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WormBase Tree Display for Variation: WBVar02127293

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Name Class

WBVar02127293EvidencePaper_evidenceWBPaper00045317
NamePublic_nameh17527
Other_nameC46H11.4c.1:c.300+1260A>T
C46H11.4f.2:c.192+1260A>T
C46H11.4e.1:c.339+1260A>T
C46H11.4f.1:c.192+1260A>T
HGVSgCHROMOSOME_I:g.5032277A>T
Sequence_detailsSMapS_parentSequenceC46H11
Flanking_sequencesTATTAGGCAACGAAAAGCACTCCTTGATATCTTAAAATTCGAAAAGTAGTGAAAAATAGTCCGAAAATATACCTTTTTCTCTCCAGAGGGGTCTATCTTGAGAGATTTCCAATCGCCAAAATTATATATAATTTCGTCGGCGATCGCCGATCGCCGACCC
Mapping_targetCHROMOSOME_I
Source_location200CHROMOSOME_I50322775032277
Type_of_mutationSubstitutionAT
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00023704
LaboratoryKR
AnalysisWGS_Rose
StatusLive
AffectsGeneWBGene00002979
TranscriptC46H11.4f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC46H11.4f.1:c.192+1260A>T
Intron_number4/10
C46H11.4c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC46H11.4c.1:c.300+1260A>T
Intron_number5/11
C46H11.4f.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC46H11.4f.2:c.192+1260A>T
Intron_number3/9
C46H11.4e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC46H11.4e.1:c.339+1260A>T
Intron_number4/9
ReferenceWBPaper00040589
WBPaper00000975
WBPaper00003985
WBPaper00000699
WBPaper00045317
MethodWGS_Rose