WormBase Tree Display for Variation: WBVar02129201

WBVar02129201 Evidence: Paper_evidence: WBPaper00045317
  Name: Public_name: h12051
    Other_name: F48A11.8:n.57C>T
      F48A11.1b.1:c.137-132G>A
      F48A11.1a.1:c.323-132G>A
      F48A11.1c.1:c.419-132G>A
    HGVSg: CHROMOSOME_II:g.205281G>A
  Sequence_details: SMap: S_parent: Sequence: F48A11
    Flanking_sequences: AATGAGTTGTTTGCTCTGAAGAGCCGTGCGGCTGCGGTAG GTGTAGGTTCGCCTAATTGAGCTGTCTCACGAAAATGGAC
    Mapping_target: CHROMOSOME_II
    Source_location: 200 CHROMOSOME_II 205281 205281
    Type_of_mutation: Substitution: G A
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023761
    Laboratory: KR
    Analysis: WGS_Rose
    Status: Live
  Affects: Gene: WBGene00000497
      WBGene00198044
    Transcript: F48A11.8 VEP_consequence: non_coding_transcript_exon_variant
        VEP_impact: MODIFIER
        HGVSc: F48A11.8:n.57C>T
        cDNA_position: 57
        Exon_number: 1/1
      F48A11.1b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F48A11.1b.1:c.137-132G>A
        Intron_number: 2/16
      F48A11.1a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F48A11.1a.1:c.323-132G>A
        Intron_number: 3/18
      F48A11.1c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F48A11.1c.1:c.419-132G>A
        Intron_number: 4/18
  Reference: WBPaper00040589
    WBPaper00000975
    WBPaper00003985
    WBPaper00000699
    WBPaper00045317
  Method: WGS_Rose