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WormBase Tree Display for Variation: WBVar01981234

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Name Class

WBVar01981234NamePublic_nameWBVar01981234
Other_namecewivar00707318
F46F6.4a.1:c.508+901_508+902insC
F46F6.4d.1:c.55+901_55+902insC
F46F6.4c.1:c.55+901_55+902insC
F46F6.4c.2:c.55+901_55+902insC
HGVSgCHROMOSOME_X:g.10382614_10382615insG
Sequence_detailsSMapS_parentSequenceF46F6
Flanking_sequencesTTAACAACTTTAAGATTTAAGAAAAAAAAAAGAAATCATTTCGCATGAGAAGATTTATTT
Mapping_targetF46F6
Source_location225CHROMOSOME_X1038255410382555From_analysisMillion_mutation_project_reanalysis
Type_of_mutationInsertionG
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004602From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00001122
TranscriptF46F6.4c.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF46F6.4c.2:c.55+901_55+902insC
Intron_number4/10
F46F6.4a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF46F6.4a.1:c.508+901_508+902insC
Intron_number5/11
F46F6.4c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF46F6.4c.1:c.55+901_55+902insC
Intron_number2/8
F46F6.4d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF46F6.4d.1:c.55+901_55+902insC
Intron_number2/9
MethodWGS_Flibotte