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WormBase Tree Display for Variation: WBVar01886651

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Name Class

WBVar01886651NamePublic_nameWBVar01886651
Other_namecewivar00601546
C25A11.4c.1:c.262-716A>T
C25A11.4a.1:c.-1014-716A>T
C25A11.4d.1:c.262-716A>T
C25A11.4b.1:c.262-716A>T
C25A11.4f.1:c.262-716A>T
HGVSgCHROMOSOME_X:g.9086863A>T
Sequence_detailsSMapS_parentSequenceH08J11
Flanking_sequencesATGTACTCGAAAAAAAATGAATAGTCAAATAGAGTGGTTACTTTTGCGTCAATAAATCTA
Mapping_targetH08J11
Source_location225CHROMOSOME_X90868079086807From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionAT
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00023072From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00000100
TranscriptC25A11.4d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC25A11.4d.1:c.262-716A>T
Intron_number3/29
C25A11.4a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC25A11.4a.1:c.-1014-716A>T
Intron_number2/30
C25A11.4f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC25A11.4f.1:c.262-716A>T
Intron_number2/28
C25A11.4c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC25A11.4c.1:c.262-716A>T
Intron_number3/23
C25A11.4b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC25A11.4b.1:c.262-716A>T
Intron_number2/18
MethodWGS_Flibotte