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WormBase Tree Display for Variation: WBVar01269759

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Name Class

WBVar01269759EvidencePaper_evidenceWBPaper00037807
NamePublic_nameWBVar01269759
Other_namecewivar00025254
Y47D3B.1.1:c.486-342T>C
HGVSgCHROMOSOME_III:g.11384377T>C
Sequence_detailsSMapS_parentSequenceY47D3B
Flanking_sequencesGCCAAAAATTGTACGCATCATATGAATGCTCCTACATCTGTTTTGAAAATAAGCAAATACCATAATTTAAAGAAAACGGGACAAAAATTTTTGAAAAGTC
Mapping_targetY47D3B
Type_of_mutationSubstitutiontCPaper_evidenceWBPaper00037807
SeqStatusSequenced
Variation_typeSNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00000032From_analysisMillion_mutation_project_reanalysis
WBStrain00006622From_analysisMillion_mutation_project_reanalysis
WBStrain00006625From_analysisMillion_mutation_project_reanalysis
WBStrain00006642From_analysisWGS_De_Bono
WBStrain00006643From_analysisMillion_mutation_project_reanalysis
WBStrain00006645From_analysisMillion_mutation_project_reanalysis
WBStrain00022850From_analysisWGS_De_Bono
Million_mutation_project_reanalysis
WBStrain00022930From_analysisMillion_mutation_project_reanalysis
WBStrain00023286From_analysisMillion_mutation_project_reanalysis
WBStrain00027652From_analysisMillion_mutation_project_reanalysis
LaboratoryAX
AnalysisWGS_De_Bono
Million_mutation_project_reanalysis
DB_infoDatabasedbSNP_ssss539104727
HistoryAcquires_mergeWBVar01334837
StatusLive
AffectsGeneWBGene00012939
TranscriptY47D3B.1.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY47D3B.1.1:c.486-342T>C
Intron_number6/12
ReferenceWBPaper00037807
MethodWGS_De_Bono