WormBase Tree Display for Variation: WBVar01698184

WBVar01698184 Name: Public_name: WBVar01698184
    Other_name: cewivar00394979
      C29F9.3a.1:c.657A>C
      CE30624:p.Glu202Asp
      C29F9.3b.1:c.*523A>C
      C29F9.3a.2:c.657A>C
      C29F9.3c.1:c.606A>C
      CE28896:p.Glu219Asp
    HGVSg: CHROMOSOME_III:g.126114A>C
  Sequence_details: SMap: S_parent: Sequence: C29F9
    Flanking_sequences: CGACGCTCGTGTTCCTCCAGAACTATTTGA TCCTTCTCGGTATCTCATTAAGGAAATTAA
    Mapping_target: C29F9
    Source_location: 225 CHROMOSOME_III 126113 126113 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Substitution: A C
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00008273 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023138 From_analysis: Million_mutation_project_reanalysis
      WBStrain00031113 From_analysis: Million_mutation_project_reanalysis
    Laboratory: VC
    Analysis: Million_mutation_project_reanalysis
    Status: Live
  Affects: Gene: WBGene00016218
    Transcript: C29F9.3b.1 VEP_consequence: 3_prime_UTR_variant
        VEP_impact: MODIFIER
        HGVSc: C29F9.3b.1:c.*523A>C
        cDNA_position: 799
        Exon_number: 6/6
      C29F9.3a.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        SIFT: 0.15 tolerated_low_confidence
        PolyPhen: 0.893 possibly_damaging
        HGVSc: C29F9.3a.1:c.657A>C
        HGVSp: CE28896:p.Glu219Asp
        cDNA_position: 684
        CDS_position: 657
        Protein_position: 219
        Exon_number: 5/9
        Codon_change: gaA/gaC
        Amino_acid_change: E/D
      C29F9.3c.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        SIFT: 0.13 tolerated_low_confidence
        PolyPhen: 0.455 possibly_damaging
        HGVSc: C29F9.3c.1:c.606A>C
        HGVSp: CE30624:p.Glu202Asp
        cDNA_position: 620
        CDS_position: 606
        Protein_position: 202
        Exon_number: 6/8
        Codon_change: gaA/gaC
        Amino_acid_change: E/D
      C29F9.3a.2 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        SIFT: 0.15 tolerated_low_confidence
        PolyPhen: 0.893 possibly_damaging
        HGVSc: C29F9.3a.2:c.657A>C
        HGVSp: CE28896:p.Glu219Asp
        cDNA_position: 671
        CDS_position: 657
        Protein_position: 219
        Exon_number: 5/9
        Codon_change: gaA/gaC
        Amino_acid_change: E/D
  Method: WGS_Flibotte