WormBase Tree Display for Variation: WBVar02132212

WBVar02132212 Evidence: Paper_evidence: WBPaper00045317
  Name: Public_name: h4670
    Other_name: R13F6.4e.1:c.832+30A>G
      R13F6.4f.1:c.610+30A>G
      R13F6.4a.2:c.-174+30A>G
      R13F6.4d.1:c.373+30A>G
    HGVSg: CHROMOSOME_III:g.6831478A>G
  Sequence_details: SMap: S_parent: Sequence: F28F5
    Flanking_sequences: AAGCGGTTCATGTAAGTTCTAAAGTCATCTGAACAAAAAG AAGGGCAGGATTTCTATAGGCAATTCTTAGAAAGTTTTAG
    Mapping_target: CHROMOSOME_III
    Source_location: 200 CHROMOSOME_III 6831415 6831415
    Type_of_mutation: Substitution: A G
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023661
    Laboratory: KR
    Analysis: WGS_Rose
    Status: Live
  Affects: Gene: WBGene00006498
    Transcript: R13F6.4f.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: R13F6.4f.1:c.610+30A>G
        Intron_number: 5/16
      R13F6.4e.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: R13F6.4e.1:c.832+30A>G
        Intron_number: 7/18
      R13F6.4a.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: R13F6.4a.2:c.-174+30A>G
        Intron_number: 4/17
      R13F6.4d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: R13F6.4d.1:c.373+30A>G
        Intron_number: 5/16
  Reference: WBPaper00040589
    WBPaper00000975
    WBPaper00003985
    WBPaper00000699
    WBPaper00045317
  Method: WGS_Rose