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WormBase Tree Display for Variation: WBVar01854385

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Name Class

WBVar01854385NamePublic_nameWBVar01854385
Other_namecewivar00567564
F42A9.6a.1:c.314-108G>T
F42A9.6b.1:c.458-108G>T
F42A9.6a.2:c.314-108G>T
F42A9.6c.2:c.248-108G>T
F42A9.6c.1:c.248-108G>T
F42A9.6a.3:c.314-108G>T
HGVSgCHROMOSOME_IV:g.8611268G>T
Sequence_detailsSMapS_parentSequenceF42A9
Flanking_sequencesGTAAAGAAACCAAATTAAGTTTATAATATTTTTGCGGTCGCGGTCATTATTATACACCCA
Mapping_targetF42A9
Source_location225CHROMOSOME_IV86112558611255From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionGT
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00023072From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00018335
TranscriptF42A9.6c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF42A9.6c.1:c.248-108G>T
Intron_number5/6
F42A9.6a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF42A9.6a.1:c.314-108G>T
Intron_number6/7
F42A9.6b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF42A9.6b.1:c.458-108G>T
Intron_number5/6
F42A9.6c.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF42A9.6c.2:c.248-108G>T
Intron_number4/5
F42A9.6a.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF42A9.6a.2:c.314-108G>T
Intron_number6/7
F42A9.6a.3VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF42A9.6a.3:c.314-108G>T
Intron_number5/6
MethodWGS_Flibotte