WormBase Tree Display for Variation: WBVar01468675

WBVar01468675 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01468675
    Other_name: cewivar00592902
      CE53186:p.Gly3804=
      F39C12.1.1:c.11412A>G
    HGVSg: CHROMOSOME_X:g.4839686T>C
  Sequence_details: SMap: S_parent: Sequence: F39C12
    Flanking_sequences: TATGCCGGAGCTGGTTGACGGTTCATCTGA CCAACGGTATTAAGTGCATCGAGAAGCGAA
    Mapping_target: F39C12
    Type_of_mutation: Substitution: t c
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023072 From_analysis: Million_mutation_project_reanalysis
          WGS_Andersen
      WBStrain00023084 From_analysis: WGS_Andersen
    Laboratory: QX
    Person: WBPerson1730
    Analysis: Million_mutation_project_reanalysis
      WGS_Andersen
    DB_info: Database: dbSNP_rs rs 193353977
        dbSNP_ss ss 295529896
    Status: Live
  Affects: Gene: WBGene00018193
    Transcript: F39C12.1.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: F39C12.1.1:c.11412A>G
        HGVSp: CE53186:p.Gly3804=
        cDNA_position: 11542
        CDS_position: 11412
        Protein_position: 3804
        Exon_number: 20/31
        Codon_change: ggA/ggG
        Amino_acid_change: G
  Reference: WBPaper00040707
  Method: WGS_Andersen