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WormBase Tree Display for Variation: WBVar01878455

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Name Class

WBVar01878455NamePublic_nameWBVar01878455
Other_namecewivar00592918
F39C12.2d.1:c.301+19A>C
F39C12.2c.1:c.301+19A>C
F39C12.2a.1:c.301+19A>C
F39C12.2e.1:c.301+19A>C
F39C12.2b.1:c.301+19A>C
HGVSgCHROMOSOME_X:g.4859408T>G
Sequence_detailsSMapS_parentSequenceF39C12
Flanking_sequencesACCAAGTTATCCGTTTTTCGAATACATTATCCAAAATATAATACAAACCATATGTGTGAA
Mapping_targetF39C12
Source_location225CHROMOSOME_X48593784859378From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionTG
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00023072From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00000072
TranscriptF39C12.2b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF39C12.2b.1:c.301+19A>C
Intron_number4/19
F39C12.2a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF39C12.2a.1:c.301+19A>C
Intron_number3/16
F39C12.2c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF39C12.2c.1:c.301+19A>C
Intron_number4/18
F39C12.2e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF39C12.2e.1:c.301+19A>C
Intron_number3/15
F39C12.2d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF39C12.2d.1:c.301+19A>C
Intron_number3/16
MethodWGS_Flibotte