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WormBase Tree Display for Variation: WBVar02001140

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Name Class

WBVar02001140NamePublic_nameWBVar02001140
Other_namecewivar00728602
F56B6.2a.1:c.1696+271del
F56B6.2j.1:c.1705+271del
F56B6.2e.1:c.211+271del
F56B6.2h.1:c.1711+271del
F56B6.2b.1:c.1585+271del
F56B6.2i.1:c.1702+271del
F56B6.2c.1:c.511+271del
HGVSgCHROMOSOME_X:g.3550542del
Sequence_detailsSMapS_parentSequenceF56B6
Flanking_sequencesGACAGTGCTATAGATTTTTCAAAAAGTGACAAAAAAACAGTAATTGCCACTTTCTGACTG
Mapping_targetF56B6
Source_location225CHROMOSOME_X35505293550529From_analysisMillion_mutation_project_reanalysis
Type_of_mutationDeletion
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00006631From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00004350
TranscriptF56B6.2j.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2j.1:c.1705+271del
Intron_number9/14
F56B6.2e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2e.1:c.211+271del
Intron_number1/7
F56B6.2i.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2i.1:c.1702+271del
Intron_number10/16
F56B6.2b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2b.1:c.1585+271del
Intron_number9/15
F56B6.2a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2a.1:c.1696+271del
Intron_number10/16
F56B6.2h.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2h.1:c.1711+271del
Intron_number10/16
F56B6.2c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF56B6.2c.1:c.511+271del
Intron_number4/9
MethodWGS_Flibotte