WormBase Tree Display for Variation: WBVar01898602

WBVar01898602 Name: Public_name: WBVar01898602
    Other_name: cewivar00614051
      CE15871:p.Asn257=
      F19H8.2.2:c.771C>T
      F19H8.2.1:c.771C>T
      F19H8.1a.1:c.2706+272G>A
    HGVSg: CHROMOSOME_II:g.14604347G>A
  Sequence_details: SMap: S_parent: Sequence: F19H8
    Flanking_sequences: ATGTCCCTTCTTCATGTGCTTCTTGTGTTG TTTGGTGGCTTTTGTGTGACTTCTGACTTT
    Mapping_target: F19H8
    Source_location: 225 CHROMOSOME_II 14604272 14604272 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Substitution: G A
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00027660 From_analysis: Million_mutation_project_reanalysis
    Laboratory: VC
    Analysis: Million_mutation_project_reanalysis
    Status: Live
  Affects: Gene: WBGene00008963
      WBGene00006603
    Transcript: F19H8.2.2 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: F19H8.2.2:c.771C>T
        HGVSp: CE15871:p.Asn257=
        cDNA_position: 951
        CDS_position: 771
        Protein_position: 257
        Exon_number: 7/8
        Codon_change: aaC/aaT
        Amino_acid_change: N
      F19H8.1a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F19H8.1a.1:c.2706+272G>A
        Intron_number: 8/15
      F19H8.2.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: F19H8.2.1:c.771C>T
        HGVSp: CE15871:p.Asn257=
        cDNA_position: 850
        CDS_position: 771
        Protein_position: 257
        Exon_number: 6/7
        Codon_change: aaC/aaT
        Amino_acid_change: N
  Method: WGS_Flibotte