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WormBase Tree Display for Variation: WBVar01446613

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Name Class

WBVar01446613EvidencePaper_evidenceWBPaper00040707
NamePublic_nameWBVar01446613
Other_nameB0361.4.1:c.387+319C>T
HGVSgCHROMOSOME_III:g.7265764C>T
Sequence_detailsSMapS_parentSequenceB0361
Flanking_sequencesGATAGGCTCAAGAGTTGAAGGAGAAAATTGCGATTTGTAGTTCAACCATCATTTTTTGAT
Mapping_targetB0361
Type_of_mutationSubstitutionct
SeqStatusSequenced
Variation_typeSNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00006618From_analysisWGS_Andersen
WBStrain00006631From_analysisWGS_Andersen
Million_mutation_project_reanalysis
WBStrain00006632From_analysisWGS_Andersen
WBStrain00006635From_analysisWGS_Andersen
WBStrain00006636From_analysisWGS_Andersen
WBStrain00006637From_analysisWGS_Andersen
Million_mutation_project_reanalysis
WBStrain00006640From_analysisWGS_Andersen
Million_mutation_project_reanalysis
WBStrain00008273From_analysisMillion_mutation_project_reanalysis
WBStrain00023018From_analysisWGS_Andersen
Million_mutation_project_reanalysis
WBStrain00023138From_analysisWGS_Andersen
Million_mutation_project_reanalysis
LaboratoryQX
PersonWBPerson1730
AnalysisWGS_Andersen
DB_infoDatabasedbSNP_rsrs193333342
dbSNP_ssss295509261
StatusLive
AffectsGeneWBGene00015158
TranscriptB0361.4.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScB0361.4.1:c.387+319C>T
Intron_number4/8
ReferenceWBPaper00040707
MethodWGS_Andersen