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WormBase Tree Display for Variation: WBVar01945166

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Name Class

WBVar01945166NamePublic_nameWBVar01945166
Other_namecewivar00666688
F39C12.3b.1:c.35+800del
F39C12.3a.1:c.-38+800del
F39C12.3a.3:c.-37-2514del
HGVSgCHROMOSOME_X:g.4873573del
Sequence_detailsSMapS_parentSequenceF39C12
Flanking_sequencesTATTGTTAATTGGAAAAAACAGGTAATTTCAAAAAAAAGTAGTAAAAGATCACATGTGTA
Mapping_targetF39C12
Source_location225CHROMOSOME_X48735434873543From_analysisMillion_mutation_project_reanalysis
Type_of_mutationDeletion
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004599From_analysisMillion_mutation_project_reanalysis
WBStrain00004602From_analysisMillion_mutation_project_reanalysis
WBStrain00022850From_analysisMillion_mutation_project_reanalysis
WBStrain00022886From_analysisMillion_mutation_project_reanalysis
WBStrain00023138From_analysisMillion_mutation_project_reanalysis
WBStrain00023139From_analysisMillion_mutation_project_reanalysis
WBStrain00027648From_analysisMillion_mutation_project_reanalysis
WBStrain00027660From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00006640
TranscriptF39C12.3a.3VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF39C12.3a.3:c.-37-2514del
Intron_number1/10
F39C12.3a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF39C12.3a.1:c.-38+800del
Intron_number1/10
F39C12.3b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF39C12.3b.1:c.35+800del
Intron_number2/9
MethodWGS_Flibotte