WormBase Tree Display for Variation: WBVar01800199

WBVar01800199 Name: Public_name: WBVar01800199
    Other_name (13)
    HGVSg: CHROMOSOME_V:g.15078714A>T
  Sequence_details: SMap: S_parent: Sequence: C01G10
    Flanking_sequences: ACATATCGATAATGCGTCGATTGCGTCTCT ATCAAAAGTGAGAAGATGAAAAGAGATATA
    Mapping_target: C01G10
    Source_location: 225 CHROMOSOME_V 15078697 15078697 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Substitution: A T
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00022930 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023286 From_analysis: Million_mutation_project_reanalysis
    Laboratory: VC
    Analysis: Million_mutation_project_reanalysis
    Status: Live
  Affects: Gene: WBGene00006808
      WBGene00305285
    Transcript: C01G10.11f.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: C01G10.11f.1:c.1065A>T
        HGVSp: CE45243:p.Leu355=
        cDNA_position: 1189
        CDS_position: 1065
        Protein_position: 355
        Exon_number: 10/12
        Codon_change: ctA/ctT
        Amino_acid_change: L
      C01G10.11d.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: C01G10.11d.1:c.615A>T
        HGVSp: CE45251:p.Leu205=
        cDNA_position: 615
        CDS_position: 615
        Protein_position: 205
        Exon_number: 4/5
        Codon_change: ctA/ctT
        Amino_acid_change: L
      C01G10.11e.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: C01G10.11e.1:c.261A>T
        HGVSp: CE45280:p.Leu87=
        cDNA_position: 261
        CDS_position: 261
        Protein_position: 87
        Exon_number: 2/3
        Codon_change: ctA/ctT
        Amino_acid_change: L
      C01G10.11b.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: C01G10.11b.1:c.1035A>T
        HGVSp: CE39211:p.Leu345=
        cDNA_position: 1046
        CDS_position: 1035
        Protein_position: 345
        Exon_number: 9/10
        Codon_change: ctA/ctT
        Amino_acid_change: L
      C01G10.11a.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: C01G10.11a.1:c.1035A>T
        HGVSp: CE39210:p.Leu345=
        cDNA_position: 1043
        CDS_position: 1035
        Protein_position: 345
        Exon_number: 9/11
        Codon_change: ctA/ctT
        Amino_acid_change: L
      C25D7.19
      C01G10.11c.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: C01G10.11c.1:c.762A>T
        HGVSp: CE45264:p.Leu254=
        cDNA_position: 762
        CDS_position: 762
        Protein_position: 254
        Exon_number: 6/7
        Codon_change: ctA/ctT
        Amino_acid_change: L
  Method: WGS_Flibotte