WormBase Tree Display for Variation: WBVar00099779

WBVar00099779 Name: Public_name: WBVar00099779
    Other_name: pas4638
      cewivar00060869
      F09B9.2b.1:c.609+140T>C
      F09B9.2a.1:c.567+140T>C
    HGVSg: CHROMOSOME_X:g.10149559T>C
  Sequence_details: SMap: S_parent: Sequence: F09B9
    Flanking_sequences: catggcacgtgtactgtttcaaatgcagcgagtgctcagcagttctccatggagagtacatgtcacatcacggaaaaccattgtgccttcgagattataacgagaaattcggtgtcaaatgttacgagtgtgaaaagttcattgctggaaaagtcttacaggtgggtatttggttgataacaaaaaataaaagtaaaaccgaacaaagttgatttgtgaacaaaacaatttagcactacattgtctacgaaaaaccataacaacatatattttcagaaaaaaagaaagtattttaatcaa ctatttataaaaaccttttggatcttcctgttccaaacttttgttacttttgcaatcaaggttaagttgtacccctgcaaaacgttgagaaaagtttttttgttaaaaaaaacaccaagatcaaaacaagttgtctattcttcttttgaccttcccaaaatattctattcagtcaatttcttttatttaggctggcggctacaaattccatccaacttgtgcccgctgttcacgatgtggatctcattttggtgacggtgaagagatgtatatgcaaggagacgagatctggcatccatc
    Mapping_target: F09B9
    Type_of_mutation: Substitution: T C
    SeqStatus: Sequenced
  Variation_type: SNP
    Predicted_SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain (37)
    Person: WBPerson6900
    Analysis: WGS_Pasadena_Quinlan
      Million_mutation_project_reanalysis
    Status: Live
  Affects: Gene: WBGene00006839
    Transcript: F09B9.2b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F09B9.2b.1:c.609+140T>C
        Intron_number: 3/10
      F09B9.2a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F09B9.2a.1:c.567+140T>C
        Intron_number: 5/13
  Method: WGS_Pasadena_Quinlan