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WormBase Tree Display for Variation: WBVar01572740

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Name Class

WBVar01572740NamePublic_nameWBVar01572740
Other_namecewivar00159319
C33G3.1b.1:c.453+640T>C
C33G3.1b.2:c.453+640T>C
HGVSgCHROMOSOME_X:g.14052721T>C
Sequence_detailsSMapS_parentSequenceC33G3
Flanking_sequencesAATCAGAATTACCATGCAATCCTAAGTATTTCACAGATTATACTTCATTTGAAAGCAAGA
Mapping_targetC33G3
Source_location225CHROMOSOME_X1405265214052652From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionTC
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004600From_analysisMillion_mutation_project_reanalysis
WBStrain00006622From_analysisMillion_mutation_project_reanalysis
WBStrain00006637From_analysisMillion_mutation_project_reanalysis
WBStrain00006643From_analysisMillion_mutation_project_reanalysis
WBStrain00006645From_analysisMillion_mutation_project_reanalysis
WBStrain00022930From_analysisMillion_mutation_project_reanalysis
WBStrain00023191From_analysisMillion_mutation_project_reanalysis
WBStrain00027652From_analysisMillion_mutation_project_reanalysis
WBStrain00027662From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00001116
TranscriptC33G3.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC33G3.1b.1:c.453+640T>C
Intron_number6/18
C33G3.1b.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC33G3.1b.2:c.453+640T>C
Intron_number5/17
MethodWGS_Flibotte