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WormBase Tree Display for Variation: WBVar01280401

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Name Class

WBVar01280401EvidencePaper_evidenceWBPaper00037807
NamePublic_nameWBVar01280401
Other_namecewivar00504578
C45E1.1a.1:c.221-281C>T
C45E1.1b.1:c.146-281C>T
C45E1.1a.2:c.221-281C>T
C45E1.1c.1:c.239-281C>T
HGVSgCHROMOSOME_I:g.3107237C>T
Sequence_detailsSMapS_parentSequenceC45E1
Flanking_sequencesGGCAAATTGGCAAACCGGCAATTTGCTGGAATTGAGAATTTCCGGCAAATGGCAAACCAGCAAATTGCAGGAAATTACGATTCCAACAATTTGCTGGTTT
Mapping_targetC45E1
Type_of_mutationSubstitutioncTPaper_evidenceWBPaper00037807
SeqStatusSequenced
Variation_typeSNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00022850From_analysisMillion_mutation_project_reanalysis
WGS_De_Bono
LaboratoryAX
AnalysisWGS_De_Bono
Million_mutation_project_reanalysis
DB_infoDatabasedbSNP_ssss539140641
StatusLive
AffectsGeneWBGene00003654
TranscriptC45E1.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC45E1.1b.1:c.146-281C>T
Intron_number1/6
C45E1.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC45E1.1c.1:c.239-281C>T
Intron_number3/8
C45E1.1a.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC45E1.1a.2:c.221-281C>T
Intron_number4/10
C45E1.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC45E1.1a.1:c.221-281C>T
Intron_number3/9
ReferenceWBPaper00037807
MethodWGS_De_Bono