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WormBase Tree Display for Variation: WBVar02020667

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Name Class

WBVar02020667NamePublic_nameWBVar02020667
Other_namecewivar00749175
C11D2.6m.1:c.34-1799del
C11D2.6n.1:c.34-1799del
C11D2.6o.1:c.34-1799del
C11D2.6p.1:c.34-1799del
HGVSgCHROMOSOME_IV:g.6181051del
Sequence_detailsSMapS_parentSequenceC11D2
Flanking_sequencesAATTTTAAAATGCTTAAATAATGAGACATCAAAAAAAATGCTCAGAAAAACTAAAAACTT
Mapping_targetC11D2
Source_location225CHROMOSOME_IV61810406181040From_analysisMillion_mutation_project_reanalysis
Type_of_mutationDeletion
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00023139From_analysisMillion_mutation_project_reanalysis
WBStrain00027648From_analysisMillion_mutation_project_reanalysis
WBStrain00027660From_analysisMillion_mutation_project_reanalysis
WBStrain00027662From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00006809
TranscriptC11D2.6o.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC11D2.6o.1:c.34-1799del
Intron_number1/28
C11D2.6p.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC11D2.6p.1:c.34-1799del
Intron_number1/28
C11D2.6n.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC11D2.6n.1:c.34-1799del
Intron_number1/27
C11D2.6m.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC11D2.6m.1:c.34-1799del
Intron_number1/29
MethodWGS_Flibotte