WormBase Tree Display for Variation: WBVar01442486

WBVar01442486 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01442486
    Other_name: F19H8.4.1:c.1640G>A
      CE32632:p.Gly547Glu
    HGVSg: CHROMOSOME_II:g.14620906G>A
  Sequence_details: SMap: S_parent: Sequence: F19H8
    Flanking_sequences: AGAAGCTGATGACCGAGCAAGGAATTCTCG GCGGGATGATATTTTCAATTTGAAAGAATA
    Mapping_target: F19H8
    Type_of_mutation: Substitution: g a
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023208 From_analysis: WGS_Andersen
    Laboratory: QX
    Person: WBPerson1730
    Analysis: WGS_Andersen
    DB_info: Database: dbSNP_rs rs 193329732
        dbSNP_ss ss 295505651
    Status: Live
  Affects: Gene: WBGene00008964
    Transcript: F19H8.4.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        SIFT: 0.23 tolerated
        PolyPhen: 0.999 probably_damaging
        HGVSc: F19H8.4.1:c.1640G>A
        HGVSp: CE32632:p.Gly547Glu
        cDNA_position: 1741
        CDS_position: 1640
        Protein_position: 547
        Exon_number: 9/12
        Codon_change: gGg/gAg
        Amino_acid_change: G/E
  Reference: WBPaper00040707
  Method: WGS_Andersen