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WormBase Tree Display for Variation: WBVar01698156

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Name Class

WBVar01698156NamePublic_nameWBVar01698156
Other_namecewivar00394951
C29F9.3c.1:c.211-108G>A
C29F9.3b.1:c.*24-55G>A
C29F9.3a.2:c.211-108G>A
C29F9.3a.1:c.211-108G>A
HGVSgCHROMOSOME_III:g.125514G>A
Sequence_detailsSMapS_parentSequenceC29F9
Flanking_sequencesAGTGCTCCTCTGCCGCTAAATTTTTTGTAGGGCCTATTTGGAAAGTGTTCTTTCAACTCA
Mapping_targetC29F9
Source_location225CHROMOSOME_III125513125513From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionGA
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00008273From_analysisMillion_mutation_project_reanalysis
WBStrain00031113From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00016218
TranscriptC29F9.3b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC29F9.3b.1:c.*24-55G>A
Intron_number4/5
C29F9.3a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC29F9.3a.1:c.211-108G>A
Intron_number3/8
C29F9.3c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC29F9.3c.1:c.211-108G>A
Intron_number3/7
C29F9.3a.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC29F9.3a.2:c.211-108G>A
Intron_number3/8
MethodWGS_Flibotte