WormBase Tree Display for Variation: WBVar00089591

WBVar00089591 Evidence: Paper_evidence: WBPaper00004497
  Name: Public_name: n538
    Other_name: CE43285:p.Pro391Ser
      T25C12.1b.1:c.1165C>T
      T25C12.1a.1:c.1171C>T
      CE03734:p.Pro389Ser
    HGVSg: CHROMOSOME_X:g.11483676C>T
  Sequence_details: SMap: S_parent: Sequence: T25C12
    Flanking_sequences: ggtctcaaccactcgaactatgcaaatctt caatcaaaggaatttgctatattcaacgta
    Mapping_target: T25C12
    Type_of_mutation: Substitution: c t Paper_evidence: WBPaper00004497
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Laboratory: MT
    Status: Live
  Linked_to: WBVar00089588
    WBVar00089592
  Affects: Gene: WBGene00003003
    Transcript: T25C12.1b.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: T25C12.1b.1:c.1165C>T
        HGVSp: CE03734:p.Pro389Ser
        cDNA_position: 1296
        CDS_position: 1165
        Protein_position: 389
        Exon_number: 8/12
        Codon_change: Cca/Tca
        Amino_acid_change: P/S
      T25C12.1a.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: T25C12.1a.1:c.1171C>T
        HGVSp: CE43285:p.Pro391Ser
        cDNA_position: 1293
        CDS_position: 1171
        Protein_position: 391
        Exon_number: 10/14
        Codon_change: Cca/Tca
        Amino_acid_change: P/S
  Isolation: Mutagen: EMS Paper_evidence: WBPaper00004497
  Genetics: Interpolated_map_position: X 3.86625
  Reference: WBPaper00004497
  Method: Substitution_allele