WormBase Tree Display for Variation: WBVar01465010

WBVar01465010 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01465010
    Other_name: Y59A8B.13d.1:c.1167+1739C>T
      Y59A8B.13b.1:c.1212+1739C>T
      Y59A8B.13e.1:c.282+1739C>T
    HGVSg: CHROMOSOME_V:g.18096143C>T
  Sequence_details: SMap: S_parent: Sequence: Y59A8B
    Flanking_sequences: TCTAGGGGCTGATTTTGGTCGGAAAATAGT GGGAAAAAATATGTGTTTATCTGTCGCTTT
    Mapping_target: Y59A8B
    Type_of_mutation: Substitution: c t
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00006618 From_analysis: WGS_Andersen
    Laboratory: QX
    Person: WBPerson1730
    Analysis: WGS_Andersen
    DB_info: Database: dbSNP_rs rs 193350666
        dbSNP_ss ss 295526585
    Status: Live
  Affects: Gene: WBGene00013350
    Transcript: Y59A8B.13b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y59A8B.13b.1:c.1212+1739C>T
        Intron_number: 9/10
      Y59A8B.13e.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y59A8B.13e.1:c.282+1739C>T
        Intron_number: 1/1
      Y59A8B.13d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y59A8B.13d.1:c.1167+1739C>T
        Intron_number: 9/10
  Reference: WBPaper00040707
  Method: WGS_Andersen