WormBase Tree Display for Variation: WBVar00210761

WBVar00210761 Name: Public_name: WBVar00210761
    Other_name (13)
    HGVSg: CHROMOSOME_V:g.6706076A>G
  Sequence_details: SMap: S_parent: Sequence: W02F12
    Flanking_sequences: aaagtgctggtttctgtaaactatt aagaattgaatcacgccgggccatt
    Mapping_target: W02F12
    Type_of_mutation: Substitution: A G
    SeqStatus: Sequenced
  Variation_type: SNP
    Predicted_SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00004602 From_analysis: Million_mutation_project_reanalysis
          WGS_Hawaiian_Waterston
      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: RW
    Person: WBPerson1562
    Analysis: WGS_Hawaiian_Waterston
      Million_mutation_project_reanalysis
    Status: Live
  Affects: Gene: WBGene00020949
    Transcript: W02F12.4c.5 VEP_consequence: 3_prime_UTR_variant
        VEP_impact: MODIFIER
        HGVSc: W02F12.4c.5:c.*366T>C
        cDNA_position: 709
        Exon_number: 6/8
      W02F12.4c.3 VEP_consequence: 3_prime_UTR_variant
        VEP_impact: MODIFIER
        HGVSc: W02F12.4c.3:c.*367T>C
        cDNA_position: 715
        Exon_number: 6/8
      W02F12.4c.2 VEP_consequence: 3_prime_UTR_variant
        VEP_impact: MODIFIER
        HGVSc: W02F12.4c.2:c.*325T>C
        cDNA_position: 673
        Exon_number: 7/9
      W02F12.4c.6 VEP_consequence: 3_prime_UTR_variant
        VEP_impact: MODIFIER
        HGVSc: W02F12.4c.6:c.*366T>C
        cDNA_position: 707
        Exon_number: 6/6
      W02F12.4c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: W02F12.4c.1:c.*245+122T>C
        Intron_number: 6/7
      W02F12.4b.2 VEP_consequence: 3_prime_UTR_variant
        VEP_impact: MODIFIER
        HGVSc: W02F12.4b.2:c.*330T>C
        cDNA_position: 665
        Exon_number: 7/9
      W02F12.4a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: W02F12.4a.1:c.541+122T>C
        Intron_number: 5/7
      W02F12.4c.4 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: W02F12.4c.4:c.*286+122T>C
        Intron_number: 5/6
      W02F12.4b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: W02F12.4b.1:c.*250+122T>C
        Intron_number: 6/7
      W02F12.4d.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: W02F12.4d.1:c.621T>C
        HGVSp: CE47068:p.Phe207=
        cDNA_position: 652
        CDS_position: 621
        Protein_position: 207
        Exon_number: 6/9
        Codon_change: ttT/ttC
        Amino_acid_change: F
  Remark: [20081124 db] this Variation was previously named hw78037
  Method: WGS_Hawaiian_Waterston