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WormBase Tree Display for Variation: WBVar01450654

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Name Class

WBVar01450654EvidencePaper_evidenceWBPaper00040707
NamePublic_nameWBVar01450654
Other_namecewivar00379043
Y104H12A.1c.1:c.48+2582T>A
Y104H12A.1a.1:c.354+2582T>A
Y104H12A.1b.1:c.150+2582T>A
HGVSgCHROMOSOME_IV:g.1391285T>A
Sequence_detailsSMapS_parentSequenceY77E11A
Flanking_sequencesTGACACACAACCGACGGTGACTAATATTTAATACGTGTCGGAATTCTTCTCGGTTTTTTG
Mapping_targetY77E11A
Type_of_mutationSubstitutionta
SeqStatusSequenced
Variation_typeSNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00006618From_analysisWGS_Andersen
WBStrain00006632From_analysisWGS_Andersen
WBStrain00006640From_analysisMillion_mutation_project_reanalysis
WGS_Andersen
WBStrain00022878From_analysisMillion_mutation_project_reanalysis
WGS_Andersen
WBStrain00022879From_analysisWGS_Andersen
WBStrain00022880From_analysisWGS_Andersen
WBStrain00022885From_analysisWGS_Andersen
WBStrain00022911From_analysisWGS_Andersen
WBStrain00023079From_analysisWGS_Andersen
WBStrain00023665From_analysisMillion_mutation_project_reanalysis
WGS_Andersen
LaboratoryQX
PersonWBPerson1730
AnalysisMillion_mutation_project_reanalysis
WGS_Andersen
DB_infoDatabasedbSNP_rsrs193336311
dbSNP_ssss295512230
StatusLive
AffectsGeneWBGene00022423
TranscriptY104H12A.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY104H12A.1a.1:c.354+2582T>A
Intron_number5/11
Y104H12A.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY104H12A.1b.1:c.150+2582T>A
Intron_number2/7
Y104H12A.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY104H12A.1c.1:c.48+2582T>A
Intron_number1/6
ReferenceWBPaper00040707
MethodWGS_Andersen