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WormBase Tree Display for Variation: WBVar01710929

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Name Class

WBVar01710929NamePublic_nameWBVar01710929
Other_namecewivar00408597
R08E3.1b.1:c.286+40A>G
R08E3.1b.2:c.286+40A>G
R08E3.1a.1:c.286+40A>G
HGVSgCHROMOSOME_X:g.4823034A>G
Sequence_detailsSMapS_parentSequenceR08E3
Flanking_sequencesAGCCACGTTTTATTATTAGCTTGAAATATGTAGTCAAAGTTTAAAAAATTGTGTAGCTGA
Mapping_targetR08E3
Source_location225CHROMOSOME_X48230044823004From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionAG
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00022850From_analysisMillion_mutation_project_reanalysis
WBStrain00022852From_analysisMillion_mutation_project_reanalysis
WBStrain00022856From_analysisMillion_mutation_project_reanalysis
WBStrain00022878From_analysisMillion_mutation_project_reanalysis
WBStrain00022902From_analysisMillion_mutation_project_reanalysis
WBStrain00023138From_analysisMillion_mutation_project_reanalysis
WBStrain00023139From_analysisMillion_mutation_project_reanalysis
WBStrain00027648From_analysisMillion_mutation_project_reanalysis
WBStrain00027660From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00019957
TranscriptR08E3.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScR08E3.1b.1:c.286+40A>G
Intron_number3/47
R08E3.1b.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScR08E3.1b.2:c.286+40A>G
Intron_number3/46
R08E3.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScR08E3.1a.1:c.286+40A>G
Intron_number3/48
MethodWGS_Flibotte