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WormBase Tree Display for Variation: WBVar02020876

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Name Class

WBVar02020876NamePublic_nameWBVar02020876
Other_namecewivar00749384
B0496.3g.1:c.-9+579_-9+580del
B0496.3d.1:c.-9+579_-9+580del
B0496.3h.1:c.-9+579_-9+580del
B0496.3e.1:c.709+579_709+580del
B0496.3a.1:c.-9+579_-9+580del
HGVSgCHROMOSOME_IV:g.7426456_7426457del
Sequence_detailsSMapS_parentSequenceB0496
Flanking_sequencesTGATCTGTTACGAGATGATATCCTACACGGTTTTTTTTCCCTTAGGCTCTTTTCCTCTTA
Mapping_targetB0496
Source_location225CHROMOSOME_IV74264457426446From_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
AffectsGeneWBGene00006814
TranscriptB0496.3e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScB0496.3e.1:c.709+579_709+580del
Intron_number6/34
B0496.3h.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScB0496.3h.1:c.-9+579_-9+580del
Intron_number2/30
B0496.3d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScB0496.3d.1:c.-9+579_-9+580del
Intron_number2/32
B0496.3g.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScB0496.3g.1:c.-9+579_-9+580del
Intron_number2/31
B0496.3a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScB0496.3a.1:c.-9+579_-9+580del
Intron_number5/32
MethodWGS_Flibotte