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WormBase Tree Display for Variation: WBVar01254725

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Name Class

WBVar01254725EvidencePaper_evidenceWBPaper00037807
NamePublic_nameWBVar01254725
Other_namecewivar00283613
Y55B1AL.3a.1:c.2173-12A>C
Y55B1AL.3b.3:c.811-12A>C
Y55B1AL.3b.2:c.811-12A>C
Y55B1AL.3b.1:c.811-12A>C
HGVSgCHROMOSOME_III:g.579605T>G
Sequence_detailsSMapS_parentSequenceY55B1AL
Flanking_sequencesGGCCAACAATTTTCGCTCGCTTGACGGGAGGGCGTTGTACTGCAAATATTGAATTTTTGGGGCTGAATTCAATTTTAAAATTAAAAAAAAAGCTTACCAT
Mapping_targetY55B1AL
Type_of_mutationSubstitutiontGPaper_evidenceWBPaper00037807
SeqStatusSequenced
Variation_typeSNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
Strain (39)
LaboratoryAX
QX
PersonWBPerson1730
AnalysisWGS_De_Bono
Million_mutation_project_reanalysis
WGS_Andersen
DB_infoDatabasedbSNP_ssss539091196
HistoryAcquires_mergeWBVar01443110
StatusLive
AffectsGeneWBGene00021905
TranscriptY55B1AL.3b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY55B1AL.3b.1:c.811-12A>C
Intron_number9/12
Y55B1AL.3b.3VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY55B1AL.3b.3:c.811-12A>C
Intron_number5/7
Y55B1AL.3a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY55B1AL.3a.1:c.2173-12A>C
Intron_number10/13
Y55B1AL.3b.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY55B1AL.3b.2:c.811-12A>C
Intron_number9/12
ReferenceWBPaper00040707
WBPaper00037807
MethodWGS_De_Bono