WormBase Tree Display for Variation: WBVar01437121

WBVar01437121 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01437121
    Other_name: cewivar00010713
      F19B10.10.2:c.1354T>G
      F19B10.10.1:c.1354T>G
      CE09477:p.Ser452Ala
    HGVSg: CHROMOSOME_II:g.3678271A>C
  Sequence_details: SMap: S_parent: Sequence: F19B10
    Flanking_sequences: ATTCCAGCAAGCCTAGGTACTTGAGCTCCG ATGTACATCTCCAACTGTGAAGCCTTTCGG
    Mapping_target: F19B10
    Type_of_mutation: Substitution: a c
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain (176)
    Laboratory: QX
    Person: WBPerson1730
    Analysis: Million_mutation_project_reanalysis
      WGS_Andersen
    DB_info: Database: dbSNP_rs rs 193325182
        dbSNP_ss ss 295501101
    Status: Live
  Affects: Gene: WBGene00017589
    Transcript: F19B10.10.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: F19B10.10.1:c.1354T>G
        HGVSp: CE09477:p.Ser452Ala
        cDNA_position: 1361
        CDS_position: 1354
        Protein_position: 452
        Exon_number: 9/11
        Codon_change: Tcg/Gcg
        Amino_acid_change: S/A
      F19B10.10.2 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: F19B10.10.2:c.1354T>G
        HGVSp: CE09477:p.Ser452Ala
        cDNA_position: 1506
        CDS_position: 1354
        Protein_position: 452
        Exon_number: 10/12
        Codon_change: Tcg/Gcg
        Amino_acid_change: S/A
  Reference: WBPaper00040707
  Method: WGS_Andersen