WormBase Tree Display for Variation: WBVar01443088

WBVar01443088 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01443088
    Other_name: cewivar00618696
      F30H5.1.1:c.1413C>T
      CE01925:p.His471=
    HGVSg: CHROMOSOME_III:g.496490C>T
  Sequence_details: SMap: S_parent: Sequence: F30H5
    Flanking_sequences: TGAGCTCATTGTTGCAACTGTTAGCAAACA GAAAGAGCTATTAATATGTTGAAAGTCGGA
    Mapping_target: F30H5
    Type_of_mutation: Substitution: c t
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00027647 From_analysis: Million_mutation_project_reanalysis
          WGS_Andersen
      WBStrain00031279 From_analysis: WGS_Andersen
      WBStrain00031284 From_analysis: WGS_Andersen
    Laboratory: QX
    Person: WBPerson1730
    Analysis: Million_mutation_project_reanalysis
      WGS_Andersen
    DB_info: Database: dbSNP_rs rs 193330249
        dbSNP_ss ss 295506168
    Status: Live
  Affects: Gene: WBGene00006781
    Transcript: F30H5.1.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: F30H5.1.1:c.1413C>T
        HGVSp: CE01925:p.His471=
        cDNA_position: 1415
        CDS_position: 1413
        Protein_position: 471
        Exon_number: 8/13
        Codon_change: caC/caT
        Amino_acid_change: H
  Reference: WBPaper00040707
  Method: WGS_Andersen