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WormBase Tree Display for Variation: WBVar02096758

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Name Class

WBVar02096758NamePublic_nameWBVar02096758
Other_namecewivar00826833
F42G9.5a.1:c.692-100_692-79delinsCTGCCAGATGGAAAAAAAATGT
F42G9.5b.2:c.140-100_140-79delinsCTGCCAGATGGAAAAAAAATGT
F42G9.5b.1:c.140-100_140-79delinsCTGCCAGATGGAAAAAAAATGT
HGVSgCHROMOSOME_III:g.776301_776322delinsACATTTTTTTTCCATCTGGCAG
Sequence_detailsSMapS_parentSequenceF42G9
Flanking_sequencesAGAAATGGAAAGATTCGATGGTTTAAAAAATTTTTTTTTTTGGAAAAAAGTCGAGAACAA
Mapping_targetF42G9
Source_location225CHROMOSOME_III776297776318From_analysisMillion_mutation_project_reanalysis
Type_of_mutationInsertionACATTTTTTTTCCATCTGGCAG
Deletion
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00006631From_analysisMillion_mutation_project_reanalysis
WBStrain00022850From_analysisMillion_mutation_project_reanalysis
WBStrain00022886From_analysisMillion_mutation_project_reanalysis
WBStrain00023072From_analysisMillion_mutation_project_reanalysis
WBStrain00024204From_analysisMillion_mutation_project_reanalysis
WBStrain00027647From_analysisMillion_mutation_project_reanalysis
WBStrain00027648From_analysisMillion_mutation_project_reanalysis
WBStrain00031113From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00000117
TranscriptF42G9.5b.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF42G9.5b.2:c.140-100_140-79delinsCTGCCAGATGGAAAAAAAATGT
Intron_number3/7
F42G9.5a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF42G9.5a.1:c.692-100_692-79delinsCTGCCAGATGGAAAAAAAATGT
Intron_number3/8
F42G9.5b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF42G9.5b.1:c.140-100_140-79delinsCTGCCAGATGGAAAAAAAATGT
Intron_number2/7
MethodWGS_Flibotte