WormBase Tree Display for Variation: WBVar01431374

WBVar01431374 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01431374
    Other_name: T21E12.4a.1:c.6261T>C
      CE23997:p.Leu2087=
      CE51690:p.Leu1155=
      T21E12.4b.1:c.3465T>C
    HGVSg: CHROMOSOME_I:g.4393746T>C
  Sequence_details: SMap: S_parent: Sequence: T21E12
    Flanking_sequences: ATCAGTCTGTGAAACTCTCGTGCCAAAACT GTAAATGAAGATATTGCCTTGTTGTTCTCT
    Mapping_target: T21E12
    Type_of_mutation: Substitution: t c
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00040481 From_analysis: WGS_Andersen
      WBStrain00040482 From_analysis: WGS_Andersen
    Laboratory: QX
    Person: WBPerson1730
    Analysis: WGS_Andersen
    DB_info: Database: dbSNP_rs rs 193319437
        dbSNP_ss ss 295495354
    Status: Live
  Affects: Gene: WBGene00000962
    Transcript: T21E12.4a.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: T21E12.4a.1:c.6261T>C
        HGVSp: CE23997:p.Leu2087=
        cDNA_position: 6266
        CDS_position: 6261
        Protein_position: 2087
        Exon_number: 8/17
        Codon_change: ctT/ctC
        Amino_acid_change: L
      T21E12.4b.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: T21E12.4b.1:c.3465T>C
        HGVSp: CE51690:p.Leu1155=
        cDNA_position: 3465
        CDS_position: 3465
        Protein_position: 1155
        Exon_number: 4/12
        Codon_change: ctT/ctC
        Amino_acid_change: L
  Reference: WBPaper00040707
  Method: WGS_Andersen