WormBase Tree Display for Variation: WBVar01914169

WBVar01914169 Name: Public_name: WBVar01914169
    Other_name: cewivar00630315
      F25C8.3b.1:c.9455A>T
      CE41563:p.Asn3173Ile
      F25C8.3a.1:c.9518A>T
      CE43592:p.Asn3211Ile
      CE47217:p.Asn3143Ile
      F25C8.3e.1:c.9323A>T
      CE47117:p.Asn3152Ile
      CE47428:p.Asn3108Ile
      F25C8.3c.1:c.9428A>T
      F25C8.3d.1:c.9632A>T
    HGVSg: CHROMOSOME_V:g.20898034A>T
  Sequence_details: SMap: S_parent: Sequence: F25C8
    Flanking_sequences: GATTAGCGAAACAATTATTATTTTAGCCAA TCGTACTCCAAATCGTCGATCGACAGAAGC
    Mapping_target: F25C8
    Source_location: 225 CHROMOSOME_V 20898003 20898003 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Substitution: A T
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00031113 From_analysis: Million_mutation_project_reanalysis
    Laboratory: VC
    Analysis: Million_mutation_project_reanalysis
    Status: Live
  Affects: Gene: WBGene00006812
    Transcript: F25C8.3d.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        SIFT: 0.03 deleterious
        PolyPhen: 0.447 benign
        HGVSc: F25C8.3d.1:c.9632A>T
        HGVSp: CE43592:p.Asn3211Ile
        cDNA_position: 9632
        CDS_position: 9632
        Protein_position: 3211
        Exon_number: 36/37
        Codon_change: aAt/aTt
        Amino_acid_change: N/I
      F25C8.3b.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        SIFT: 0.04 deleterious
        PolyPhen: 0.447 benign
        HGVSc: F25C8.3b.1:c.9455A>T
        HGVSp: CE47117:p.Asn3152Ile
        cDNA_position: 9708
        CDS_position: 9455
        Protein_position: 3152
        Exon_number: 34/36
        Codon_change: aAt/aTt
        Amino_acid_change: N/I
      F25C8.3e.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        SIFT: 0.04 deleterious_low_confidence
        PolyPhen: 0.447 benign
        HGVSc: F25C8.3e.1:c.9323A>T
        HGVSp: CE47428:p.Asn3108Ile
        cDNA_position: 9323
        CDS_position: 9323
        Protein_position: 3108
        Exon_number: 32/34
        Codon_change: aAt/aTt
        Amino_acid_change: N/I
      F25C8.3c.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        SIFT: 0.03 deleterious
        PolyPhen: 0.447 benign
        HGVSc: F25C8.3c.1:c.9428A>T
        HGVSp: CE47217:p.Asn3143Ile
        cDNA_position: 9428
        CDS_position: 9428
        Protein_position: 3143
        Exon_number: 34/35
        Codon_change: aAt/aTt
        Amino_acid_change: N/I
      F25C8.3a.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        SIFT: 0.03 deleterious
        PolyPhen: 0.447 benign
        HGVSc: F25C8.3a.1:c.9518A>T
        HGVSp: CE41563:p.Asn3173Ile
        cDNA_position: 9518
        CDS_position: 9518
        Protein_position: 3173
        Exon_number: 35/37
        Codon_change: aAt/aTt
        Amino_acid_change: N/I
  Method: WGS_Flibotte