WormBase Tree Display for Variation: WBVar01466317

WBVar01466317 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01466317
    Other_name: Y116F11B.12a.1:c.863-165G>C
      Y116F11B.12c.1:c.863-165G>C
      Y116F11B.12b.1:c.863-165G>C
      Y116F11B.12a.2:c.863-165G>C
    HGVSg: CHROMOSOME_V:g.19888820C>G
  Sequence_details: SMap: S_parent: Sequence: Y116F11B
    Flanking_sequences: GAATTCCCCGTGCCAATTAACCCCTAAACC CAGTTTTCAGAATTTTAGTGCGAAATCCCG
    Mapping_target: Y116F11B
    Type_of_mutation: Substitution: c g
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain (98)
    Laboratory: QX
    Person: WBPerson1730
    Analysis: WGS_Andersen
    DB_info: Database: dbSNP_rs rs 193351902
        dbSNP_ss ss 295527821
    Status: Live
  Affects: Gene: WBGene00001629
    Transcript: Y116F11B.12b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y116F11B.12b.1:c.863-165G>C
        Intron_number: 3/7
      Y116F11B.12a.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y116F11B.12a.2:c.863-165G>C
        Intron_number: 4/10
      Y116F11B.12a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y116F11B.12a.1:c.863-165G>C
        Intron_number: 5/11
      Y116F11B.12c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y116F11B.12c.1:c.863-165G>C
        Intron_number: 3/6
  Reference: WBPaper00040707
  Method: WGS_Andersen