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WormBase Tree Display for Variation: WBVar01553589

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Name Class

WBVar01553589NamePublic_nameWBVar01553589
Other_namecewivar00130899
K09E9.1a.1:c.649-131G>C
K09E9.1b.1:c.679-131G>C
K09E9.1a.2:c.649-131G>C
K09E9.1c.1:c.457-131G>C
HGVSgCHROMOSOME_X:g.15624257G>C
Sequence_detailsSMapS_parentSequenceK09E9
Flanking_sequencesAAATTTCCGGAACGTCTCATTTCAAAATTTGTAGATTTGGATCATTTTAAGTATAAAAAA
Mapping_targetK09E9
Source_location225CHROMOSOME_X1562418915624189From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionGC
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004599From_analysisMillion_mutation_project_reanalysis
WBStrain00006622From_analysisMillion_mutation_project_reanalysis
WBStrain00006631From_analysisMillion_mutation_project_reanalysis
WBStrain00006643From_analysisMillion_mutation_project_reanalysis
WBStrain00006645From_analysisMillion_mutation_project_reanalysis
WBStrain00008273From_analysisMillion_mutation_project_reanalysis
WBStrain00023138From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00010724
TranscriptK09E9.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScK09E9.1a.1:c.649-131G>C
Intron_number6/12
K09E9.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScK09E9.1c.1:c.457-131G>C
Intron_number3/8
K09E9.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScK09E9.1b.1:c.679-131G>C
Intron_number5/10
K09E9.1a.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScK09E9.1a.2:c.649-131G>C
Intron_number5/11
MethodWGS_Flibotte