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WormBase Tree Display for Variation: WBVar02118939

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Name Class

WBVar02118939NamePublic_nameWBVar02118939
Other_namecewivar00849794
M142.1a.1:c.554-46_554-25delinsATATGTTTTTTTGTTGTAAAATTA
M142.1c.1:c.629-46_629-25delinsATATGTTTTTTTGTTGTAAAATTA
M142.1b.1:c.494-46_494-25delinsATATGTTTTTTTGTTGTAAAATTA
HGVSgCHROMOSOME_III:g.10908602_10908623delinsATATGTTTTTTTGTTGTAAAATTA
Sequence_detailsSMapS_parentSequenceM142
Flanking_sequencesGAAAGTAAAATGAAATTTGCAAAAAAAAAAAAAAAAAAAACTGTATATTTTCAGTGGACG
Mapping_targetM142
Source_location225CHROMOSOME_III1090850310908524From_analysisMillion_mutation_project_reanalysis
Type_of_mutationInsertionATATGTTTTTTTGTTGTAAAATTA
Deletion
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00027648From_analysisMillion_mutation_project_reanalysis
WBStrain00027662From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00006843
TranscriptM142.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScM142.1a.1:c.554-46_554-25delinsATATGTTTTTTTGTTGTAAAATTA
Intron_number4/5
M142.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScM142.1c.1:c.629-46_629-25delinsATATGTTTTTTTGTTGTAAAATTA
Intron_number5/6
M142.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScM142.1b.1:c.494-46_494-25delinsATATGTTTTTTTGTTGTAAAATTA
Intron_number2/3
MethodWGS_Flibotte