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WormBase Tree Display for Variation: WBVar01689783

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Name Class

WBVar01689783NamePublic_nameWBVar01689783
Other_namecewivar00381792
Y59A8B.22b.1:c.439-541A>C
Y59A8B.22a.1:c.730-541A>C
Y59A8B.22c.1:c.340-541A>C
HGVSgCHROMOSOME_V:g.17975479T>G
Sequence_detailsSMapS_parentSequenceY59A8B
Flanking_sequencesGTAGATTTACGAAATGTTCGGATGCTGATTTCGTTTTTCAACGAGTTTCCTTCATTTTCG
Mapping_targetY59A8B
Source_location225CHROMOSOME_V1797545317975453From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionTG
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00006640From_analysisMillion_mutation_project_reanalysis
WBStrain00022899From_analysisMillion_mutation_project_reanalysis
WBStrain00022930From_analysisMillion_mutation_project_reanalysis
WBStrain00023191From_analysisMillion_mutation_project_reanalysis
WBStrain00031113From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00013354
TranscriptY59A8B.22b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY59A8B.22b.1:c.439-541A>C
Intron_number4/8
Y59A8B.22a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY59A8B.22a.1:c.730-541A>C
Intron_number6/11
Y59A8B.22c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScY59A8B.22c.1:c.340-541A>C
Intron_number3/7
MethodWGS_Flibotte