WormBase Tree Display for Variation: WBVar02137224

WBVar02137224 Evidence: Paper_evidence: WBPaper00045317
  Name: Public_name: h7653
    Other_name: F57F5.5c.1:c.147-203C>T
      F57F5.5a.2:c.-22-203C>T
      F57F5.5a.3:c.-22-203C>T
      F10C2.10:n.152G>A
    HGVSg: CHROMOSOME_V:g.12024363G>A
  Sequence_details: SMap: S_parent: Sequence: F10C2
    Flanking_sequences: CGACGGCGGCGACACAGCGGAGCGAGAAGCCGTCGATGCG ACGCGACGAAGGCAGAGGGGAAATGGGCGGAGCGCGGCCT
    Mapping_target: CHROMOSOME_V
    Source_location: 200 CHROMOSOME_V 12024341 12024341
    Type_of_mutation: Substitution: G A
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023700
    Laboratory: KR
    Analysis: WGS_Rose
    Status: Live
  Affects: Gene: WBGene00196303
      WBGene00004032
    Transcript: F57F5.5a.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F57F5.5a.2:c.-22-203C>T
        Intron_number: 2/15
      F57F5.5c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F57F5.5c.1:c.147-203C>T
        Intron_number: 2/13
      F10C2.10 VEP_consequence: non_coding_transcript_exon_variant
        VEP_impact: MODIFIER
        HGVSc: F10C2.10:n.152G>A
        cDNA_position: 152
        Exon_number: 1/1
      F57F5.5a.3 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F57F5.5a.3:c.-22-203C>T
        Intron_number: 1/14
  Reference: WBPaper00040589
    WBPaper00000975
    WBPaper00003985
    WBPaper00000699
    WBPaper00045317
  Method: WGS_Rose