WormBase Tree Display for Variation: WBVar01518629

WBVar01518629 Name: Public_name: WBVar01518629
    Other_name: cewivar00043136
      CE35608:p.Ala383=
      T01G6.6b.1:c.1155C>G
      T01G6.6a.1:c.1149C>G
      CE42457:p.Ala385=
    HGVSg: CHROMOSOME_V:g.486784C>G
  Sequence_details: SMap: S_parent: Sequence: T01G6
    Flanking_sequences: CTGGGAAAAACGTTGGAAAAGAGAGTTGGC GAGAAATTCGATATCTTCCATTTGCATTTT
    Mapping_target: T01G6
    Source_location: 225 CHROMOSOME_V 486785 486785 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Substitution: C G
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00000032 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023191 From_analysis: Million_mutation_project_reanalysis
    Laboratory: VC
    Analysis: Million_mutation_project_reanalysis
    Status: Live
  Affects: Gene: WBGene00020153
    Transcript: T01G6.6b.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: T01G6.6b.1:c.1155C>G
        HGVSp: CE42457:p.Ala385=
        cDNA_position: 1188
        CDS_position: 1155
        Protein_position: 385
        Exon_number: 7/8
        Codon_change: gcC/gcG
        Amino_acid_change: A
      T01G6.6a.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: T01G6.6a.1:c.1149C>G
        HGVSp: CE35608:p.Ala383=
        cDNA_position: 1226
        CDS_position: 1149
        Protein_position: 383
        Exon_number: 7/8
        Codon_change: gcC/gcG
        Amino_acid_change: A
  Method: WGS_Flibotte