WormBase Tree Display for Variation: WBVar00088033

WBVar00088033 Evidence: Paper_evidence: WBPaper00002189
  Name: Public_name: it90
    Other_name (25)
    HGVSg: CHROMOSOME_V:g.14126130_14126131delinsTT
  Sequence_details (5)
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Laboratory: KK
    Status: Live
  Affects: Gene: WBGene00003916
    Transcript: H39E23.1e.3 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: H39E23.1e.3:c.337_338delinsAA
        HGVSp: CE44733:p.Gly113Lys
        cDNA_position: 337-338
        CDS_position: 337-338
        Protein_position: 113
        Exon_number: 2/12
        Codon_change: GGa/AAa
        Amino_acid_change: G/K
      H39E23.1e.2 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: H39E23.1e.2:c.337_338delinsAA
        HGVSp: CE44733:p.Gly113Lys
        cDNA_position: 337-338
        CDS_position: 337-338
        Protein_position: 113
        Exon_number: 2/15
        Codon_change: GGa/AAa
        Amino_acid_change: G/K
      H39E23.1g.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: H39E23.1g.1:c.76_77delinsAA
        HGVSp: CE45263:p.Gly26Lys
        cDNA_position: 76-77
        CDS_position: 76-77
        Protein_position: 26
        Exon_number: 1/12
        Codon_change: GGa/AAa
        Amino_acid_change: G/K
      H39E23.1a.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: H39E23.1a.1:c.529_530delinsAA
        HGVSp: CE23838:p.Gly177Lys
        cDNA_position: 529-530
        CDS_position: 529-530
        Protein_position: 177
        Exon_number: 5/17
        Codon_change: GGa/AAa
        Amino_acid_change: G/K
      H39E23.1d.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: H39E23.1d.1:c.337_338delinsAA
        HGVSp: CE44808:p.Gly113Lys
        cDNA_position: 337-338
        CDS_position: 337-338
        Protein_position: 113
        Exon_number: 2/15
        Codon_change: GGa/AAa
        Amino_acid_change: G/K
      H39E23.1l.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: H39E23.1l.1:c.271_272delinsAA
        HGVSp: CE48381:p.Gly91Lys
        cDNA_position: 538-539
        CDS_position: 271-272
        Protein_position: 91
        Exon_number: 3/15
        Codon_change: GGa/AAa
        Amino_acid_change: G/K
      H39E23.1e.4 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: H39E23.1e.4:c.337_338delinsAA
        HGVSp: CE44733:p.Gly113Lys
        cDNA_position: 337-338
        CDS_position: 337-338
        Protein_position: 113
        Exon_number: 2/13
        Codon_change: GGa/AAa
        Amino_acid_change: G/K
      H39E23.1e.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: H39E23.1e.1:c.337_338delinsAA
        HGVSp: CE44733:p.Gly113Lys
        cDNA_position: 337-338
        CDS_position: 337-338
        Protein_position: 113
        Exon_number: 2/16
        Codon_change: GGa/AAa
        Amino_acid_change: G/K
      H39E23.1c.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: H39E23.1c.1:c.139_140delinsAA
        HGVSp: CE40085:p.Gly47Lys
        cDNA_position: 139-140
        CDS_position: 139-140
        Protein_position: 47
        Exon_number: 2/13
        Codon_change: GGa/AAa
        Amino_acid_change: G/K
      H39E23.1m.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: H39E23.1m.1:c.826_827delinsAA
        HGVSp: CE52350:p.Gly276Lys
        cDNA_position: 826-827
        CDS_position: 826-827
        Protein_position: 276
        Exon_number: 5/19
        Codon_change: GGa/AAa
        Amino_acid_change: G/K
      H39E23.1j.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: H39E23.1j.1:c.529_530delinsAA
        HGVSp: CE46555:p.Gly177Lys
        cDNA_position: 529-530
        CDS_position: 529-530
        Protein_position: 177
        Exon_number: 5/17
        Codon_change: GGa/AAa
        Amino_acid_change: G/K
      H39E23.1f.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: H39E23.1f.1:c.262_263delinsAA
        HGVSp: CE45159:p.Gly88Lys
        cDNA_position: 262-263
        CDS_position: 262-263
        Protein_position: 88
        Exon_number: 2/13
        Codon_change: GGa/AAa
        Amino_acid_change: G/K
      H39E23.1e.5 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: H39E23.1e.5:c.337_338delinsAA
        HGVSp: CE44733:p.Gly113Lys
        cDNA_position: 337-338
        CDS_position: 337-338
        Protein_position: 113
        Exon_number: 2/12
        Codon_change: GGa/AAa
        Amino_acid_change: G/K
      H39E23.1b.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: H39E23.1b.1:c.385_386delinsAA
        HGVSp: CE27768:p.Gly129Lys
        cDNA_position: 401-402
        CDS_position: 385-386
        Protein_position: 129
        Exon_number: 4/15
        Codon_change: GGa/AAa
        Amino_acid_change: G/K
      H39E23.1e.6 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: H39E23.1e.6:c.337_338delinsAA
        HGVSp: CE44733:p.Gly113Lys
        cDNA_position: 337-338
        CDS_position: 337-338
        Protein_position: 113
        Exon_number: 2/12
        Codon_change: GGa/AAa
        Amino_acid_change: G/K
  Genetics: Interpolated_map_position: V 6.16562
  Reference: WBPaper00002189
  Method: Substitution_allele