WormBase Tree Display for Variation: WBVar02133988

WBVar02133988 Evidence: Paper_evidence: WBPaper00045317
  Name: Public_name: h16359
    Other_name: H16O14.1d.1:c.1835+509G>T
      H16O14.1c.1:c.1754+509G>T
      H16O14.1a.1:c.1631+509G>T
      H16O14.1e.1:c.1463+509G>T
      H16O14.1b.1:c.1685+509G>T
    HGVSg: CHROMOSOME_IV:g.6069608G>T
  Sequence_details: SMap: S_parent: Sequence: H16O14
    Flanking_sequences: AACTACATACACAGTCAGTTCTTCAATTCTTTTATTGATT TTGCAAATTTCTAAAAATTTATACCGAGAAATTTTATTTC
    Mapping_target: CHROMOSOME_IV
    Source_location: 200 CHROMOSOME_IV 6069591 6069591
    Type_of_mutation: Substitution: G T
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023752
    Laboratory: KR
    Analysis: WGS_Rose
    Status: Live
  Affects: Gene: WBGene00019205
    Transcript: H16O14.1e.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: H16O14.1e.1:c.1463+509G>T
        Intron_number: 5/11
      H16O14.1d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: H16O14.1d.1:c.1835+509G>T
        Intron_number: 8/14
      H16O14.1b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: H16O14.1b.1:c.1685+509G>T
        Intron_number: 8/15
      H16O14.1a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: H16O14.1a.1:c.1631+509G>T
        Intron_number: 7/14
      H16O14.1c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: H16O14.1c.1:c.1754+509G>T
        Intron_number: 8/15
  Reference: WBPaper00040589
    WBPaper00000975
    WBPaper00003985
    WBPaper00000699
    WBPaper00045317
  Method: WGS_Rose