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WormBase Tree Display for Variation: WBVar01566652

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Name Class

WBVar01566652NamePublic_nameWBVar01566652
Other_namecewivar00150669
F47D12.1b.1:c.734+109T>A
F47D12.1c.1:c.734+109T>A
F47D12.1a.1:c.734+109T>A
HGVSgCHROMOSOME_III:g.6315528T>A
Sequence_detailsSMapS_parentSequenceF47D12
Flanking_sequencesTCCTGTTTCCAAAGATTGCCTGAAAATCAAAGTTTTCGTGATTCTTTAACGTTATTTTCC
Mapping_targetF47D12
Source_location225CHROMOSOME_III63154766315476From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionTA
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004600From_analysisMillion_mutation_project_reanalysis
WBStrain00006631From_analysisMillion_mutation_project_reanalysis
WBStrain00006637From_analysisMillion_mutation_project_reanalysis
WBStrain00006640From_analysisMillion_mutation_project_reanalysis
WBStrain00008273From_analysisMillion_mutation_project_reanalysis
WBStrain00023018From_analysisMillion_mutation_project_reanalysis
WBStrain00023138From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00001518
TranscriptF47D12.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF47D12.1b.1:c.734+109T>A
Intron_number6/12
F47D12.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF47D12.1a.1:c.734+109T>A
Intron_number6/13
F47D12.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF47D12.1c.1:c.734+109T>A
Intron_number6/12
MethodWGS_Flibotte