WormBase Tree Display for Variation: WBVar02139428

WBVar02139428 Evidence: Paper_evidence: WBPaper00045317
  Name: Public_name: h18291
    Other_name: T07H6.5c.1:c.1451-673T>C
      T07H6.5a.1:c.1451-673T>C
      T07H6.5b.1:c.1451-673T>C
    HGVSg: CHROMOSOME_X:g.6287718A>G
  Sequence_details: SMap: S_parent: Sequence: T07H6
    Flanking_sequences: AGTGCAACTTAAATTGGTCAGTGCAACTGCAACTGGTCAGTGCAACTTAAATTGGTCAGTGCAACTGCAACTGGTCAGTGCAACTTAAATTGGTCAGTGCAACTGCAACTGGTCAGTGCACTGCAACTGGTCAGTGCACTACAACTGGTCAGTGCACTGCAACTGGTCAGTGCACTACAACTGGTCAGTGCACTGCAACTGGTCAGTGCACTACAACTGGTCAGTGCACTGCAACTGGTCAGTGCACTACAACTGGTCAGTGCACTGCAACTGGTCAGTGCACTACAACTGGTCAGTGCACTGCAACTGGTCAGTGCACT CAACTGGTCAGTGCACTGCAACTGGTCAGTGCACTACAACTGGTCATGGTCAGTGCACTGCAACTGGTCAGTGCACTAAT
    Mapping_target: CHROMOSOME_X
    Source_location: 200 CHROMOSOME_X 6287676 6287676
    Type_of_mutation: Substitution: A G
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023671
    Laboratory: KR
    Analysis: WGS_Rose
    Status: Live
  Affects: Gene: WBGene00002976
    Transcript: T07H6.5b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T07H6.5b.1:c.1451-673T>C
        Intron_number: 10/28
      T07H6.5a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T07H6.5a.1:c.1451-673T>C
        Intron_number: 10/13
      T07H6.5c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: T07H6.5c.1:c.1451-673T>C
        Intron_number: 9/12
  Reference: WBPaper00040589
    WBPaper00000975
    WBPaper00003985
    WBPaper00000699
    WBPaper00045317
  Method: WGS_Rose