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WormBase Tree Display for Variation: WBVar01829931

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Name Class

WBVar01829931NamePublic_nameWBVar01829931
Other_namecewivar00542025
F25C8.3d.1:c.5848+262G>T
F25C8.3a.1:c.5734+262G>T
F25C8.3e.1:c.5575+262G>T
F25C8.3c.1:c.5680+262G>T
F25C8.3b.1:c.5707+262G>T
HGVSgCHROMOSOME_V:g.20892895G>T
Sequence_detailsSMapS_parentSequenceF25C8
Flanking_sequencesAGATTTTGAACACTAAACAGTCATTTTAATAACAATTTTCTCTTTTCAAGTTCAAAATGT
Mapping_targetF25C8
Source_location225CHROMOSOME_V2089286420892864From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionGT
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00022886From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00006812
TranscriptF25C8.3d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF25C8.3d.1:c.5848+262G>T
Intron_number24/36
F25C8.3b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF25C8.3b.1:c.5707+262G>T
Intron_number23/35
F25C8.3e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF25C8.3e.1:c.5575+262G>T
Intron_number21/33
F25C8.3c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF25C8.3c.1:c.5680+262G>T
Intron_number23/34
F25C8.3a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF25C8.3a.1:c.5734+262G>T
Intron_number23/36
MethodWGS_Flibotte