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WormBase Tree Display for Variation: WBVar01668476

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Name Class

WBVar01668476NamePublic_nameWBVar01668476
Other_namecewivar00358401
Y37E11C.1c.1:c.89+664T>G
Y37E11C.1b.1:c.557+664T>G
Y37E11C.1a.1:c.1082+664T>G
HGVSgCHROMOSOME_IV:g.3520436T>G
Sequence_detailsSMapS_parentSequenceM57
Flanking_sequencesAAAATATTTTTTCTACAAAAATCCCATTTTAACATTTTTTTCTATTTTGAGTTCAAAAAT
Mapping_targetM57
Source_location225CHROMOSOME_IV35204333520433From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionTG
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00006637From_analysisMillion_mutation_project_reanalysis
WBStrain00022883From_analysisMillion_mutation_project_reanalysis
WBStrain00022930From_analysisMillion_mutation_project_reanalysis
WBStrain00023139From_analysisMillion_mutation_project_reanalysis
WBStrain00023286From_analysisMillion_mutation_project_reanalysis
WBStrain00027660From_analysisMillion_mutation_project_reanalysis
WBStrain00027662From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00006769
TranscriptY37E11C.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY37E11C.1c.1:c.89+664T>G
Intron_number1/3
Y37E11C.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY37E11C.1b.1:c.557+664T>G
Intron_number3/5
Y37E11C.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY37E11C.1a.1:c.1082+664T>G
Intron_number7/10
MethodWGS_Flibotte