WormBase Tree Display for Variation: WBVar00075318

WBVar00075318 Name: Public_name: WBVar00075318
    Other_name (16)
    HGVSg: CHROMOSOME_X:g.1558909C>A
  Sequence_details: SMap: S_parent: Sequence: H02F09
    Flanking_sequences: ttcaatttcgctctactggttgctt caaattgaacaatgaatcaattttg
    Mapping_target: H02F09
    Type_of_mutation: Substitution: C A
    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.3671C>A
        HGVSp: CE53511:p.Ser1224Tyr
        cDNA_position: 3671
        CDS_position: 3671
        Protein_position: 1224
        Exon_number: 10/13
        Codon_change: tCc/tAc
        Amino_acid_change: S/Y
      K06A9.1c.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: K06A9.1c.1:c.2033C>A
        HGVSp: CE34576:p.Ser678Tyr
        cDNA_position: 3674
        CDS_position: 2033
        Protein_position: 678
        Exon_number: 11/15
        Codon_change: tCc/tAc
        Amino_acid_change: S/Y
      K06A9.1b.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: K06A9.1b.1:c.7346C>A
        HGVSp: CE53577:p.Ser2449Tyr
        cDNA_position: 7346
        CDS_position: 7346
        Protein_position: 2449
        Exon_number: 11/14
        Codon_change: tCc/tAc
        Amino_acid_change: S/Y
      K06A9.1g.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: K06A9.1g.1:c.5240C>A
        HGVSp: CE53575:p.Ser1747Tyr
        cDNA_position: 5240
        CDS_position: 5240
        Protein_position: 1747
        Exon_number: 10/13
        Codon_change: tCc/tAc
        Amino_acid_change: S/Y
      K06A9.1e.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: K06A9.1e.1:c.4418C>A
        HGVSp: CE53667:p.Ser1473Tyr
        cDNA_position: 4418
        CDS_position: 4418
        Protein_position: 1473
        Exon_number: 10/13
        Codon_change: tCc/tAc
        Amino_acid_change: S/Y
      K06A9.1f.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: K06A9.1f.1:c.4964C>A
        HGVSp: CE53628:p.Ser1655Tyr
        cDNA_position: 4964
        CDS_position: 4964
        Protein_position: 1655
        Exon_number: 10/13
        Codon_change: tCc/tAc
        Amino_acid_change: S/Y
      K06A9.1a.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: K06A9.1a.1:c.2909C>A
        HGVSp: CE53677:p.Ser970Tyr
        cDNA_position: 2913
        CDS_position: 2909
        Protein_position: 970
        Exon_number: 11/15
        Codon_change: tCc/tAc
        Amino_acid_change: S/Y
  Remark: [20081124 db] this Variation was previously named hw99678
  Method: WGS_Hawaiian_Waterston