WormBase Tree Display for Variation: WBVar02128171

WBVar02128171 Evidence: Paper_evidence: WBPaper00045317
  Name: Public_name: h15086
    Other_name: CE44414:p.Pro1538Ser
      CE37103:p.Pro1466Ser
      F16A11.3d.1:c.4612C>T
      CE37104:p.Pro1340Ser
      F16A11.3b.1:c.4018C>T
      F16A11.3a.1:c.4396C>T
    HGVSg: CHROMOSOME_I:g.9364898G>A
  Sequence_details: SMap: S_parent: Sequence: M04C9
    Flanking_sequences: TTGAACATTTTTTGTTTAAAAATTGACCTCACCACTGGTG TGGAAGAGTAGGTGCAGGATCCATAGGTATATCCAGTTCA
    Mapping_target: CHROMOSOME_I
    Source_location: 200 CHROMOSOME_I 9364889 9364889
    Type_of_mutation: Substitution: G A
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023875
    Laboratory: KR
    Analysis: WGS_Rose
    Status: Live
  Affects: Gene: WBGene00008878
    Transcript: F16A11.3a.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: F16A11.3a.1:c.4396C>T
        HGVSp: CE37103:p.Pro1466Ser
        cDNA_position: 4445
        CDS_position: 4396
        Protein_position: 1466
        Exon_number: 24/26
        Codon_change: Cca/Tca
        Amino_acid_change: P/S
      F16A11.3b.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: F16A11.3b.1:c.4018C>T
        HGVSp: CE37104:p.Pro1340Ser
        cDNA_position: 4073
        CDS_position: 4018
        Protein_position: 1340
        Exon_number: 23/25
        Codon_change: Cca/Tca
        Amino_acid_change: P/S
      F16A11.3d.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: F16A11.3d.1:c.4612C>T
        HGVSp: CE44414:p.Pro1538Ser
        cDNA_position: 4612
        CDS_position: 4612
        Protein_position: 1538
        Exon_number: 25/26
        Codon_change: Cca/Tca
        Amino_acid_change: P/S
  Reference: WBPaper00040589
    WBPaper00000975
    WBPaper00003985
    WBPaper00000699
    WBPaper00045317
  Method: WGS_Rose