WormBase Tree Display for Variation: WBVar00075284

WBVar00075284 Name: Public_name: WBVar00075284
    Other_name (16)
    HGVSg: CHROMOSOME_X:g.1550176T>C
  Sequence_details: SMap: S_parent: Sequence: K06A9
    Flanking_sequences: atctggttctactgtcaccgttgtc caggatcttccagcacatacggatc
    Mapping_target: K06A9
    Type_of_mutation: Substitution: T C
    SeqStatus: Sequenced
  Variation_type: SNP
    Predicted_SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00004602 From_analysis: Million_mutation_project_reanalysis
          WGS_Hawaiian_Waterston
      WBStrain00006622 From_analysis: Million_mutation_project_reanalysis
      WBStrain00006640 From_analysis: Million_mutation_project_reanalysis
      WBStrain00022850 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023072 From_analysis: Million_mutation_project_reanalysis
    Laboratory: RW
    Person: WBPerson1562
    Analysis: WGS_Hawaiian_Waterston
      Million_mutation_project_reanalysis
    Status: Live
  Affects: Gene: WBGene00019435
    Transcript: K06A9.1d.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: K06A9.1d.1:c.2368T>C
        HGVSp: CE53511:p.Ser790Pro
        cDNA_position: 2368
        CDS_position: 2368
        Protein_position: 790
        Exon_number: 7/13
        Codon_change: Tca/Cca
        Amino_acid_change: S/P
      K06A9.1c.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: K06A9.1c.1:c.730T>C
        HGVSp: CE34576:p.Ser244Pro
        cDNA_position: 2371
        CDS_position: 730
        Protein_position: 244
        Exon_number: 8/15
        Codon_change: Tca/Cca
        Amino_acid_change: S/P
      K06A9.1b.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: K06A9.1b.1:c.2368T>C
        HGVSp: CE53577:p.Ser790Pro
        cDNA_position: 2368
        CDS_position: 2368
        Protein_position: 790
        Exon_number: 7/14
        Codon_change: Tca/Cca
        Amino_acid_change: S/P
      K06A9.1g.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: K06A9.1g.1:c.2368T>C
        HGVSp: CE53575:p.Ser790Pro
        cDNA_position: 2368
        CDS_position: 2368
        Protein_position: 790
        Exon_number: 7/13
        Codon_change: Tca/Cca
        Amino_acid_change: S/P
      K06A9.1e.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: K06A9.1e.1:c.2368T>C
        HGVSp: CE53667:p.Ser790Pro
        cDNA_position: 2368
        CDS_position: 2368
        Protein_position: 790
        Exon_number: 7/13
        Codon_change: Tca/Cca
        Amino_acid_change: S/P
      K06A9.1f.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: K06A9.1f.1:c.2368T>C
        HGVSp: CE53628:p.Ser790Pro
        cDNA_position: 2368
        CDS_position: 2368
        Protein_position: 790
        Exon_number: 7/13
        Codon_change: Tca/Cca
        Amino_acid_change: S/P
      K06A9.1a.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: K06A9.1a.1:c.2368T>C
        HGVSp: CE53677:p.Ser790Pro
        cDNA_position: 2372
        CDS_position: 2368
        Protein_position: 790
        Exon_number: 8/15
        Codon_change: Tca/Cca
        Amino_acid_change: S/P
  Remark: [20081124 db] this Variation was previously named hw99644
  Method: WGS_Hawaiian_Waterston