WormBase Tree Display for Variation: WBVar00073461

WBVar00073461 Name: Public_name: WBVar00073461
    Other_name: haw97821
      cewivar00266367
      F26F2.7c.1:c.897C>T
      CE52915:p.Phe509=
      F26F2.7b.1:c.1527C>T
      CE52844:p.Phe163=
      CE52948:p.Phe299=
      F26F2.7a.1:c.1521C>T
      F26F2.7d.1:c.489C>T
      CE19819:p.Phe507=
    HGVSg: CHROMOSOME_V:g.20588459C>T
  Sequence_details: SMap: S_parent: Sequence: F26F2
    Flanking_sequences: caggaatcggctggcttctggtgtt gccgtgaaaatctgcaatggagtag
    Mapping_target: F26F2
    Type_of_mutation: Substitution: C T
    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.1527C>T
        HGVSp: CE52915:p.Phe509=
        cDNA_position: 1578
        CDS_position: 1527
        Protein_position: 509
        Exon_number: 13/17
        Codon_change: ttC/ttT
        Amino_acid_change: F
      F26F2.7d.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: F26F2.7d.1:c.489C>T
        HGVSp: CE52844:p.Phe163=
        cDNA_position: 685
        CDS_position: 489
        Protein_position: 163
        Exon_number: 5/9
        Codon_change: ttC/ttT
        Amino_acid_change: F
      F26F2.7c.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: F26F2.7c.1:c.897C>T
        HGVSp: CE52948:p.Phe299=
        cDNA_position: 897
        CDS_position: 897
        Protein_position: 299
        Exon_number: 6/9
        Codon_change: ttC/ttT
        Amino_acid_change: F
      F26F2.7a.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: F26F2.7a.1:c.1521C>T
        HGVSp: CE19819:p.Phe507=
        cDNA_position: 1566
        CDS_position: 1521
        Protein_position: 507
        Exon_number: 13/17
        Codon_change: ttC/ttT
        Amino_acid_change: F
  Remark: [20081124 db] this Variation was previously named hw97821
  Method: WGS_Hawaiian_Waterston