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WormBase Tree Display for Variation: WBVar01698158

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Name Class

WBVar01698158NamePublic_nameWBVar01698158
Other_namecewivar00394953
C29F9.3a.1:c.211-23T>C
C29F9.3c.1:c.211-23T>C
C29F9.3a.2:c.211-23T>C
C29F9.3b.1:c.*54T>C
HGVSgCHROMOSOME_III:g.125599T>C
Sequence_detailsSMapS_parentSequenceC29F9
Flanking_sequencesGATTAGGCCGAAATACTTCCCTTGGTGTTCTTATTACATTACTTTTATGCAGAACTTTGC
Mapping_targetC29F9
Source_location225CHROMOSOME_III125598125598From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionTC
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00008273From_analysisMillion_mutation_project_reanalysis
WBStrain00023138From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00016218
TranscriptC29F9.3b.1VEP_consequence3_prime_UTR_variant
VEP_impactMODIFIER
HGVScC29F9.3b.1:c.*54T>C
cDNA_position330
Exon_number5/6
C29F9.3a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC29F9.3a.1:c.211-23T>C
Intron_number3/8
C29F9.3c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC29F9.3c.1:c.211-23T>C
Intron_number3/7
C29F9.3a.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC29F9.3a.2:c.211-23T>C
Intron_number3/8
MethodWGS_Flibotte