WormBase Tree Display for Variation: WBVar01793442

WBVar01793442 Name: Public_name: WBVar01793442
    Other_name (16)
    HGVSg: CHROMOSOME_III:g.9552710C>T
  Sequence_details: SMap: S_parent: Sequence: ZK1098
    Flanking_sequences: CACTTCCGAATGTTGAAGCTGAAGTATCAT TGTTCCGATTCCTGTCTGTTGTCGTCCACT
    Mapping_target: ZK1098
    Source_location: 225 CHROMOSOME_III 9552625 9552625 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Substitution: C T
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023286 From_analysis: Million_mutation_project_reanalysis
    Laboratory: VC
    Analysis: Million_mutation_project_reanalysis
    Status: Live
  Affects: Gene: WBGene00006755
    Transcript: ZK1098.10g.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: ZK1098.10g.1:c.734C>T
        HGVSp: CE48500:p.Ser245Phe
        cDNA_position: 734
        CDS_position: 734
        Protein_position: 245
        Exon_number: 5/14
        Codon_change: tCt/tTt
        Amino_acid_change: S/F
      ZK1098.10b.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: ZK1098.10b.1:c.1685C>T
        HGVSp: CE31846:p.Ser562Phe
        cDNA_position: 1749
        CDS_position: 1685
        Protein_position: 562
        Exon_number: 12/22
        Codon_change: tCt/tTt
        Amino_acid_change: S/F
      ZK1098.10a.2 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: ZK1098.10a.2:c.1631C>T
        HGVSp: CE00363:p.Ser544Phe
        cDNA_position: 1775
        CDS_position: 1631
        Protein_position: 544
        Exon_number: 13/23
        Codon_change: tCt/tTt
        Amino_acid_change: S/F
      ZK1098.10o.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: ZK1098.10o.1:c.752C>T
        HGVSp: CE48464:p.Ser251Phe
        cDNA_position: 752
        CDS_position: 752
        Protein_position: 251
        Exon_number: 6/15
        Codon_change: tCt/tTt
        Amino_acid_change: S/F
      ZK1098.10a.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: ZK1098.10a.1:c.1631C>T
        HGVSp: CE00363:p.Ser544Phe
        cDNA_position: 1840
        CDS_position: 1631
        Protein_position: 544
        Exon_number: 14/24
        Codon_change: tCt/tTt
        Amino_acid_change: S/F
      ZK1098.10f.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: ZK1098.10f.1:c.938C>T
        HGVSp: CE44092:p.Ser313Phe
        cDNA_position: 938
        CDS_position: 938
        Protein_position: 313
        Exon_number: 7/16
        Codon_change: tCt/tTt
        Amino_acid_change: S/F
      ZK1098.10e.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: ZK1098.10e.1:c.1784C>T
        HGVSp: CE43483:p.Ser595Phe
        cDNA_position: 1848
        CDS_position: 1784
        Protein_position: 595
        Exon_number: 13/23
        Codon_change: tCt/tTt
        Amino_acid_change: S/F
      ZK1098.10d.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: ZK1098.10d.1:c.1685C>T
        HGVSp: CE41491:p.Ser562Phe
        cDNA_position: 1749
        CDS_position: 1685
        Protein_position: 562
        Exon_number: 12/23
        Codon_change: tCt/tTt
        Amino_acid_change: S/F
  Method: WGS_Flibotte