WormBase Tree Display for Variation: WBVar01431991

WBVar01431991 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01431991
    Other_name: CE30258:p.Thr1454=
      C48B6.6b.1:c.4368C>T
      C48B6.6a.1:c.4362C>T
      CE53740:p.Thr1456=
    HGVSg: CHROMOSOME_I:g.6905887G>A
  Sequence_details: SMap: S_parent: Sequence: C48B6
    Flanking_sequences: AAGTTCTAGAATTCTCAATGTCGCCAAAGT GTCTCCTCTTTTTTCTAAAAAAATTATCAA
    Mapping_target: C48B6
    Type_of_mutation: Substitution: g a
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00031279 From_analysis: WGS_Andersen
      WBStrain00031284 From_analysis: WGS_Andersen
    Laboratory: QX
    Person: WBPerson1730
    Analysis: WGS_Andersen
    DB_info: Database: dbSNP_rs rs 193320054
        dbSNP_ss ss 295495971
    Status: Live
  Affects: Gene: WBGene00004879
    Transcript: C48B6.6b.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: C48B6.6b.1:c.4368C>T
        HGVSp: CE53740:p.Thr1456=
        cDNA_position: 4368
        CDS_position: 4368
        Protein_position: 1456
        Exon_number: 27/42
        Codon_change: acC/acT
        Amino_acid_change: T
      C48B6.6a.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: C48B6.6a.1:c.4362C>T
        HGVSp: CE30258:p.Thr1454=
        cDNA_position: 4390
        CDS_position: 4362
        Protein_position: 1454
        Exon_number: 28/44
        Codon_change: acC/acT
        Amino_acid_change: T
  Reference: WBPaper00040707
  Method: WGS_Andersen