WormBase Tree Display for Variation: WBVar02135577

WBVar02135577 Evidence: Paper_evidence: WBPaper00045317
  Name: Public_name: h6661
    Other_name: C14C6.4.1:c.382C>T
      CE50872:p.Pro128Ser
    HGVSg: CHROMOSOME_V:g.540269C>T
  Sequence_details: SMap: S_parent: Sequence: C14C6
    Flanking_sequences: ATTACCTTCGAGCAACTCGACAAGCTCAGTGGAATCAACA CATTATCCTCTCCAGTGGACTCTACAGCAGACCCTTCCCC
    Mapping_target: CHROMOSOME_V
    Source_location: 200 CHROMOSOME_V 540270 540270
    Type_of_mutation: Substitution: C T
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023687
    Laboratory: KR
    Analysis: WGS_Rose
    Status: Live
  Affects: Gene: WBGene00015758
    Transcript: C14C6.4.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: C14C6.4.1:c.382C>T
        HGVSp: CE50872:p.Pro128Ser
        cDNA_position: 382
        CDS_position: 382
        Protein_position: 128
        Exon_number: 5/10
        Codon_change: Cca/Tca
        Amino_acid_change: P/S
  Reference: WBPaper00040589
    WBPaper00000975
    WBPaper00003985
    WBPaper00000699
    WBPaper00045317
  Method: WGS_Rose