WormBase Tree Display for Variation: WBVar02141296

WBVar02141296 Evidence: Paper_evidence: WBPaper00045884
  Name: Public_name: js1288
    Other_name: C52E12.2b.1:c.631T>G
      CE47855:p.Ser211Ala
      CE48050:p.Ser211Ala
      C52E12.2a.2:c.631T>G
      C52E12.2a.1:c.631T>G
    HGVSg: CHROMOSOME_II:g.7001752T>G
  Sequence_details: SMap: S_parent: Sequence: C52E12
    Flanking_sequences: actgttgctgcaacaaatatgaattcgaca catcaagatcccatgcggtattcacaatag
    Mapping_target: C52E12
    Type_of_mutation: Substitution: t g Paper_evidence: WBPaper00045884
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Laboratory: NM
    Status: Live
  Affects: Gene: WBGene00006831
    Transcript: C52E12.2a.2 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: C52E12.2a.2:c.631T>G
        HGVSp: CE48050:p.Ser211Ala
        cDNA_position: 633
        CDS_position: 631
        Protein_position: 211
        Exon_number: 6/24
        Codon_change: Tca/Gca
        Amino_acid_change: S/A
      C52E12.2b.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: C52E12.2b.1:c.631T>G
        HGVSp: CE47855:p.Ser211Ala
        cDNA_position: 831
        CDS_position: 631
        Protein_position: 211
        Exon_number: 6/25
        Codon_change: Tca/Gca
        Amino_acid_change: S/A
      C52E12.2a.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: C52E12.2a.1:c.631T>G
        HGVSp: CE48050:p.Ser211Ala
        cDNA_position: 767
        CDS_position: 631
        Protein_position: 211
        Exon_number: 6/24
        Codon_change: Tca/Gca
        Amino_acid_change: S/A
  Genetics: Interpolated_map_position: II 0.210226
  Reference: WBPaper00045884
  Method: Substitution_allele