WormBase Tree Display for Variation: WBVar00305005

WBVar00305005 Evidence: Paper_evidence: WBPaper00036201
  Name: Public_name: otn8184
    Other_name: OH7677_21651
      T22H2.5a.1:c.405+35C>T
      T22H2.5c.1:c.405+35C>T
      T22H2.5b.1:c.405+35C>T
      T22H2.5a.2:c.405+35C>T
    HGVSg: CHROMOSOME_I:g.11690382G>A
  Sequence_details: SMap: S_parent: Sequence: T22H2
    Flanking_sequences: GGATCAATTTTGGCTTGGTAGGCCTGAAAATTTGGGCTCAGGATTGCTCC CGAGCTTGTTGAACCAGATGCTCCGTGAGCTTACCCTCTTAAAGTTATCC
    Mapping_target: T22H2
    Type_of_mutation: Substitution: G A
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00029537
    Laboratory: OTN
    Analysis: WGS_Hobert
    Status: Live
  Affects: Gene: WBGene00011935
    Transcript: T22H2.5a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T22H2.5a.1:c.405+35C>T
        Intron_number: 2/7
      T22H2.5b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T22H2.5b.1:c.405+35C>T
        Intron_number: 2/7
      T22H2.5a.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T22H2.5a.2:c.405+35C>T
        Intron_number: 2/8
      T22H2.5c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T22H2.5c.1:c.405+35C>T
        Intron_number: 2/6
  Genetics: Map: I
  Reference: WBPaper00036201
  Method: WGS_Hobert