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WormBase Tree Display for Variation: WBVar01533968

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Name Class

WBVar01533968NamePublic_nameWBVar01533968
Other_namecewivar00080086
F56D12.1b.1:c.679-250A>G
F56D12.1c.1:c.679-250A>G
F56D12.1a.2:c.679-250A>G
F56D12.1d.1:c.259-250A>G
F56D12.1a.1:c.679-250A>G
HGVSgCHROMOSOME_II:g.1308265T>C
Sequence_detailsSMapS_parentSequenceF56D12
Flanking_sequencesCTTGTAGTTTGTAGTCTAGCAGACCAAATTTCTTCAAAACACTTGGGTCTGCTAAATCGAAACTTGTAGTTTGTAGCCTA
Mapping_targetF56D12
Source_location225CHROMOSOME_II13082721308272From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionTC
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00000034From_analysisMillion_mutation_project_reanalysis
WBStrain00023665From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00000112
TranscriptF56D12.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56D12.1b.1:c.679-250A>G
Intron_number5/7
F56D12.1a.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56D12.1a.2:c.679-250A>G
Intron_number6/9
F56D12.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56D12.1a.1:c.679-250A>G
Intron_number5/8
F56D12.1d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56D12.1d.1:c.259-250A>G
Intron_number1/3
F56D12.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56D12.1c.1:c.679-250A>G
Intron_number4/5
MethodWGS_Flibotte