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WormBase Tree Display for Variation: WBVar01401359

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Name Class

WBVar01401359EvidencePaper_evidenceWBPaper00037807
NamePublic_nameWBVar01401359
Other_namecewivar00735264
H14E04.2a.1:c.893+339_893+341del
H14E04.2c.1:c.914+339_914+341del
H14E04.2b.1:c.902+339_902+341del
H14E04.2d.1:c.527+339_527+341del
HGVSgCHROMOSOME_III:g.2381241_2381243del
Sequence_detailsSMapS_parentSequenceH14E04
Flanking_sequencesTACTGACGCGCTGAATTTGAATTTCTGTGTATGAATGAATAATCTTAAAATTTTTTTTTTTTGATTTAAAAAAAAACTTCTTTTTTTTAATCTTCAAAAT
Mapping_targetH14E04
Type_of_mutationDeletionTTTPaper_evidenceWBPaper00037807
SeqStatusSequenced
Variation_typeSNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00006640From_analysisMillion_mutation_project_reanalysis
WBStrain00008273From_analysisMillion_mutation_project_reanalysis
WBStrain00022850From_analysisMillion_mutation_project_reanalysis
WGS_De_Bono
WBStrain00022852From_analysisMillion_mutation_project_reanalysis
WBStrain00022902From_analysisMillion_mutation_project_reanalysis
WBStrain00022930From_analysisMillion_mutation_project_reanalysis
LaboratoryAX
AnalysisWGS_De_Bono
Million_mutation_project_reanalysis
DB_infoDatabasedbSNP_ssss539196246
StatusLive
AffectsGeneWBGene00019199
TranscriptH14E04.2a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH14E04.2a.1:c.893+339_893+341del
Intron_number7/11
H14E04.2c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH14E04.2c.1:c.914+339_914+341del
Intron_number8/12
H14E04.2b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH14E04.2b.1:c.902+339_902+341del
Intron_number7/11
H14E04.2d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScH14E04.2d.1:c.527+339_527+341del
Intron_number4/8
ReferenceWBPaper00037807
MethodWGS_De_Bono