WormBase Tree Display for Variation: WBVar02126090

WBVar02126090 Evidence: Paper_evidence: WBPaper00045317
  Name: Public_name: h13655
    Other_name: Y95B8A.12d.1:c.493-53G>A
      Y95B8A.12b.1:c.466-53G>A
      Y95B8A.12a.1:c.490-53G>A
      Y95B8A.12f.1:c.487-53G>A
      Y95B8A.12e.1:c.469-53G>A
      Y95B8A.12c.1:c.511-53G>A
    HGVSg: CHROMOSOME_I:g.916459C>T
  Sequence_details: SMap: S_parent: Sequence: Y95B8A
    Flanking_sequences: TTTTTTTTTGGTATTGGAGCTCGTCTCTGGGCTCGTTTTG AGTTTGTACCCTTAAAAAGACATTAAAAAGACATCAGCAA
    Mapping_target: CHROMOSOME_I
    Source_location: 200 CHROMOSOME_I 916461 916461
    Type_of_mutation: Substitution: C T
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023809
    Laboratory: KR
    Analysis: WGS_Rose
    Status: Live
  Affects: Gene: WBGene00022391
    Transcript: Y95B8A.12f.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y95B8A.12f.1:c.487-53G>A
        Intron_number: 4/11
      Y95B8A.12d.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y95B8A.12d.1:c.493-53G>A
        Intron_number: 4/10
      Y95B8A.12a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y95B8A.12a.1:c.490-53G>A
        Intron_number: 5/12
      Y95B8A.12e.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y95B8A.12e.1:c.469-53G>A
        Intron_number: 4/11
      Y95B8A.12c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y95B8A.12c.1:c.511-53G>A
        Intron_number: 5/12
      Y95B8A.12b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: Y95B8A.12b.1:c.466-53G>A
        Intron_number: 4/11
  Reference: WBPaper00040589
    WBPaper00000975
    WBPaper00003985
    WBPaper00000699
    WBPaper00045317
  Method: WGS_Rose