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WormBase Tree Display for Variation: WBVar01533970

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Name Class

WBVar01533970NamePublic_nameWBVar01533970
Other_namecewivar00080088
F56D12.1b.1:c.678+185A>G
F56D12.1a.1:c.678+185A>G
F56D12.1d.1:c.258+185A>G
F56D12.1c.1:c.678+185A>G
F56D12.1a.2:c.678+185A>G
HGVSgCHROMOSOME_II:g.1308560T>C
Sequence_detailsSMapS_parentSequenceF56D12
Flanking_sequencesTTGTAGTTTGTAGTCCAGCAGACCCAATCTATCAAAATCACATTGGTCTGCTAAATCGAA
Mapping_targetF56D12
Source_location225CHROMOSOME_II13085671308567From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionTC
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00000034From_analysisMillion_mutation_project_reanalysis
WBStrain00004599From_analysisMillion_mutation_project_reanalysis
WBStrain00006625From_analysisMillion_mutation_project_reanalysis
WBStrain00023665From_analysisMillion_mutation_project_reanalysis
WBStrain00027652From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00000112
TranscriptF56D12.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56D12.1b.1:c.678+185A>G
Intron_number5/7
F56D12.1a.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56D12.1a.2:c.678+185A>G
Intron_number6/9
F56D12.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56D12.1a.1:c.678+185A>G
Intron_number5/8
F56D12.1d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56D12.1d.1:c.258+185A>G
Intron_number1/3
F56D12.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56D12.1c.1:c.678+185A>G
Intron_number4/5
MethodWGS_Flibotte