WormBase Tree Display for Variation: WBVar00090766

WBVar00090766 Evidence: Paper_evidence: WBPaper00029251
  Name: Public_name: n3736
    Other_name: CE37542:p.Phe247Ser
      R06C7.7b.1:c.1103T>C
      R06C7.7a.1:c.740T>C
      CE31573:p.Phe368Ser
    HGVSg: CHROMOSOME_I:g.7249853A>G
  Sequence_details: SMap: S_parent: Sequence: R06C7
    Flanking_sequences: attggatagacgagggaagcttcttcatat tcctgttggatttgcagcagtcaatggata
    Mapping_target: R06C7
    Type_of_mutation: Substitution: t c Paper_evidence: WBPaper00029251
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Laboratory: MT
    Status: Live
  Affects: Gene: WBGene00003041
    Transcript: R06C7.7b.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: R06C7.7b.1:c.1103T>C
        HGVSp: CE31573:p.Phe368Ser
        cDNA_position: 1103
        CDS_position: 1103
        Protein_position: 368
        Exon_number: 5/7
        Codon_change: tTt/tCt
        Amino_acid_change: F/S
      R06C7.7a.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: R06C7.7a.1:c.740T>C
        HGVSp: CE37542:p.Phe247Ser
        cDNA_position: 740
        CDS_position: 740
        Protein_position: 247
        Exon_number: 4/7
        Codon_change: tTt/tCt
        Amino_acid_change: F/S
  Genetics: Interpolated_map_position: I 1.85882
  Reference: WBPaper00029251
  Method: Substitution_allele