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WormBase Tree Display for Variation: WBVar01854384

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Name Class

WBVar01854384NamePublic_nameWBVar01854384
Other_namecewivar00567563
F42A9.6a.1:c.313+404T>C
F42A9.6a.3:c.313+404T>C
F42A9.6c.1:c.248-523T>C
F42A9.6c.2:c.248-523T>C
F42A9.6b.1:c.458-523T>C
F42A9.6a.2:c.313+404T>C
HGVSgCHROMOSOME_IV:g.8610853T>C
Sequence_detailsSMapS_parentSequenceF42A9
Flanking_sequencesCAAAAGTGGATTTTGCAGATATTTATTGAATGAAATTATTTGTGATAGGAAAGCAATTTG
Mapping_targetF42A9
Source_location225CHROMOSOME_IV86108408610840From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionTC
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00023072From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00018335
TranscriptF42A9.6c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF42A9.6c.1:c.248-523T>C
Intron_number5/6
F42A9.6a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF42A9.6a.1:c.313+404T>C
Intron_number6/7
F42A9.6b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF42A9.6b.1:c.458-523T>C
Intron_number5/6
F42A9.6c.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF42A9.6c.2:c.248-523T>C
Intron_number4/5
F42A9.6a.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF42A9.6a.2:c.313+404T>C
Intron_number6/7
F42A9.6a.3VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF42A9.6a.3:c.313+404T>C
Intron_number5/6
MethodWGS_Flibotte