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WormBase Tree Display for Variation: WBVar00276355

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Name Class

WBVar00276355EvidencePaper_evidenceWBPaper00036200
NamePublic_namegk1771
Other_nameF18A1.3l.1:c.67-719G>A
F18A1.3c.1:c.67-719G>A
F18A1.3i.1:c.67-719G>A
F18A1.3d.1:c.67-719G>A
F18A1.3b.1:c.67-719G>A
F18A1.3a.1:c.67-719G>A
HGVSgCHROMOSOME_II:g.7680332G>A
Sequence_detailsSMapS_parentSequenceF18A1
Flanking_sequencesTGTAGAATGAGTTTCGCTCTTCCACGGAACCCACGCCCATCATCTCAACGTAGGTTCCAT
Mapping_targetF18A1
Type_of_mutationSubstitutionGA
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00036970
LaboratoryVC
PersonWBPerson427
AnalysisMillion_Mutation_Pilot_Project
KO_consortium_allele
StatusLive
AffectsGeneWBGene00003044
TranscriptF18A1.3l.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF18A1.3l.1:c.67-719G>A
Intron_number2/6
F18A1.3b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF18A1.3b.1:c.67-719G>A
Intron_number2/6
F18A1.3a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF18A1.3a.1:c.67-719G>A
Intron_number2/5
F18A1.3c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF18A1.3c.1:c.67-719G>A
Intron_number2/4
F18A1.3i.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF18A1.3i.1:c.67-719G>A
Intron_number2/6
F18A1.3d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF18A1.3d.1:c.67-719G>A
Intron_number2/6
IsolationMutagenEMS
ReferenceWBPaper00036200
RemarkAllele identified through whole-genome sequencing by the Gene Knockout ConsortiumPaper_evidenceWBPaper00036200
Sequenced by the C. elegans Gene Knockout ConsortiumPaper_evidenceWBPaper00041807
MethodKO_consortium_allele