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WormBase Tree Display for Variation: WBVar01549465

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Name Class

WBVar01549465NamePublic_nameWBVar01549465
Other_namecewivar00125627
F39C12.2a.1:c.444+23T>A
F39C12.2d.1:c.444+23T>A
F39C12.2c.1:c.444+23T>A
F39C12.2e.1:c.444+23T>A
F39C12.2b.1:c.444+23T>A
HGVSgCHROMOSOME_X:g.4858939A>T
Sequence_detailsSMapS_parentSequenceF39C12
Flanking_sequencesAAGTTTTAAATTTTTGTGGTAATTTTAAAAGTCAATACTTCAAGCACCCTACCGAGATTT
Mapping_targetF39C12
Source_location225CHROMOSOME_X48589094858909From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionAT
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
Strain (12)
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00000072
TranscriptF39C12.2b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF39C12.2b.1:c.444+23T>A
Intron_number5/19
F39C12.2a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF39C12.2a.1:c.444+23T>A
Intron_number4/16
F39C12.2c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF39C12.2c.1:c.444+23T>A
Intron_number5/18
F39C12.2e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF39C12.2e.1:c.444+23T>A
Intron_number4/15
F39C12.2d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF39C12.2d.1:c.444+23T>A
Intron_number4/16
MethodWGS_Flibotte