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WormBase Tree Display for Variation: WBVar01305081

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Name Class

WBVar01305081EvidencePaper_evidenceWBPaper00037807
NamePublic_nameWBVar01305081
Other_namecewivar00012723
R03H10.2.1:c.165+878G>A
HGVSgCHROMOSOME_II:g.4156817G>A
Sequence_detailsSMapS_parentSequenceR03H10
Flanking_sequencesAAGTTTTTGTTAGATCAAAAAGTGAAGAGGAAGTCAGAAAAGTTGGGTTCAATAGTGATATGGTCTATTAGAGAAATAATTGAATCTTTGAATCTGTGAG
Mapping_targetR03H10
Type_of_mutationSubstitutiongAPaper_evidenceWBPaper00037807
SeqStatusSequenced
Variation_typeSNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00000032From_analysisMillion_mutation_project_reanalysis
WBStrain00006622From_analysisMillion_mutation_project_reanalysis
WBStrain00006637From_analysisMillion_mutation_project_reanalysis
WBStrain00022850From_analysisMillion_mutation_project_reanalysis
WGS_De_Bono
WBStrain00022852From_analysisMillion_mutation_project_reanalysis
WBStrain00022856From_analysisMillion_mutation_project_reanalysis
WBStrain00022886From_analysisMillion_mutation_project_reanalysis
WBStrain00022902From_analysisMillion_mutation_project_reanalysis
WBStrain00022930From_analysisMillion_mutation_project_reanalysis
WBStrain00023072From_analysisMillion_mutation_project_reanalysis
LaboratoryAX
AnalysisWGS_De_Bono
Million_mutation_project_reanalysis
DB_infoDatabasedbSNP_ssss539162853
StatusLive
AffectsGeneWBGene00019855
TranscriptR03H10.2.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScR03H10.2.1:c.165+878G>A
Intron_number2/10
ReferenceWBPaper00037807
MethodWGS_De_Bono