WormBase Tree Display for Variation: WBVar01307407

WBVar01307407 Evidence: Paper_evidence: WBPaper00037807
  Name: Public_name: WBVar01307407
    Other_name: cewivar00306834
      CE05121:p.Phe220Ser
      ZK1127.11.1:c.2233+303A>G
      ZK1127.1.1:c.659T>C
    HGVSg: CHROMOSOME_II:g.7066524T>C
  Sequence_details: SMap: S_parent: Sequence: ZK1127
    Flanking_sequences: CTAACGTGAGCATTTCAGGTACTGCCCAATGAAGCCGTCGAGCCAGTTGT CTTCAATGAGGATTTCAGCCGAGACTTCGAAAACCGACGATTCCAGCGCA
    Mapping_target: ZK1127
    Type_of_mutation: Substitution: t C Paper_evidence: WBPaper00037807
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00006625 From_analysis: Million_mutation_project_reanalysis
      WBStrain00022850 From_analysis: Million_mutation_project_reanalysis
          WGS_De_Bono
      WBStrain00023286 From_analysis: Million_mutation_project_reanalysis
      WBStrain00027652 From_analysis: Million_mutation_project_reanalysis
    Laboratory: AX
    Analysis: WGS_De_Bono
      Million_mutation_project_reanalysis
    DB_info: Database: dbSNP_ss ss 539164946
    Status: Live
  Affects: Gene: WBGene00003784
      WBGene00001872
    Transcript: ZK1127.1.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: ZK1127.1.1:c.659T>C
        HGVSp: CE05121:p.Phe220Ser
        cDNA_position: 715
        CDS_position: 659
        Protein_position: 220
        Exon_number: 6/7
        Codon_change: tTc/tCc
        Amino_acid_change: F/S
      ZK1127.11.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: ZK1127.11.1:c.2233+303A>G
        Intron_number: 15/18
  Reference: WBPaper00037807
  Method: WGS_De_Bono