WormBase Tree Display for Variation: WBVar01386813

WBVar01386813 Evidence: Paper_evidence: WBPaper00037807
  Name: Public_name: WBVar01386813
    Other_name: cewivar00189783
      CE19488:p.Phe385=
      H10E21.3b.1:c.1155C>T
      CE28733:p.Phe367=
      H10E21.3a.1:c.1101C>T
    HGVSg: CHROMOSOME_III:g.12623G>A
  Sequence_details: SMap: S_parent: Sequence: H10E21
    Flanking_sequences: CTGTTAACTTGTTGGGTGATTAGGTGACGTTTCGCCTCTGACACGTTTTC AAACCTGGAATTTTTTAGAGTTTTGCAAAGATTTTCAATAACACAAGCGT
    Mapping_target: H10E21
    Type_of_mutation: Substitution: g A 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
      WBStrain00023138 From_analysis: Million_mutation_project_reanalysis
      WBStrain00027647 From_analysis: Million_mutation_project_reanalysis
    Laboratory: AX
    Analysis: WGS_De_Bono
      Million_mutation_project_reanalysis
    DB_info: Database: dbSNP_ss ss 539062264
    Status: Live
  Affects: Gene: WBGene00003670
    Transcript: H10E21.3b.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: H10E21.3b.1:c.1155C>T
        HGVSp: CE19488:p.Phe385=
        cDNA_position: 1155
        CDS_position: 1155
        Protein_position: 385
        Exon_number: 5/7
        Codon_change: ttC/ttT
        Amino_acid_change: F
      H10E21.3a.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: H10E21.3a.1:c.1101C>T
        HGVSp: CE28733:p.Phe367=
        cDNA_position: 1217
        CDS_position: 1101
        Protein_position: 367
        Exon_number: 7/9
        Codon_change: ttC/ttT
        Amino_acid_change: F
  Reference: WBPaper00037807
  Method: WGS_De_Bono