WormBase Tree Display for Variation: WBVar00145043

WBVar00145043 Name: Public_name: e2901
    Other_name: F23H12.4b.1:c.671A>G
      CE05707:p.Asp290Gly
      F23H12.4a.1:c.869A>G
      CE46560:p.Asp224Gly
    HGVSg: CHROMOSOME_V:g.12354043A>G
  Sequence_details: SMap: S_parent: Sequence: F23H12
    Flanking_sequences: atttgtaatatttcaggtattgcgctctcg tggaggagtcttcttcgaggacggaaccag
    Mapping_target: F23H12
    Type_of_mutation: Substitution: a g Paper_evidence: WBPaper00024637
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Laboratory: CB
    Status: Live
  Affects: Gene: WBGene00005018
    Transcript: F23H12.4a.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        SIFT: 0.02 deleterious
        PolyPhen: 0 unknown
        HGVSc: F23H12.4a.1:c.869A>G
        HGVSp: CE05707:p.Asp290Gly
        cDNA_position: 1145
        CDS_position: 869
        Protein_position: 290
        Exon_number: 4/5
        Codon_change: gAt/gGt
        Amino_acid_change: D/G
      F23H12.4b.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        SIFT: 0 deleterious
        PolyPhen: 0 unknown
        HGVSc: F23H12.4b.1:c.671A>G
        HGVSp: CE46560:p.Asp224Gly
        cDNA_position: 671
        CDS_position: 671
        Protein_position: 224
        Exon_number: 2/2
        Codon_change: gAt/gGt
        Amino_acid_change: D/G
  Isolation: Mutagen: ENU Paper_evidence: WBPaper00024637
  Genetics: Interpolated_map_position: V 4.00901
  Method: Substitution_allele