WormBase Tree Display for Variation: WBVar02140505

WBVar02140505 Evidence: Paper_evidence: WBPaper00045317
  Name: Public_name: h7695
    Other_name: C33G3.1b.1:c.498+52C>T
      C33G3.1a.1:c.216+52C>T
      C33G3.1b.2:c.498+52C>T
    HGVSg: CHROMOSOME_X:g.14056642C>T
  Sequence_details: SMap: S_parent: Sequence: C33G3
    Flanking_sequences: TGAATGATGATGATCGTTGTCATCGTTATAATAAATGACT CCATTATCCATGTAGTTGTCAGCTGTGAAAGAGAAGATCA
    Mapping_target: CHROMOSOME_X
    Source_location: 200 CHROMOSOME_X 14056564 14056564
    Type_of_mutation: Substitution: C T
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023700
    Laboratory: KR
    Analysis: WGS_Rose
    Status: Live
  Affects: Gene: WBGene00001116
    Transcript: C33G3.1b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C33G3.1b.1:c.498+52C>T
        Intron_number: 7/18
      C33G3.1b.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C33G3.1b.2:c.498+52C>T
        Intron_number: 6/17
      C33G3.1a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C33G3.1a.1:c.216+52C>T
        Intron_number: 3/14
  Reference: WBPaper00040589
    WBPaper00000975
    WBPaper00003985
    WBPaper00000699
    WBPaper00045317
  Method: WGS_Rose