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WormBase Tree Display for Variation: WBVar01443033

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Name Class

WBVar01443033EvidencePaper_evidenceWBPaper00040707
NamePublic_nameWBVar01443033
Other_namecewivar00468665
W07B3.3:n.101+822G>C
W07B3.2d.1:c.-28+1519C>G
W07B3.2c.2:c.-28+1519C>G
W07B3.2b.2:c.-28+1519C>G
W07B3.2a.2:c.-28+1519C>G
HGVSgCHROMOSOME_III:g.353144G>C
Sequence_detailsSMapS_parentSequenceW07B3
Flanking_sequencesTGCTGGTGAGATATTTCATCACACGTTGTTTCACTTATTAATTATACTAATGGAGAGGTA
Mapping_targetW07B3
Type_of_mutationSubstitutiongc
SeqStatusSequenced
Variation_typeSNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00023191From_analysisMillion_mutation_project_reanalysis
WGS_Andersen
WBStrain00027653From_analysisWGS_Andersen
WBStrain00027656From_analysisWGS_Andersen
LaboratoryQX
PersonWBPerson1730
AnalysisMillion_mutation_project_reanalysis
WGS_Andersen
DB_infoDatabasedbSNP_rsrs193330194
dbSNP_ssss295506113
StatusLive
AffectsGeneWBGene00001561
WBGene00219745
TranscriptW07B3.3VEP_consequenceintron_variant,non_coding_transcript_variant
VEP_impactMODIFIER
HGVScW07B3.3:n.101+822G>C
Intron_number1/1
W07B3.2b.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW07B3.2b.2:c.-28+1519C>G
Intron_number1/11
W07B3.2c.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW07B3.2c.2:c.-28+1519C>G
Intron_number1/10
W07B3.2a.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW07B3.2a.2:c.-28+1519C>G
Intron_number1/10
W07B3.2d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW07B3.2d.1:c.-28+1519C>G
Intron_number1/10
ReferenceWBPaper00040707
MethodWGS_Andersen