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: WBVar00277913

expand all nodes | collapse all nodes | view schema

Name Class

WBVar00277913EvidencePaper_evidenceWBPaper00036200
NamePublic_namegk2384
Other_nameY54G2A.17b.1:c.889+209T>G
Y54G2A.17a.2:c.829+209T>G
Y54G2A.17a.1:c.829+209T>G
Y54G2A.17a.3:c.829+209T>G
HGVSgCHROMOSOME_IV:g.2880500A>C
Sequence_detailsSMapS_parentSequenceY54G2A
Flanking_sequencesAAAAAAAAATCGGGTTTTTTCGATTTTTCTCAGGCGCCTCTCACACGTGTATCGCGTGTG
Mapping_targetY54G2A
Type_of_mutationSubstitutionAC
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00037339
LaboratoryVC
PersonWBPerson427
AnalysisMillion_Mutation_Pilot_Project
KO_consortium_allele
StatusLive
AffectsGeneWBGene00021882
TranscriptY54G2A.17a.3VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY54G2A.17a.3:c.829+209T>G
Intron_number3/7
Y54G2A.17b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY54G2A.17b.1:c.889+209T>G
Intron_number4/7
Y54G2A.17a.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY54G2A.17a.2:c.829+209T>G
Intron_number4/8
Y54G2A.17a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY54G2A.17a.1:c.829+209T>G
Intron_number4/8
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