WormBase Tree Display for Variation: WBVar01895354

WBVar01895354 Name: Public_name: WBVar01895354
    Other_name (13)
    HGVSg: CHROMOSOME_II:g.11073491A>C
  Sequence_details: SMap: S_parent: Sequence: C09H10
    Flanking_sequences: GTGGAAAGTTGGAATTTGGGTTAGTTGCTG AGCGGTTGCTGACGTGGCGACACGTGGCGA
    Mapping_target: C09H10
    Source_location: 225 CHROMOSOME_II 11073433 11073433 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Substitution: A C
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00024204 From_analysis: Million_mutation_project_reanalysis
    Laboratory: VC
    Analysis: Million_mutation_project_reanalysis
    Status: Live
  Affects: Gene: WBGene00006788
    Transcript: F45E10.1c.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: F45E10.1c.1:c.460T>G
        HGVSp: CE33783:p.Ser154Ala
        cDNA_position: 460
        CDS_position: 460
        Protein_position: 154
        Exon_number: 6/24
        Codon_change: Tca/Gca
        Amino_acid_change: S/A
      F45E10.1b.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: F45E10.1b.1:c.460T>G
        HGVSp: CE31347:p.Ser154Ala
        cDNA_position: 460
        CDS_position: 460
        Protein_position: 154
        Exon_number: 6/23
        Codon_change: Tca/Gca
        Amino_acid_change: S/A
      F45E10.1d.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: F45E10.1d.1:c.58T>G
        HGVSp: CE34019:p.Ser20Ala
        cDNA_position: 255
        CDS_position: 58
        Protein_position: 20
        Exon_number: 4/21
        Codon_change: Tca/Gca
        Amino_acid_change: S/A
      F45E10.1g.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: F45E10.1g.1:c.460T>G
        HGVSp: CE44133:p.Ser154Ala
        cDNA_position: 460
        CDS_position: 460
        Protein_position: 154
        Exon_number: 6/22
        Codon_change: Tca/Gca
        Amino_acid_change: S/A
      F45E10.1a.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: F45E10.1a.1:c.460T>G
        HGVSp: CE31346:p.Ser154Ala
        cDNA_position: 501
        CDS_position: 460
        Protein_position: 154
        Exon_number: 7/24
        Codon_change: Tca/Gca
        Amino_acid_change: S/A
      F45E10.1h.1 VEP_consequence: missense_variant
        VEP_impact: MODERATE
        HGVSc: F45E10.1h.1:c.460T>G
        HGVSp: CE44088:p.Ser154Ala
        cDNA_position: 460
        CDS_position: 460
        Protein_position: 154
        Exon_number: 6/22
        Codon_change: Tca/Gca
        Amino_acid_change: S/A
  Method: WGS_Flibotte