WormBase Tree Display for Variation: WBVar00050501

WBVar00050501 Name: Public_name: WBVar00050501
    Other_name: pas21697
      cewivar00058483
      K09F5.6a.1:c.2398-177T>C
      K09F5.6b.1:c.*21-177T>C
    HGVSg: CHROMOSOME_X:g.7724860T>C
  Sequence_details: SMap: S_parent: Sequence: K09F5
    Flanking_sequences: cacccactggagcacttaaccaaaatgactttgctaccagcattgtgtgaatatttgttttacatttttggtaggtcttaattcaaaagtaactagaaatgtttacaaattcaaaattttcaaacggaatgattgcaactctgaaatatagaaatcatcaaaaaaattgaaacaattgaaagcgatatcataactatctgcatcgaattatgaaaaaaaaaccgagatattttactattaatttacaaaaatgttatgattcaccgtatttcctctattagtattgcattaccctttaaa agaaataaggaacacgattaaaccgaaattgtatatcatgtaacctgatcatgtaagcctaataaaattagttcagaaaacggtttcaaagcccatataattttaggatgaaattgataagtttcactgttcacagagtttgcattcttaacttttgacaaagatacattttacaggaaccctactgatcccgatgaactattcccccaattaacacatgaaccaaatcaactccgtgacaatgcacttcttctcgccaaacacttaaacagttaaccgccaaacaaacacatcatccca
    Mapping_target: K09F5
    Type_of_mutation: Substitution: T C
    SeqStatus: Sequenced
  Variation_type: SNP
    Predicted_SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain (27)
    Person: WBPerson6900
    Analysis: WGS_Pasadena_Quinlan
      Million_mutation_project_reanalysis
    Status: Live
  Affects: Gene: WBGene00044698
    Transcript: K09F5.6b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: K09F5.6b.1:c.*21-177T>C
        Intron_number: 14/14
      K09F5.6a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: K09F5.6a.1:c.2398-177T>C
        Intron_number: 12/13
  Method: WGS_Pasadena_Quinlan