WormBase Tree Display for Variation: WBVar01869502

WBVar01869502 Name: Public_name: WBVar01869502
    Other_name (21)
    HGVSg: CHROMOSOME_V:g.13370975G>A
  Sequence_details: SMap: S_parent: Sequence: M04G12
    Flanking_sequences: TACCTGTGCAGCTGCCGCGGCTGCCGCGGC AGAGTCGCTGCGTTGGCACCCATCGGTGGA
    Mapping_target: M04G12
    Source_location: 225 CHROMOSOME_V 13370962 13370962 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Substitution: G A
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023072 From_analysis: Million_mutation_project_reanalysis
    Laboratory: VC
    Analysis: Million_mutation_project_reanalysis
    Status: Live
  Affects: Gene: WBGene00010867
    Transcript: M04G12.1j.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: M04G12.1j.1:c.168C>T
        HGVSp: CE53001:p.Leu56=
        cDNA_position: 168
        CDS_position: 168
        Protein_position: 56
        Exon_number: 1/2
        Codon_change: ctC/ctT
        Amino_acid_change: L
      M04G12.1i.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: M04G12.1i.1:c.627C>T
        HGVSp: CE53124:p.Leu209=
        cDNA_position: 627
        CDS_position: 627
        Protein_position: 209
        Exon_number: 3/5
        Codon_change: ctC/ctT
        Amino_acid_change: L
      M04G12.1b.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: M04G12.1b.1:c.1101C>T
        HGVSp: CE21079:p.Leu367=
        cDNA_position: 1298
        CDS_position: 1101
        Protein_position: 367
        Exon_number: 6/8
        Codon_change: ctC/ctT
        Amino_acid_change: L
      M04G12.1f.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: M04G12.1f.1:c.1101C>T
        HGVSp: CE52967:p.Leu367=
        cDNA_position: 1101
        CDS_position: 1101
        Protein_position: 367
        Exon_number: 5/7
        Codon_change: ctC/ctT
        Amino_acid_change: L
      M04G12.1g.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: M04G12.1g.1:c.1182C>T
        HGVSp: CE12422:p.Leu394=
        cDNA_position: 1182
        CDS_position: 1182
        Protein_position: 394
        Exon_number: 4/6
        Codon_change: ctC/ctT
        Amino_acid_change: L
      M04G12.1a.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: M04G12.1a.1:c.1182C>T
        HGVSp: CE32470:p.Leu394=
        cDNA_position: 1304
        CDS_position: 1182
        Protein_position: 394
        Exon_number: 5/8
        Codon_change: ctC/ctT
        Amino_acid_change: L
      M04G12.1h.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: M04G12.1h.1:c.1071C>T
        HGVSp: CE53042:p.Leu357=
        cDNA_position: 1071
        CDS_position: 1071
        Protein_position: 357
        Exon_number: 4/5
        Codon_change: ctC/ctT
        Amino_acid_change: L
      M04G12.1d.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: M04G12.1d.1:c.627C>T
        HGVSp: CE45375:p.Leu209=
        cDNA_position: 627
        CDS_position: 627
        Protein_position: 209
        Exon_number: 3/4
        Codon_change: ctC/ctT
        Amino_acid_change: L
      M04G12.1c.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: M04G12.1c.1:c.1071C>T
        HGVSp: CE42519:p.Leu357=
        cDNA_position: 1071
        CDS_position: 1071
        Protein_position: 357
        Exon_number: 4/6
        Codon_change: ctC/ctT
        Amino_acid_change: L
      M04G12.1e.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: M04G12.1e.1:c.168C>T
        HGVSp: CE48395:p.Leu56=
        cDNA_position: 168
        CDS_position: 168
        Protein_position: 56
        Exon_number: 1/3
        Codon_change: ctC/ctT
        Amino_acid_change: L
  Method: WGS_Flibotte