WormBase Tree Display for Variation: WBVar00073451

WBVar00073451 Name: Public_name: WBVar00073451
    Other_name: haw97811
      cewivar00266336
      F26F2.7d.1:c.27T>C
      F26F2.7a.1:c.1059T>C
      CE52948:p.Leu145=
      F26F2.7c.1:c.435T>C
      CE19819:p.Leu353=
      CE52844:p.Leu9=
      F26F2.7b.1:c.1065T>C
      CE52915:p.Leu355=
    HGVSg: CHROMOSOME_V:g.20584889T>C
  Sequence_details: SMap: S_parent: Sequence: F26F2
    Flanking_sequences: tgatgagcaataatttcgttgaact aaaggatcggttttcaagaaattcg
    Mapping_target: F26F2
    Type_of_mutation: Substitution: T C
    SeqStatus: Sequenced
  Variation_type: SNP
    Predicted_SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00004602 From_analysis: Million_mutation_project_reanalysis
          WGS_Hawaiian_Waterston
      WBStrain00023072 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023139 From_analysis: Million_mutation_project_reanalysis
      WBStrain00027648 From_analysis: Million_mutation_project_reanalysis
      WBStrain00027660 From_analysis: Million_mutation_project_reanalysis
      WBStrain00027662 From_analysis: Million_mutation_project_reanalysis
    Laboratory: RW
    Person: WBPerson1562
    Analysis: WGS_Hawaiian_Waterston
      Million_mutation_project_reanalysis
    Status: Live
  Affects: Gene: WBGene00009172
    Transcript: F26F2.7b.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: F26F2.7b.1:c.1065T>C
        HGVSp: CE52915:p.Leu355=
        cDNA_position: 1116
        CDS_position: 1065
        Protein_position: 355
        Exon_number: 10/17
        Codon_change: ctT/ctC
        Amino_acid_change: L
      F26F2.7d.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: F26F2.7d.1:c.27T>C
        HGVSp: CE52844:p.Leu9=
        cDNA_position: 223
        CDS_position: 27
        Protein_position: 9
        Exon_number: 2/9
        Codon_change: ctT/ctC
        Amino_acid_change: L
      F26F2.7c.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: F26F2.7c.1:c.435T>C
        HGVSp: CE52948:p.Leu145=
        cDNA_position: 435
        CDS_position: 435
        Protein_position: 145
        Exon_number: 3/9
        Codon_change: ctT/ctC
        Amino_acid_change: L
      F26F2.7a.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: F26F2.7a.1:c.1059T>C
        HGVSp: CE19819:p.Leu353=
        cDNA_position: 1104
        CDS_position: 1059
        Protein_position: 353
        Exon_number: 10/17
        Codon_change: ctT/ctC
        Amino_acid_change: L
  Remark: [20081124 db] this Variation was previously named hw97811
  Method: WGS_Hawaiian_Waterston