WormBase Tree Display for Variation: WBVar00310443

WBVar00310443 Evidence: Paper_evidence: WBPaper00036201
  Name: Public_name: otn13622
    Other_name: OH8547_235881
      C34F6.10a.1:c.-16-1461G>T
      C34F6.10d.1:c.-16-1461G>T
      C34F6.10c.1:c.101+1668G>T
      C34F6.10b.1:c.101+1668G>T
    HGVSg: CHROMOSOME_X:g.11238842C>A
  Sequence_details: SMap: S_parent: Sequence: C03A3
    Flanking_sequences: TTGTAATTTTCATGCTTTTTTACTACGAATTACCACCGTAGTGGCTGTAA AATGTTTTTCAAATATTTTTTTGCAGGTGTTATGTCTCCCACTCAATCTG
    Mapping_target: C03A3
    Type_of_mutation: Substitution: C A
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00029556
    Laboratory: OTN
    Analysis: WGS_Hobert
    Status: Live
  Affects: Gene: WBGene00007944
    Transcript: C34F6.10d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C34F6.10d.1:c.-16-1461G>T
        Intron_number: 1/16
      C34F6.10c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C34F6.10c.1:c.101+1668G>T
        Intron_number: 2/15
      C34F6.10b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C34F6.10b.1:c.101+1668G>T
        Intron_number: 2/16
      C34F6.10a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C34F6.10a.1:c.-16-1461G>T
        Intron_number: 1/17
  Genetics: Map: X
  Reference: WBPaper00036201
  Method: WGS_Hobert