WormBase Tree Display for Variation: WBVar01644033

WBVar01644033 Name: Public_name: WBVar01644033
    Other_name (17)
    HGVSg: CHROMOSOME_III:g.4257986G>C
  Sequence_details: SMap: S_parent: Sequence: T08A11
    Flanking_sequences: TCAATTGTTCCACGTCGTGAGGGAGATGTG CACGAAGTTTGGTTAGAGCTGCTGGAACTA
    Mapping_target: T08A11
    Source_location: 225 CHROMOSOME_III 4257959 4257959 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Substitution: G C
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00006629 From_analysis: Million_mutation_project_reanalysis
      WBStrain00006637 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023018 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023072 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023191 From_analysis: Million_mutation_project_reanalysis
      WBStrain00024204 From_analysis: Million_mutation_project_reanalysis
    Laboratory: VC
    Analysis: Million_mutation_project_reanalysis
    Status: Live
  Affects: Gene: WBGene00011604
    Transcript: T08A11.1e.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: T08A11.1e.1:c.2312C>G
        HGVSp: CE54607:p.Ala771Gly
        cDNA_position: 2312
        CDS_position: 2312
        Protein_position: 771
        Exon_number: 9/18
        Codon_change: gCc/gGc
        Amino_acid_change: A/G
      T08A11.1g.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: T08A11.1g.1:c.2312C>G
        HGVSp: CE54616:p.Ala771Gly
        cDNA_position: 2408
        CDS_position: 2312
        Protein_position: 771
        Exon_number: 10/19
        Codon_change: gCc/gGc
        Amino_acid_change: A/G
      T08A11.1h.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: T08A11.1h.1:c.2318C>G
        HGVSp: CE54610:p.Ala773Gly
        cDNA_position: 2414
        CDS_position: 2318
        Protein_position: 773
        Exon_number: 10/19
        Codon_change: gCc/gGc
        Amino_acid_change: A/G
      T08A11.1d.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: T08A11.1d.1:c.2318C>G
        HGVSp: CE54612:p.Ala773Gly
        cDNA_position: 2414
        CDS_position: 2318
        Protein_position: 773
        Exon_number: 10/19
        Codon_change: gCc/gGc
        Amino_acid_change: A/G
      T08A11.1f.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: T08A11.1f.1:c.2318C>G
        HGVSp: CE54622:p.Ala773Gly
        cDNA_position: 2318
        CDS_position: 2318
        Protein_position: 773
        Exon_number: 9/18
        Codon_change: gCc/gGc
        Amino_acid_change: A/G
      T08A11.1c.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: T08A11.1c.1:c.2312C>G
        HGVSp: CE54609:p.Ala771Gly
        cDNA_position: 2312
        CDS_position: 2312
        Protein_position: 771
        Exon_number: 9/18
        Codon_change: gCc/gGc
        Amino_acid_change: A/G
      T08A11.1b.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: T08A11.1b.1:c.2318C>G
        HGVSp: CE54613:p.Ala773Gly
        cDNA_position: 2414
        CDS_position: 2318
        Protein_position: 773
        Exon_number: 10/19
        Codon_change: gCc/gGc
        Amino_acid_change: A/G
      T08A11.1a.1 (12)
  Method: WGS_Flibotte