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WormBase Tree Display for Variation: WBVar01269562

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Name Class

WBVar01269562EvidencePaper_evidenceWBPaper00037807
NamePublic_nameWBVar01269562
Other_namecewivar00658245
Y46E12BL.2a.2:c.3794+338del
Y46E12BL.2a.1:c.3794+338del
HGVSgCHROMOSOME_II:g.15243412del
Sequence_detailsSMapS_parentSequenceY46E12BL
Flanking_sequencesGCCAATGGAACAAAAATCGATTTTTCGATGAATTTTGAGATTTTTTTCCGAAAAAAAAATGCTTGTCATCACTTTTTTTCGAGCTGGAATAGGCTTGAAA
Mapping_targetY46E12BL
Type_of_mutationDeletionAPaper_evidenceWBPaper00037807
SeqStatusSequenced
Variation_typeSNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00000034From_analysisMillion_mutation_project_reanalysis
WBStrain00004602From_analysisMillion_mutation_project_reanalysis
WGS_De_Bono
WBStrain00022850From_analysisMillion_mutation_project_reanalysis
WBStrain00023665From_analysisMillion_mutation_project_reanalysis
WBStrain00024204From_analysisMillion_mutation_project_reanalysis
WBStrain00031113From_analysisMillion_mutation_project_reanalysis
LaboratoryAX
AnalysisWGS_De_Bono
Million_mutation_project_reanalysis
DB_infoDatabasedbSNP_ssss539008593
StatusLive
AffectsGeneWBGene00021595
TranscriptY46E12BL.2a.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY46E12BL.2a.2:c.3794+338del
Intron_number10/11
Y46E12BL.2a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY46E12BL.2a.1:c.3794+338del
Intron_number9/10
ReferenceWBPaper00037807
MethodWGS_De_Bono