WormBase Tree Display for Variation: WBVar02138932

WBVar02138932 Evidence: Paper_evidence: WBPaper00045317
  Name: Public_name: h10007
    Other_name: F53B3.5.1:c.594+152C>T
    HGVSg: CHROMOSOME_X:g.2876234G>A
  Sequence_details: SMap: S_parent: Sequence: F53B3
    Flanking_sequences: TGCCTACGTAATTTTCACCGATTTTGTTTTTTTTGTTGTT AAATAGTGAAATAGTGAAATGAAAATTATTTCAAGTGTTG
    Mapping_target: CHROMOSOME_X
    Source_location: 200 CHROMOSOME_X 2876228 2876228
    Type_of_mutation: Substitution: G A
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023744
    Laboratory: KR
    Analysis: WGS_Rose
    Status: Live
  Affects: Gene: WBGene00018743
    Transcript: F53B3.5.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F53B3.5.1:c.594+152C>T
        Intron_number: 6/8
  Reference: WBPaper00040589
    WBPaper00000975
    WBPaper00003985
    WBPaper00000699
    WBPaper00045317
  Method: WGS_Rose