WormBase Tree Display for Variation: WBVar00320885

WBVar00320885 Evidence: Paper_evidence: WBPaper00037659
  Name: Public_name: snx3313
    Other_name: IS657_3671
      Y59A8B.22d.1:c.19-531C>A
      Y59A8B.22a.1:c.1054-531C>A
      Y59A8B.22b.1:c.763-531C>A
      Y59A8B.22c.1:c.664-531C>A
    HGVSg: CHROMOSOME_V:g.17972112G>T
  Sequence_details: SMap: S_parent: Sequence: Y59A8B
    Flanking_sequences: AAAATGCGGAAAATCTTTTTTGTTTTTTTTTTTTTTTTTGGGATTTTCAG GAAAATTTCAGATTTTTAATTAGAAAATTGATTTTTTTTTTCACATTTTC
    Mapping_target: Y59A8B
    Type_of_mutation: Substitution: G T
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00022164
    Laboratory: IS
    Analysis: WGS_Jarriault
    Status: Live
  Affects: Gene: WBGene00013354
    Transcript: Y59A8B.22b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y59A8B.22b.1:c.763-531C>A
        Intron_number: 6/8
      Y59A8B.22d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y59A8B.22d.1:c.19-531C>A
        Intron_number: 1/3
      Y59A8B.22a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y59A8B.22a.1:c.1054-531C>A
        Intron_number: 8/11
      Y59A8B.22c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y59A8B.22c.1:c.664-531C>A
        Intron_number: 5/7
  Genetics: Map: V
  Reference: WBPaper00037659
  Method: WGS_Jarriault