WormBase Tree Display for Variation: WBVar02127963

WBVar02127963 Evidence: Paper_evidence: WBPaper00045317
  Name: Public_name: h8650
    Other_name: F18C12.3.1:c.1105-11C>T
    HGVSg: CHROMOSOME_I:g.8097648C>T
  Sequence_details: SMap: S_parent: Sequence: F18C12
    Flanking_sequences: GACCAGATACCGTATTTTTTGCGTCTGGTCTATTTATCTC GAATTTATAGGTGAAAAACCCCAAAAAGTCGAATAAAAGT
    Mapping_target: CHROMOSOME_I
    Source_location: 200 CHROMOSOME_I 8097642 8097642
    Type_of_mutation: Substitution: C T
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023676
    Laboratory: KR
    Analysis: WGS_Rose
    Status: Live
  Affects: Gene: WBGene00008934
    Transcript: F18C12.3.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F18C12.3.1:c.1105-11C>T
        Intron_number: 4/7
  Reference: WBPaper00040589
    WBPaper00000975
    WBPaper00003985
    WBPaper00000699
    WBPaper00045317
  Method: WGS_Rose