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WormBase Tree Display for Variation: WBVar01588331

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Name Class

WBVar01588331NamePublic_nameWBVar01588331
Other_namecewivar00234279
F26F12.3a.1:c.39-482T>C
F26F12.3c.1:c.-1612-482T>C
HGVSgCHROMOSOME_V:g.5844714A>G
Sequence_detailsSMapS_parentSequenceF26F12
Flanking_sequencesGAATAATATATTCGTCAGGGACAAACAACCCAACTGAACTATGTTGATCGGAGAAAAAAA
Mapping_targetF26F12
Source_location225CHROMOSOME_V58446975844697From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionAG
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004602From_analysisMillion_mutation_project_reanalysis
WBStrain00006629From_analysisMillion_mutation_project_reanalysis
WBStrain00022850From_analysisMillion_mutation_project_reanalysis
WBStrain00023072From_analysisMillion_mutation_project_reanalysis
WBStrain00023139From_analysisMillion_mutation_project_reanalysis
WBStrain00027648From_analysisMillion_mutation_project_reanalysis
WBStrain00027660From_analysisMillion_mutation_project_reanalysis
WBStrain00027662From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00017834
TranscriptF26F12.3a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF26F12.3a.1:c.39-482T>C
Intron_number2/6
F26F12.3c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF26F12.3c.1:c.-1612-482T>C
Intron_number1/6
MethodWGS_Flibotte