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WormBase Tree Display for Variation: WBVar01933394

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Name Class

WBVar01933394NamePublic_nameWBVar01933394
Other_namecewivar00652886
F56D12.1c.1:c.177+18dup
F56D12.1b.1:c.177+18dup
F56D12.1a.1:c.177+18dup
F56D12.1a.2:c.177+18dup
HGVSgCHROMOSOME_II:g.1309556_1309557insT
Sequence_detailsSMapS_parentSequenceF56D12
Flanking_sequencesTCTCTCACTATTCGATAACTTTTTTCGCACTTTTTTTGAAGAATTAACCTTGCTGTAGAA
Mapping_targetF56D12
Source_location225CHROMOSOME_II13095631309564From_analysisMillion_mutation_project_reanalysis
Type_of_mutationInsertionT
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.177+18dup
Intron_number2/7
F56D12.1a.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56D12.1a.2:c.177+18dup
Intron_number3/9
F56D12.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56D12.1a.1:c.177+18dup
Intron_number2/8
F56D12.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56D12.1c.1:c.177+18dup
Intron_number1/5
MethodWGS_Flibotte