WormBase Tree Display for Variation: WBVar02138481

WBVar02138481 Evidence: Paper_evidence: WBPaper00045317
  Name: Public_name: h12674
    Other_name: F26F2.7d.1:c.361-335C>T
      F26F2.7a.1:c.1393-335C>T
      F26F2.7b.1:c.1399-335C>T
      F26F2.7c.1:c.769-335C>T
    HGVSg: CHROMOSOME_V:g.20587344C>T
  Sequence_details: SMap: S_parent: Sequence: F26F2
    Flanking_sequences: TGCCGGAATTGAAATTTCCGGCAAATCGGCAAATCGGCAA CTGCCGGAATTGAACGTTACCGGCAAATCGGCAAGCTGCCGGAATTGAACGTTACCGGCAAATCGGCGAATTGCTGGTATTGAGCATTTCCGGCAAATCGGCGAATTGCCGGAATTGAACGTTACCGGCAAATCGGCGAATTGCTGGATTTGAACATTTC
    Mapping_target: CHROMOSOME_V
    Source_location: 200 CHROMOSOME_V 20587307 20587307
    Type_of_mutation: Substitution: C T
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023858
    Laboratory: KR
    Analysis: WGS_Rose
    Status: Live
  Affects: Gene: WBGene00009172
    Transcript: F26F2.7b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F26F2.7b.1:c.1399-335C>T
        Intron_number: 11/16
      F26F2.7d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F26F2.7d.1:c.361-335C>T
        Intron_number: 3/8
      F26F2.7c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F26F2.7c.1:c.769-335C>T
        Intron_number: 4/8
      F26F2.7a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F26F2.7a.1:c.1393-335C>T
        Intron_number: 11/16
  Reference: WBPaper00040589
    WBPaper00000975
    WBPaper00003985
    WBPaper00000699
    WBPaper00045317
  Method: WGS_Rose