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WormBase Tree Display for Variation: WBVar00272623

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Name Class

WBVar00272623EvidencePaper_evidenceWBPaper00005369
NamePublic_nameWBVar00272623
Other_nameuCE5-2024
M04G12.4c.1:c.666+29del
M04G12.4b.1:c.579+29del
M04G12.4a.1:c.666+29del
M04G12.4d.1:c.579+29del
HGVSgCHROMOSOME_V:g.13388877del
Sequence_detailsSMapS_parentSequenceM04G12
Flanking_sequencesTAGAAAAAATCAAATATTTTGTCAGCTCACTTATTGATTAAAAAAAAATTTTCAAGATATGATCTGCAGAAGATGAGCAATGCAACAAGCTAACACTTTTAATTATAAAATTTCAAATGAAAACTCACATCGTCTGAGGGTGAAACAGTTGCAGCTGAAACAGAATTATTCCTTAATGTTTCTGCGCTACTGTTACTGGT
Mapping_targetM04G12
Type_of_mutationDeletionT
SeqStatusSequenced
Variation_typeSNP
Predicted_SNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004602From_analysisSNP_Swan
AnalysisSNP_Swan
StatusLive
AffectsGeneWBGene00010868
TranscriptM04G12.4b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScM04G12.4b.1:c.579+29del
Intron_number2/5
M04G12.4a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScM04G12.4a.1:c.666+29del
Intron_number3/6
M04G12.4c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScM04G12.4c.1:c.666+29del
Intron_number3/6
M04G12.4d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScM04G12.4d.1:c.579+29del
Intron_number1/3
ReferenceWBPaper00005369
MethodSNP_Swan