WormBase Tree Display for Variation: WBVar00946167

WBVar00946167 Name: Public_name: gk522375
    Other_name (18)
    HGVSg: CHROMOSOME_IV:g.11986964G>A
  Sequence_details: SMap: S_parent: Sequence: ZK617
    Flanking_sequences: CTAGCATCAGATGGATCAGATGGGCCTCCCTTGTTAACAGCAACAACACG AATTCGTATTCCTCATTTGGTGTGAGGTCTGGAACGGTTGCAGTTGTCTG
    Mapping_target: ZK617
    Type_of_mutation: Substitution: G A
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00039206
    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.8754C>T
        HGVSp: CE49956:p.Phe2918=
        cDNA_position: 8754
        CDS_position: 8754
        Protein_position: 2918
        Exon_number: 25/33
        Codon_change: ttC/ttT
        Amino_acid_change: F
      ZK617.1a.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: ZK617.1a.1:c.7872C>T
        HGVSp: CE33017:p.Phe2624=
        cDNA_position: 7999
        CDS_position: 7872
        Protein_position: 2624
        Exon_number: 24/33
        Codon_change: ttC/ttT
        Amino_acid_change: F
      ZK617.1g.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: ZK617.1g.1:c.7899C>T
        HGVSp: CE46868:p.Phe2633=
        cDNA_position: 7899
        CDS_position: 7899
        Protein_position: 2633
        Exon_number: 24/32
        Codon_change: ttC/ttT
        Amino_acid_change: F
      ZK617.1f.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: ZK617.1f.1:c.8136C>T
        HGVSp: CE46948:p.Phe2712=
        cDNA_position: 8136
        CDS_position: 8136
        Protein_position: 2712
        Exon_number: 23/31
        Codon_change: ttC/ttT
        Amino_acid_change: F
      ZK617.1d.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: ZK617.1d.1:c.6711C>T
        HGVSp: CE49926:p.Phe2237=
        cDNA_position: 6711
        CDS_position: 6711
        Protein_position: 2237
        Exon_number: 14/22
        Codon_change: ttC/ttT
        Amino_acid_change: F
      ZK617.1c.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: ZK617.1c.1:c.7212C>T
        HGVSp: CE47057:p.Phe2404=
        cDNA_position: 7473
        CDS_position: 7212
        Protein_position: 2404
        Exon_number: 18/26
        Codon_change: ttC/ttT
        Amino_acid_change: F
      ZK617.1h.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: ZK617.1h.1:c.8781C>T
        HGVSp: CE49973:p.Phe2927=
        cDNA_position: 8781
        CDS_position: 8781
        Protein_position: 2927
        Exon_number: 26/34
        Codon_change: ttC/ttT
        Amino_acid_change: F
      ZK617.1b.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: ZK617.1b.1:c.8829C>T
        HGVSp: CE33018:p.Phe2943=
        cDNA_position: 8829
        CDS_position: 8829
        Protein_position: 2943
        Exon_number: 26/34
        Codon_change: ttC/ttT
        Amino_acid_change: F
      ZK617.1e.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: ZK617.1e.1:c.6660C>T
        HGVSp: CE44668:p.Phe2220=
        cDNA_position: 6660
        CDS_position: 6660
        Protein_position: 2220
        Exon_number: 13/21
        Codon_change: ttC/ttT
        Amino_acid_change: F
  Reference: WBPaper00042537
  Method: Million_mutation