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WormBase Tree Display for Variation: WBVar00267931

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Name Class

WBVar00267931EvidencePaper_evidenceWBPaper00005369
NamePublic_nameWBVar00267931
Other_nameuCE2-755
F56D12.4e.1:c.1123+379dup
F56D12.4c.1:c.646+379dup
F56D12.4a.1:c.2545+379dup
F56D12.4f.1:c.661+379dup
F56D12.4d.1:c.2530+379dup
F56D12.4b.1:c.1108+379dup
HGVSgCHROMOSOME_II:g.1348082dup
Sequence_detailsSMapS_parentSequenceC13A10
Flanking_sequencesTGAAAAATTGGAAATCGGCGCAGTTGCATATAGGATTTTCATTGATGTAGATTTTGAAATGTGCCGTCCTATAATTTTCGAGTAATGACACGATTAAGAATTGGCTGAGTAGCGACTCAGGCTACGTATCGCCCTTGAAATTAATTTCAAAAAATGTAAAATTTGATCTTCCACAGTTTTGTCTCTGACGCCATGTTTCTA
Mapping_targetC13A10
Type_of_mutationInsertionA
SeqStatusSequenced
Variation_typeSNP
Predicted_SNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004602From_analysisSNP_Swan
AnalysisSNP_Swan
StatusLive
AffectsGeneWBGene00002176
TranscriptF56D12.4e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56D12.4e.1:c.1123+379dup
Intron_number7/10
F56D12.4a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56D12.4a.1:c.2545+379dup
Intron_number16/20
F56D12.4b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56D12.4b.1:c.1108+379dup
Intron_number7/11
F56D12.4f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56D12.4f.1:c.661+379dup
Intron_number5/8
F56D12.4d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56D12.4d.1:c.2530+379dup
Intron_number16/20
F56D12.4c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56D12.4c.1:c.646+379dup
Intron_number5/8
ReferenceWBPaper00005369
MethodSNP_Swan