WormBase Tree Display for Variation: WBVar02128744

WBVar02128744 Evidence: Paper_evidence: WBPaper00045317
  Name: Public_name: h4904
    Other_name: K11D2.4a.1:c.105+1378C>T
      K11D2.4a.2:c.105+1378C>T
    HGVSg: CHROMOSOME_I:g.12520676C>T
  Sequence_details: SMap: S_parent: Sequence: K11D2
    Flanking_sequences: ACAGAGCTCTCCAGAGGGCACACACAGAGAGAGAGACCTC GAGAGATTTTTGTGTGTGTGTGAGCATGAATGTACGCTGC
    Mapping_target: CHROMOSOME_I
    Source_location: 200 CHROMOSOME_I 12520665 12520665
    Type_of_mutation: Substitution: C T
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023666
    Laboratory: KR
    Analysis: WGS_Rose
    Status: Live
  Affects: Gene: WBGene00010770
    Transcript: K11D2.4a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: K11D2.4a.1:c.105+1378C>T
        Intron_number: 3/9
      K11D2.4a.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: K11D2.4a.2:c.105+1378C>T
        Intron_number: 2/8
  Reference: WBPaper00040589
    WBPaper00000975
    WBPaper00003985
    WBPaper00000699
    WBPaper00045317
  Method: WGS_Rose