WormBase Tree Display for Variation: WBVar01386802

WBVar01386802 Evidence: Paper_evidence: WBPaper00037807
  Name: Public_name: WBVar01386802
    Other_name: cewivar00189771
      CE19488:p.Leu496=
      H10E21.3a.1:c.1434T>C
      CE28733:p.Leu478=
      H10E21.3b.1:c.1488T>C
    HGVSg: CHROMOSOME_III:g.12216A>G
  Sequence_details: SMap: S_parent: Sequence: H10E21
    Flanking_sequences: AAAGCCCAAAAATTCATTTATTCTCATTTTTCAAGCTTTGCCTGACCCAA AGCACATCATTATTATTATTAACAACATTAATCCCATTCCGCATCGCCCG
    Mapping_target: H10E21
    Type_of_mutation: Substitution: a G Paper_evidence: WBPaper00037807
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00004602 From_analysis: Million_mutation_project_reanalysis
          WGS_De_Bono
      WBStrain00027647 From_analysis: Million_mutation_project_reanalysis
    Laboratory: AX
    Analysis: WGS_De_Bono
      Million_mutation_project_reanalysis
    DB_info: Database: dbSNP_ss ss 539062253
    Status: Live
  Affects: Gene: WBGene00003670
    Transcript: H10E21.3b.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: H10E21.3b.1:c.1488T>C
        HGVSp: CE19488:p.Leu496=
        cDNA_position: 1488
        CDS_position: 1488
        Protein_position: 496
        Exon_number: 6/7
        Codon_change: ctT/ctC
        Amino_acid_change: L
      H10E21.3a.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: H10E21.3a.1:c.1434T>C
        HGVSp: CE28733:p.Leu478=
        cDNA_position: 1550
        CDS_position: 1434
        Protein_position: 478
        Exon_number: 8/9
        Codon_change: ctT/ctC
        Amino_acid_change: L
  Reference: WBPaper00037807
  Method: WGS_De_Bono