WormBase Tree Display for Variation: WBVar01449022

WBVar01449022 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01449022
    Other_name: C18D11.2.1:c.678+334T>A
    HGVSg: CHROMOSOME_III:g.11820351A>T
  Sequence_details: SMap: S_parent: Sequence: C18D11
    Flanking_sequences: TAAGCCTAATTGGCAAACAAACAAATTTTT AAAAAGTCGTGAGAGCCAATTTGAAAACAC
    Mapping_target: C18D11
    Type_of_mutation: Substitution: a t
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain (89)
    Laboratory: QX
    Person: WBPerson1730
    Analysis: WGS_Andersen
    DB_info: Database: dbSNP_rs rs 193334989
        dbSNP_ss ss 295510908
    Status: Live
  Affects: Gene: WBGene00007680
    Transcript: C18D11.2.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C18D11.2.1:c.678+334T>A
        Intron_number: 4/5
  Reference: WBPaper00040707
  Method: WGS_Andersen