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WormBase Tree Display for Variation: WBVar02049959

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Name Class

WBVar02049959NamePublic_nameWBVar02049959
Other_namecewivar00779136
W08A12.1c.1:c.1212+353del
W08A12.1a.1:c.1401+353del
W08A12.1b.1:c.1230+353del
W08A12.1e.1:c.1155+353del
W08A12.1b.3:c.1230+353del
W08A12.1d.1:c.1353+353del
W08A12.1b.2:c.1230+353del
HGVSgCHROMOSOME_V:g.3700357del
Sequence_detailsSMapS_parentSequenceW08A12
Flanking_sequencesCGAGAAATTGGTGAAAATTATTGAAATTAATTTTTTTTTACATTCGATAAAAATCATAAA
Mapping_targetW08A12
Source_location225CHROMOSOME_V37003443700344From_analysisMillion_mutation_project_reanalysis
Type_of_mutationDeletion
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00022886From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00021078
TranscriptW08A12.1b.3VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW08A12.1b.3:c.1230+353del
Intron_number6/7
W08A12.1a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW08A12.1a.1:c.1401+353del
Intron_number6/7
W08A12.1c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW08A12.1c.1:c.1212+353del
Intron_number6/7
W08A12.1b.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW08A12.1b.2:c.1230+353del
Intron_number7/8
W08A12.1b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW08A12.1b.1:c.1230+353del
Intron_number7/8
W08A12.1d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW08A12.1d.1:c.1353+353del
Intron_number4/5
W08A12.1e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW08A12.1e.1:c.1155+353del
Intron_number4/4
MethodWGS_Flibotte