WormBase Tree Display for Variation: WBVar02136658

WBVar02136658 Evidence: Paper_evidence: WBPaper00045317
  Name: Public_name: h17641
    Other_name: C37C3.6a.1:c.*1881+1418T>C
      C37C3.6b.1:c.5322+1418T>C
      C37C3.7.1:c.256+39A>G
      C37C3.6a.2:c.*1881+1418T>C
    HGVSg: CHROMOSOME_V:g.7836776T>C
  Sequence_details: SMap: S_parent: Sequence: C37C3
    Flanking_sequences: AAACTGTCGAGTTTTTAAGTTCTACAAATCTCTTATAACA CGCTACATCTACTATCAAACTTTGAAAAAAAACCATACCA
    Mapping_target: CHROMOSOME_V
    Source_location: 200 CHROMOSOME_V 7836757 7836757
    Type_of_mutation: Substitution: T C
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023704
    Laboratory: KR
    Analysis: WGS_Rose
    Status: Live
  Affects: Gene: WBGene00016499
      WBGene00003242
    Transcript: C37C3.7.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C37C3.7.1:c.256+39A>G
        Intron_number: 2/7
      C37C3.6b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C37C3.6b.1:c.5322+1418T>C
        Intron_number: 16/19
      C37C3.6a.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C37C3.6a.2:c.*1881+1418T>C
        Intron_number: 15/17
      C37C3.6a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C37C3.6a.1:c.*1881+1418T>C
        Intron_number: 15/17
  Reference: WBPaper00040589
    WBPaper00000975
    WBPaper00003985
    WBPaper00000699
    WBPaper00045317
  Method: WGS_Rose