WormBase Tree Display for Variation: WBVar02132368

WBVar02132368 Evidence: Paper_evidence: WBPaper00045317
  Name: Public_name: h11692
    Other_name: F10E9.6a.1:c.534+398T>A
      F10E9.6b.1:c.483+398T>A
      F10E9.6a.3:c.534+398T>A
      F10E9.6c.1:c.870+398T>A
      F10E9.6a.2:c.534+398T>A
    HGVSg: CHROMOSOME_III:g.8302576T>A
  Sequence_details: SMap: S_parent: Sequence: F10E9
    Flanking_sequences: TGCAATTTTTTAGCTGGAAGTTTTGCTCTTACACTAAGAA AATCTTTGTAAAGTAGGTTTTGCCAAATTCCATTCAGTTT
    Mapping_target: CHROMOSOME_III
    Source_location: 200 CHROMOSOME_III 8302496 8302496
    Type_of_mutation: Substitution: T A
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023706
    Laboratory: KR
    Analysis: WGS_Rose
    Status: Live
  Affects: Gene: WBGene00003243
    Transcript: F10E9.6a.3 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F10E9.6a.3:c.534+398T>A
        Intron_number: 7/12
      F10E9.6a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F10E9.6a.1:c.534+398T>A
        Intron_number: 5/10
      F10E9.6c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F10E9.6c.1:c.870+398T>A
        Intron_number: 6/10
      F10E9.6b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F10E9.6b.1:c.483+398T>A
        Intron_number: 5/10
      F10E9.6a.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F10E9.6a.2:c.534+398T>A
        Intron_number: 6/11
  Reference: WBPaper00040589
    WBPaper00000975
    WBPaper00003985
    WBPaper00000699
    WBPaper00045317
  Method: WGS_Rose