WormBase Tree Display for Variation: WBVar02134984

WBVar02134984 Evidence: Paper_evidence: WBPaper00045317
  Name: Public_name: h7625
    Other_name: F52G2.2d.1:c.1343+64G>A
      F52G2.2a.1:c.2687+64G>A
      F52G2.2b.1:c.2117+64G>A
    HGVSg: CHROMOSOME_IV:g.13529187C>T
  Sequence_details: SMap: S_parent: Sequence: F52G2
    Flanking_sequences: TAGTGACTGATAAAAAGTGAATAAGTATTAATGCACACTT TTCTCGGGGAGTACACGAACCCTGCGTTAATCTACATGCT
    Mapping_target: CHROMOSOME_IV
    Source_location: 200 CHROMOSOME_IV 13529154 13529154
    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: WBGene00004681
    Transcript: F52G2.2a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F52G2.2a.1:c.2687+64G>A
        Intron_number: 15/21
      F52G2.2d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F52G2.2d.1:c.1343+64G>A
        Intron_number: 8/13
      F52G2.2b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F52G2.2b.1:c.2117+64G>A
        Intron_number: 12/17
  Reference: WBPaper00040589
    WBPaper00000975
    WBPaper00003985
    WBPaper00000699
    WBPaper00045317
  Method: WGS_Rose