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: WBVar00276588

expand all nodes | collapse all nodes | view schema

Name Class

WBVar00276588EvidencePaper_evidenceWBPaper00036200
NamePublic_nameok5285
Other_nameF45H7.2a.1:c.697-71A>G
F45H7.2d.1:c.190-71A>G
F45H7.2b.1:c.697-71A>G
F45H7.2d.3:c.190-71A>G
F45H7.2d.2:c.190-71A>G
HGVSgCHROMOSOME_III:g.3346945A>G
Sequence_detailsSMapS_parentSequenceF45H7
Flanking_sequencesCTTAGGCTTAGGCTTAGGCTTAGGCTTAGGCTTACCCATGACGTAGGCTTGGCCAATGCCTCTAATTTTTACACCAGGAAATGGGGTAACTTGCGATTCA
Mapping_targetF45H7
Type_of_mutationSubstitutionAG
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00033305
LaboratoryRB
PersonWBPerson46
AnalysisMillion_Mutation_Pilot_Project
KO_consortium_allele
StatusLiveCurator_confirmedWBPerson4025
AffectsGeneWBGene00001559
TranscriptF45H7.2d.3VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF45H7.2d.3:c.190-71A>G
Intron_number3/23
F45H7.2a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF45H7.2a.1:c.697-71A>G
Intron_number7/27
F45H7.2d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF45H7.2d.1:c.190-71A>G
Intron_number6/25
F45H7.2b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF45H7.2b.1:c.697-71A>G
Intron_number7/25
F45H7.2d.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF45H7.2d.2:c.190-71A>G
Intron_number4/23
IsolationMutagenENU
ReferenceWBPaper00036200
RemarkAllele identified through whole-genome sequencing by the Gene Knockout ConsortiumPaper_evidenceWBPaper00036200
This was suppressed because it overlapped with a corrected genome sequence error featureFeature_evidenceWBsf268561
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