WormBase Tree Display for Variation: WBVar02133905

WBVar02133905 Evidence: Paper_evidence: WBPaper00045317
  Name: Public_name: h4034
    Other_name: Y4C6A.2d.1:c.2746+234C>T
      Y4C6A.2g.1:c.922+234C>T
      Y4C6A.2a.1:c.2740+234C>T
      Y4C6A.2f.1:c.1510+234C>T
      Y4C6A.2e.1:c.1516+234C>T
      Y4C6A.2h.1:c.916+234C>T
    HGVSg: CHROMOSOME_IV:g.5448717C>T
  Sequence_details: SMap: S_parent: Sequence: Y4C6A
    Flanking_sequences: AAATTATGATTTTTAAAAACACGCAATGGAAACTGACTAA ATATAAACAGTTGGGCAAATGAAAACATTATGAAGTAGTC
    Mapping_target: CHROMOSOME_IV
    Source_location: 200 CHROMOSOME_IV 5448704 5448704
    Type_of_mutation: Substitution: C T
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023775
    Laboratory: KR
    Analysis: WGS_Rose
    Status: Live
  Affects: Gene: WBGene00021152
    Transcript: Y4C6A.2f.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y4C6A.2f.1:c.1510+234C>T
        Intron_number: 11/11
      Y4C6A.2a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y4C6A.2a.1:c.2740+234C>T
        Intron_number: 18/19
      Y4C6A.2h.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y4C6A.2h.1:c.916+234C>T
        Intron_number: 7/7
      Y4C6A.2e.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y4C6A.2e.1:c.1516+234C>T
        Intron_number: 11/11
      Y4C6A.2g.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y4C6A.2g.1:c.922+234C>T
        Intron_number: 7/7
      Y4C6A.2d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y4C6A.2d.1:c.2746+234C>T
        Intron_number: 18/19
  Reference: WBPaper00040589
    WBPaper00000975
    WBPaper00003985
    WBPaper00000699
    WBPaper00045317
  Method: WGS_Rose