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WormBase Tree Display for Variation: WBVar01991778

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Name Class

WBVar01991778NamePublic_nameWBVar01991778
Other_namecewivar00718525
E01B7.1.2:c.1657-31del
E01B7.1.1:c.1657-31del
HGVSgCHROMOSOME_V:g.17930521del
Sequence_detailsSMapS_parentSequenceY59A8B
Flanking_sequencesAATTTCAGAATTTTCAGCCATGTTTTTGTGAAATCGGCATTTTTAACATTTTTCTTGCAG
Mapping_targetY59A8B
Source_location225CHROMOSOME_V1793049517930495From_analysisMillion_mutation_project_reanalysis
Type_of_mutationDeletion
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00006625From_analysisMillion_mutation_project_reanalysis
WBStrain00022868From_analysisMillion_mutation_project_reanalysis
WBStrain00022878From_analysisMillion_mutation_project_reanalysis
WBStrain00022886From_analysisMillion_mutation_project_reanalysis
WBStrain00023139From_analysisMillion_mutation_project_reanalysis
WBStrain00023192From_analysisMillion_mutation_project_reanalysis
WBStrain00027648From_analysisMillion_mutation_project_reanalysis
WBStrain00027652From_analysisMillion_mutation_project_reanalysis
WBStrain00027660From_analysisMillion_mutation_project_reanalysis
WBStrain00027662From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00008441
TranscriptE01B7.1.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScE01B7.1.1:c.1657-31del
Intron_number11/18
E01B7.1.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScE01B7.1.2:c.1657-31del
Intron_number12/19
MethodWGS_Flibotte