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y18H1A.3d.1:c.775-96G>A
        Intron_number: 3/6
      Y18H1A.3e.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y18H1A.3e.1:c.1792-96G>A
        Intron_number: 8/11
  Reference: WBPaper00040589
    WBPaper00000975
    WBPaper00003985
    WBPaper00000699
    WBPaper00045317
  Method: WGS_Rose