WormBase Tree Display for Variation: WBVar01259441

WBVar01259441 Evidence: Paper_evidence: WBPaper00037807
  Name: Public_name: WBVar01259441
    Other_name: cewivar00608308
      H14E04.2b.1:c.1669-83A>G
      H14E04.2c.1:c.1681-83A>G
      H14E04.2a.1:c.1660-83A>G
      H14E04.2d.1:c.1294-83A>G
    HGVSg: CHROMOSOME_III:g.2384419A>G
  Sequence_details: SMap: S_parent: Sequence: H14E04
    Flanking_sequences: TTCAAAATTCACGGAAATTGGGCGTGTTGGGGGTCATTTTGAAGGTCTCG TGAGATCAATACGAATTTTAATGATGCGAACCAAAAAATCAATAATTAAA
    Mapping_target: H14E04
    Type_of_mutation: Substitution: a G Paper_evidence: WBPaper00037807
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00006642 From_analysis: WGS_De_Bono
      WBStrain00023665 From_analysis: Million_mutation_project_reanalysis
      WBStrain00027647 From_analysis: Million_mutation_project_reanalysis
    Laboratory: AX
    Analysis: WGS_De_Bono
      Million_mutation_project_reanalysis
    DB_info: Database: dbSNP_ss ss 539095441
    Status: Live
  Affects: Gene: WBGene00019199
    Transcript: H14E04.2a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: H14E04.2a.1:c.1660-83A>G
        Intron_number: 10/11
      H14E04.2c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: H14E04.2c.1:c.1681-83A>G
        Intron_number: 11/12
      H14E04.2b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: H14E04.2b.1:c.1669-83A>G
        Intron_number: 10/11
      H14E04.2d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: H14E04.2d.1:c.1294-83A>G
        Intron_number: 7/8
  Reference: WBPaper00037807
  Method: WGS_De_Bono