WormBase Tree Display for Variation: WBVar02136660

WBVar02136660 Evidence: Paper_evidence: WBPaper00045317
  Name: Public_name: h11106
    Other_name: C37C3.6a.1:c.*1881+2342C>T
      C37C3.6b.1:c.5322+2342C>T
      C37C3.6a.2:c.*1881+2342C>T
      C37C3.13.1:c.154+47G>A
    HGVSg: CHROMOSOME_V:g.7837700C>T
  Sequence_details: SMap: S_parent: Sequence: C37C3
    Flanking_sequences: TGTGTAAGATTCGGTCTAATTAGAACATCAATTTTTAACG AGCTGATAAAAAACTTTAATTTCAAGCTTCACATAATTCT
    Mapping_target: CHROMOSOME_V
    Source_location: 200 CHROMOSOME_V 7837681 7837681
    Type_of_mutation: Substitution: C T
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023707
    Laboratory: KR
    Analysis: WGS_Rose
    Status: Live
  Affects: Gene: WBGene00003242
      WBGene00016505
    Transcript: C37C3.6b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C37C3.6b.1:c.5322+2342C>T
        Intron_number: 16/19
      C37C3.6a.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C37C3.6a.2:c.*1881+2342C>T
        Intron_number: 15/17
      C37C3.6a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C37C3.6a.1:c.*1881+2342C>T
        Intron_number: 15/17
      C37C3.13.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C37C3.13.1:c.154+47G>A
        Intron_number: 2/3
  Reference: WBPaper00040589
    WBPaper00000975
    WBPaper00003985
    WBPaper00000699
    WBPaper00045317
  Method: WGS_Rose