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WormBase Tree Display for Variation: WBVar01914168

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Name Class

WBVar01914168NamePublic_nameWBVar01914168
Other_namecewivar00630314
F25C8.3d.1:c.4932+73G>T
F25C8.3e.1:c.4659+180G>T
F25C8.3a.1:c.4818+73G>T
F25C8.3c.1:c.4764+73G>T
F25C8.3b.1:c.4791+180G>T
HGVSgCHROMOSOME_V:g.20891518G>T
Sequence_detailsSMapS_parentSequenceF25C8
Flanking_sequencesCCAACACAATACCTTGTAATCTTATTGTATTTCCCACTTCTCAATCAGCAAGCTTAATAC
Mapping_targetF25C8
Source_location225CHROMOSOME_V2089148720891487From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionGT
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00031113From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00006812
TranscriptF25C8.3d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF25C8.3d.1:c.4932+73G>T
Intron_number23/36
F25C8.3b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF25C8.3b.1:c.4791+180G>T
Intron_number22/35
F25C8.3e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF25C8.3e.1:c.4659+180G>T
Intron_number20/33
F25C8.3c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF25C8.3c.1:c.4764+73G>T
Intron_number22/34
F25C8.3a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF25C8.3a.1:c.4818+73G>T
Intron_number22/36
MethodWGS_Flibotte