WormBase Tree Display for Variation: WBVar02129517

WBVar02129517 Evidence: Paper_evidence: WBPaper00045317
  Name: Public_name: h4920
    Other_name: K02F6.9.1:c.744G>T
      CE21017:p.Ala248=
      K02F6.9.2:c.744G>T
    HGVSg: CHROMOSOME_II:g.2561205C>A
  Sequence_details: SMap: S_parent: Sequence: Y47G7C
    Flanking_sequences: CCGTCAGATTTCTCGATTTCGACATGTTATCATTGTCCAG GCCAGGTTTCTATAGTCGGCAAGCTCAAAAATTGGTTGGA
    Mapping_target: CHROMOSOME_II
    Source_location: 200 CHROMOSOME_II 2561206 2561206
    Type_of_mutation: Substitution: C A
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023666
    Laboratory: KR
    Analysis: WGS_Rose
    Status: Live
  Affects: Gene: WBGene00019343
    Transcript: K02F6.9.2 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: K02F6.9.2:c.744G>T
        HGVSp: CE21017:p.Ala248=
        cDNA_position: 1000
        CDS_position: 744
        Protein_position: 248
        Exon_number: 8/15
        Codon_change: gcG/gcT
        Amino_acid_change: A
      K02F6.9.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: K02F6.9.1:c.744G>T
        HGVSp: CE21017:p.Ala248=
        cDNA_position: 1069
        CDS_position: 744
        Protein_position: 248
        Exon_number: 8/15
        Codon_change: gcG/gcT
        Amino_acid_change: A
  Reference: WBPaper00040589
    WBPaper00000975
    WBPaper00003985
    WBPaper00000699
    WBPaper00045317
  Method: WGS_Rose