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WormBase Tree Display for Variation: WBVar01607160

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Name Class

WBVar01607160NamePublic_nameWBVar01607160
Other_namecewivar00285732
F10E9.6a.3:c.369+236A>G
F10E9.6c.1:c.705+236A>G
F10E9.6b.1:c.318+236A>G
F10E9.6a.2:c.369+236A>G
F10E9.6a.1:c.369+236A>G
HGVSgCHROMOSOME_III:g.8300966A>G
Sequence_detailsSMapS_parentSequenceF10E9
Flanking_sequencesTAAAGTGAATACGAACGCCTTTTGCTCACATCCCCCTCTCCTTTTGCACAAGAAATTTGA
Mapping_targetF10E9
Source_location225CHROMOSOME_III83008958300895From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionAG
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00006622From_analysisMillion_mutation_project_reanalysis
WBStrain00022852From_analysisMillion_mutation_project_reanalysis
WBStrain00022856From_analysisMillion_mutation_project_reanalysis
WBStrain00022878From_analysisMillion_mutation_project_reanalysis
WBStrain00023286From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00003243
TranscriptF10E9.6a.3VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF10E9.6a.3:c.369+236A>G
Intron_number6/12
F10E9.6a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF10E9.6a.1:c.369+236A>G
Intron_number4/10
F10E9.6c.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF10E9.6c.1:c.705+236A>G
Intron_number5/10
F10E9.6b.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF10E9.6b.1:c.318+236A>G
Intron_number4/10
F10E9.6a.2VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF10E9.6a.2:c.369+236A>G
Intron_number5/11
MethodWGS_Flibotte