WormBase Tree Display for Variation: WBVar02139132

WBVar02139132 Evidence: Paper_evidence: WBPaper00045317
  Name: Public_name: h11142
    Other_name: F09F9.4.1:c.934+603G>A
    HGVSg: CHROMOSOME_X:g.4125388C>T
  Sequence_details: SMap: S_parent: Sequence: F09F9
    Flanking_sequences: GTGTCTCCTTGACCCTAGGCTCATCTGTGCACATCTGCTT ACGCATGTCATACAATAGAAGCACAGGTAACGTCTGTCGA
    Mapping_target: CHROMOSOME_X
    Source_location: 200 CHROMOSOME_X 4125364 4125364
    Type_of_mutation: Substitution: C T
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023707
    Laboratory: KR
    Analysis: WGS_Rose
    Status: Live
  Affects: Gene: WBGene00017309
    Transcript: F09F9.4.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F09F9.4.1:c.934+603G>A
        Intron_number: 6/14
  Reference: WBPaper00040589
    WBPaper00000975
    WBPaper00003985
    WBPaper00000699
    WBPaper00045317
  Method: WGS_Rose