WormBase Tree Display for Variation: WBVar00142896

WBVar00142896 Evidence: Paper_evidence: WBPaper00004647
  Name: Public_name: dx87
    Other_name: T01H8.5d.2:c.4394C>T
      CE42821:p.Ser1160Phe
      T01H8.5e.1:c.3479C>T
      CE41002:p.Ser1505Phe
      CE41003:p.Ser1465Phe
      T01H8.5d.1:c.4394C>T
      CE30390:p.Ser1566Phe
      T01H8.5a.1:c.4697C>T
      T01H8.5c.1:c.4514C>T
    HGVSg: CHROMOSOME_I:g.8551870G>A
  Sequence_details: SMap: S_parent: Sequence: T01H8
    Flanking_sequences: gtcacatcttcgacgccaccgatgagatgt tcagcaaatttggcttttccagcgttacaa
    Mapping_target: T01H8
    Type_of_mutation: Substitution: c t
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Laboratory: EJ
    Status: Live
  Affects: Gene: WBGene00001651
    Transcript: T01H8.5e.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: T01H8.5e.1:c.3479C>T
        HGVSp: CE42821:p.Ser1160Phe
        cDNA_position: 3479
        CDS_position: 3479
        Protein_position: 1160
        Exon_number: 15/20
        Codon_change: tCt/tTt
        Amino_acid_change: S/F
      T01H8.5a.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: T01H8.5a.1:c.4697C>T
        HGVSp: CE30390:p.Ser1566Phe
        cDNA_position: 4738
        CDS_position: 4697
        Protein_position: 1566
        Exon_number: 25/31
        Codon_change: tCt/tTt
        Amino_acid_change: S/F
      T01H8.5d.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: T01H8.5d.1:c.4394C>T
        HGVSp: CE41003:p.Ser1465Phe
        cDNA_position: 4665
        CDS_position: 4394
        Protein_position: 1465
        Exon_number: 23/29
        Codon_change: tCt/tTt
        Amino_acid_change: S/F
      T01H8.5c.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: T01H8.5c.1:c.4514C>T
        HGVSp: CE41002:p.Ser1505Phe
        cDNA_position: 4514
        CDS_position: 4514
        Protein_position: 1505
        Exon_number: 21/26
        Codon_change: tCt/tTt
        Amino_acid_change: S/F
      T01H8.5d.2 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: T01H8.5d.2:c.4394C>T
        HGVSp: CE41003:p.Ser1465Phe
        cDNA_position: 4527
        CDS_position: 4394
        Protein_position: 1465
        Exon_number: 21/27
        Codon_change: tCt/tTt
        Amino_acid_change: S/F
  Isolation: Mutagen: UV
  Genetics: Interpolated_map_position: I 2.94445
  Reference: WBPaper00004647
  Remark: Identical to dx154 Paper_evidence: WBPaper00048884
  Method: Substitution_allele