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WormBase Tree Display for Variation: WBVar01719889

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Name Class

WBVar01719889NamePublic_nameWBVar01719889
Other_namecewivar00418024
F59E12.6b.1:c.343-27T>G
F59E12.6a.2:c.484-27T>G
F59E12.6a.1:c.484-27T>G
F59E12.16c.1:n.931-27T>G
HGVSgCHROMOSOME_II:g.5628776A>C
Sequence_detailsSMapS_parentSequenceF59E12
Flanking_sequencesGAACCTGTAAATATAGTTGAATTATTTAAAACCACAGAAACTCAGTTTTTGTAGTAGAAA
Mapping_targetF59E12
Source_location225CHROMOSOME_II56287585628758From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionAC
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00023139From_analysisMillion_mutation_project_reanalysis
WBStrain00027648From_analysisMillion_mutation_project_reanalysis
WBStrain00027660From_analysisMillion_mutation_project_reanalysis
WBStrain00027662From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00305468
WBGene00019122
WBGene00235270
TranscriptF59E12.6a.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF59E12.6a.2:c.484-27T>G
Intron_number3/5
F59E12.18
F59E12.6b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF59E12.6b.1:c.343-27T>G
Intron_number4/5
F59E12.6a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF59E12.6a.1:c.484-27T>G
Intron_number6/8
PseudogeneF59E12.16cVEP_consequenceintron_variant,non_coding_transcript_variant
VEP_impactMODIFIER
HGVScF59E12.16c.1:n.931-27T>G
Intron_number4/7
MethodWGS_Flibotte