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WormBase Tree Display for Variation: WBVar01626650

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Name Class

WBVar01626650NamePublic_nameWBVar01626650
Other_namecewivar00306806
F22D3.2j.1:c.939+92C>A
F22D3.2g.1:c.948+92C>A
F22D3.2f.1:c.948+92C>A
F22D3.2e.1:c.939+92C>A
F22D3.2d.1:c.948+92C>A
HGVSgCHROMOSOME_II:g.6933228C>A
Sequence_detailsSMapS_parentSequenceF22D3
Flanking_sequencesGAGAGTACGCAGAGAAATGATGATGAATGATCGCGCATGCATTTTTTGTTGACAGTCTTC
Mapping_targetF22D3
Source_location225CHROMOSOME_II69331846933184From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionCA
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00006625From_analysisMillion_mutation_project_reanalysis
WBStrain00027652From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00017699
TranscriptF22D3.2g.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF22D3.2g.1:c.948+92C>A
Intron_number11/18
F22D3.2e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF22D3.2e.1:c.939+92C>A
Intron_number11/18
F22D3.2d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF22D3.2d.1:c.948+92C>A
Intron_number11/18
F22D3.2f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF22D3.2f.1:c.948+92C>A
Intron_number9/10
F22D3.2j.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF22D3.2j.1:c.939+92C>A
Intron_number11/18
MethodWGS_Flibotte