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WormBase Tree Display for Variation: WBVar01602078

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Name Class

WBVar01602078NamePublic_nameWBVar01602078
Other_namecewivar00275255
C25A11.4d.1:c.261+1498T>C
C25A11.4c.1:c.261+1498T>C
C25A11.4b.1:c.261+1498T>C
C25A11.4a.1:c.-1015+1498T>C
C25A11.4f.1:c.261+1498T>C
HGVSgCHROMOSOME_X:g.9085559T>C
Sequence_detailsSMapS_parentSequenceF47E1
Flanking_sequencesACAACTCAATAGTGAAAGTGAATTTTACTTTACATAATTTTCCTTAGTGAAACTAAGTTG
Mapping_targetF47E1
Source_location225CHROMOSOME_X90855039085503From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionTC
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004602From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00000100
TranscriptC25A11.4d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC25A11.4d.1:c.261+1498T>C
Intron_number3/29
C25A11.4a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC25A11.4a.1:c.-1015+1498T>C
Intron_number2/30
C25A11.4f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC25A11.4f.1:c.261+1498T>C
Intron_number2/28
C25A11.4c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC25A11.4c.1:c.261+1498T>C
Intron_number3/23
C25A11.4b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC25A11.4b.1:c.261+1498T>C
Intron_number2/18
MethodWGS_Flibotte