WormBase Tree Display for Variation: WBVar02130693

WBVar02130693 Evidence: Paper_evidence: WBPaper00045317
  Name: Public_name: h6953
    Other_name: F45E10.1h.1:c.30+2704C>T
      F45E10.1a.1:c.30+2704C>T
      F45E10.1g.1:c.30+2704C>T
      F45E10.1c.1:c.30+2704C>T
      F45E10.1b.1:c.30+2704C>T
    HGVSg: CHROMOSOME_II:g.11086682G>A
  Sequence_details: SMap: S_parent: Sequence: C09H10
    Flanking_sequences: TAGAATCCACTGCCAAGTTTGCGGAATTCATCCGCGGAAG GTGTCCATGAATCCGCATAAAATGTTTTCTACTAAAGCCA
    Mapping_target: CHROMOSOME_II
    Source_location: 200 CHROMOSOME_II 11086607 11086607
    Type_of_mutation: Substitution: G A
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023732
    Laboratory: KR
    Analysis: WGS_Rose
    Status: Live
  Affects: Gene: WBGene00006788
    Transcript: F45E10.1c.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F45E10.1c.1:c.30+2704C>T
        Intron_number: 1/23
      F45E10.1b.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F45E10.1b.1:c.30+2704C>T
        Intron_number: 1/22
      F45E10.1g.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F45E10.1g.1:c.30+2704C>T
        Intron_number: 1/21
      F45E10.1a.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F45E10.1a.1:c.30+2704C>T
        Intron_number: 2/23
      F45E10.1h.1 VEP_consequence: intron_variant
        VEP_impact: MODIFIER
        HGVSc: F45E10.1h.1:c.30+2704C>T
        Intron_number: 1/21
  Reference: WBPaper00040589
    WBPaper00000975
    WBPaper00003985
    WBPaper00000699
    WBPaper00045317
  Method: WGS_Rose