WormBase Tree Display for Variation: WBVar01438316

WBVar01438316 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01438316
    Other_name: F22D3.2g.1:c.1102-549A>G
      F22D3.2j.1:c.1093-549A>G
      F22D3.2e.1:c.1093-549A>G
      F22D3.2d.1:c.1102-549A>G
    HGVSg: CHROMOSOME_II:g.6942163A>G
  Sequence_details: SMap: S_parent: Sequence: F22D3
    Flanking_sequences: TTCTCAGTGTCGGCGGAGCGCACCAACACC AAAGTCATGATTTGAGAAGGACGTTCCCTA
    Mapping_target: F22D3
    Type_of_mutation: Substitution: a g
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00031279 From_analysis: WGS_Andersen
      WBStrain00031284 From_analysis: WGS_Andersen
    Laboratory: QX
    Person: WBPerson1730
    Analysis: WGS_Andersen
    DB_info: Database: dbSNP_rs rs 193326377
        dbSNP_ss ss 295502296
    Status: Live
  Affects: Gene: WBGene00017699
    Transcript: F22D3.2g.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F22D3.2g.1:c.1102-549A>G
        Intron_number: 13/18
      F22D3.2e.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F22D3.2e.1:c.1093-549A>G
        Intron_number: 13/18
      F22D3.2d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F22D3.2d.1:c.1102-549A>G
        Intron_number: 13/18
      F22D3.2j.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F22D3.2j.1:c.1093-549A>G
        Intron_number: 13/18
  Reference: WBPaper00040707
  Method: WGS_Andersen