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WormBase Tree Display for Variation: WBVar01604111

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Name Class

WBVar01604111NamePublic_nameWBVar01604111
Other_namecewivar00280756
C15F1.1b.1:c.428+49T>C
C15F1.1a.1:c.381-161T>C
HGVSgCHROMOSOME_II:g.6990972T>C
Sequence_detailsSMapS_parentSequenceC15F1
Flanking_sequencesTTGTTTTTATTTATTTTCCAAAAAAACCTATTTTTTGTTTCGAACTGTTGAGTGTTTTGT
Mapping_targetC15F1
Source_location225CHROMOSOME_II69909306990930From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionTC
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00006622From_analysisMillion_mutation_project_reanalysis
WBStrain00022852From_analysisMillion_mutation_project_reanalysis
WBStrain00022856From_analysisMillion_mutation_project_reanalysis
WBStrain00022886From_analysisMillion_mutation_project_reanalysis
WBStrain00022902From_analysisMillion_mutation_project_reanalysis
WBStrain00022930From_analysisMillion_mutation_project_reanalysis
WBStrain00023018From_analysisMillion_mutation_project_reanalysis
WBStrain00023072From_analysisMillion_mutation_project_reanalysis
WBStrain00023191From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00015794
TranscriptC15F1.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC15F1.1b.1:c.428+49T>C
Intron_number6/8
C15F1.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC15F1.1a.1:c.381-161T>C
Intron_number5/7
MethodWGS_Flibotte