WormBase Tree Display for Variation: WBVar02134006

WBVar02134006 Evidence: Paper_evidence: WBPaper00045317
  Name: Public_name: h6198
    Other_name: F58F9.9b.1:c.190C>T
      CE49170:p.Pro64Ser
      CE38613:p.Pro64Ser
      F58F9.9a.1:c.190C>T
    HGVSg: CHROMOSOME_IV:g.6240539C>T
  Sequence_details: SMap: S_parent: Sequence: F58F9
    Flanking_sequences: AAAGATTTTGTACACGAGGAAGTGCCTATCCACAAATATT CAAACTGTGCATGTGTGTAAGTTCTAGCAAATTTTGCTGA
    Mapping_target: CHROMOSOME_IV
    Source_location: 200 CHROMOSOME_IV 6240523 6240523
    Type_of_mutation: Substitution: C T
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023699
    Laboratory: KR
    Analysis: WGS_Rose
    Status: Live
  Affects: Gene: WBGene00044307
    Transcript: F58F9.9a.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: F58F9.9a.1:c.190C>T
        HGVSp: CE38613:p.Pro64Ser
        cDNA_position: 203
        CDS_position: 190
        Protein_position: 64
        Exon_number: 3/5
        Codon_change: Cca/Tca
        Amino_acid_change: P/S
      F58F9.9b.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: F58F9.9b.1:c.190C>T
        HGVSp: CE49170:p.Pro64Ser
        cDNA_position: 190
        CDS_position: 190
        Protein_position: 64
        Exon_number: 2/5
        Codon_change: Cca/Tca
        Amino_acid_change: P/S
  Reference: WBPaper00040589
    WBPaper00000975
    WBPaper00003985
    WBPaper00000699
    WBPaper00045317
  Method: WGS_Rose