WormBase Tree Display for Variation: WBVar01460158

WBVar01460158 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01460158
    Other_name (17)
    HGVSg: CHROMOSOME_V:g.6185194G>C
  Sequence_details: SMap: S_parent: Sequence: H05O09
    Flanking_sequences: CAAAGTTTTGACAAGTGTCAGCTTGTTTTC GTTTTTAAACCAATTTCGACTGGAATTTCA
    Mapping_target: H05O09
    Type_of_mutation: Substitution: g c
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00031279 From_analysis: WGS_Andersen
      WBStrain00031284 From_analysis: WGS_Andersen
    Laboratory: QX
    Person: WBPerson1730
    Analysis: WGS_Andersen
    DB_info: Database: dbSNP_rs rs 193345815
        dbSNP_ss ss 295521734
    Status: Live
  Affects: Gene: WBGene00006436
    Transcript: W06H8.8f.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: W06H8.8f.1:c.8751C>G
        HGVSp: CE52428:p.Thr2917=
        cDNA_position: 8751
        CDS_position: 8751
        Protein_position: 2917
        Exon_number: 21/60
        Codon_change: acC/acG
        Amino_acid_change: T
      W06H8.8b.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: W06H8.8b.1:c.7473C>G
        HGVSp: CE52423:p.Thr2491=
        cDNA_position: 7566
        CDS_position: 7473
        Protein_position: 2491
        Exon_number: 21/58
        Codon_change: acC/acG
        Amino_acid_change: T
      W06H8.8a.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: W06H8.8a.1:c.8751C>G
        HGVSp: CE52437:p.Thr2917=
        cDNA_position: 8844
        CDS_position: 8751
        Protein_position: 2917
        Exon_number: 22/61
        Codon_change: acC/acG
        Amino_acid_change: T
      W06H8.8i.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: W06H8.8i.1:c.7473C>G
        HGVSp: CE52442:p.Thr2491=
        cDNA_position: 7473
        CDS_position: 7473
        Protein_position: 2491
        Exon_number: 20/57
        Codon_change: acC/acG
        Amino_acid_change: T
      W06H8.8a.2 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: W06H8.8a.2:c.8751C>G
        HGVSp: CE52437:p.Thr2917=
        cDNA_position: 8844
        CDS_position: 8751
        Protein_position: 2917
        Exon_number: 22/60
        Codon_change: acC/acG
        Amino_acid_change: T
      W06H8.8h.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: W06H8.8h.1:c.8751C>G
        HGVSp: CE52451:p.Thr2917=
        cDNA_position: 8751
        CDS_position: 8751
        Protein_position: 2917
        Exon_number: 21/58
        Codon_change: acC/acG
        Amino_acid_change: T
      W06H8.8d.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: W06H8.8d.1:c.8751C>G
        HGVSp: CE52449:p.Thr2917=
        cDNA_position: 8751
        CDS_position: 8751
        Protein_position: 2917
        Exon_number: 21/58
        Codon_change: acC/acG
        Amino_acid_change: T
      W06H8.8e.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: W06H8.8e.1:c.7473C>G
        HGVSp: CE52441:p.Thr2491=
        cDNA_position: 7473
        CDS_position: 7473
        Protein_position: 2491
        Exon_number: 20/56
        Codon_change: acC/acG
        Amino_acid_change: T
      W06H8.8g.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: W06H8.8g.1:c.7473C>G
        HGVSp: CE52417:p.Thr2491=
        cDNA_position: 7473
        CDS_position: 7473
        Protein_position: 2491
        Exon_number: 20/58
        Codon_change: acC/acG
        Amino_acid_change: T
  Reference: WBPaper00040707
  Method: WGS_Andersen