Questions, Feedback & Help
Send us an email and we'll get back to you ASAP. Or you can read our Frequently Asked Questions.

WormBase Tree Display for Variation: WBVar00091219

expand all nodes | collapse all nodes | view schema

Name Class

WBVar00091219EvidencePaper_evidenceWBPaper00029073
NamePublic_nameWBVar00091219
Other_nameniDf198(IV)
HGVSgCHROMOSOME_IV:g.14547815_14550314del
Sequence_detailsSMapS_parentSequenceT27E7
Flanking_sequencesTAATTAACTTACCAAATCAAAAACTCTTGGCTATCTGAAATTACCAGTTTGTAAAATTTT
Mapping_targetT27E7
CGH_deleted_probesATATGTAAGTTGAGCTCTCACTGACACCTCTTCAGTATTCATGCTCACGAATCATATAGTTGTTCAGCCTCAATTTTTGGATCTTTGCCATCGACCAGTT
Type_of_mutationDeletion
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00022850
LaboratoryVC
PersonWBPerson427
Detection_methodOligo Array CGH
StatusLive
AffectsGeneWBGene00013294
WBGene00166559
WBGene00168987
WBGene00012093
WBGene00048387
WBGene00048535
TranscriptY57G11B.1.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,3_prime_UTR_variant,intron_variant
VEP_impactHIGH
cDNA_position873-?
CDS_position860-?
Protein_position287-?
Intron_number8/9
Exon_number8-10/10
T27E7.27
T27E7.46
T27E7.52
T27E7.26
T27E7.9.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,5_prime_UTR_variant,intron_variant
VEP_impactHIGH
cDNA_position?-661
CDS_position?-639
Protein_position?-213
Intron_number2-3/7
Exon_number1-4/8
ReferenceWBPaper00029073
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