WormBase Tree Display for Variation: WBVar00144112

WBVar00144112 Evidence: Paper_evidence: WBPaper00027217
  Name: Public_name: e1563
    Other_name: T10H9.4.1:c.289_290delinsGA
      CE18252:p.Ile97Asp
    HGVSg: CHROMOSOME_V:g.6656049_6656050delinsTC
  Sequence_details: SMap: S_parent: Sequence: T10H9
    Flanking_sequences: atgatgatcatcatgtgcgctatcgtcgtc tcttattatcatcatcgttttatgggctgg
    Mapping_target: T10H9
    Type_of_mutation: Substitution: at ga Paper_evidence: WBPaper00027217
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00004434
      WBStrain00033412
      WBStrain00033414
    Laboratory: CB
    Status: Live
  Affects: Gene: WBGene00004897
    Transcript: T10H9.4.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: T10H9.4.1:c.289_290delinsGA
        HGVSp: CE18252:p.Ile97Asp
        cDNA_position: 319-320
        CDS_position: 289-290
        Protein_position: 97
        Exon_number: 3/4
        Codon_change: ATt/GAt
        Amino_acid_change: I/D
  Genetics: Interpolated_map_position: V 0.132255
    Mapping_data: In_2_point: 233
        234
  Description: Phenotype: WBPhenotype:0002256 Paper_evidence: WBPaper00041069
        Curator_confirmed: WBPerson1754
        Remark: Blocks the increased sensitivity of unc-17(e245) to selenium induced movement decline Paper_evidence: WBPaper00041069
            Curator_confirmed: WBPerson1754
        Affected_by: Molecule: WBMol:00001915 Paper_evidence: WBPaper00041069
              Curator_confirmed: WBPerson1754
  Reference: WBPaper00041069
    WBPaper00018307
  Method: Substitution_allele