WormBase Tree Display for Variation: WBVar00275617

WBVar00275617 Evidence: Paper_evidence: WBPaper00036200
  Name: Public_name: gk2533
    Other_name: CE44996:p.Asn2747=
      B0228.4a.1:c.3772+5468T>C
      B0228.4c.1:c.8241T>C
    HGVSg: CHROMOSOME_II:g.7735628T>C
  Sequence_details: SMap: S_parent: Sequence: B0228
    Flanking_sequences: AGTGGTTGCTGCTGAATTTGGAATTGCAAA GAAAGTGTTCAAAAGGCATTGGAAGTTTTG
    Mapping_target: B0228
    Type_of_mutation: Substitution: T C
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00037340
    Laboratory: VC
    Person: WBPerson427
    Analysis: Million_Mutation_Pilot_Project
    KO_consortium_allele
    Status: Live
  Affects: Gene: WBGene00015061
    Transcript: B0228.4c.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: B0228.4c.1:c.8241T>C
        HGVSp: CE44996:p.Asn2747=
        cDNA_position: 8241
        CDS_position: 8241
        Protein_position: 2747
        Exon_number: 13/25
        Codon_change: aaT/aaC
        Amino_acid_change: N
      B0228.4a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: B0228.4a.1:c.3772+5468T>C
        Intron_number: 11/21
  Isolation: Mutagen: ENU
  Reference: WBPaper00036200
  Remark: Allele identified through whole-genome sequencing by the Gene Knockout Consortium Paper_evidence: WBPaper00036200
    Sequenced by the C. elegans Gene Knockout Consortium Paper_evidence: WBPaper00041807
  Method: KO_consortium_allele