WormBase Tree Display for Variation: WBVar02140759

WBVar02140759 Evidence: Paper_evidence: WBPaper00045317
  Name: Public_name: h12539
    Other_name: ZK662.3a.1:c.2201+49G>C
      ZK662.3d.1:c.2186+49G>C
      ZK662.3c.1:c.2219+49G>C
      ZK662.3b.1:c.2168+49G>C
    HGVSg: CHROMOSOME_X:g.15715214G>C
  Sequence_details: SMap: S_parent: Sequence: ZK662
    Flanking_sequences: TGTCACATGAATAAATGTTTTGGAAAACAATCAGCAAAAG AACTTAAAGGTGGAGTAGCGCCAGTGGGGAAAGTGCAAAA
    Mapping_target: CHROMOSOME_X
    Source_location: 200 CHROMOSOME_X 15715136 15715136
    Type_of_mutation: Substitution: G C
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023780
    Laboratory: KR
    Analysis: WGS_Rose
    Status: Live
  Affects: Gene: WBGene00003638
    Transcript: ZK662.3c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: ZK662.3c.1:c.2219+49G>C
        Intron_number: 14/15
      ZK662.3d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: ZK662.3d.1:c.2186+49G>C
        Intron_number: 14/15
      ZK662.3a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: ZK662.3a.1:c.2201+49G>C
        Intron_number: 15/17
      ZK662.3b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: ZK662.3b.1:c.2168+49G>C
        Intron_number: 15/17
  Reference: WBPaper00040589
    WBPaper00000975
    WBPaper00003985
    WBPaper00000699
    WBPaper00045317
  Method: WGS_Rose