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WormBase Tree Display for Variation: WBVar02074514

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Name Class

WBVar02074514NamePublic_nameWBVar02074514
Other_namecewivar00803826
F56B6.5d.1:c.140+251del
F56B6.5a.1:c.110+251del
F56B6.5c.1:c.140+251del
F56B6.5b.1:c.110+251del
F56B6.5a.2:c.110+251del
HGVSgCHROMOSOME_X:g.3529178del
Sequence_detailsSMapS_parentSequenceF56B6
Flanking_sequencesTTTCCTAATTCACGTTTTATTATTTAAAAATGAAAACATGTTGGGATGCAGCTAATACAC
Mapping_targetF56B6
Source_location225CHROMOSOME_X35291653529165From_analysisMillion_mutation_project_reanalysis
Type_of_mutationDeletion
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00031113From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00006864
TranscriptF56B6.5d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.5d.1:c.140+251del
Intron_number2/10
F56B6.5c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.5c.1:c.140+251del
Intron_number2/10
F56B6.5a.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.5a.2:c.110+251del
Intron_number3/12
F56B6.5b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.5b.1:c.110+251del
Intron_number2/11
F56B6.5a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.5a.1:c.110+251del
Intron_number2/11
MethodWGS_Flibotte