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WormBase Tree Display for Variation: WBVar01952267

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Name Class

WBVar01952267NamePublic_nameWBVar01952267
Other_namecewivar00674602
F47D12.1e.1:c.721-226_721-225insT
F47D12.1b.1:c.1561-226_1561-225insT
F47D12.1c.1:c.1711-226_1711-225insT
F47D12.1a.1:c.1600-226_1600-225insT
HGVSgCHROMOSOME_III:g.6320093_6320094insT
Sequence_detailsSMapS_parentSequenceF47D12
Flanking_sequencesCCATAAGTTCAAGCTGATAAAGTACAGTAGTTTTTTTTTGCATTTTTTGTTTCTTTGAAA
Mapping_targetF47D12
Source_location225CHROMOSOME_III63200416320042From_analysisMillion_mutation_project_reanalysis
Type_of_mutationInsertionT
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
WBStrain00023138From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00001518
TranscriptF47D12.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF47D12.1b.1:c.1561-226_1561-225insT
Intron_number11/12
F47D12.1e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF47D12.1e.1:c.721-226_721-225insT
Intron_number6/7
F47D12.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF47D12.1a.1:c.1600-226_1600-225insT
Intron_number12/13
F47D12.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF47D12.1c.1:c.1711-226_1711-225insT
Intron_number11/12
MethodWGS_Flibotte