WormBase Tree Display for Variation: WBVar02136534

WBVar02136534 Evidence: Paper_evidence: WBPaper00045317
  Name: Public_name: h9983
    Other_name: W02F12.5.1:c.1173C>T
      CE31083:p.Phe391=
    HGVSg: CHROMOSOME_V:g.6707658G>A
  Sequence_details: SMap: S_parent: Sequence: W02F12
    Flanking_sequences: CCAAAATTGCACTTTGTGGTGGATTGATGATTGGGGTTCC AACATGGATCCGAAGACTCCACCGTTAGAAATCGTGAAGG
    Mapping_target: CHROMOSOME_V
    Source_location: 200 CHROMOSOME_V 6707641 6707641
    Type_of_mutation: Substitution: G A
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023744
    Laboratory: KR
    Analysis: WGS_Rose
    Status: Live
  Affects: Gene: WBGene00020950
    Transcript: W02F12.5.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: W02F12.5.1:c.1173C>T
        HGVSp: CE31083:p.Phe391=
        cDNA_position: 1184
        CDS_position: 1173
        Protein_position: 391
        Exon_number: 7/9
        Codon_change: ttC/ttT
        Amino_acid_change: F
  Reference: WBPaper00040589
    WBPaper00000975
    WBPaper00003985
    WBPaper00000699
    WBPaper00045317
  Method: WGS_Rose