WormBase Tree Display for Variation: WBVar02136234

WBVar02136234 Evidence: Paper_evidence: WBPaper00045317
  Name: Public_name: h6844
    Other_name: Y47D7A.14b.1:c.1014+689C>T
      Y47D7A.14d.1:c.150+689C>T
      Y47D7A.14c.1:c.606+689C>T
      Y47D7A.14a.1:c.975+689C>T
    HGVSg: CHROMOSOME_V:g.4445368G>A
  Sequence_details: SMap: S_parent: Sequence: Y47D7A
    Flanking_sequences: ACACCCGTAATCGACACAAGCGCTACAGTAGTCATTTAAA AATTACTGTAATTTTCGCTACGAGATATTTTGCGCGTCAAATATGTTGCACAATACGCATTTTGTGTTCCTGTAATAAAA
    Mapping_target: CHROMOSOME_V
    Source_location: 200 CHROMOSOME_V 4445354 4445354
    Type_of_mutation: Substitution: G A
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023729
    Laboratory: KR
    Analysis: WGS_Rose
    Status: Live
  Affects: Gene: WBGene00021626
    Transcript: Y47D7A.14d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y47D7A.14d.1:c.150+689C>T
        Intron_number: 1/3
      Y47D7A.14b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y47D7A.14b.1:c.1014+689C>T
        Intron_number: 5/8
      Y47D7A.14a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y47D7A.14a.1:c.975+689C>T
        Intron_number: 4/7
      Y47D7A.14c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y47D7A.14c.1:c.606+689C>T
        Intron_number: 2/4
  Reference: WBPaper00040589
    WBPaper00000975
    WBPaper00003985
    WBPaper00000699
    WBPaper00045317
  Method: WGS_Rose