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WormBase Tree Display for Variation: WBVar01596466

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Name Class

WBVar01596466NamePublic_nameWBVar01596466
Other_namecewivar00259800
Y59A8B.21b.1:c.1365+423G>T
Y59A8B.21a.1:c.1227+423G>T
HGVSgCHROMOSOME_V:g.17993613G>T
Sequence_detailsSMapS_parentSequenceY59A8B
Flanking_sequencesAATAATTTTTTTGCATAGAATCGATTAAATTCCGTTATCTAACAAAAAATCTCTATGTAAAATTCTATGAAAACCAACAC
Mapping_targetY59A8B
Source_location225CHROMOSOME_V1799358517993585From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionGT
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004602From_analysisMillion_mutation_project_reanalysis
WBStrain00006629From_analysisMillion_mutation_project_reanalysis
WBStrain00006637From_analysisMillion_mutation_project_reanalysis
WBStrain00022868From_analysisMillion_mutation_project_reanalysis
WBStrain00022878From_analysisMillion_mutation_project_reanalysis
WBStrain00022930From_analysisMillion_mutation_project_reanalysis
WBStrain00023072From_analysisMillion_mutation_project_reanalysis
WBStrain00023191From_analysisMillion_mutation_project_reanalysis
WBStrain00023286From_analysisMillion_mutation_project_reanalysis
WBStrain00024204From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00013353
TranscriptY59A8B.21a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY59A8B.21a.1:c.1227+423G>T
Intron_number10/11
Y59A8B.21b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY59A8B.21b.1:c.1365+423G>T
Intron_number11/11
MethodWGS_Flibotte