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WormBase Tree Display for Variation: WBVar01710869

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Name Class

WBVar01710869NamePublic_nameWBVar01710869
Other_namecewivar00408536
F43C9.2b.1:c.298+155T>C
F43C9.9:n.59A>G
F43C9.2a.1:c.343+155T>C
HGVSgCHROMOSOME_X:g.4789783T>C
Sequence_detailsSMapS_parentSequenceF43C9
Flanking_sequencesCGGTCTCCCAAAGTTCATTTTATTTCATTGGCAGAAGGAGAGCCAGCGAGCGAGCAAAGC
Mapping_targetF43C9
Source_location225CHROMOSOME_X47897534789753From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionTC
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00022850From_analysisMillion_mutation_project_reanalysis
WBStrain00022852From_analysisMillion_mutation_project_reanalysis
WBStrain00022856From_analysisMillion_mutation_project_reanalysis
WBStrain00022878From_analysisMillion_mutation_project_reanalysis
WBStrain00022886From_analysisMillion_mutation_project_reanalysis
WBStrain00022902From_analysisMillion_mutation_project_reanalysis
WBStrain00023138From_analysisMillion_mutation_project_reanalysis
WBStrain00023139From_analysisMillion_mutation_project_reanalysis
WBStrain00027648From_analysisMillion_mutation_project_reanalysis
WBStrain00027660From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00018376
WBGene00202168
TranscriptF43C9.2a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF43C9.2a.1:c.343+155T>C
Intron_number4/5
F43C9.9VEP_consequencenon_coding_transcript_exon_variant
VEP_impactMODIFIER
HGVScF43C9.9:n.59A>G
cDNA_position59
Exon_number1/1
F43C9.2b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF43C9.2b.1:c.298+155T>C
Intron_number4/5
MethodWGS_Flibotte