WormBase Tree Display for Variation: WBVar01878453

WBVar01878453 Name: Public_name: WBVar01878453
    Other_name (11)
    HGVSg: CHROMOSOME_X:g.4856093A>C
  Sequence_details: SMap: S_parent: Sequence: F39C12
    Flanking_sequences: CAAAATCTGGCTTTGTGGTCCAGCAGAAAG GTTCCCAGTCTGTTGTTTTCTTTGATAGCT
    Mapping_target: F39C12
    Source_location: 225 CHROMOSOME_X 4856063 4856063 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Substitution: A C
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023072 From_analysis: Million_mutation_project_reanalysis
    Laboratory: VC
    Analysis: Million_mutation_project_reanalysis
    Status: Live
  Affects: Gene: WBGene00000072
    Transcript: F39C12.2b.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: F39C12.2b.1:c.1503T>G
        HGVSp: CE28309:p.Thr501=
        cDNA_position: 1510
        CDS_position: 1503
        Protein_position: 501
        Exon_number: 13/20
        Codon_change: acT/acG
        Amino_acid_change: T
      F39C12.2a.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: F39C12.2a.1:c.1503T>G
        HGVSp: CE28308:p.Thr501=
        cDNA_position: 1503
        CDS_position: 1503
        Protein_position: 501
        Exon_number: 12/17
        Codon_change: acT/acG
        Amino_acid_change: T
      F39C12.2c.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: F39C12.2c.1:c.1503T>G
        HGVSp: CE29794:p.Thr501=
        cDNA_position: 1512
        CDS_position: 1503
        Protein_position: 501
        Exon_number: 13/19
        Codon_change: acT/acG
        Amino_acid_change: T
      F39C12.2e.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: F39C12.2e.1:c.1503T>G
        HGVSp: CE34553:p.Thr501=
        cDNA_position: 1503
        CDS_position: 1503
        Protein_position: 501
        Exon_number: 12/16
        Codon_change: acT/acG
        Amino_acid_change: T
      F39C12.2d.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: F39C12.2d.1:c.1503T>G
        HGVSp: CE30979:p.Thr501=
        cDNA_position: 1503
        CDS_position: 1503
        Protein_position: 501
        Exon_number: 12/17
        Codon_change: acT/acG
        Amino_acid_change: T
  Method: WGS_Flibotte