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WormBase Tree Display for Variation: WBVar01794824

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Name Class

WBVar01794824NamePublic_nameWBVar01794824
Other_namecewivar00497199
B0496.3d.1:c.-8-756G>A
B0496.3a.1:c.-8-756G>A
B0496.3g.1:c.-8-756G>A
B0496.3e.1:c.710-756G>A
B0496.3h.1:c.-8-756G>A
HGVSgCHROMOSOME_IV:g.7428170G>A
Sequence_detailsSMapS_parentSequenceB0496
Flanking_sequencesTTCTATAGACTCACAAGCTTGAATTTTCCTATAATTTTTAAAATAACGAGGTTCAAAATT
Mapping_targetB0496
Source_location225CHROMOSOME_IV74281597428159From_analysisMillion_mutation_project_reanalysis
Type_of_mutationSubstitutionGA
SeqStatusSequenced
Variation_typeNatural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00022899From_analysisMillion_mutation_project_reanalysis
WBStrain00023286From_analysisMillion_mutation_project_reanalysis
LaboratoryVC
AnalysisMillion_mutation_project_reanalysis
StatusLive
AffectsGeneWBGene00006814
TranscriptB0496.3e.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScB0496.3e.1:c.710-756G>A
Intron_number6/34
B0496.3h.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScB0496.3h.1:c.-8-756G>A
Intron_number2/30
B0496.3d.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScB0496.3d.1:c.-8-756G>A
Intron_number2/32
B0496.3g.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScB0496.3g.1:c.-8-756G>A
Intron_number2/31
B0496.3a.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScB0496.3a.1:c.-8-756G>A
Intron_number5/32
MethodWGS_Flibotte