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WormBase Tree Display for Variation: WBVar01566651

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Name Class

WBVar01566651NamePublic_nameWBVar01566651
Other_namecewivar00150668
F47D12.1a.1:c.157-358T>G
F47D12.1c.1:c.157-358T>G
F47D12.1d.1:c.157-358T>G
F47D12.1b.1:c.157-358T>G
HGVSgCHROMOSOME_III:g.6313838T>G
Sequence_detailsSMapS_parentSequenceF47D12
Flanking_sequencesCAATCGAGGTCTACAAGCTTAAAAGTGGGGGCATGAGGTCAATTGGAGGAAGCGCACGCG
Mapping_targetF47D12
Source_location225CHROMOSOME_III63137866313786From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionTG
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
TranscriptF47D12.1d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF47D12.1d.1:c.157-358T>G
Intron_number1/4
F47D12.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF47D12.1b.1:c.157-358T>G
Intron_number2/12
F47D12.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF47D12.1a.1:c.157-358T>G
Intron_number2/13
F47D12.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF47D12.1c.1:c.157-358T>G
Intron_number2/12
MethodWGS_Flibotte