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WormBase Tree Display for Variation: WBVar01945162

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Name Class

WBVar01945162NamePublic_nameWBVar01945162
Other_namecewivar00666684
F39C12.3b.1:c.199-276del
F39C12.3a.2:c.127-276del
F39C12.3a.1:c.127-276del
F39C12.3a.3:c.127-276del
HGVSgCHROMOSOME_X:g.4869858del
Sequence_detailsSMapS_parentSequenceF39C12
Flanking_sequencesACAAACACCGAAAAGGCAATTTGGATGAGAGGGGGGGGGGGAAGGTGAAGCCTAACGCAC
Mapping_targetF39C12
Source_location225CHROMOSOME_X48698284869828From_analysisMillion_mutation_project_reanalysis
Type_of_mutationDeletion
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004599From_analysisMillion_mutation_project_reanalysis
WBStrain00004602From_analysisMillion_mutation_project_reanalysis
WBStrain00027662From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00006640
TranscriptF39C12.3a.3VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF39C12.3a.3:c.127-276del
Intron_number3/10
F39C12.3a.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF39C12.3a.2:c.127-276del
Intron_number2/9
F39C12.3a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF39C12.3a.1:c.127-276del
Intron_number3/10
F39C12.3b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF39C12.3b.1:c.199-276del
Intron_number3/9
MethodWGS_Flibotte