WormBase Tree Display for Variation: WBVar00090748

WBVar00090748 Evidence: Paper_evidence: WBPaper00013412
      WBPaper00027336
  Name: Public_name: n3681
    Other_name (2)
    HGVSg: CHROMOSOME_V:g.7083011C>T
  Sequence_details: SMap: S_parent: Sequence: VC5
    Flanking_sequences: tatgaactctcgaaaattgaacagaagaca gatcacccgaaaaaccactatcagatttgg
    Mapping_target: VC5
    Type_of_mutation: Substitution: g a Paper_evidence: WBPaper00027336
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00027398
    Laboratory: MT
    Status: Live
  Affects: Gene: WBGene00007029
    Transcript: VC5.4.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        SIFT: 0 deleterious
        PolyPhen: 1 probably_damaging
        HGVSc: VC5.4.1:c.1021G>A
        HGVSp: CE21225:p.Gly341Arg
        cDNA_position: 1030
        CDS_position: 1021
        Protein_position: 341
        Exon_number: 5/7
        Codon_change: Gga/Aga
        Amino_acid_change: G/R
    Interactor: WBInteraction000503733
  Genetics: Interpolated_map_position: V 0.546172
  Reference: WBPaper00027336
    WBPaper00013412
  Remark: Manually curated Gene associations preserved as a text remark so that VEP is the canonical predictor of consequence: WBGene00007029 Missense 341 G to R Person_evidence: WBPerson31184"
        WBPerson31184
  Method: Substitution_allele