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WormBase Tree Display for Variation: WBVar00267201

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Name Class

WBVar00267201EvidencePaper_evidenceWBPaper00005369
NamePublic_nameWBVar00267201
Other_nameuCE1-1045
cewivar00681176
C16C2.2b.1:c.398+108_398+109insGA
C16C2.2a.1:c.398+108_398+109insGA
C16C2.3a.1:c.-61-2673_-61-2672dup
HGVSgCHROMOSOME_I:g.9723577_9723578insGA
Sequence_detailsSMapS_parentSequenceC16C2
Flanking_sequencesACATTATTTCGGACATTAGGAAAAATTATTTAGTCAGAAAATATTGAACAATCCTCACGACTTAGAAATAAATTGGTAAAGCTTCGCCAAGAAATCTTACTGAGATCACGAAAAATGTCAAAGTGTACAGAGATTAGTTTTGGCATTTTTATGATTTCAGTTTTGGAGTCGAAAGCTATTATTTTTAACCTTTTAAAAATT
Mapping_targetC16C2
Type_of_mutationInsertionGA
SeqStatusSequenced
Variation_typeSNP
Predicted_SNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004602From_analysisSNP_Swan
Million_mutation_project_reanalysis
WBStrain00027652From_analysisMillion_mutation_project_reanalysis
AnalysisSNP_Swan
Million_mutation_project_reanalysis
HistoryAcquires_mergeWBVar01957568
StatusLive
AffectsGeneWBGene00007620
WBGene00001145
TranscriptC16C2.2b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC16C2.2b.1:c.398+108_398+109insGA
Intron_number6/11
C16C2.2a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC16C2.2a.1:c.398+108_398+109insGA
Intron_number6/11
C16C2.3a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC16C2.3a.1:c.-61-2673_-61-2672dup
Intron_number1/14
ReferenceWBPaper00005369
MethodSNP_Swan