WormBase Tree Display for Variation: WBVar01471076

WBVar01471076 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01471076
    Other_name: cewivar00544237
      F13D2.1b.1:c.1374+1096A>G
      F13D2.1a.1:c.1374+1096A>G
    HGVSg: CHROMOSOME_X:g.11172945T>C
  Sequence_details: SMap: S_parent: Sequence: F13D2
    Flanking_sequences: TTACCAAGTATTCGCCCGCTTAAACGAAAT TTTACCATCCACTATTCTACGGAATTCCTT
    Mapping_target: F13D2
    Type_of_mutation: Substitution: t c
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00022887 From_analysis: Million_mutation_project_reanalysis
          WGS_Andersen
      WBStrain00022893 From_analysis: WGS_Andersen
      WBStrain00023049 From_analysis: WGS_Andersen
    Laboratory: QX
    Person: WBPerson1730
    Analysis: Million_mutation_project_reanalysis
      WGS_Andersen
    DB_info: Database: dbSNP_rs rs 193356378
        dbSNP_ss ss 295532297
    Status: Live
  Affects: Gene: WBGene00008735
    Transcript: F13D2.1b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F13D2.1b.1:c.1374+1096A>G
        Intron_number: 13/38
      F13D2.1a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F13D2.1a.1:c.1374+1096A>G
        Intron_number: 12/37
  Reference: WBPaper00040707
  Method: WGS_Andersen