WormBase Tree Display for Variation: WBVar01306174

WBVar01306174 Evidence: Paper_evidence: WBPaper00037807
  Name: Public_name: WBVar01306174
    Other_name: cewivar00466448
      F59E12.2.1:c.1310+755T>C
      F59E12.12.1:c.318A>G
      CE11540:p.Lys106=
    HGVSg: CHROMOSOME_II:g.5652057T>C
  Sequence_details: SMap: S_parent: Sequence: F59E12
    Flanking_sequences: GATGGTCCGGTTTTGCAAGAACAGCATTGTCCTCCTGGAGCCAAAGAGGA TTGCTGCTACTGAATCCGGACTCGGCATTTGTATTCGATTCAGCGAAATC
    Mapping_target: F59E12
    Type_of_mutation: Substitution: t C Paper_evidence: WBPaper00037807
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00022850 From_analysis: Million_mutation_project_reanalysis
          WGS_De_Bono
      WBStrain00023191 From_analysis: Million_mutation_project_reanalysis
    Laboratory: AX
    Analysis: WGS_De_Bono
      Million_mutation_project_reanalysis
    DB_info: Database: dbSNP_ss ss 539163836
    Status: Live
  Affects: Gene: WBGene00000252
      WBGene00006988
    Transcript: F59E12.12.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: F59E12.12.1:c.318A>G
        HGVSp: CE11540:p.Lys106=
        cDNA_position: 331
        CDS_position: 318
        Protein_position: 106
        Exon_number: 3/4
        Codon_change: aaA/aaG
        Amino_acid_change: K
      F59E12.2.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F59E12.2.1:c.1310+755T>C
        Intron_number: 5/8
  Reference: WBPaper00037807
  Method: WGS_De_Bono