WormBase Tree Display for Variation: WBVar01858891

WBVar01858891 Name: Public_name: WBVar01858891
    Other_name (19)
    HGVSg: CHROMOSOME_IV:g.11983584G>A
  Sequence_details: SMap: S_parent: Sequence: ZK617
    Flanking_sequences: AAGCTTATTAACCTTGGCTGTACAATCTGG AAAGTTCCGACTTCCTGCCATGTTCCACGA
    Mapping_target: ZK617
    Source_location: 225 CHROMOSOME_IV 11983561 11983561 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Substitution: G A
    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: WBGene00006759
    Transcript: ZK617.1i.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: ZK617.1i.1:c.11937C>T
        HGVSp: CE49956:p.Phe3979=
        cDNA_position: 11937
        CDS_position: 11937
        Protein_position: 3979
        Exon_number: 29/33
        Codon_change: ttC/ttT
        Amino_acid_change: F
      ZK617.1a.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: ZK617.1a.1:c.11055C>T
        HGVSp: CE33017:p.Phe3685=
        cDNA_position: 11182
        CDS_position: 11055
        Protein_position: 3685
        Exon_number: 28/33
        Codon_change: ttC/ttT
        Amino_acid_change: F
      ZK617.1g.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: ZK617.1g.1:c.11082C>T
        HGVSp: CE46868:p.Phe3694=
        cDNA_position: 11082
        CDS_position: 11082
        Protein_position: 3694
        Exon_number: 28/32
        Codon_change: ttC/ttT
        Amino_acid_change: F
      ZK617.1f.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: ZK617.1f.1:c.11319C>T
        HGVSp: CE46948:p.Phe3773=
        cDNA_position: 11319
        CDS_position: 11319
        Protein_position: 3773
        Exon_number: 27/31
        Codon_change: ttC/ttT
        Amino_acid_change: F
      ZK617.1d.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: ZK617.1d.1:c.9894C>T
        HGVSp: CE49926:p.Phe3298=
        cDNA_position: 9894
        CDS_position: 9894
        Protein_position: 3298
        Exon_number: 18/22
        Codon_change: ttC/ttT
        Amino_acid_change: F
      ZK617.1c.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: ZK617.1c.1:c.10395C>T
        HGVSp: CE47057:p.Phe3465=
        cDNA_position: 10656
        CDS_position: 10395
        Protein_position: 3465
        Exon_number: 22/26
        Codon_change: ttC/ttT
        Amino_acid_change: F
      ZK617.1h.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: ZK617.1h.1:c.11964C>T
        HGVSp: CE49973:p.Phe3988=
        cDNA_position: 11964
        CDS_position: 11964
        Protein_position: 3988
        Exon_number: 30/34
        Codon_change: ttC/ttT
        Amino_acid_change: F
      ZK617.1b.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: ZK617.1b.1:c.12012C>T
        HGVSp: CE33018:p.Phe4004=
        cDNA_position: 12012
        CDS_position: 12012
        Protein_position: 4004
        Exon_number: 30/34
        Codon_change: ttC/ttT
        Amino_acid_change: F
      ZK617.1e.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: ZK617.1e.1:c.9843C>T
        HGVSp: CE44668:p.Phe3281=
        cDNA_position: 9843
        CDS_position: 9843
        Protein_position: 3281
        Exon_number: 17/21
        Codon_change: ttC/ttT
        Amino_acid_change: F
  Method: WGS_Flibotte