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WormBase Tree Display for Variation: WBVar00145628

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Name Class

WBVar00145628NamePublic_namegk221
HGVSgCHROMOSOME_V:g.9707259_9709310del
Sequence_detailsSMapS_parentSequenceF40F9
Flanking_sequencesGTAACATTGTGCCAATTTAAATGAATGTGTATTATCGAAAAAATACGATCAACCAAAAGTTTGCTTAAACACGTGAAAACTCGGAATTTAGGAGAAACTT
Mapping_targetF40F9
Type_of_mutationDeletion
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00035757
LaboratoryVC
PersonWBPerson427
KO_consortium_allele
StatusLiveCurator_confirmedWBPerson4025
AffectsGeneWBGene00006470
WBGene00009580
TranscriptF40F9.1a.1VEP_consequencesplice_acceptor_variant,coding_sequence_variant,3_prime_UTR_variant,intron_variant
VEP_impactHIGH
Intron_number7/8
Exon_number8-9/9
F40F9.1a.2VEP_consequencesplice_acceptor_variant,coding_sequence_variant,3_prime_UTR_variant,intron_variant
VEP_impactHIGH
Intron_number8/9
Exon_number9-10/10
F40F9.1b.3VEP_consequencesplice_acceptor_variant,3_prime_UTR_variant,intron_variant
VEP_impactHIGH
Intron_number8/8
Exon_number9/9
F40F9.2.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,3_prime_UTR_variant,intron_variant
VEP_impactHIGH
Intron_number2-5/6
Exon_number3-7/7
F40F9.1b.1VEP_consequencesplice_acceptor_variant,3_prime_UTR_variant,intron_variant
VEP_impactHIGH
Intron_number9/9
Exon_number10/10
F40F9.1b.2VEP_consequence3_prime_UTR_variant
VEP_impactMODIFIER
cDNA_position1060-?
Exon_number9/9
IsolationMutagenTMP/UV
GeneticsMapping_dataIn_multi_point5142
RemarkThis was suppressed because it overlapped with a corrected genome sequence error featureFeature_evidenceWBsf898404
This was un-suppressed after examination showed it is not changed by the corrected genome sequence errorCurator_confirmedWBPerson4025
Sequenced by the C. elegans Gene Knockout ConsortiumPaper_evidenceWBPaper00041807
MethodKO_consortium_allele