WormBase Tree Display for Variation: WBVar00089179

WBVar00089179 Evidence: Paper_evidence: WBPaper00004764
  Name: Public_name: mn602
    Other_name: CE15742:p.Ser223Pro
      CC4.3.2:c.667T>C
      CC4.3.1:c.667T>C
    HGVSg: CHROMOSOME_I:g.12997983T>C
  Sequence_details: SMap: S_parent: Sequence: CC4
    Flanking_sequences: tcagaaagttatcccgaatcggcagttttc caccggacgctaattatcttgtttctggct
    Mapping_target: CC4
    Type_of_mutation: Substitution: t c Paper_evidence: WBPaper00004764
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00034402
    Laboratory: SP
    Status: Live
  Affects: Gene: WBGene00004895
    Transcript: CC4.3.2 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: CC4.3.2:c.667T>C
        HGVSp: CE15742:p.Ser223Pro
        cDNA_position: 753
        CDS_position: 667
        Protein_position: 223
        Exon_number: 6/14
        Codon_change: Tca/Cca
        Amino_acid_change: S/P
      CC4.3.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: CC4.3.1:c.667T>C
        HGVSp: CE15742:p.Ser223Pro
        cDNA_position: 753
        CDS_position: 667
        Protein_position: 223
        Exon_number: 6/13
        Codon_change: Tca/Cca
        Amino_acid_change: S/P
  Genetics: Interpolated_map_position: I 16.8334
  Reference: WBPaper00004764
  Method: Substitution_allele