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WormBase Tree Display for Variation: WBVar00276389

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Name Class

WBVar00276389EvidencePaper_evidenceWBPaper00036200
NamePublic_namegk2324
Other_nameF22D3.2c.1:c.306+124G>A
F22D3.2j.1:c.1281+124G>A
F22D3.2d.1:c.1278+124G>A
F22D3.2i.1:c.201+124G>A
F22D3.2g.1:c.1290+124G>A
F22D3.2e.1:c.1269+124G>A
HGVSgCHROMOSOME_II:g.6944972G>A
Sequence_detailsSMapS_parentSequenceF22D3
Flanking_sequencesGTATCGTTAACGCGCATTTCTGATCATCTTATCAAATCGCACTTGCCCACAAAAATCGTATCAATACCGTATCCCGGTTATTTCGTCCAAAAAGCATACA
Mapping_targetF22D3
Type_of_mutationSubstitutionGA
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00037339
LaboratoryVC
PersonWBPerson427
AnalysisMillion_Mutation_Pilot_Project
KO_consortium_allele
StatusLive
AffectsGeneWBGene00017699
TranscriptF22D3.2g.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF22D3.2g.1:c.1290+124G>A
Intron_number15/18
F22D3.2e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF22D3.2e.1:c.1269+124G>A
Intron_number15/18
F22D3.2c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF22D3.2c.1:c.306+124G>A
Intron_number3/6
F22D3.2i.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF22D3.2i.1:c.201+124G>A
Intron_number2/4
F22D3.2d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF22D3.2d.1:c.1278+124G>A
Intron_number15/18
F22D3.2j.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF22D3.2j.1:c.1281+124G>A
Intron_number15/18
IsolationMutagenENU
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