WormBase Tree Display for Variation: WBVar02137897

WBVar02137897 Evidence: Paper_evidence: WBPaper00045317
  Name: Public_name: h3661
    Other_name: T25E12.4e.1:c.928+400C>T
      T25E12.4a.1:c.928+400C>T
      T25E12.4f.1:c.928+400C>T
      T25E12.4d.1:c.262+400C>T
    HGVSg: CHROMOSOME_V:g.16759645C>T
  Sequence_details: SMap: S_parent: Sequence: F14D1
    Flanking_sequences: TGTAAAGCCTATTCAAAATAGTATACATTCCTAGAGTAGA ACTATTAAAATAAAATCGAATTATAGTGGATTTTGTCCTA
    Mapping_target: CHROMOSOME_V
    Source_location: 200 CHROMOSOME_V 16759617 16759617
    Type_of_mutation: Substitution: C T
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023882
    Laboratory: KR
    Analysis: WGS_Rose
    Status: Live
  Affects: Gene: WBGene00012019
    Transcript: T25E12.4f.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T25E12.4f.1:c.928+400C>T
        Intron_number: 6/18
      T25E12.4d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T25E12.4d.1:c.262+400C>T
        Intron_number: 2/13
      T25E12.4a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T25E12.4a.1:c.928+400C>T
        Intron_number: 6/18
      T25E12.4e.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T25E12.4e.1:c.928+400C>T
        Intron_number: 6/17
  Reference: WBPaper00040589
    WBPaper00000975
    WBPaper00003985
    WBPaper00000699
    WBPaper00045317
  Method: WGS_Rose