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WormBase Tree Display for Variation: WBVar00273004

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Name Class

WBVar00273004EvidencePaper_evidenceWBPaper00005369
NamePublic_nameWBVar00273004
Other_nameuCE5-2455
cewivar00702627
T25E12.4a.1:c.2101+7375_2101+7376insAAT
T25E12.4d.1:c.1435+7375_1435+7376insAAT
T25E12.4e.1:c.2095+7375_2095+7376insAAT
T25E12.4f.1:c.2176+7375_2176+7376insAAT
T25E12.4c.1:c.1507+7375_1507+7376insAAT
HGVSgCHROMOSOME_V:g.16777186_16777187insAAT
Sequence_detailsSMapS_parentSequenceF14D1
Flanking_sequencesAGAATGGCAGTTCGCGAAGTGGCGCGGTTTTTTTTGTCAAATTTTCTTGAAATTCATTAGAACGGCGTATAAATAGCTTTAAACATTCCCAGAGCTCCCAATTTTTTCTGGAATAAAAAAAAGTAATTTTTCGACCTCGCTATCAACATGTTTTCAGAGCCAAAACGTCATTCAAATGAATATTTCATTCTGTCGCTTTTA
Mapping_targetF14D1
Type_of_mutationInsertionAAT
SeqStatusSequenced
Variation_typeSNP
Predicted_SNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004602From_analysisSNP_Swan
Million_mutation_project_reanalysis
AnalysisSNP_Swan
Million_mutation_project_reanalysis
HistoryAcquires_mergeWBVar01976619
StatusLive
AffectsGeneWBGene00012019
TranscriptT25E12.4f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT25E12.4f.1:c.2176+7375_2176+7376insAAT
Intron_number15/18
T25E12.4d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT25E12.4d.1:c.1435+7375_1435+7376insAAT
Intron_number10/13
T25E12.4c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT25E12.4c.1:c.1507+7375_1507+7376insAAT
Intron_number10/13
T25E12.4a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT25E12.4a.1:c.2101+7375_2101+7376insAAT
Intron_number14/18
T25E12.4e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT25E12.4e.1:c.2095+7375_2095+7376insAAT
Intron_number14/17
ReferenceWBPaper00005369
MethodSNP_Swan