WormBase Tree Display for Variation: WBVar00143969

WBVar00143969 Evidence: Paper_evidence: WBPaper00035610
  Name: Public_name: e1393
    Other_name: CE06236:p.Ser391Trp
      R05D11.1.1:c.1172C>A
      CE06236:p.Ser391Ter
      R05D11.1.1:c.1172C>G
    HGVSg: CHROMOSOME_I:g.8585234G>T
  Sequence_details: SMap: S_parent: Sequence: R05D11
    Flanking_sequences: tatcaaaataacatcattacagccgtttct gcttggttggtacaacaatccaaaccgctc
    Mapping_target: R05D11
    Type_of_mutation: Substitution: c r Paper_evidence: WBPaper00035610
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00003964
      WBStrain00003965
      WBStrain00003971
      WBStrain00004321
      WBStrain00006203
      WBStrain00006206
      WBStrain00006213
      WBStrain00006216
      WBStrain00006268
      WBStrain00006331
      WBStrain00006339
      WBStrain00006342
      WBStrain00008453
      WBStrain00030741
      WBStrain00030759
      WBStrain00035146
    Laboratory: CB
    Status: Live
  Affects: Gene: WBGene00000904
    Transcript: R05D11.1.1 VEP_consequence: missense_variant
          stop_gained
        VEP_impact: MODERATE
          HIGH
        HGVSc: R05D11.1.1:c.1172C>A
          R05D11.1.1:c.1172C>G
        HGVSp: CE06236:p.Ser391Trp
          CE06236:p.Ser391Ter
        cDNA_position: 1190
        CDS_position: 1172
        Protein_position: 391
        Exon_number: 6/8
        Codon_change: tCg/tAg
          tCg/tGg
        Amino_acid_change: S/*
          S/W
    Interactor (54)
  Genetics: Interpolated_map_position: I 2.97492
    Mapping_data: In_2_point: 28
        424
        703
        2509
        3738
      In_multi_point (20)
      In_pos_neg_data: 2508
        2510
        2511
        6821
        6824
        7283
        7286
  Description (2)
  Reference (13)
  Method: Substitution_allele