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WormBase Tree Display for Variation: WBVar01949168

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Name Class

WBVar01949168NamePublic_nameWBVar01949168
Other_namecewivar00671011
F18A1.3l.1:c.66+2553_66+2563del
F18A1.3d.1:c.66+2553_66+2563del
F18A1.3a.1:c.66+2553_66+2563del
F18A1.3b.1:c.66+2553_66+2563del
F18A1.3i.1:c.66+2553_66+2563del
F18A1.3c.1:c.66+2553_66+2563del
HGVSgCHROMOSOME_II:g.7674661_7674671del
Sequence_detailsSMapS_parentSequenceF18A1
Flanking_sequencesGTTTTCTTTTTAACTCAAAGTAACGTATTAGAAGATCCTGTTAGAGTATCCGTGTCGTCT
Mapping_targetF18A1
Source_location225CHROMOSOME_II76746107674620From_analysisMillion_mutation_project_reanalysis
Type_of_mutationDeletion
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
Strain (12)
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00003044
TranscriptF18A1.3l.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF18A1.3l.1:c.66+2553_66+2563del
Intron_number2/6
F18A1.3b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF18A1.3b.1:c.66+2553_66+2563del
Intron_number2/6
F18A1.3a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF18A1.3a.1:c.66+2553_66+2563del
Intron_number2/5
F18A1.3c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF18A1.3c.1:c.66+2553_66+2563del
Intron_number2/4
F18A1.3i.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF18A1.3i.1:c.66+2553_66+2563del
Intron_number2/6
F18A1.3d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF18A1.3d.1:c.66+2553_66+2563del
Intron_number2/6
MethodWGS_Flibotte