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WormBase Tree Display for Variation: WBVar01933392

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Name Class

WBVar01933392NamePublic_nameWBVar01933392
Other_namecewivar00652884
F56D12.1b.1:c.678+92_678+93del
F56D12.1d.1:c.258+92_258+93del
F56D12.1a.2:c.678+92_678+93del
F56D12.1a.1:c.678+92_678+93del
F56D12.1c.1:c.678+92_678+93del
HGVSgCHROMOSOME_II:g.1308652_1308653del
Sequence_detailsSMapS_parentSequenceF56D12
Flanking_sequencesTCTACAAAACCAAATCGGCAAATTTGAGGATTCAGCTTAATTTAGCAATTTTTCTCGGAA
Mapping_targetF56D12
Source_location225CHROMOSOME_II13086591308660From_analysisMillion_mutation_project_reanalysis
Type_of_mutationDeletion
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00000034From_analysisMillion_mutation_project_reanalysis
WBStrain00004599From_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+92_678+93del
Intron_number5/7
F56D12.1a.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56D12.1a.2:c.678+92_678+93del
Intron_number6/9
F56D12.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56D12.1a.1:c.678+92_678+93del
Intron_number5/8
F56D12.1d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56D12.1d.1:c.258+92_258+93del
Intron_number1/3
F56D12.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56D12.1c.1:c.678+92_678+93del
Intron_number4/5
MethodWGS_Flibotte