WormBase Tree Display for Variation: WBVar01879523

WBVar01879523 Name: Public_name: WBVar01879523
    Other_name: cewivar00594041
      C54G7.3e.1:c.1724-418A>G
      C54G7.3b.1:c.1868-418A>G
      C54G7.3d.1:c.1715-418A>G
      C54G7.3g.1:c.1868-418A>G
      C54G7.3h.1:c.1715-418A>G
      C54G7.3i.1:c.1724-418A>G
      C54G7.3a.1:c.1571-418A>G
      C54G7.3c.1:c.1868-418A>G
      C54G7.3f.1:c.1571-418A>G
    HGVSg: CHROMOSOME_X:g.5531659T>C
  Sequence_details: SMap: S_parent: Sequence: C54G7
    Flanking_sequences: CAATTGATTTCAGACAATTTTCAGTACTAT ATCACAAACACATACATACTCTTGACATTT
    Mapping_target: C54G7
    Source_location: 225 CHROMOSOME_X 5531624 5531624 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Substitution: T C
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023072 From_analysis: Million_mutation_project_reanalysis
    Laboratory: VC
    Analysis: Million_mutation_project_reanalysis
    Status: Live
  Affects: Gene: WBGene00002983
    Transcript: C54G7.3i.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C54G7.3i.1:c.1724-418A>G
        Intron_number: 10/29
      C54G7.3c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C54G7.3c.1:c.1868-418A>G
        Intron_number: 11/30
      C54G7.3h.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C54G7.3h.1:c.1715-418A>G
        Intron_number: 10/29
      C54G7.3f.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C54G7.3f.1:c.1571-418A>G
        Intron_number: 9/28
      C54G7.3d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C54G7.3d.1:c.1715-418A>G
        Intron_number: 10/29
      C54G7.3e.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C54G7.3e.1:c.1724-418A>G
        Intron_number: 10/29
      C54G7.3a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C54G7.3a.1:c.1571-418A>G
        Intron_number: 10/30
      C54G7.3b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C54G7.3b.1:c.1868-418A>G
        Intron_number: 12/21
      C54G7.3g.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: C54G7.3g.1:c.1868-418A>G
        Intron_number: 11/30
  Method: WGS_Flibotte