WormBase Tree Display for Variation: WBVar01744126

WBVar01744126 Name: Public_name: WBVar01744126
    Other_name: cewivar00443402
      CE38513:p.Phe487Ser
      CE38512:p.Phe487Ser
      F35E12.7b.1:c.1446+62T>C
      F35E12.7d.1:c.1460T>C
      F35E12.7a.1:c.1460T>C
      F35E12.7c.1:c.1460T>C
      CE09922:p.Phe487Ser
    HGVSg: CHROMOSOME_V:g.13728638A>G
  Sequence_details: SMap: S_parent: Sequence: F35E12
    Flanking_sequences: GAGACTGAGGTAACTATCGGTGCAGTTGAA AGCTTCCCGAAGGCTAAAACAAAAGAATGC
    Mapping_target: F35E12
    Source_location: 225 CHROMOSOME_V 13728625 13728625 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Substitution: A G
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: 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: VC
    Analysis: Million_mutation_project_reanalysis
    Status: Live
  Affects: Gene: WBGene00009431
    Transcript: F35E12.7c.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: F35E12.7c.1:c.1460T>C
        HGVSp: CE38512:p.Phe487Ser
        cDNA_position: 1471
        CDS_position: 1460
        Protein_position: 487
        Exon_number: 12/14
        Codon_change: tTt/tCt
        Amino_acid_change: F/S
      F35E12.7b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F35E12.7b.1:c.1446+62T>C
        Intron_number: 11/12
      F35E12.7a.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: F35E12.7a.1:c.1460T>C
        HGVSp: CE09922:p.Phe487Ser
        cDNA_position: 1463
        CDS_position: 1460
        Protein_position: 487
        Exon_number: 12/14
        Codon_change: tTt/tCt
        Amino_acid_change: F/S
      F35E12.7d.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: F35E12.7d.1:c.1460T>C
        HGVSp: CE38513:p.Phe487Ser
        cDNA_position: 1471
        CDS_position: 1460
        Protein_position: 487
        Exon_number: 12/14
        Codon_change: tTt/tCt
        Amino_acid_change: F/S
  Method: WGS_Flibotte