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: WBVar02099498

expand all nodes | collapse all nodes | view schema

Name Class

WBVar02099498NamePublic_nameWBVar02099498
Other_namecewivar00829668
F53A3.4b.1:c.1167+121_1167+142delinsTCTGCAAAAATGCGGAAAATTTT
F53A3.4c.1:c.1167+121_1167+142delinsTCTGCAAAAATGCGGAAAATTTT
F53A3.4a.1:c.1167+121_1167+142delinsTCTGCAAAAATGCGGAAAATTTT
HGVSgCHROMOSOME_III:g.1908442_1908463delinsTCTGCAAAAATGCGGAAAATTTT
Sequence_detailsSMapS_parentSequenceB0524
Flanking_sequencesTCACTTTTTAACCTTTAGAAATTGAAAAAAAATCTCAAAATTTTGAGATTTTTGGTTCCA
Mapping_targetB0524
Source_location225CHROMOSOME_III19084331908454From_analysisMillion_mutation_project_reanalysis
Type_of_mutationInsertionTCTGCAAAAATGCGGAAAATTTT
Deletion
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00006640From_analysisMillion_mutation_project_reanalysis
WBStrain00023138From_analysisMillion_mutation_project_reanalysis
WBStrain00031113From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00004128
TranscriptF53A3.4c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF53A3.4c.1:c.1167+121_1167+142delinsTCTGCAAAAATGCGGAAAATTTT
Intron_number5/16
F53A3.4b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF53A3.4b.1:c.1167+121_1167+142delinsTCTGCAAAAATGCGGAAAATTTT
Intron_number5/23
F53A3.4a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF53A3.4a.1:c.1167+121_1167+142delinsTCTGCAAAAATGCGGAAAATTTT
Intron_number6/23
MethodWGS_Flibotte