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WormBase Tree Display for Variation: WBVar01661003

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Name Class

WBVar01661003NamePublic_nameWBVar01661003
Other_namecewivar00348970
C49C3.8a.1:c.206+18A>T
C49C3.8b.1:c.50+18A>T
HGVSgCHROMOSOME_IV:g.17335867A>T
Sequence_detailsSMapS_parentSequenceC49C3
Flanking_sequencesGCTTGTATTACAGGTACCAATTTGTTTTATCGGAAGTTTTTAAAGTTAAAACTAATTCAG
Mapping_targetC49C3
Source_location225CHROMOSOME_IV1733583017335830From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionAT
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00006631From_analysisMillion_mutation_project_reanalysis
WBStrain00006637From_analysisMillion_mutation_project_reanalysis
WBStrain00022850From_analysisMillion_mutation_project_reanalysis
WBStrain00022886From_analysisMillion_mutation_project_reanalysis
WBStrain00022899From_analysisMillion_mutation_project_reanalysis
WBStrain00023072From_analysisMillion_mutation_project_reanalysis
WBStrain00023286From_analysisMillion_mutation_project_reanalysis
WBStrain00027647From_analysisMillion_mutation_project_reanalysis
WBStrain00027652From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00008198
TranscriptC49C3.8a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC49C3.8a.1:c.206+18A>T
Intron_number3/5
C49C3.8b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScC49C3.8b.1:c.50+18A>T
Intron_number1/2
MethodWGS_Flibotte