WormBase Tree Display for Variation: WBVar00277246

WBVar00277246 Evidence: Paper_evidence: WBPaper00036200
  Name: Public_name: gk2398
    Other_name: T11B7.4d.1:c.390T>C
      CE39401:p.Leu130=
      CE35946:p.Leu59=
      CE35944:p.Leu130=
      T11B7.4a.1:c.390T>C
      T11B7.4b.1:c.390T>C
      T11B7.4c.1:c.177T>C
      CE03650:p.Leu130=
      CE35945:p.Leu130=
      T11B7.4e.1:c.390T>C
    HGVSg: CHROMOSOME_IV:g.8854934T>C
  Sequence_details: SMap: S_parent: Sequence: T11B7
    Flanking_sequences: TCCACCACAAGGTTTCAACAATTCAGCACT CCTTTTGAAACAGATCAACGTGTGAAACAT
    Mapping_target: T11B7
    Type_of_mutation: Substitution: T C
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00037339
    Laboratory: VC
    Person: WBPerson427
    Analysis: Million_Mutation_Pilot_Project
    KO_consortium_allele
    Status: Live
  Affects: Gene: WBGene00001132
    Transcript: T11B7.4e.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: T11B7.4e.1:c.390T>C
        HGVSp: CE39401:p.Leu130=
        cDNA_position: 410
        CDS_position: 390
        Protein_position: 130
        Exon_number: 5/16
        Codon_change: ctT/ctC
        Amino_acid_change: L
      T11B7.4d.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: T11B7.4d.1:c.390T>C
        HGVSp: CE03650:p.Leu130=
        cDNA_position: 404
        CDS_position: 390
        Protein_position: 130
        Exon_number: 5/18
        Codon_change: ctT/ctC
        Amino_acid_change: L
      T11B7.4c.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: T11B7.4c.1:c.177T>C
        HGVSp: CE35946:p.Leu59=
        cDNA_position: 193
        CDS_position: 177
        Protein_position: 59
        Exon_number: 4/16
        Codon_change: ctT/ctC
        Amino_acid_change: L
      T11B7.4b.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: T11B7.4b.1:c.390T>C
        HGVSp: CE35945:p.Leu130=
        cDNA_position: 404
        CDS_position: 390
        Protein_position: 130
        Exon_number: 5/15
        Codon_change: ctT/ctC
        Amino_acid_change: L
      T11B7.4a.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: T11B7.4a.1:c.390T>C
        HGVSp: CE35944:p.Leu130=
        cDNA_position: 404
        CDS_position: 390
        Protein_position: 130
        Exon_number: 5/12
        Codon_change: ctT/ctC
        Amino_acid_change: L
  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