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WormBase Tree Display for Variation: WBVar01340901

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Name Class

WBVar01340901EvidencePaper_evidenceWBPaper00037807
NamePublic_nameWBVar01340901
Other_namecewivar00680798
F08A10.1f.2:c.593-1797_593-1796insC
F08A10.1f.1:c.593-1797_593-1796insC
F08A10.1k.1:c.680-1797_680-1796insC
F08A10.1a.1:c.494-1797_494-1796insC
F08A10.1h.1:c.494-1797_494-1796insC
F08A10.1d.1:c.473-1797_473-1796insC
F08A10.1j.1:c.1103-1797_1103-1796insC
F08A10.1i.1:c.494-1797_494-1796insC
F08A10.1e.1:c.596-1797_596-1796insC
HGVSgCHROMOSOME_I:g.8204475_8204476insC
Sequence_detailsSMapS_parentSequenceT02E1
Flanking_sequencesCTCTTTCTGTTTTAGTTTTTGTGTTAGATTATTGCATTTTTTAGAAAAAAGTTTTTATTCTAAATTCAAAAACTAGTATCTTCCAGACACCCATAGTCTT
Mapping_targetT02E1
Type_of_mutationInsertionCPaper_evidenceWBPaper00037807
SeqStatusSequenced
Variation_typeSNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004602From_analysisWGS_De_Bono
Million_mutation_project_reanalysis
WBStrain00027652From_analysisMillion_mutation_project_reanalysis
LaboratoryAX
AnalysisWGS_De_Bono
Million_mutation_project_reanalysis
DB_infoDatabasedbSNP_ssss539016279
HistoryAcquires_mergeWBVar01957329
StatusLive
AffectsGeneWBGene00008570
TranscriptF08A10.1h.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF08A10.1h.1:c.494-1797_494-1796insC
Intron_number5/13
F08A10.1k.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF08A10.1k.1:c.680-1797_680-1796insC
Intron_number8/16
F08A10.1e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF08A10.1e.1:c.596-1797_596-1796insC
Intron_number6/14
F08A10.1f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF08A10.1f.1:c.593-1797_593-1796insC
Intron_number12/21
F08A10.1f.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF08A10.1f.2:c.593-1797_593-1796insC
Intron_number9/18
F08A10.1j.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF08A10.1j.1:c.1103-1797_1103-1796insC
Intron_number11/19
F08A10.1i.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF08A10.1i.1:c.494-1797_494-1796insC
Intron_number5/13
F08A10.1d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF08A10.1d.1:c.473-1797_473-1796insC
Intron_number5/13
F08A10.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF08A10.1a.1:c.494-1797_494-1796insC
Intron_number6/15
ReferenceWBPaper00037807
MethodWGS_De_Bono