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WormBase Tree Display for Variation: WBVar01418412

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Name Class

WBVar01418412EvidencePaper_evidenceWBPaper00037807
NamePublic_nameWBVar01418412
Other_namecewivar00680246
B0041.2a.1:c.1135+81del
B0041.2d.1:c.1261+81del
B0041.2a.2:c.1135+81del
B0041.2c.1:c.1135+81del
B0041.2b.1:c.1261+81del
B0041.2e.1:c.1261+81del
B0041.2f.1:c.1261+81del
B0041.2g.1:c.1135+81del
HGVSgCHROMOSOME_I:g.4656861del
Sequence_detailsSMapS_parentSequenceB0041
Flanking_sequencesTATTTGGTGGTAAAACCATTAATTTATTCGTTTAAAATTAATTATACCAATTTTTTGTTGCGTTTTCCGTTTTTTTAAATATTTTTTTACATCGAAATTG
Mapping_targetB0041
Type_of_mutationDeletionTPaper_evidenceWBPaper00037807
SeqStatusSequenced
Variation_typeSNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004602From_analysisMillion_mutation_project_reanalysis
WGS_De_Bono
WBStrain00006629From_analysisMillion_mutation_project_reanalysis
WBStrain00022850From_analysisMillion_mutation_project_reanalysis
WBStrain00023018From_analysisMillion_mutation_project_reanalysis
WBStrain00027652From_analysisMillion_mutation_project_reanalysis
WBStrain00031113From_analysisMillion_mutation_project_reanalysis
LaboratoryAX
AnalysisWGS_De_Bono
Million_mutation_project_reanalysis
DB_infoDatabasedbSNP_ssss539069365
StatusLive
AffectsGeneWBGene00015007
TranscriptB0041.2f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScB0041.2f.1:c.1261+81del
Intron_number6/10
B0041.2d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScB0041.2d.1:c.1261+81del
Intron_number5/8
B0041.2c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScB0041.2c.1:c.1135+81del
Intron_number4/8
B0041.2e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScB0041.2e.1:c.1261+81del
Intron_number6/10
B0041.2a.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScB0041.2a.2:c.1135+81del
Intron_number4/8
B0041.2a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScB0041.2a.1:c.1135+81del
Intron_number6/10
B0041.2g.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScB0041.2g.1:c.1135+81del
Intron_number4/8
B0041.2b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScB0041.2b.1:c.1261+81del
Intron_number6/10
ReferenceWBPaper00037807
MethodWGS_De_Bono