WormBase Tree Display for Variation: WBVar01468311

WBVar01468311 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01468311
    Other_name: F56B6.2a.1:c.1206-12T>G
      F56B6.2c.1:c.21-12T>G
      F56B6.2i.1:c.1212-12T>G
      F56B6.2h.1:c.1212-12T>G
      F56B6.2b.1:c.1095-12T>G
      F56B6.2j.1:c.1206-12T>G
    HGVSg: CHROMOSOME_X:g.3547557T>G
  Sequence_details: SMap: S_parent: Sequence: F56B6
    Flanking_sequences: TTATTTTTCCATAAATCCATCTGTAAAACT AATATTTTCAGAAAGAAACGAATCCTGGGA
    Mapping_target: F56B6
    Type_of_mutation: Substitution: t g
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00031279 From_analysis: WGS_Andersen
      WBStrain00031284 From_analysis: WGS_Andersen
    Laboratory: QX
    Person: WBPerson1730
    Analysis: WGS_Andersen
    DB_info: Database: dbSNP_rs rs 193353613
        dbSNP_ss ss 295529532
    Status: Live
  Affects: Gene: WBGene00004350
    Transcript: F56B6.2j.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F56B6.2j.1:c.1206-12T>G
        Intron_number: 6/14
      F56B6.2i.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F56B6.2i.1:c.1212-12T>G
        Intron_number: 7/16
      F56B6.2b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F56B6.2b.1:c.1095-12T>G
        Intron_number: 6/15
      F56B6.2a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F56B6.2a.1:c.1206-12T>G
        Intron_number: 7/16
      F56B6.2h.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F56B6.2h.1:c.1212-12T>G
        Intron_number: 7/16
      F56B6.2c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F56B6.2c.1:c.21-12T>G
        Intron_number: 1/9
  Reference: WBPaper00040707
  Method: WGS_Andersen