WormBase Tree Display for Variation: WBVar00270994

WBVar00270994 Evidence: Paper_evidence: WBPaper00005369
  Name: Public_name: WBVar00270994
    Other_name: uCE4-1396
      cewivar00500342
      Y57G11C.1134:n.767A>C
    HGVSg: CHROMOSOME_IV:g.14936300T>G
  Sequence_details: SMap: S_parent: Sequence: Y57G11C
    Flanking_sequences: ATTTGCTTACATTAAGTACTGAAAGAAGTTACAGTTTCCAATAAAATCAACCTGTTTCATGGTTTTTTTTCAACTTACCGGAAACCAATTATTCTGAAAA ATTTCCAGAGGAATTGAAAAAATTGCAAATAATTAAAAGCGTTGTGCTCGGTTTTTGAAAAAAAAACCGGGAAAAGATATCATCACATTTGGTACTTAAA
    Mapping_target: Y57G11C
    Type_of_mutation: Substitution: T G
    SeqStatus: Sequenced
  Variation_type: SNP
    Predicted_SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00004602 From_analysis: SNP_Swan
      WBStrain00023286 From_analysis: Million_mutation_project_reanalysis
      WBStrain00027662 From_analysis: Million_mutation_project_reanalysis
    Analysis: SNP_Swan
      Million_mutation_project_reanalysis
    Status: Live
  Affects: Gene: WBGene00194923
    Transcript: Y57G11C.1134 VEP_consequence: non_coding_transcript_exon_variant
        VEP_impact: MODIFIER
        HGVSc: Y57G11C.1134:n.767A>C
        cDNA_position: 767
        Exon_number: 2/2
  Reference: WBPaper00005369
  Method: SNP_Swan