WormBase Tree Display for Variation: WBVar02130446

WBVar02130446 Evidence: Paper_evidence: WBPaper00045317
  Name: Public_name: h7382
    Other_name: T24H10.7h.1:c.509+3288C>T
      T24H10.7f.1:c.551+3288C>T
      T24H10.7g.1:c.275+3288C>T
      T24H10.7i.1:c.398+3288C>T
      T24H10.7b.1:c.647+3288C>T
      T24H10.7a.1:c.707+3288C>T
    HGVSg: CHROMOSOME_II:g.9126624C>T
  Sequence_details: SMap: S_parent: Sequence: T24H10
    Flanking_sequences: GAAATTAATTATGGGAAGTAATTCGAATTACATTTGATGC AAAACATGATACGGTTTAAAAAAATTATTTCAATCGTTTC
    Mapping_target: CHROMOSOME_II
    Source_location: 200 CHROMOSOME_II 9126544 9126544
    Type_of_mutation: Substitution: C T
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023691
    Laboratory: KR
    Analysis: WGS_Rose
    Status: Live
  Affects: Gene: WBGene00012005
    Transcript: T24H10.7g.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T24H10.7g.1:c.275+3288C>T
        Intron_number: 2/3
      T24H10.7f.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T24H10.7f.1:c.551+3288C>T
        Intron_number: 6/8
      T24H10.7i.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T24H10.7i.1:c.398+3288C>T
        Intron_number: 3/4
      T24H10.7h.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T24H10.7h.1:c.509+3288C>T
        Intron_number: 4/5
      T24H10.7a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T24H10.7a.1:c.707+3288C>T
        Intron_number: 7/9
      T24H10.7b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T24H10.7b.1:c.647+3288C>T
        Intron_number: 7/9
  Reference: WBPaper00040589
    WBPaper00000975
    WBPaper00003985
    WBPaper00000699
    WBPaper00045317
  Method: WGS_Rose