WormBase Tree Display for Variation: WBVar01453079

WBVar01453079 Evidence: Paper_evidence: WBPaper00040707
  Name: Public_name: WBVar01453079
    Other_name (18)
    HGVSg: CHROMOSOME_IV:g.7432742A>G
  Sequence_details: SMap: S_parent: Sequence: B0496
    Flanking_sequences: GAATCTTCTGACAACATTCTGTGGAAGTCC TTGTATGCATCTCCAGAAATTATCAACGGA
    Mapping_target: B0496
    Type_of_mutation: Substitution: a g
    SeqStatus: Sequenced
  Variation_type: SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00031279 From_analysis: WGS_Andersen
      WBStrain00031284 From_analysis: WGS_Andersen
    Laboratory: QX
    Person: WBPerson1730
    Analysis: WGS_Andersen
    DB_info: Database: dbSNP_rs rs 193338736
        dbSNP_ss ss 295514655
    Status: Live
  Affects: Gene: WBGene00006814
    Transcript: B0496.3h.2 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: B0496.3h.2:c.657A>G
        HGVSp: CE44339:p.Pro219=
        cDNA_position: 657
        CDS_position: 657
        Protein_position: 219
        Exon_number: 5/28
        Codon_change: ccA/ccG
        Amino_acid_change: P
      B0496.3a.2 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: B0496.3a.2:c.657A>G
        HGVSp: CE44329:p.Pro219=
        cDNA_position: 671
        CDS_position: 657
        Protein_position: 219
        Exon_number: 6/28
        Codon_change: ccA/ccG
        Amino_acid_change: P
      B0496.3b.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: B0496.3b.1:c.657A>G
        HGVSp: CE44280:p.Pro219=
        cDNA_position: 657
        CDS_position: 657
        Protein_position: 219
        Exon_number: 5/31
        Codon_change: ccA/ccG
        Amino_acid_change: P
      B0496.3i.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: B0496.3i.1:c.708A>G
        HGVSp: CE49580:p.Pro236=
        cDNA_position: 708
        CDS_position: 708
        Protein_position: 236
        Exon_number: 5/30
        Codon_change: ccA/ccG
        Amino_acid_change: P
      B0496.3g.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: B0496.3g.1:c.657A>G
        HGVSp: CE44297:p.Pro219=
        cDNA_position: 762
        CDS_position: 657
        Protein_position: 219
        Exon_number: 8/32
        Codon_change: ccA/ccG
        Amino_acid_change: P
      B0496.3a.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: B0496.3a.1:c.657A>G
        HGVSp: CE44329:p.Pro219=
        cDNA_position: 1126
        CDS_position: 657
        Protein_position: 219
        Exon_number: 11/33
        Codon_change: ccA/ccG
        Amino_acid_change: P
      B0496.3e.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: B0496.3e.1:c.1374A>G
        HGVSp: CE44360:p.Pro458=
        cDNA_position: 1376
        CDS_position: 1374
        Protein_position: 458
        Exon_number: 11/35
        Codon_change: ccA/ccG
        Amino_acid_change: P
      B0496.3f.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: B0496.3f.1:c.657A>G
        HGVSp: CE44278:p.Pro219=
        cDNA_position: 657
        CDS_position: 657
        Protein_position: 219
        Exon_number: 5/29
        Codon_change: ccA/ccG
        Amino_acid_change: P
      B0496.3h.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: B0496.3h.1:c.657A>G
        HGVSp: CE44339:p.Pro219=
        cDNA_position: 762
        CDS_position: 657
        Protein_position: 219
        Exon_number: 8/31
        Codon_change: ccA/ccG
        Amino_acid_change: P
      B0496.3d.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: B0496.3d.1:c.657A>G
        HGVSp: CE44346:p.Pro219=
        cDNA_position: 762
        CDS_position: 657
        Protein_position: 219
        Exon_number: 8/33
        Codon_change: ccA/ccG
        Amino_acid_change: P
  Reference: WBPaper00040707
  Method: WGS_Andersen