WormBase Tree Display for Variation: WBVar01438341

WBVar01438341 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01438341
    Other_name: C52E12.2a.1:c.2214-37G>A
      C52E12.2a.2:c.2214-37G>A
      C52E12.2b.1:c.2214-37G>A
    HGVSg: CHROMOSOME_II:g.7004622G>A
  Sequence_details: SMap: S_parent: Sequence: C52E12
    Flanking_sequences: AATAATAAATTGAGCAATTTTGAAAACTTT TTAACTGAGAATTCTCTTAAATATCGAATA
    Mapping_target: C52E12
    Type_of_mutation: Substitution: g a
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00031279 From_analysis: WGS_Andersen
      WBStrain00031284 From_analysis: WGS_Andersen
    Laboratory: QX
    Person: WBPerson1730
    Analysis: WGS_Andersen
    DB_info: Database: dbSNP_rs rs 193326402
        dbSNP_ss ss 295502321
    Status: Live
  Affects: Gene: WBGene00006831
    Transcript: C52E12.2a.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C52E12.2a.2:c.2214-37G>A
        Intron_number: 12/23
      C52E12.2b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C52E12.2b.1:c.2214-37G>A
        Intron_number: 12/24
      C52E12.2a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C52E12.2a.1:c.2214-37G>A
        Intron_number: 12/23
  Reference: WBPaper00040707
  Method: WGS_Andersen