WormBase Tree Display for Variation: WBVar00023246

WBVar00023246 Name: Public_name: WBVar00023246
    Other_name: pas16246
      F12B6.2c.1:c.171-337T>C
      F12B6.2a.1:c.296+294T>C
    HGVSg: CHROMOSOME_I:g.2251130T>C
  Sequence_details: SMap: S_parent: Sequence: F12B6
    Flanking_sequences: ccaaaaagtgagtatgtcagctgattatttgagaagaagaagtgctactgataagaaatatgttcagaaattatttccgattaaacggggtgaatttattgaaaaatcacgaagaaattatgattggaagtgggaaatttcttaaattttgcacaaaaatttaaaaaaaaattgaagtttggtggactaagaaaagttaggccaccaaactttggtgaactaagaaaagttaggccaccaaacattggtggactaagaaaagttaggccaccaaactttggcgaattaagaaaagttaag cacaaaatttttggtggactaagaaaagttaggccaccaaactttggtggattaagaaatgttaggccaccaaactttgatcgactaggtggcctaactttttttaggccaaccaaactttggtggacttttctgaaaagcattttttcggtttatgaaaactttcaataaaaaattagaatttcgctccaatttttcaaattttaaattttaattttccaagaaaattgggagaatataaaatttcaactttgcgcgccaaaattttctcaaaaaattttctcaaaatttttttttcga
    Mapping_target: F12B6
    Type_of_mutation: Substitution: T C
    SeqStatus: Sequenced
  Variation_type: SNP
    Predicted_SNP
    Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00004604 From_analysis: WGS_Pasadena_Quinlan
    Person: WBPerson6900
    Analysis: WGS_Pasadena_Quinlan
    Status: Live
  Affects: Gene: WBGene00017398
    Transcript: F12B6.2c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F12B6.2c.1:c.171-337T>C
        Intron_number: 2/10
      F12B6.2a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F12B6.2a.1:c.296+294T>C
        Intron_number: 4/13
  Method: WGS_Pasadena_Quinlan