Questions, Feedback & Help
Send us an email and we'll get back to you ASAP. Or you can read our Frequently Asked Questions.

WormBase Tree Display for Variation: WBVar01396718

expand all nodes | collapse all nodes | view schema

Name Class

WBVar01396718EvidencePaper_evidenceWBPaper00037807
NamePublic_nameWBVar01396718
Other_namecewivar00738541
T08A11.1f.1:c.4450-200del
T08A11.1g.1:c.4450-200del
T08A11.1e.1:c.4444-200del
T08A11.1c.1:c.4444-200del
T08A11.1d.1:c.4450-200del
T08A11.1a.1:c.4438-200del
T08A11.1b.1:c.4444-200del
T08A11.1h.1:c.4456-200del
HGVSgCHROMOSOME_III:g.4250283del
Sequence_detailsSMapS_parentSequenceT08A11
Flanking_sequencesCAAAATAGTTAATCCTTACTAGTTAGAATGCGTACAATTTTGAATTTTCCAAAAAAAAAAAGTACAAAACCACAATTTGCCGGAGGTTTTCAATTCCGGC
Mapping_targetT08A11
Type_of_mutationDeletionAPaper_evidenceWBPaper00037807
SeqStatusSequenced
Variation_typeSNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00006642From_analysisWGS_De_Bono
WBStrain00006643From_analysisMillion_mutation_project_reanalysis
WBStrain00006645From_analysisMillion_mutation_project_reanalysis
WBStrain00023665From_analysisMillion_mutation_project_reanalysis
LaboratoryAX
AnalysisWGS_De_Bono
Million_mutation_project_reanalysis
DB_infoDatabasedbSNP_ssss539115841
StatusLive
AffectsGeneWBGene00011604
TranscriptT08A11.1e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT08A11.1e.1:c.4444-200del
Intron_number15/17
T08A11.1g.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT08A11.1g.1:c.4450-200del
Intron_number16/18
T08A11.1h.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT08A11.1h.1:c.4456-200del
Intron_number16/18
T08A11.1d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT08A11.1d.1:c.4450-200del
Intron_number16/18
T08A11.1f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT08A11.1f.1:c.4450-200del
Intron_number15/17
T08A11.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT08A11.1c.1:c.4444-200del
Intron_number15/17
T08A11.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT08A11.1b.1:c.4444-200del
Intron_number16/18
T08A11.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT08A11.1a.1:c.4438-200del
Intron_number16/18
ReferenceWBPaper00037807
MethodWGS_De_Bono