WormBase Tree Display for Variation: WBVar00272081

WBVar00272081 Evidence: Paper_evidence: WBPaper00005369
  Name: Public_name: WBVar00272081
    Other_name (18)
    HGVSg: CHROMOSOME_V:g.6180792C>T
  Sequence_details: SMap: S_parent: Sequence: Y38B5A
    Flanking_sequences: TAAGTTTCTCAACTGTTGGTTCGACTGTAGGTGCACTAGTCTCTGGCACTGGAACATCCTTTTGCTCAACAATTTCAGCTGGTTCTACTTCAGATGTTTC TTGGATTCCACAGGAGCAAGTTTCTCAACTGTTGGTTCTTGGGCGGGTGCGGCAGTTGAACCTTTTTGGATAGAAGTTGTTACGTATTCAGAACATTCCA
    Mapping_target: Y38B5A
    Type_of_mutation: Substitution: C T
    SeqStatus: Sequenced
  Variation_type: SNP
    Predicted_SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00004602 From_analysis: SNP_Swan
    Analysis: SNP_Swan
    Status: Live
  Affects: Gene: WBGene00006436
    Transcript: W06H8.8f.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: W06H8.8f.1:c.12120G>A
        HGVSp: CE52428:p.Lys4040=
        cDNA_position: 12120
        CDS_position: 12120
        Protein_position: 4040
        Exon_number: 25/60
        Codon_change: aaG/aaA
        Amino_acid_change: K
      W06H8.8b.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: W06H8.8b.1:c.10842G>A
        HGVSp: CE52423:p.Lys3614=
        cDNA_position: 10935
        CDS_position: 10842
        Protein_position: 3614
        Exon_number: 25/58
        Codon_change: aaG/aaA
        Amino_acid_change: K
      W06H8.8a.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: W06H8.8a.1:c.12120G>A
        HGVSp: CE52437:p.Lys4040=
        cDNA_position: 12213
        CDS_position: 12120
        Protein_position: 4040
        Exon_number: 26/61
        Codon_change: aaG/aaA
        Amino_acid_change: K
      W06H8.8i.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: W06H8.8i.1:c.10842G>A
        HGVSp: CE52442:p.Lys3614=
        cDNA_position: 10842
        CDS_position: 10842
        Protein_position: 3614
        Exon_number: 24/57
        Codon_change: aaG/aaA
        Amino_acid_change: K
      W06H8.8a.2 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: W06H8.8a.2:c.12120G>A
        HGVSp: CE52437:p.Lys4040=
        cDNA_position: 12213
        CDS_position: 12120
        Protein_position: 4040
        Exon_number: 26/60
        Codon_change: aaG/aaA
        Amino_acid_change: K
      W06H8.8h.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: W06H8.8h.1:c.12120G>A
        HGVSp: CE52451:p.Lys4040=
        cDNA_position: 12120
        CDS_position: 12120
        Protein_position: 4040
        Exon_number: 25/58
        Codon_change: aaG/aaA
        Amino_acid_change: K
      W06H8.8d.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: W06H8.8d.1:c.12120G>A
        HGVSp: CE52449:p.Lys4040=
        cDNA_position: 12120
        CDS_position: 12120
        Protein_position: 4040
        Exon_number: 25/58
        Codon_change: aaG/aaA
        Amino_acid_change: K
      W06H8.8e.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: W06H8.8e.1:c.10842G>A
        HGVSp: CE52441:p.Lys3614=
        cDNA_position: 10842
        CDS_position: 10842
        Protein_position: 3614
        Exon_number: 24/56
        Codon_change: aaG/aaA
        Amino_acid_change: K
      W06H8.8g.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: W06H8.8g.1:c.10842G>A
        HGVSp: CE52417:p.Lys3614=
        cDNA_position: 10842
        CDS_position: 10842
        Protein_position: 3614
        Exon_number: 24/58
        Codon_change: aaG/aaA
        Amino_acid_change: K
  Reference: WBPaper00005369
  Method: SNP_Swan