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WormBase Tree Display for Variation: WBVar01700286

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Name Class

WBVar01700286NamePublic_nameWBVar01700286
Other_namecewivar00397086
W07B3.2b.2:c.-28+1622T>C
W07B3.3:n.101+719A>G
W07B3.2d.1:c.-28+1622T>C
W07B3.2c.2:c.-28+1622T>C
W07B3.2a.2:c.-28+1622T>C
HGVSgCHROMOSOME_III:g.353041A>G
Sequence_detailsSMapS_parentSequenceW07B3
Flanking_sequencesTCCCTCAATAGTAGATCAAAAGATAAACTATAGTATGTCTACATATCCGTTAGATTAGCT
Mapping_targetW07B3
Source_location225CHROMOSOME_III353040353040From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionAG
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00008273From_analysisMillion_mutation_project_reanalysis
WBStrain00023138From_analysisMillion_mutation_project_reanalysis
WBStrain00023191From_analysisMillion_mutation_project_reanalysis
WBStrain00027647From_analysisMillion_mutation_project_reanalysis
WBStrain00031113From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00001561
WBGene00219745
TranscriptW07B3.3VEP_consequenceintron_variant,non_coding_transcript_variant
VEP_impactMODIFIER
HGVScW07B3.3:n.101+719A>G
Intron_number1/1
W07B3.2b.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW07B3.2b.2:c.-28+1622T>C
Intron_number1/11
W07B3.2c.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW07B3.2c.2:c.-28+1622T>C
Intron_number1/10
W07B3.2a.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW07B3.2a.2:c.-28+1622T>C
Intron_number1/10
W07B3.2d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScW07B3.2d.1:c.-28+1622T>C
Intron_number1/10
MethodWGS_Flibotte