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WormBase Tree Display for Variation: WBVar01425300

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Name Class

WBVar01425300EvidencePaper_evidenceWBPaper00037807
NamePublic_nameWBVar01425300
Other_namecewivar00652008
Y47H9C.4a.1:c.1026+286del
Y47H9C.4b.1:c.1026+286del
Y47H9C.4c.1:c.1026+286del
HGVSgCHROMOSOME_I:g.11862507del
Sequence_detailsSMapS_parentSequenceY47H9C
Flanking_sequencesGATTGTTCAGTTGTTGGCTAAATTGCTCGATTTTGGACCATTTTTACAGATTTTTTTTTTTCGTATTTAACTTGGAAATCGCCAAATTTATATAAAAATC
Mapping_targetY47H9C
Type_of_mutationDeletionTPaper_evidenceWBPaper00037807
SeqStatusSequenced
Variation_typeSNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00000034From_analysisMillion_mutation_project_reanalysis
WBStrain00004602From_analysisMillion_mutation_project_reanalysis
WGS_De_Bono
WBStrain00006625From_analysisMillion_mutation_project_reanalysis
WBStrain00006637From_analysisMillion_mutation_project_reanalysis
LaboratoryAX
AnalysisWGS_De_Bono
Million_mutation_project_reanalysis
DB_infoDatabasedbSNP_ssss539070053
StatusLive
AffectsGeneWBGene00000415
TranscriptY47H9C.4a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY47H9C.4a.1:c.1026+286del
Intron_number6/12
Y47H9C.4c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY47H9C.4c.1:c.1026+286del
Intron_number6/11
Y47H9C.4b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY47H9C.4b.1:c.1026+286del
Intron_number6/12
ReferenceWBPaper00037807
MethodWGS_De_Bono