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WormBase Tree Display for Variation: WBVar00091228

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Name Class

WBVar00091228EvidencePaper_evidenceWBPaper00029073
NamePublic_nameWBVar00091228
Other_nameniDf207(V)
HGVSgCHROMOSOME_V:g.2009484_2011867del
Sequence_detailsSMapS_parentSequenceF59A7
Flanking_sequencesACCGACCTCACGGAGACGCCCGACGGCTTCTGAAAAGCCAAATATCATAGTGTCAAGTAA
Mapping_targetF59A7
CGH_deleted_probesCTTGTCGATCTCATGCCCCATCAGAAAGCAGGACTTTGCTGGCTCCTTTGAGGTCCGGTTCTCCGTCACTTAAAGGTGTCTACATTTATTTCTATGAATC
Type_of_mutationDeletion
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00022850
LaboratoryVC
PersonWBPerson427
Detection_methodOligo Array CGH
StatusLive
AffectsGeneWBGene00019095
WBGene00305467
TranscriptF59A7.15
PseudogeneF59A7.8VEP_consequencesplice_acceptor_variant,splice_donor_variant,non_coding_transcript_exon_variant,intron_variant
VEP_impactHIGH
cDNA_position694-?
Intron_number3-5/5
Exon_number3-6/6
ReferenceWBPaper00029073
WBPaper00042533
RemarkFlanking sequences represent the nearest array oligo sequences present in the deletion chromsome on the basis of fluorescence ratio. These should not be considered hard breakpoints in the absence of actual sequence data. Original data available on-line at http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE6294.
MethodCGH_allele