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WormBase Tree Display for Variation: WBVar01819579

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Name Class

WBVar01819579NamePublic_nameWBVar01819579
Other_namecewivar00531182
F39C12.3a.1:c.-38+1026G>A
F39C12.3a.3:c.-37-2288G>A
F39C12.3b.1:c.35+1026G>A
HGVSgCHROMOSOME_X:g.4873347C>T
Sequence_detailsSMapS_parentSequenceF39C12
Flanking_sequencesAAAAAATAATAAATCGGTTTTTCTTTTTATTTGTGCCTATTGAAACAAGGTAACAATCAT
Mapping_targetF39C12
Source_location225CHROMOSOME_X48733174873317From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionCT
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00022852From_analysisMillion_mutation_project_reanalysis
WBStrain00022856From_analysisMillion_mutation_project_reanalysis
WBStrain00022878From_analysisMillion_mutation_project_reanalysis
WBStrain00022902From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00006640
TranscriptF39C12.3a.3VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF39C12.3a.3:c.-37-2288G>A
Intron_number1/10
F39C12.3a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF39C12.3a.1:c.-38+1026G>A
Intron_number1/10
F39C12.3b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF39C12.3b.1:c.35+1026G>A
Intron_number2/9
MethodWGS_Flibotte