WormBase Tree Display for Variation: WBVar01069153

WBVar01069153 Name: Public_name: gk427870
    Other_name: C47E8.4b.1:c.312C>T
      CE44798:p.Phe104=
      C47E8.4a.1:c.732C>T
      CE44805:p.Phe244=
      CE44813:p.Phe12=
      C47E8.4c.1:c.36C>T
    HGVSg: CHROMOSOME_V:g.14684073G>A
  Sequence_details: SMap: S_parent: Sequence: C47E8
    Flanking_sequences: GGACCAGTCTTTCCCATTGCTTTTGTGACTATAAAGTCTTGGAACGTGTA AAATGTGGTATGATGAGATCCTCTTTGACGAACATCAGATTCTCGGCTGT
    Mapping_target: C47E8
    Type_of_mutation: Substitution: G A
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00038886
    Laboratory: VC
    Analysis: Million_Mutation_Project
    Status: Live
  Affects: Gene: WBGene00008143
    Transcript: C47E8.4c.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: C47E8.4c.1:c.36C>T
        HGVSp: CE44813:p.Phe12=
        cDNA_position: 36
        CDS_position: 36
        Protein_position: 12
        Exon_number: 1/1
        Codon_change: ttC/ttT
        Amino_acid_change: F
      C47E8.4b.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: C47E8.4b.1:c.312C>T
        HGVSp: CE44798:p.Phe104=
        cDNA_position: 312
        CDS_position: 312
        Protein_position: 104
        Exon_number: 3/3
        Codon_change: ttC/ttT
        Amino_acid_change: F
      C47E8.4a.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: C47E8.4a.1:c.732C>T
        HGVSp: CE44805:p.Phe244=
        cDNA_position: 740
        CDS_position: 732
        Protein_position: 244
        Exon_number: 8/9
        Codon_change: ttC/ttT
        Amino_acid_change: F
  Reference: WBPaper00042537
  Method: Million_mutation