WormBase Tree Display for Variation: WBVar01909767

WBVar01909767 Name: Public_name: WBVar01909767
    Other_name: cewivar00625664
      CE42754:p.Ala43=
      F07A5.7a.2:c.1086C>T
      F07A5.7b.1:c.129C>T
      CE09197:p.Ala362=
      F07A5.7a.1:c.1086C>T
    HGVSg: CHROMOSOME_I:g.7379200G>A
  Sequence_details: SMap: S_parent: Sequence: F07A5
    Flanking_sequences: GGCACGCTCCAAGAGAGCAATGGTGTTCTG GCCTTCTCAAGATCAACGATAAGAACCTCG
    Mapping_target: F07A5
    Source_location: 225 CHROMOSOME_I 7379197 7379197 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Substitution: G A
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00027652 From_analysis: Million_mutation_project_reanalysis
    Laboratory: VC
    Analysis: Million_mutation_project_reanalysis
    Status: Live
  Affects: Gene: WBGene00006754
    Transcript: F07A5.7a.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: F07A5.7a.1:c.1086C>T
        HGVSp: CE09197:p.Ala362=
        cDNA_position: 1200
        CDS_position: 1086
        Protein_position: 362
        Exon_number: 9/14
        Codon_change: gcC/gcT
        Amino_acid_change: A
      F07A5.7a.2 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: F07A5.7a.2:c.1086C>T
        HGVSp: CE09197:p.Ala362=
        cDNA_position: 1200
        CDS_position: 1086
        Protein_position: 362
        Exon_number: 9/13
        Codon_change: gcC/gcT
        Amino_acid_change: A
      F07A5.7b.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: F07A5.7b.1:c.129C>T
        HGVSp: CE42754:p.Ala43=
        cDNA_position: 129
        CDS_position: 129
        Protein_position: 43
        Exon_number: 1/4
        Codon_change: gcC/gcT
        Amino_acid_change: A
  Method: WGS_Flibotte