WormBase Tree Display for Variation: WBVar00395671

WBVar00395671 Name: Public_name: gk172428
    Other_name (16)
    HGVSg: CHROMOSOME_III:g.4250915C>T
  Sequence_details: SMap: S_parent: Sequence: T08A11
    Flanking_sequences: TTCAACCATCATGAATCTCGATACTTTCGAATTTTCGGGAAAGTCAGGAT CGAGATATAACACAGTTGGAATCCATATTCAGCTTTGAATTTGAACATTT
    Mapping_target: T08A11
    Type_of_mutation: Substitution: C T
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00038151
    Laboratory: VC
    Analysis: Million_Mutation_Project
    Status: Live
  Affects: Gene: WBGene00011604
    Transcript: T08A11.1e.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: T08A11.1e.1:c.4276G>A
        HGVSp: CE54607:p.Asp1426Asn
        cDNA_position: 4276
        CDS_position: 4276
        Protein_position: 1426
        Exon_number: 15/18
        Codon_change: Gat/Aat
        Amino_acid_change: D/N
      T08A11.1g.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: T08A11.1g.1:c.4282G>A
        HGVSp: CE54616:p.Asp1428Asn
        cDNA_position: 4378
        CDS_position: 4282
        Protein_position: 1428
        Exon_number: 16/19
        Codon_change: Gat/Aat
        Amino_acid_change: D/N
      T08A11.1h.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: T08A11.1h.1:c.4288G>A
        HGVSp: CE54610:p.Asp1430Asn
        cDNA_position: 4384
        CDS_position: 4288
        Protein_position: 1430
        Exon_number: 16/19
        Codon_change: Gat/Aat
        Amino_acid_change: D/N
      T08A11.1d.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: T08A11.1d.1:c.4282G>A
        HGVSp: CE54612:p.Asp1428Asn
        cDNA_position: 4378
        CDS_position: 4282
        Protein_position: 1428
        Exon_number: 16/19
        Codon_change: Gat/Aat
        Amino_acid_change: D/N
      T08A11.1f.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: T08A11.1f.1:c.4282G>A
        HGVSp: CE54622:p.Asp1428Asn
        cDNA_position: 4282
        CDS_position: 4282
        Protein_position: 1428
        Exon_number: 15/18
        Codon_change: Gat/Aat
        Amino_acid_change: D/N
      T08A11.1c.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: T08A11.1c.1:c.4276G>A
        HGVSp: CE54609:p.Asp1426Asn
        cDNA_position: 4276
        CDS_position: 4276
        Protein_position: 1426
        Exon_number: 15/18
        Codon_change: Gat/Aat
        Amino_acid_change: D/N
      T08A11.1b.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: T08A11.1b.1:c.4276G>A
        HGVSp: CE54613:p.Asp1426Asn
        cDNA_position: 4372
        CDS_position: 4276
        Protein_position: 1426
        Exon_number: 16/19
        Codon_change: Gat/Aat
        Amino_acid_change: D/N
      T08A11.1a.1 (12)
  Reference: WBPaper00042537
  Method: Million_mutation