WormBase Tree Display for Variation: WBVar01726527

WBVar01726527 Name: Public_name: WBVar01726527
    Other_name: cewivar00424899
      CE37292:p.Val501=
      Y54G2A.2d.1:c.138C>T
      CE48868:p.Val222=
      CE48618:p.Val46=
      CE26776:p.Val501=
      Y54G2A.2b.1:c.1503C>T
      Y54G2A.2a.1:c.1503C>T
      Y54G2A.2c.1:c.666C>T
    HGVSg: CHROMOSOME_IV:g.2795845C>T
  Sequence_details: SMap: S_parent: Sequence: Y54G2A
    Flanking_sequences: ACTCTGTCTTGTGATTGGAGCTCTCGGCGT TGGGCTTATTCTCGTTATTCTGGACATCTT
    Mapping_target: Y54G2A
    Source_location: 225 CHROMOSOME_IV 2795843 2795843 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Substitution: C T
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00022850 From_analysis: Million_mutation_project_reanalysis
      WBStrain00023139 From_analysis: Million_mutation_project_reanalysis
      WBStrain00027648 From_analysis: Million_mutation_project_reanalysis
      WBStrain00027660 From_analysis: Million_mutation_project_reanalysis
      WBStrain00027662 From_analysis: Million_mutation_project_reanalysis
    Laboratory: VC
    Analysis: Million_mutation_project_reanalysis
    Status: Live
  Affects: Gene: WBGene00021868
    Transcript: Y54G2A.2c.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: Y54G2A.2c.1:c.666C>T
        HGVSp: CE48868:p.Val222=
        cDNA_position: 666
        CDS_position: 666
        Protein_position: 222
        Exon_number: 4/5
        Codon_change: gtC/gtT
        Amino_acid_change: V
      Y54G2A.2a.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: Y54G2A.2a.1:c.1503C>T
        HGVSp: CE26776:p.Val501=
        cDNA_position: 1512
        CDS_position: 1503
        Protein_position: 501
        Exon_number: 10/12
        Codon_change: gtC/gtT
        Amino_acid_change: V
      Y54G2A.2d.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: Y54G2A.2d.1:c.138C>T
        HGVSp: CE48618:p.Val46=
        cDNA_position: 138
        CDS_position: 138
        Protein_position: 46
        Exon_number: 1/2
        Codon_change: gtC/gtT
        Amino_acid_change: V
      Y54G2A.2b.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: Y54G2A.2b.1:c.1503C>T
        HGVSp: CE37292:p.Val501=
        cDNA_position: 1515
        CDS_position: 1503
        Protein_position: 501
        Exon_number: 10/12
        Codon_change: gtC/gtT
        Amino_acid_change: V
  Method: WGS_Flibotte