WormBase Tree Display for Variation: WBVar01415619

WBVar01415619 Evidence: Paper_evidence: WBPaper00037807
  Name: Public_name: WBVar01415619
    Other_name: cewivar00687941
      H14E04.2c.1:c.1518+71_1518+72insCG
      H14E04.2d.1:c.1131+71_1131+72insCG
      H14E04.2a.1:c.1497+71_1497+72insCG
      H14E04.2b.1:c.1506+71_1506+72insCG
    HGVSg: CHROMOSOME_III:g.2382878_2382879insCG
  Sequence_details: SMap: S_parent: Sequence: H14E04
    Flanking_sequences: AAATTTAAAAAAAAAAAACGGAGAAATTTGAGCCAAAAATCGAGAAAAAA ATTTTTCAAGTCCAAATTCGAATTCCCCACCAATTTTCACCCCAAGTGTC
    Mapping_target: H14E04
    Type_of_mutation: Insertion: CG Paper_evidence: WBPaper00037807
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain (19)
    Laboratory: AX
    Analysis: WGS_De_Bono
      Million_mutation_project_reanalysis
    DB_info: Database: dbSNP_ss ss 539201366
    History: Acquires_merge: WBVar01962131
    Status: Live
  Affects: Gene: WBGene00019199
    Transcript: H14E04.2a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: H14E04.2a.1:c.1497+71_1497+72insCG
        Intron_number: 9/11
      H14E04.2c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: H14E04.2c.1:c.1518+71_1518+72insCG
        Intron_number: 10/12
      H14E04.2b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: H14E04.2b.1:c.1506+71_1506+72insCG
        Intron_number: 9/11
      H14E04.2d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: H14E04.2d.1:c.1131+71_1131+72insCG
        Intron_number: 6/8
  Reference: WBPaper00037807
  Method: WGS_De_Bono