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WormBase Tree Display for Variation: WBVar01567585

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Name Class

WBVar01567585NamePublic_nameWBVar01567585
Other_namecewivar00152142
M142.1a.1:c.554-46T>A
M142.1b.1:c.494-46T>A
M142.1c.1:c.629-46T>A
HGVSgCHROMOSOME_III:g.10908602T>A
Sequence_detailsSMapS_parentSequenceM142
Flanking_sequencesGAAAGTAAAATGAAATTTGCAAAAAAAAAAATGTTTTTTTGTTGTAAAATTAAAAAAAAA
Mapping_targetM142
Source_location225CHROMOSOME_III1090850310908503From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionTA
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004600From_analysisMillion_mutation_project_reanalysis
WBStrain00008273From_analysisMillion_mutation_project_reanalysis
WBStrain00022886From_analysisMillion_mutation_project_reanalysis
WBStrain00023072From_analysisMillion_mutation_project_reanalysis
WBStrain00027647From_analysisMillion_mutation_project_reanalysis
WBStrain00031113From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00006843
TranscriptM142.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScM142.1a.1:c.554-46T>A
Intron_number4/5
M142.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScM142.1c.1:c.629-46T>A
Intron_number5/6
M142.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScM142.1b.1:c.494-46T>A
Intron_number2/3
MethodWGS_Flibotte