WormBase Tree Display for Variation: WBVar00946174

WBVar00946174 Name: Public_name: gk769182
    Other_name (18)
    HGVSg: CHROMOSOME_IV:g.11987812G>A
  Sequence_details: SMap: S_parent: Sequence: ZK617
    Flanking_sequences: ACCTTGACAGTTGTATCAGAAAGATCTTCACGATGAATTCTTGGAGCAAG TTTCTTGGCTTCGCAACAACACGATCAGAAGGATCAGAAGGATCTCCAGT
    Mapping_target: ZK617
    Type_of_mutation: Substitution: G A
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00039672
    Laboratory: VC
    Analysis: Million_Mutation_Project
    Status: Live
  Affects: Gene: WBGene00006759
    Transcript: ZK617.1i.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: ZK617.1i.1:c.7953C>T
        HGVSp: CE49956:p.Asn2651=
        cDNA_position: 7953
        CDS_position: 7953
        Protein_position: 2651
        Exon_number: 24/33
        Codon_change: aaC/aaT
        Amino_acid_change: N
      ZK617.1a.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: ZK617.1a.1:c.7071C>T
        HGVSp: CE33017:p.Asn2357=
        cDNA_position: 7198
        CDS_position: 7071
        Protein_position: 2357
        Exon_number: 23/33
        Codon_change: aaC/aaT
        Amino_acid_change: N
      ZK617.1g.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: ZK617.1g.1:c.7098C>T
        HGVSp: CE46868:p.Asn2366=
        cDNA_position: 7098
        CDS_position: 7098
        Protein_position: 2366
        Exon_number: 23/32
        Codon_change: aaC/aaT
        Amino_acid_change: N
      ZK617.1f.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: ZK617.1f.1:c.7335C>T
        HGVSp: CE46948:p.Asn2445=
        cDNA_position: 7335
        CDS_position: 7335
        Protein_position: 2445
        Exon_number: 22/31
        Codon_change: aaC/aaT
        Amino_acid_change: N
      ZK617.1d.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: ZK617.1d.1:c.5910C>T
        HGVSp: CE49926:p.Asn1970=
        cDNA_position: 5910
        CDS_position: 5910
        Protein_position: 1970
        Exon_number: 13/22
        Codon_change: aaC/aaT
        Amino_acid_change: N
      ZK617.1c.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: ZK617.1c.1:c.6411C>T
        HGVSp: CE47057:p.Asn2137=
        cDNA_position: 6672
        CDS_position: 6411
        Protein_position: 2137
        Exon_number: 17/26
        Codon_change: aaC/aaT
        Amino_acid_change: N
      ZK617.1h.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: ZK617.1h.1:c.7980C>T
        HGVSp: CE49973:p.Asn2660=
        cDNA_position: 7980
        CDS_position: 7980
        Protein_position: 2660
        Exon_number: 25/34
        Codon_change: aaC/aaT
        Amino_acid_change: N
      ZK617.1b.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: ZK617.1b.1:c.8028C>T
        HGVSp: CE33018:p.Asn2676=
        cDNA_position: 8028
        CDS_position: 8028
        Protein_position: 2676
        Exon_number: 25/34
        Codon_change: aaC/aaT
        Amino_acid_change: N
      ZK617.1e.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: ZK617.1e.1:c.5859C>T
        HGVSp: CE44668:p.Asn1953=
        cDNA_position: 5859
        CDS_position: 5859
        Protein_position: 1953
        Exon_number: 12/21
        Codon_change: aaC/aaT
        Amino_acid_change: N
  Reference: WBPaper00042537
  Method: Million_mutation