WormBase Tree Display for Variation: WBVar02139790

WBVar02139790 Evidence: Paper_evidence: WBPaper00045317
  Name: Public_name: h16777
    Other_name: F47E1.20.1:c.200-62T>C
    HGVSg: CHROMOSOME_X:g.9049256T>C
  Sequence_details: SMap: S_parent: Sequence: F47E1
    Flanking_sequences: ATTGAATTATTCAAATGCCATGTATACTTTTCATTTACTA GTTTTCCATGATTTTCTAATCACTGACATTCTATTCTATA
    Mapping_target: CHROMOSOME_X
    Source_location: 200 CHROMOSOME_X 9049194 9049194
    Type_of_mutation: Substitution: T C
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023759
    Laboratory: KR
    Analysis: WGS_Rose
    Status: Live
  Affects: Gene: WBGene00304808
    Transcript: F47E1.20.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F47E1.20.1:c.200-62T>C
        Intron_number: 2/8
  Reference: WBPaper00040589
    WBPaper00000975
    WBPaper00003985
    WBPaper00000699
    WBPaper00045317
  Method: WGS_Rose