WormBase Tree Display for Variation: WBVar02135092

WBVar02135092 Evidence: Paper_evidence: WBPaper00045317
  Name: Public_name: h16688
    Other_name: Y64G10A.7d.1:c.4004+310G>C
      Y64G10A.7e.1:c.3878+310G>C
      Y64G10A.7c.1:c.4025+310G>C
      Y64G10A.7b.1:c.4331+310G>C
      Y64G10A.7a.1:c.4151+310G>C
    HGVSg: CHROMOSOME_IV:g.14316694G>C
  Sequence_details: SMap: S_parent: Sequence: Y64G10A
    Flanking_sequences: AGCTGTGGTACATTTTGAGCTCTTTTCAATGTATTTTAAT GTCTGGAAAATCACTTTTTAAAAATTTTAACTTCTGTACA
    Mapping_target: CHROMOSOME_IV
    Source_location: 200 CHROMOSOME_IV 14316659 14316659
    Type_of_mutation: Substitution: G C
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023759
    Laboratory: KR
    Analysis: WGS_Rose
    Status: Live
  Affects: Gene: WBGene00013416
    Transcript: Y64G10A.7e.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y64G10A.7e.1:c.3878+310G>C
        Intron_number: 18/20
      Y64G10A.7c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y64G10A.7c.1:c.4025+310G>C
        Intron_number: 20/23
      Y64G10A.7b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y64G10A.7b.1:c.4331+310G>C
        Intron_number: 21/23
      Y64G10A.7a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y64G10A.7a.1:c.4151+310G>C
        Intron_number: 21/24
      Y64G10A.7d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y64G10A.7d.1:c.4004+310G>C
        Intron_number: 20/23
  Reference: WBPaper00040589
    WBPaper00000975
    WBPaper00003985
    WBPaper00000699
    WBPaper00045317
  Method: WGS_Rose