WormBase Tree Display for Variation: WBVar00241571

WBVar00241571 Evidence: Paper_evidence: WBPaper00006014
  Name: Public_name: rh191
    Other_name: K08C7.3f.1:c.6086G>A
      CE43544:p.Cys2029Tyr
      CE25049:p.Cys2018Tyr
      K08C7.3c.1:c.6086G>A
      CE06136:p.Cys2018Tyr
      K08C7.3b.1:c.6053G>A
      K08C7.3e.1:c.6026G>A
      CE43590:p.Cys2009Tyr
      CE49945:p.Cys2029Tyr
      CE49858:p.Cys2009Tyr
      K08C7.3a.1:c.6053G>A
      K08C7.3d.1:c.6026G>A
    HGVSg: CHROMOSOME_IV:g.10673601G>A
  Sequence_details: SMap: S_parent: Sequence: K08C7
    Flanking_sequences: aatgcaagatcaatgtagaaggagactcct cgatagatgcaaaccagatcattggggttt
    Mapping_target: K08C7
    Type_of_mutation: Substitution: g a Paper_evidence: WBPaper00006014
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Laboratory: NJ
    Status: Live
  Affects: Gene: WBGene00001328
    Transcript: K08C7.3a.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        SIFT: 0 deleterious
        PolyPhen: 1 probably_damaging
        HGVSc: K08C7.3a.1:c.6053G>A
        HGVSp: CE25049:p.Cys2018Tyr
        cDNA_position: 6059
        CDS_position: 6053
        Protein_position: 2018
        Exon_number: 10/17
        Codon_change: tGc/tAc
        Amino_acid_change: C/Y
      K08C7.3e.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        SIFT: 0 deleterious
        PolyPhen: 1 probably_damaging
        HGVSc: K08C7.3e.1:c.6026G>A
        HGVSp: CE49858:p.Cys2009Tyr
        cDNA_position: 6036
        CDS_position: 6026
        Protein_position: 2009
        Exon_number: 10/17
        Codon_change: tGc/tAc
        Amino_acid_change: C/Y
      K08C7.3d.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        SIFT: 0 deleterious
        PolyPhen: 1 probably_damaging
        HGVSc: K08C7.3d.1:c.6026G>A
        HGVSp: CE43590:p.Cys2009Tyr
        cDNA_position: 6032
        CDS_position: 6026
        Protein_position: 2009
        Exon_number: 10/16
        Codon_change: tGc/tAc
        Amino_acid_change: C/Y
      K08C7.3f.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        SIFT: 0 deleterious
        PolyPhen: 1 probably_damaging
        HGVSc: K08C7.3f.1:c.6086G>A
        HGVSp: CE49945:p.Cys2029Tyr
        cDNA_position: 6086
        CDS_position: 6086
        Protein_position: 2029
        Exon_number: 10/17
        Codon_change: tGc/tAc
        Amino_acid_change: C/Y
      K08C7.3c.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        SIFT: 0 deleterious
        PolyPhen: 1 probably_damaging
        HGVSc: K08C7.3c.1:c.6086G>A
        HGVSp: CE43544:p.Cys2029Tyr
        cDNA_position: 6092
        CDS_position: 6086
        Protein_position: 2029
        Exon_number: 11/17
        Codon_change: tGc/tAc
        Amino_acid_change: C/Y
      K08C7.3b.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        SIFT: 0 deleterious
        PolyPhen: 1 probably_damaging
        HGVSc: K08C7.3b.1:c.6053G>A
        HGVSp: CE06136:p.Cys2018Tyr
        cDNA_position: 6053
        CDS_position: 6053
        Protein_position: 2018
        Exon_number: 9/15
        Codon_change: tGc/tAc
        Amino_acid_change: C/Y
  Genetics: Interpolated_map_position: IV 4.64492
  Reference: WBPaper00006014
  Method: Substitution_allele