WormBase Tree Display for Variation: WBVar01439787

WBVar01439787 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01439787
    Other_name: F45E10.1h.1:c.149-1191G>T
      F45E10.1g.1:c.149-1191G>T
      F45E10.1c.1:c.149-1191G>T
      F45E10.1b.1:c.149-1191G>T
      F45E10.1a.1:c.149-1191G>T
    HGVSg: CHROMOSOME_II:g.11081731C>A
  Sequence_details: SMap: S_parent: Sequence: C09H10
    Flanking_sequences: CAAACACTGAGAGCGTAATACTCGATAAAT ACCAATTAACTTCTCAATGGATAGTTGTGC
    Mapping_target: C09H10
    Type_of_mutation: Substitution: c a
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00004602 From_analysis: WGS_Andersen
    Laboratory: QX
    Person: WBPerson1730
    Analysis: WGS_Andersen
    DB_info: Database: dbSNP_rs rs 193327819
        dbSNP_ss ss 295503738
    Status: Live
  Affects: Gene: WBGene00006788
    Transcript: F45E10.1c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F45E10.1c.1:c.149-1191G>T
        Intron_number: 2/23
      F45E10.1b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F45E10.1b.1:c.149-1191G>T
        Intron_number: 2/22
      F45E10.1g.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F45E10.1g.1:c.149-1191G>T
        Intron_number: 2/21
      F45E10.1a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F45E10.1a.1:c.149-1191G>T
        Intron_number: 3/23
      F45E10.1h.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F45E10.1h.1:c.149-1191G>T
        Intron_number: 2/21
  Reference: WBPaper00040707
  Method: WGS_Andersen