WormBase Tree Display for Variation: WBVar01134602

WBVar01134602 Name: Public_name: gk435574
    Other_name: F56B6.2j.1:c.1706-996C>T
      F56B6.2h.1:c.1712-996C>T
      F56B6.2a.1:c.1697-996C>T
      F56B6.2c.1:c.512-996C>T
      F56B6.2b.1:c.1586-996C>T
      F56B6.2i.1:c.1703-996C>T
      F56B6.2e.1:c.212-996C>T
    HGVSg: CHROMOSOME_X:g.3551551C>T
  Sequence_details: SMap: S_parent: Sequence: F56B6
    Flanking_sequences: CCCACGCCTGTTTTTGGAACAACACATCACTGCCACGCATTTTGTATCGA CGATAGAAATGAGGGGATGCACAGTTTTTATTGAGGACAACTTTCTTTAG
    Mapping_target: F56B6
    Type_of_mutation: Substitution: C T
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin (5)
  Affects: Gene: WBGene00004350
    Transcript: F56B6.2j.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F56B6.2j.1:c.1706-996C>T
        Intron_number: 9/14
      F56B6.2e.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F56B6.2e.1:c.212-996C>T
        Intron_number: 1/7
      F56B6.2i.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F56B6.2i.1:c.1703-996C>T
        Intron_number: 10/16
      F56B6.2b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F56B6.2b.1:c.1586-996C>T
        Intron_number: 9/15
      F56B6.2a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F56B6.2a.1:c.1697-996C>T
        Intron_number: 10/16
      F56B6.2h.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F56B6.2h.1:c.1712-996C>T
        Intron_number: 10/16
      F56B6.2c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F56B6.2c.1:c.512-996C>T
        Intron_number: 4/9
  Reference: WBPaper00042537
  Method: Million_mutation