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WormBase Tree Display for Variation: WBVar01949169

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Name Class

WBVar01949169NamePublic_nameWBVar01949169
Other_namecewivar00671012
F18A1.3l.1:c.66+4429_66+4434del
F18A1.3a.1:c.66+4429_66+4434del
F18A1.3i.1:c.66+4429_66+4434del
F18A1.3b.1:c.66+4429_66+4434del
F18A1.3d.1:c.66+4429_66+4434del
F18A1.3c.1:c.66+4429_66+4434del
HGVSgCHROMOSOME_II:g.7676537_7676542del
Sequence_detailsSMapS_parentSequenceF18A1
Flanking_sequencesACGCGGAGAGAATTGAAGAAGGCTATGCGCGACAGTAGTCGTCGAAAAATAAAAGAAGAT
Mapping_targetF18A1
Source_location225CHROMOSOME_II76764867676491From_analysisMillion_mutation_project_reanalysis
Type_of_mutationDeletion
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
Strain (13)
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00003044
TranscriptF18A1.3l.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF18A1.3l.1:c.66+4429_66+4434del
Intron_number2/6
F18A1.3b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF18A1.3b.1:c.66+4429_66+4434del
Intron_number2/6
F18A1.3a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF18A1.3a.1:c.66+4429_66+4434del
Intron_number2/5
F18A1.3c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF18A1.3c.1:c.66+4429_66+4434del
Intron_number2/4
F18A1.3i.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF18A1.3i.1:c.66+4429_66+4434del
Intron_number2/6
F18A1.3d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF18A1.3d.1:c.66+4429_66+4434del
Intron_number2/6
MethodWGS_Flibotte