WormBase Tree Display for Variation: WBVar01438340

WBVar01438340 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01438340
    Other_name: C52E12.2a.2:c.2014+62T>C
      C52E12.2a.1:c.2014+62T>C
      C52E12.2b.1:c.2014+62T>C
    HGVSg: CHROMOSOME_II:g.7004094T>C
  Sequence_details: SMap: S_parent: Sequence: C52E12
    Flanking_sequences: GTTTTCAAAGATATTACAATTTATTCATTT TGAAAACTGCTTAACACCAGTGAAACTTTT
    Mapping_target: C52E12
    Type_of_mutation: Substitution: t c
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00005305 From_analysis: WGS_Andersen
      WBStrain00005315 From_analysis: WGS_Andersen
      WBStrain00030851 From_analysis: WGS_Andersen
    Laboratory: QX
    Person: WBPerson1730
    Analysis: WGS_Andersen
    DB_info: Database: dbSNP_rs rs 193326401
        dbSNP_ss ss 295502320
    Status: Live
  Affects: Gene: WBGene00006831
    Transcript: C52E12.2a.2 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C52E12.2a.2:c.2014+62T>C
        Intron_number: 11/23
      C52E12.2b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C52E12.2b.1:c.2014+62T>C
        Intron_number: 11/24
      C52E12.2a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C52E12.2a.1:c.2014+62T>C
        Intron_number: 11/23
  Reference: WBPaper00040707
  Method: WGS_Andersen