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WormBase Tree Display for Variation: WBVar01794949

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Name Class

WBVar01794949NamePublic_nameWBVar01794949
Other_namecewivar00497339
F20C5.11.1:c.-88+15G>A
F20C5.2d.1:c.98+15G>A
F20C5.2a.1:c.2276+15G>A
F20C5.11.2:c.-88+15G>A
F20C5.2c.1:c.293+15G>A
F20C5.2f.1:c.11+15G>A
HGVSgCHROMOSOME_IV:g.8757122C>T
Sequence_detailsSMapS_parentSequenceF20C5
Flanking_sequencesATTAAAACAGAATATTCATGACAATAATTCACAAAAAAACGTACTTTAATATCATAGTCG
Mapping_targetF20C5
Source_location225CHROMOSOME_IV87571098757109From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionCT
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00023286From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00303015
WBGene00002222
TranscriptF20C5.2f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF20C5.2f.1:c.11+15G>A
Intron_number1/1
F20C5.2a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF20C5.2a.1:c.2276+15G>A
Intron_number14/14
F20C5.2c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF20C5.2c.1:c.293+15G>A
Intron_number3/3
F20C5.11.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF20C5.11.1:c.-88+15G>A
Intron_number3/9
F20C5.2d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF20C5.2d.1:c.98+15G>A
Intron_number2/2
F20C5.11.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF20C5.11.2:c.-88+15G>A
Intron_number13/19
MethodWGS_Flibotte