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WormBase Tree Display for Variation: WBVar01620208

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Name Class

WBVar01620208NamePublic_nameWBVar01620208
Other_namecewivar00299877
F09B9.2b.1:c.1432+14C>A
F09B9.2a.1:c.1390+14C>A
HGVSgCHROMOSOME_X:g.10151123C>A
Sequence_detailsSMapS_parentSequenceF09B9
Flanking_sequencesCGTCCCAATCAATGCTTGTATGTTTTTGTGGCTTTCCTAATTGAATCAGTAGCTGGCTAT
Mapping_targetF09B9
Source_location225CHROMOSOME_X1015106410151064From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionCA
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00006622From_analysisMillion_mutation_project_reanalysis
WBStrain00022852From_analysisMillion_mutation_project_reanalysis
WBStrain00022856From_analysisMillion_mutation_project_reanalysis
WBStrain00022868From_analysisMillion_mutation_project_reanalysis
WBStrain00022878From_analysisMillion_mutation_project_reanalysis
WBStrain00022930From_analysisMillion_mutation_project_reanalysis
WBStrain00023191From_analysisMillion_mutation_project_reanalysis
WBStrain00027652From_analysisMillion_mutation_project_reanalysis
WBStrain00027662From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00006839
TranscriptF09B9.2b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF09B9.2b.1:c.1432+14C>A
Intron_number8/10
F09B9.2a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF09B9.2a.1:c.1390+14C>A
Intron_number10/13
MethodWGS_Flibotte