WormBase Tree Display for Variation: WBVar01327560

WBVar01327560 Evidence: Paper_evidence: WBPaper00037807
  Name: Public_name: WBVar01327560
    Other_name: cewivar00378194
      H14E04.2d.1:c.389+174C>T
      H14E04.2a.1:c.755+174C>T
      H14E04.2c.1:c.776+174C>T
      H14E04.2b.1:c.764+174C>T
    HGVSg: CHROMOSOME_III:g.2380042C>T
  Sequence_details: SMap: S_parent: Sequence: H14E04
    Flanking_sequences: GACCCCCATATCGGTTATATTCCGTTCACTTTGAAAATTCTGGGTCCTGC ACGAAAACTACAGTACCCCCCTTCGCGGCGAGACCCAGAATTTTGAAATG
    Mapping_target: H14E04
    Type_of_mutation: Substitution: c T Paper_evidence: WBPaper00037807
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00006640 From_analysis: Million_mutation_project_reanalysis
      WBStrain00008273 From_analysis: Million_mutation_project_reanalysis
      WBStrain00022850 From_analysis: Million_mutation_project_reanalysis
          WGS_De_Bono
      WBStrain00022930 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023138 From_analysis: Million_mutation_project_reanalysis
    Laboratory: AX
    Analysis: WGS_De_Bono
      Million_mutation_project_reanalysis
    DB_info: Database: dbSNP_ss ss 539183085
    Status: Live
  Affects: Gene: WBGene00019199
    Transcript: H14E04.2a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: H14E04.2a.1:c.755+174C>T
        Intron_number: 6/11
      H14E04.2c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: H14E04.2c.1:c.776+174C>T
        Intron_number: 7/12
      H14E04.2b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: H14E04.2b.1:c.764+174C>T
        Intron_number: 6/11
      H14E04.2d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: H14E04.2d.1:c.389+174C>T
        Intron_number: 3/8
  Reference: WBPaper00037807
  Method: WGS_De_Bono