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WormBase Tree Display for Variation: WBVar02046568

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Name Class

WBVar02046568NamePublic_nameWBVar02046568
Other_namecewivar00775703
C47C12.6d.1:c.1106-182del
C47C12.6b.1:c.1327+104del
C47C12.6f.1:c.1076-182del
C47C12.6a.1:c.1130-182del
C47C12.6c.1:c.1160-182del
C47C12.6e.1:c.1297+104del
C47C12.6g.1:c.1070-182del
C47C12.6a.2:c.1130-182del
HGVSgCHROMOSOME_X:g.7766358del
Sequence_detailsSMapS_parentSequenceC47C12
Flanking_sequencesAATCTTTTTGTTAACTGCATGGTTATGTTGTTTTTTTTAATCTCACATGTTGAATAATTA
Mapping_targetC47C12
Source_location225CHROMOSOME_X77663077766307From_analysisMillion_mutation_project_reanalysis
Type_of_mutationDeletion
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00022852From_analysisMillion_mutation_project_reanalysis
WBStrain00022856From_analysisMillion_mutation_project_reanalysis
WBStrain00022878From_analysisMillion_mutation_project_reanalysis
WBStrain00022930From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00000950
TranscriptC47C12.6e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC47C12.6e.1:c.1297+104del
Intron_number9/16
C47C12.6c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC47C12.6c.1:c.1160-182del
Intron_number9/16
C47C12.6a.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC47C12.6a.2:c.1130-182del
Intron_number8/16
C47C12.6b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC47C12.6b.1:c.1327+104del
Intron_number10/17
C47C12.6a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC47C12.6a.1:c.1130-182del
Intron_number9/17
C47C12.6d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC47C12.6d.1:c.1106-182del
Intron_number8/15
C47C12.6f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC47C12.6f.1:c.1076-182del
Intron_number7/14
C47C12.6g.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC47C12.6g.1:c.1070-182del
Intron_number11/18
MethodWGS_Flibotte