WormBase Tree Display for Variation: WBVar01281858

WBVar01281858 Evidence: Paper_evidence: WBPaper00037807
  Name: Public_name: WBVar01281858
    Other_name: cewivar00505526
      ZK973.6c.1:c.1931C>T
      CE52179:p.Ala644Val
      ZK973.6a.1:c.1952C>T
      CE33588:p.Ala651Val
    HGVSg: CHROMOSOME_I:g.4327104C>T
  Sequence_details: SMap: S_parent: Sequence: ZK973
    Flanking_sequences: ACGACGTAGAAACGGAGTTCCACCGACTCCGGAAGACGAACAAGCACTTG TGTTATCACTGCTGGAGCCGATCAGTTGGCTCCAAAGTTGGGAGCTTCTG
    Mapping_target: ZK973
    Type_of_mutation: Substitution: c T Paper_evidence: WBPaper00037807
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00022850 From_analysis: Million_mutation_project_reanalysis
          WGS_De_Bono
    Laboratory: AX
    Analysis: WGS_De_Bono
      Million_mutation_project_reanalysis
    DB_info: Database: dbSNP_ss ss 539141952
    Status: Live
  Affects: Gene: WBGene00000140
    Transcript: ZK973.6c.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: ZK973.6c.1:c.1931C>T
        HGVSp: CE52179:p.Ala644Val
        cDNA_position: 1931
        CDS_position: 1931
        Protein_position: 644
        Exon_number: 8/30
        Codon_change: gCt/gTt
        Amino_acid_change: A/V
      ZK973.6a.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: ZK973.6a.1:c.1952C>T
        HGVSp: CE33588:p.Ala651Val
        cDNA_position: 1952
        CDS_position: 1952
        Protein_position: 651
        Exon_number: 8/31
        Codon_change: gCt/gTt
        Amino_acid_change: A/V
  Reference: WBPaper00037807
  Method: WGS_De_Bono