WormBase Tree Display for Variation: WBVar00317940

WBVar00317940 Evidence: Paper_evidence: WBPaper00037659
  Name: Public_name: snx368
    Other_name: IS656_1013
      F22D3.2c.1:c.306+124G>A
      F22D3.2j.1:c.1281+124G>A
      F22D3.2d.1:c.1278+124G>A
      F22D3.2i.1:c.201+124G>A
      F22D3.2g.1:c.1290+124G>A
      F22D3.2e.1:c.1269+124G>A
    HGVSg: CHROMOSOME_II:g.6944972G>A
  Sequence_details: SMap: S_parent: Sequence: F22D3
    Flanking_sequences: GTATCGTTAACGCGCATTTCTGATCATCTTATCAAATCGCACTTGCCCAC AAAAATCGTATCAATACCGTATCCCGGTTATTTCGTCCAAAAAGCATACA
    Mapping_target: F22D3
    Type_of_mutation: Substitution: G A
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00022163
    Laboratory: IS
    Analysis: WGS_Jarriault
    Status: Live
  Affects: Gene: WBGene00017699
    Transcript: F22D3.2g.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F22D3.2g.1:c.1290+124G>A
        Intron_number: 15/18
      F22D3.2e.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F22D3.2e.1:c.1269+124G>A
        Intron_number: 15/18
      F22D3.2c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F22D3.2c.1:c.306+124G>A
        Intron_number: 3/6
      F22D3.2i.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F22D3.2i.1:c.201+124G>A
        Intron_number: 2/4
      F22D3.2d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F22D3.2d.1:c.1278+124G>A
        Intron_number: 15/18
      F22D3.2j.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F22D3.2j.1:c.1281+124G>A
        Intron_number: 15/18
  Genetics: Map: II
  Reference: WBPaper00037659
  Method: WGS_Jarriault