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WormBase Tree Display for Variation: WBVar01980166

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Name Class

WBVar01980166NamePublic_nameWBVar01980166
Other_namecewivar00706244
F56B6.2i.1:c.1831-51_1831-50insT
F56B6.2c.1:c.640-51_640-50insT
F56B6.2a.1:c.1825-51_1825-50insT
F56B6.2e.1:c.340-51_340-50insT
F56B6.2j.1:c.1834-51_1834-50insT
F56B6.2b.1:c.1714-51_1714-50insT
F56B6.2h.1:c.1840-51_1840-50insT
HGVSgCHROMOSOME_X:g.3552763_3552764insT
Sequence_detailsSMapS_parentSequenceF56B6
Flanking_sequencesCTGACTTTGAGTTTGTTCTTTTATTTATTCTTTTTTTTGTGCTTCAAAAACTCTTCATGT
Mapping_targetF56B6
Source_location225CHROMOSOME_X35527503552751From_analysisMillion_mutation_project_reanalysis
Type_of_mutationInsertionT
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004602From_analysisMillion_mutation_project_reanalysis
WBStrain00022850From_analysisMillion_mutation_project_reanalysis
WBStrain00022868From_analysisMillion_mutation_project_reanalysis
WBStrain00022878From_analysisMillion_mutation_project_reanalysis
WBStrain00022886From_analysisMillion_mutation_project_reanalysis
WBStrain00023072From_analysisMillion_mutation_project_reanalysis
WBStrain00023139From_analysisMillion_mutation_project_reanalysis
WBStrain00027648From_analysisMillion_mutation_project_reanalysis
WBStrain00027660From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00004350
TranscriptF56B6.2j.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2j.1:c.1834-51_1834-50insT
Intron_number10/14
F56B6.2e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2e.1:c.340-51_340-50insT
Intron_number2/7
F56B6.2i.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2i.1:c.1831-51_1831-50insT
Intron_number11/16
F56B6.2b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2b.1:c.1714-51_1714-50insT
Intron_number10/15
F56B6.2a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2a.1:c.1825-51_1825-50insT
Intron_number11/16
F56B6.2h.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2h.1:c.1840-51_1840-50insT
Intron_number11/16
F56B6.2c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2c.1:c.640-51_640-50insT
Intron_number5/9
MethodWGS_Flibotte