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WormBase Tree Display for Variation: WBVar01405462

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Name Class

WBVar01405462EvidencePaper_evidenceWBPaper00037807
NamePublic_nameWBVar01405462
Other_namecewivar00671165
C01G6.1b.1:c.690-238dup
C01G6.1a.1:c.690-238dup
C01G6.1b.2:c.690-238dup
HGVSgCHROMOSOME_II:g.9260066_9260067insT
Sequence_detailsSMapS_parentSequenceC01G6
Flanking_sequencesTTCCCCTTACGGAAATGGGCCAAGATTCTATGTTTGTTCTCAAAAATTTCTTTTTTTTTGATTTCCCTCAAAATTCGTTGACCGAGAAGGGAGTTGGCAA
Mapping_targetC01G6
Type_of_mutationInsertionTPaper_evidenceWBPaper00037807
SeqStatusSequenced
Variation_typeSNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004600From_analysisMillion_mutation_project_reanalysis
WBStrain00006629From_analysisMillion_mutation_project_reanalysis
WBStrain00006631From_analysisMillion_mutation_project_reanalysis
WBStrain00006637From_analysisMillion_mutation_project_reanalysis
WBStrain00006640From_analysisMillion_mutation_project_reanalysis
WBStrain00006642From_analysisWGS_De_Bono
WBStrain00006643From_analysisMillion_mutation_project_reanalysis
WBStrain00006645From_analysisMillion_mutation_project_reanalysis
WBStrain00022878From_analysisMillion_mutation_project_reanalysis
WBStrain00023138From_analysisMillion_mutation_project_reanalysis
WBStrain00023139From_analysisMillion_mutation_project_reanalysis
WBStrain00023192From_analysisMillion_mutation_project_reanalysis
WBStrain00027647From_analysisMillion_mutation_project_reanalysis
WBStrain00027648From_analysisMillion_mutation_project_reanalysis
WBStrain00027660From_analysisMillion_mutation_project_reanalysis
WBStrain00027662From_analysisMillion_mutation_project_reanalysis
LaboratoryAX
AnalysisWGS_De_Bono
Million_mutation_project_reanalysis
DB_infoDatabasedbSNP_ssss539120237
HistoryAcquires_mergeWBVar01949257
StatusLive
AffectsGeneWBGene00000170
TranscriptC01G6.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC01G6.1b.1:c.690-238dup
Intron_number4/7
C01G6.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC01G6.1a.1:c.690-238dup
Intron_number4/6
C01G6.1b.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC01G6.1b.2:c.690-238dup
Intron_number4/6
ReferenceWBPaper00037807
MethodWGS_De_Bono