WormBase Tree Display for Variation: WBVar01431125

WBVar01431125 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01431125
    Other_name: Y47G6A.23c.1:c.2830-140C>A
      Y47G6A.23d.1:c.2836-140C>A
      Y47G6A.23b.1:c.2836-140C>A
      Y47G6A.23a.1:c.2830-140C>A
    HGVSg: CHROMOSOME_I:g.3588425G>T
  Sequence_details: SMap: S_parent: Sequence: Y47G6A
    Flanking_sequences: CAGCCTGCCGATTTCTCGGTTTTTTTTTTT GTTTTCAATTATTCGGTTTTTCTGAAAAAC
    Mapping_target: Y47G6A
    Type_of_mutation: Substitution: g t
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain (38)
    Laboratory: QX
    Person: WBPerson1730
    Analysis: WGS_Andersen
    DB_info: Database: dbSNP_rs rs 193319188
        dbSNP_ss ss 295495105
    Status: Live
  Affects: Gene: WBGene00003060
    Transcript: Y47G6A.23c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y47G6A.23c.1:c.2830-140C>A
        Intron_number: 13/31
      Y47G6A.23b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y47G6A.23b.1:c.2836-140C>A
        Intron_number: 14/31
      Y47G6A.23a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y47G6A.23a.1:c.2830-140C>A
        Intron_number: 14/32
      Y47G6A.23d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y47G6A.23d.1:c.2836-140C>A
        Intron_number: 14/32
  Reference: WBPaper00040707
  Method: WGS_Andersen