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WormBase Tree Display for Variation: WBVar00143986

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Name Class

WBVar00143986EvidencePaper_evidenceWBPaper00016044
NamePublic_namee1411
Other_nameCE27761:p.Pro91Ser
F54B11.3b.1:c.271C>T
CE28236:p.Pro91Ser
F54B11.3a.1:c.271C>T
HGVSgCHROMOSOME_X:g.13585544C>T
Sequence_detailsSMapS_parentSequenceF54B11
Flanking_sequencesgatccatccttgccggaccactgggaagtgcaaaccttggtggtactacttcaggatcac
Mapping_targetF54B11
Type_of_mutationSubstitutionctPaper_evidenceWBPaper00003628
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
LaboratoryCB
StatusLive
Affects (3)
GeneticsInterpolated_map_positionX13.7256
DescriptionPhenotypeWBPhenotype:0000511Paper_evidenceWBPaper00045548
Curator_confirmedWBPerson24422
RemarkIntermediate nuclear migration defect where 48.7% of nuclei fail to migrate.Paper_evidenceWBPaper00045548
Curator_confirmedWBPerson24422
ReferenceWBPaper00003628
WBPaper00016044
WBPaper00045548
MethodSubstitution_allele