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WormBase Tree Display for Variation: WBVar01374800

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Name Class

WBVar01374800EvidencePaper_evidenceWBPaper00037807
NamePublic_nameWBVar01374800
Other_namecewivar00654612
F22D3.2j.1:c.1010+3125_1010+3126insGT
F22D3.2d.1:c.1019+3125_1019+3126insGT
F22D3.2g.1:c.1019+3125_1019+3126insGT
F22D3.2e.1:c.1010+3125_1010+3126insGT
HGVSgCHROMOSOME_II:g.6937280_6937281insGT
Sequence_detailsSMapS_parentSequenceF22D3
Flanking_sequencesTAATATTTGTATATGTGTCCTCTCGCGCTCTATTATGTTATACTACCTCGGTGTGTGTGTGTGTATGTGTGCAAAATGTCGTACAAATATTAGAAGCGTT
Mapping_targetF22D3
Type_of_mutationInsertionGTPaper_evidenceWBPaper00037807
SeqStatusSequenced
Variation_typeSNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
Strain (19)
LaboratoryAX
AnalysisWGS_De_Bono
Million_mutation_project_reanalysis
DB_infoDatabasedbSNP_ssss539050202
HistoryAcquires_mergeWBVar01934861
StatusLive
AffectsGeneWBGene00017699
TranscriptF22D3.2g.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF22D3.2g.1:c.1019+3125_1019+3126insGT
Intron_number12/18
F22D3.2e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF22D3.2e.1:c.1010+3125_1010+3126insGT
Intron_number12/18
F22D3.2d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF22D3.2d.1:c.1019+3125_1019+3126insGT
Intron_number12/18
F22D3.2j.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF22D3.2j.1:c.1010+3125_1010+3126insGT
Intron_number12/18
ReferenceWBPaper00037807
MethodWGS_De_Bono